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1. Baricitinib in juvenile idiopathic arthritis: an international, phase 3, randomised, double-blind, placebo-controlled, withdrawal, efficacy, and safety trial

Author

Viola, Diego, Spindler, Alberto, Akikusa, Jonathan, Chaitow, Jeffrey, Huemer, Christian, Dehoorne, Joke, Wouters, Carine, Lauwerys, Bernard, Boulanger, Cecile, Saad Magalhães, Claudia, Terreri, Maria, Li, Caifeng, Tang, Xuemei, Feng, Qihua, Yu, Haiguo, Zhou, Zhixuan, Dolezalova, Pavla, Horvath, Rudolf, Herlin, Troels, Glerup, Mia, Quartier Dit Maire, Pierre, Kone Paut, Isabelle, Gervais, Elisabeth, Belot, Alexandre, Name, Investigator, Horneff, Gerd, Minden, Kirsten, Trauzeddel, Ralf, Foeldvari, Ivan, Lutz, Thomas, Helling-Bakki, Astrid, Grulich-Henn, Jürgen, Kümmerle-Deschner, Jasmin, Sawhney, Sujata, Kumar, Sathish, Janarthanan, Mahesh, Amarilyo, Gil, Butbul, Yonatan, Uziel, Yosef, Tirosh, Irit, Harel, Liora, Caorsi, Roberta, Pastore, Serena, Tommasini, Alberto, Alessio, Maria, Breda, Luciana, Cattalini, Marco, Cimaz, Rolando, Giani, Teresa, Simonini, Gabriele, Filocamo, Giovanni, Umebayashi, Hiroaki, Kaneko, Utako, Kawano, Yutaka, Sato, Satoshi, Mori, Masaaki, Shimizu, Masaki, Yamaguchi, Kenichi, Ito, Shuichi, Imagawa, Tomoyuki, Inoue, Natsumi, Yokoyama, Tadafumi, Shabana, Kosuke, Ozeki, Yuka, Kawano, Yoshifumi, Yamasaki, Yuichi, Miyamae, Takako, Vega Cornejo, Gabriel, Rubio Perez, Nadina, Vargas, Edgar, Pacheco-Tena, Cesar, Edmundo Enriquez Sosa, Favio, Smolewska, Elzbieta, Zuber, Zbigniew, Gietka, Piotr, Alexeeva, Ekaterina, Nikishina, Irina, Valieva, Sania, Antón López, Jordi, Murias Loza, Sara, Maria Alcobendas Rueda, Rosa, Calvo Penades, Inmaculada, Grana, Genaro, Lucica Boteanu, Alina, Kasapcopur, Ozgur, Unsal, Erbil, Vaidyanathan Ramanan, Athimalaipet, Lacassagne, Sandrine, Hawley, Daniel, Mahmood, Kamran, Almeida, Beverley, Ramanan, Athimalaipet V, Quartier, Pierre, Okamoto, Nami, Fingerhutová, Šárka, Antón, Jordi, Wang, Zhongkai, Meszaros, Gabriella, Araújo, Joana, Liao, Ran, Keller, Stuart, Brunner, Hermine I, and Ruperto, Nicolino

Published
2023
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2. Tofacitinib for Refractory Uveitis and Scleritis in Children: A Case Series.

Author

Dutta Majumder, Parthopratim, Abraham, Sharanya, Sudharshan, Sridharan, Janarthanan, Mahesh, and Ramanan, Athimalaipet V.

Subjects
JUVENILE idiopathic arthritis, CHILD patients, MIDDLE-income countries, PEDIATRIC therapy, UVEITIS, IRIDOCYCLITIS
Abstract

Purpose: This study analyzes the efficacy and safety of tofacitinib in pediatric patients presenting with treatment-resistant uveitis and scleritis. Method: Retrospective Chart Review Result: Nine children diagnosed with uveitis and one with scleritis received oral tofacitinib treatment. The median age of these patients was 9 years, with bilateral involvement observed in nine of them. Juvenile idiopathic arthritis was the most identifiable cause of uveitis, with anterior uveitis (50%) being the most frequent subtype of inflammation among these children. The median duration of immunosuppressive treatment before switching to tofacitinib was 18 (16–49) months. Remission of uveitis was achieved in all but two children, who experienced recurrence – manifesting as anterior uveitis. The median duration of follow-up in these children after tofacitinib treatment was 277.5 (183–549) days. At the end of follow-up, topical steroids could be withdrawn in six children, and two children were on topical steroids once a day. None of the children developed any systemic side-effect during the follow-up period. The mean BCVA at presentation was 0.62 ± 0.55, which improved to a mean of 0.27 ± 0.325 at the final follow-up (p = 0.0014) Conclusion: Treatment of pediatric uveitis with tofacitinib can be a valuable second-line treatment option and useful alternative in low- and middle-income countries. [ABSTRACT FROM AUTHOR]

Published
2024
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3. Differences Sustained Between Diffuse and Limited Forms of Juvenile Systemic Sclerosis in an Expanded International Cohort

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Terreri, Maria Teresa, Sakamoto, Ana Paula, Stanevicha, Valda, Sztajnbok, Flavio, Anton, Jordi, Feldman, Brian, Alexeeva, Ekaterina, Katsicas, Maria, Smith, Vanessa, Avcin, Tadej, Marrani, Edoardo, Kostik, Mikhail, Lehman, Thomas, Sifuentes‐Giraldo, Walter‐Alberto, Vasquez‐Canizares, Natalia, Appenzeller, Simone, Janarthanan, Mahesh, Moll, Monika, Nemcova, Dana, Patwardhan, Anjali, Santos, Maria Jose, Sawhney, Sujata, Schonenberg‐Meinema, Dieneke, Battagliotti, Cristina, Berntson, Lillemor, Bica, Blanca, Brunner, Jürgen, Costa‐Reis, Patricia, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Kaiser, Daniela, Kallinich, Tilmann, Lazarevic, Dragana, Minden, Kirsten, Nielsen, Susan, Nuruzzaman, Farzana, Uziel, Yosef, Helmus, Nicola, and Torok, Kathryn S.

Published
2022
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4. Exploring clinical features and therapeutic outcomes in Indian children with mixed connective tissue disease: A multicenter study.

Author

Guha, Suparna, Suri, Deepti, Balan, Suma, Janarthanan, Mahesh, Agarwal, Manjari, Viswanathan, Vijay, Gupta, Aman, Hazarika, Rashna Dass, Gummadi, Anjani, Sudhakar, Murugan, Pal, Samar Ranjan, Raghuram, Jyothi, Rao, Anand Prahalad, Singh, Neha, Aggarwal, Amita, and Bhattad, Sagar

Subjects
CONNECTIVE tissue diseases, TREATMENT effectiveness, RAYNAUD'S disease, MACROPHAGE activation syndrome, PEDIATRIC rheumatology, JUVENILE diseases
Abstract

Introduction: Mixed connective tissue disease (MCTD) is a rare entity in children. There is a paucity of studies on juvenile‐onset MCTD (jMCTD) worldwide especially from Southeast Asia. Objectives: To describe clinical and laboratory features of jMCTD diagnosed at pediatric rheumatology centers across India. Methods: A predesigned detailed case proforma in an excel format was prepared and was sent to all the Pediatric Rheumatology centers in India. Eleven centers provided the clinical and laboratory data of their jMCTD patients, which was then compiled and analyzed in detail. Results: Thirty‐one jMCTD patients from 11 centers were included in the study. Our cohort had 27 females and four male patients over 12 months (August 2021 to July 2022). The median age at presentation was 12 years (range 5–18 years) and the median duration of symptoms was 24 months at diagnosis (range 2–96 months). The common features included arthritis (90%), malar rash (70.9%), and Raynaud's phenomenon (70.9%). At a mean follow‐up of 43 months (range 1–168 months), 45% of them were in remission. There were two deaths reported, due to macrophage activation syndrome and sepsis respectively. Conclusion: We present the largest multicenter experience on jMCTD from the Indian subcontinent. The study's findings serve as a crucial stepping stone toward unraveling the complexities of jMCTD and improving patient care and management strategies. [ABSTRACT FROM AUTHOR]

Published
2024
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6. Rheumatological Presentation of Inborn Errors of Immunity in Children: A Case Series from a Tertiary Care Center.

Author

Koneru, Shree Hasitha, Kumaresan, Maithrayie, Jayaraman, Dhaarani, Janarthanan, Mahesh, Harshita, Bhogavalli Lakshmi, and Scott, Julius Xavier

Subjects
PRIMARY immunodeficiency diseases, KILLER cells, IMMUNOLOGICAL deficiency syndromes, AUTOIMMUNITY, DISEASE relapse
Abstract

Copyright of Annals of African Medicine is the property of Wolters Kluwer India Pvt Ltd and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Published
2024
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8. Baricitinib in juvenile idiopathic arthritis: an international, phase 3, randomised, double-blind, placebo-controlled, withdrawal, efficacy, and safety trial

Author

Ramanan, Athimalaipet V, primary, Quartier, Pierre, additional, Okamoto, Nami, additional, Foeldvari, Ivan, additional, Spindler, Alberto, additional, Fingerhutová, Šárka, additional, Antón, Jordi, additional, Wang, Zhongkai, additional, Meszaros, Gabriella, additional, Araújo, Joana, additional, Liao, Ran, additional, Keller, Stuart, additional, Brunner, Hermine I, additional, Ruperto, Nicolino, additional, Viola, Diego, additional, Akikusa, Jonathan, additional, Chaitow, Jeffrey, additional, Huemer, Christian, additional, Dehoorne, Joke, additional, Wouters, Carine, additional, Lauwerys, Bernard, additional, Boulanger, Cecile, additional, Saad Magalhães, Claudia, additional, Terreri, Maria, additional, Li, Caifeng, additional, Tang, Xuemei, additional, Feng, Qihua, additional, Yu, Haiguo, additional, Zhou, Zhixuan, additional, Dolezalova, Pavla, additional, Horvath, Rudolf, additional, Herlin, Troels, additional, Glerup, Mia, additional, Quartier Dit Maire, Pierre, additional, Kone Paut, Isabelle, additional, Gervais, Elisabeth, additional, Belot, Alexandre, additional, Name, Investigator, additional, Horneff, Gerd, additional, Minden, Kirsten, additional, Trauzeddel, Ralf, additional, Lutz, Thomas, additional, Helling-Bakki, Astrid, additional, Grulich-Henn, Jürgen, additional, Kümmerle-Deschner, Jasmin, additional, Sawhney, Sujata, additional, Kumar, Sathish, additional, Janarthanan, Mahesh, additional, Amarilyo, Gil, additional, Butbul, Yonatan, additional, Uziel, Yosef, additional, Tirosh, Irit, additional, Harel, Liora, additional, Caorsi, Roberta, additional, Pastore, Serena, additional, Tommasini, Alberto, additional, Alessio, Maria, additional, Breda, Luciana, additional, Cattalini, Marco, additional, Cimaz, Rolando, additional, Giani, Teresa, additional, Simonini, Gabriele, additional, Filocamo, Giovanni, additional, Umebayashi, Hiroaki, additional, Kaneko, Utako, additional, Kawano, Yutaka, additional, Sato, Satoshi, additional, Mori, Masaaki, additional, Shimizu, Masaki, additional, Yamaguchi, Kenichi, additional, Ito, Shuichi, additional, Imagawa, Tomoyuki, additional, Inoue, Natsumi, additional, Yokoyama, Tadafumi, additional, Shabana, Kosuke, additional, Ozeki, Yuka, additional, Kawano, Yoshifumi, additional, Yamasaki, Yuichi, additional, Miyamae, Takako, additional, Vega Cornejo, Gabriel, additional, Rubio Perez, Nadina, additional, Vargas, Edgar, additional, Pacheco-Tena, Cesar, additional, Edmundo Enriquez Sosa, Favio, additional, Smolewska, Elzbieta, additional, Zuber, Zbigniew, additional, Gietka, Piotr, additional, Alexeeva, Ekaterina, additional, Nikishina, Irina, additional, Valieva, Sania, additional, Antón López, Jordi, additional, Murias Loza, Sara, additional, Maria Alcobendas Rueda, Rosa, additional, Calvo Penades, Inmaculada, additional, Grana, Genaro, additional, Lucica Boteanu, Alina, additional, Kasapcopur, Ozgur, additional, Unsal, Erbil, additional, Vaidyanathan Ramanan, Athimalaipet, additional, Lacassagne, Sandrine, additional, Hawley, Daniel, additional, Mahmood, Kamran, additional, and Almeida, Beverley, additional

Published
2023
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12. Gender differences in juvenile systemic sclerosis patients : Results from the international juvenile scleroderma inception cohort

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Terreri, Maria Teresa, Sakamoto, Ana Paula, Stanevicha, Valda, Anton, Jordi, Feldman, Brian M., Sztajnbok, Flavio, Khubchandani, Raju, Alexeeva, Ekaterina, Katsicas, Maria, Sawhney, Sujata, Smith, Vanessa, Appenzeller, Simone, Avcin, Tadej, Kostik, Mikhail, Lehman, Thomas, Marrani, Edoardo, Schonenberg-Meinema, Dieneke, Sifuentes-Giraldo, Walter-Alberto, Vasquez-Canizares, Natalia, Janarthanan, Mahesh, Moll, Monika, Nemcova, Dana, Patwardhan, Anjali, Santos, Maria Jose, Battagliotti, Cristina, Berntson, Lillemor, Bica, Blanca, Brunner, Jürgen, Cimaz, Rolando, Costa-Reis, Patricia, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Johnson, Sindhu R., Kaiser, Daniela, Kallinich, Tilmann, Lazarevic, Dragana, Minden, Kirsten, Nielsen, Susan, Nuruzzaman, Farzana, Opsahl Hetlevik, Siri, Uziel, Yosef, Helmus, Nicola, Torok, Kathryn S., Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Terreri, Maria Teresa, Sakamoto, Ana Paula, Stanevicha, Valda, Anton, Jordi, Feldman, Brian M., Sztajnbok, Flavio, Khubchandani, Raju, Alexeeva, Ekaterina, Katsicas, Maria, Sawhney, Sujata, Smith, Vanessa, Appenzeller, Simone, Avcin, Tadej, Kostik, Mikhail, Lehman, Thomas, Marrani, Edoardo, Schonenberg-Meinema, Dieneke, Sifuentes-Giraldo, Walter-Alberto, Vasquez-Canizares, Natalia, Janarthanan, Mahesh, Moll, Monika, Nemcova, Dana, Patwardhan, Anjali, Santos, Maria Jose, Battagliotti, Cristina, Berntson, Lillemor, Bica, Blanca, Brunner, Jürgen, Cimaz, Rolando, Costa-Reis, Patricia, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Johnson, Sindhu R., Kaiser, Daniela, Kallinich, Tilmann, Lazarevic, Dragana, Minden, Kirsten, Nielsen, Susan, Nuruzzaman, Farzana, Opsahl Hetlevik, Siri, Uziel, Yosef, Helmus, Nicola, and Torok, Kathryn S.

Abstract

Objective: To compare organ involvement and disease severity between male and female patients with juvenile onset systemic sclerosis. Methods: Demographics, organ involvement, laboratory evaluation, patient-reported outcomes and physician assessment variables were compared between male and female juvenile onset systemic sclerosis patients enrolled in the prospective international juvenile systemic sclerosis cohort at their baseline visit and after 12 months. Results: One hundred and seventy-five juvenile onset systemic sclerosis patients were evaluated, 142 females and 33 males. Race, age of onset, disease duration, and disease subtypes (70% diffuse cutaneous) were similar between males and females. Active digital ulceration, very low body mass index, and tendon friction rubs were significantly more frequent in males. Physician global assessment of disease severity and digital ulcer activity was significantly higher in males. Composite pulmonary involvement was also more frequent in males, though not statistically significantly. After 12 months, they are the pattern of differences changed female patients had significantly more frequent pulmonary involvement. Conclusion: In this cohort, juvenile onset systemic sclerosis had a more severe course in males at baseline and but the pattern changed after 12 months. Some differences from adult findings persisted, there is no increased signal of pulmonary arterial hypertension or heart failure in male pediatric patients. While monitoring protocols of organ involvement in juvenile onset systemic sclerosis need to be identical for males and females.

Published
2023
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15. Gender differences in juvenile systemic sclerosis patients: Results from the international juvenile scleroderma inception cohort

Author

Foeldvari, Ivan, primary, Klotsche, Jens, additional, Kasapcopur, Ozgur, additional, Adrovic, Amra, additional, Terreri, Maria Teresa, additional, Sakamoto, Ana Paula, additional, Stanevicha, Valda, additional, Anton, Jordi, additional, Feldman, Brian M, additional, Sztajnbok, Flavio, additional, Khubchandani, Raju, additional, Alexeeva, Ekaterina, additional, Katsicas, Maria, additional, Sawhney, Sujata, additional, Smith, Vanessa, additional, Appenzeller, Simone, additional, Avcin, Tadej, additional, Kostik, Mikhail, additional, Lehman, Thomas, additional, Marrani, Edoardo, additional, Schonenberg-Meinema, Dieneke, additional, Sifuentes-Giraldo, Walter-Alberto, additional, Vasquez-Canizares, Natalia, additional, Janarthanan, Mahesh, additional, Moll, Monika, additional, Nemcova, Dana, additional, Patwardhan, Anjali, additional, Santos, Maria Jose, additional, Battagliotti, Cristina, additional, Berntson, Lillemor, additional, Bica, Blanca, additional, Brunner, Jürgen, additional, Cimaz, Rolando, additional, Costa-Reis, Patricia, additional, Eleftheriou, Despina, additional, Harel, Liora, additional, Horneff, Gerd, additional, Johnson, Sindhu R, additional, Kaiser, Daniela, additional, Kallinich, Tilmann, additional, Lazarevic, Dragana, additional, Minden, Kirsten, additional, Nielsen, Susan, additional, Nuruzzaman, Farzana, additional, Opsahl Hetlevik, Siri, additional, Uziel, Yosef, additional, Helmus, Nicola, additional, and Torok, Kathryn S, additional

Published
2022
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18. Diffuse juvenile systemic sclerosis patients show distinct organ involvement and have more severe disease in the largest jSSc cohort of the world. Results from the the juvenile scleroderma inception cohort

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Torok, Kathryn, Terreri, Maria Teresa, Sakamoto, Ana Paula, Feldman, Brian, Sztajnbok, Flavio, Stanevicha, Valda, Anton, Jordi, Johnson, Sindhu, Khubchandani, Raju, Alexeeva, Ekaterina, Katsicas, Maria, Sawhney, Sujata, Smith, Vanessa, Appenzeller, Simone, Avcin, Tadey, Kostik, Mikhail, Lehman, Thomas, Malcova, Hana, Marrani, Edoardo, Pain, Clare, Schonenberg, Dieneke, Sifuentes-Giraldo, W.-Alberto, Vasquez-Canizares, Natalia, Costa Reis, Patricia, Janarthanan, Mahesh, Moll, Monika, Nemcova, Dana, Patwardhan, Anjali, Santos, Maria Jose, Abu Al-Saoud, Sima, Battagliotti, Christina, Berntson, Lillemor, Bica, Blanca, Brunner, Juergen, Cimaz, Rolando, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Kaiser, Daniela, Kallinich, Tilmann, Lazarevic, Dragana, Minden, Kirsten, Nuruzzaman, Farzana, Opsahl Hetlevik, Siri, Uziel, Yosef, and Helmus, Nicola

Subjects
Medicine and health
Abstract

Introduction: Juvenile systemic sclerosis (jSSc) is an orphan disease with a prevalence of 3 in 1,000,000 children [ref:1]. In adult patients there are significant differences between the clinical presentation of diffuse and limited subtypes [ref:2]. We reviewed clinical differences [for full text, please go to the a.m. URL]

Published
2022
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19. Juvenile systemic sclerosis treatment practices in an international cohort and comparison to recent SHARE consensus guidelines

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Torok, Kathryn, Terreri, Maria Teresa, Sakamoto, Ana Paula, Feldman, Brian, Anton, Jordi, Sztajnbok, Flavio, Stanevicha, Valda, Appenzeller, Simone, Avcin, Tadey, Johnson, Sindhu, Khubchandani, Raju, Kostik, Mikhail, Marrani, Edoardo, Sifuentes-Giraldo, W.-Alberto, Nemcova, Dana, Santos, Maria Jose, Schonenberg, Dieneke, Battagliotti, Christina, Berntson, Lillemor, Bica, Blanca, Brunner, Juergen, Cimaz, Rolando, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Janarthanan, Mahesh, Kallinich, Tilmann, Lehman, Thomas, Moll, Monika, Nuruzzaman, Farzana, Patwardhan, Anjali, Smith, Vanessa, and Helmus, Nicola

Subjects
Medicine and health
Abstract

Introduction: Juvenile systemic scleroderma (jSSc) is an orphan disease with a prevalence of 3 in 1,000,000 children [ref:1]. Currently no medications are licensed for the treatment of jSSc. Due to its rarity, only recently have the first management and treatment guidelines been published, [for full text, please go to the a.m. URL]

Published
2022
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20. Clinical characteristics of juvenile onset systemic sclerosis patients from the juvenile scleroderma inception cohort compared to adult age juvenile-onset patients from EUSTAR. Are these differences suggesting risk for mortality?

Author

Foeldvari, Ivan, Klotsche, Jens, Carreira, Patricia E., Kasapcopur, Ozgur, Adrovic, Amra, Torok, Kathryn, Airò, Paolo, Iannone, Florenzo, Allanore, Yannick, Balbir-Gurman, Alexandra, Schmeiser, Tim, Sztajnbok, Flavio, Terreri, Maria Teresa, Stanevicha, Valda, Anton, Jordi, Feldman, Brian, Khubchandani, Raju, Alexeeva, Ekaterina, Johnson, Sindhu, Katsicas, Maria, Sawhney, Sujata, Smith, Vanessa, Appenzeller, Simone, Avcin, Tadey, Campochiaro, Corrado, De Vries-Bouwstra, Jeska, Kostik, Mikhail, Lehman, Thomas, Marrani, Edoardo, Schonenberg, Dieneke, Sifuentes-Giraldo, W.-Alberto, Vasquez-Canizares, Natalia, Janarthanan, Mahesh, Malcova, Hana, Moll, Monika, Nemcova, Dana, Patwardhan, Anjali, Santos, Maria Jose, Seskute, Goda, Truchetet, Marie-Elise, Veale, Douglas, Hoffmann-Vold, Anna-Maria, Gabrielli, Armando, and Distler, Oliver

Subjects
Medicine and health
Abstract

Introduction: Juvenile systemic sclerosis (jSSc) is an orphan autoimmune disease with a prevalence of 3 in 1,000,000 children. Information on long-term development of organ involvement and clinical characteristics of jSSc patients in adulthood are lacking. It was believed that patients in adult cohorts [for full text, please go to the a.m. URL]

Published
2022
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21. Patient and physician reported outcomes of juvenile systemic sclerosis patients significantly improve over 12 months observation period in the juvenile systemic scleroderma inception cohort

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Torok, Kathryn, Terreri, Maria Teresa, Feldman, Brian, Anton, Jordi, Katsicas, Maria, Stanevicha, Valda, Sztajnbok, Flavio, Appenzeller, Simone, Avcin, Tadey, Kostik, Mikhail, Marrani, Edoardo, Sifuentes-Giraldo, W.-Alberto, Johnson, Sindhu, Khubchandani, Raju, Nemcova, Dana, Santos, Maria Jose, Battagliotti, Christina, Berntson, Lillemor, Bica, Blanca, Brunner, Juergen, Cimaz, Rolando, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Janarthanan, Mahesh, Kallinich, Tilmann, Minden, Kirsten, Moll, Monika, Nielsen, Susan, Patwardhan, Anjali, Schonenberg, Dieneke, Smith, Vanessa, and Helmus, Nicola

Subjects
Medicine and health
Abstract

Introduction: Juvenile systemic sclerosis (jSSc) is an orphan disease with a prevalence of 3 in 1,000,000 children [ref:1]. The Juvenile Systemic Scleroderma Inception cohort (jSScC) is the largest cohort of jSSc patients in the world. The jSScC collects longitudinal data prospectively in [for full text, please go to the a.m. URL]

Published
2022
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22. Underdetection of Interstitial Lung Disease in Juvenile Systemic Sclerosis

Author

Foeldvari, Ivan, Klotsche, Jens, Hinrichs, Bernd, Helmus, Nicola, Kasapcopur, Ozgur, Adrovic, Amra, Sztajnbok, Flavio, Terreri, Maria Teresa, Anton, Jordi, Smith, Vanessa, Katsicas, Maria, Kostik, Mikhail, Vasquez-Canizares, Natalia, Avcin, Tadej, Feldman, Brian, Janarthanan, Mahesh, Santos, Maria Jose, Sawhney, Sujata, Schonenberg-Meinema, Dieneke, Sifuentes-Giraldo, Walter-Alberto, Alexeeva, Ekaterina, Appenzeller, Simone, Battagliotti, Cristina, Berntson, Lillemor, Bica, Blanca, Costa-Reis, Patricia, Eleftheriou, Despina, Kallinich, Tilmann, Lehman, Thomas, Marrani, Edoardo, Minden, Kirsten, Nielsen, Susan, Nuruzzaman, Farzana, Patwardhan, Anjali, Khubchandani, Raju, Stanevicha, Valda, Uziel, Yosef, Torok, Kathryn S., Foeldvari, Ivan, Klotsche, Jens, Hinrichs, Bernd, Helmus, Nicola, Kasapcopur, Ozgur, Adrovic, Amra, Sztajnbok, Flavio, Terreri, Maria Teresa, Anton, Jordi, Smith, Vanessa, Katsicas, Maria, Kostik, Mikhail, Vasquez-Canizares, Natalia, Avcin, Tadej, Feldman, Brian, Janarthanan, Mahesh, Santos, Maria Jose, Sawhney, Sujata, Schonenberg-Meinema, Dieneke, Sifuentes-Giraldo, Walter-Alberto, Alexeeva, Ekaterina, Appenzeller, Simone, Battagliotti, Cristina, Berntson, Lillemor, Bica, Blanca, Costa-Reis, Patricia, Eleftheriou, Despina, Kallinich, Tilmann, Lehman, Thomas, Marrani, Edoardo, Minden, Kirsten, Nielsen, Susan, Nuruzzaman, Farzana, Patwardhan, Anjali, Khubchandani, Raju, Stanevicha, Valda, Uziel, Yosef, and Torok, Kathryn S.

Abstract

Objective. Utilizing data obtained from a prospective, international, juvenile systemic sclerosis (SSc) cohort, the present study was undertaken to determine if pulmonary screening with forced vital capacity (FVC) and diffusing capacity for carbon monoxide (DLco) is sufficient to assess the presence of interstitial lung disease (ILD) in comparison to high-resolution computed tomography (HRCT) in juvenile SSc. Methods. The juvenile SSc cohort database was queried for patients enrolled from January 2008 to January 2020 with recorded pulmonary function tests (PFTs) parameters and HRCT to determine the discriminatory properties of P FT parameters, FVC, and DLco in detecting ILD. Results. Eighty-six juvenile SSc patients had both computed tomography imaging and FVC values for direct comparison. Using findings on HRCT as the standard measure of ILD presence, the sensitivity of FVC in detecting ILD in juvenile SSc was only 40%, the specificity was 77%, and area under the curve (AUC) was 0.58. Fifty-eight juvenile SSc patients had both CT imaging and DLco values for comparison. The sensitivity of DLco in detecting ILD was 76%, the specificity was 70%, and AUC was 0.73. Conclusion. The performance of PFTs in juvenile SSc to detect underlying ILD was quite limited. Specifically, the FVC, which is one of the main clinical parameters in adult SSc to detect and monitor ILD, would miss -60% of children who had ILD changes on their accompanying HRCT. The DLco was more sensitive in detecting potential abnormalities on HRCT, but with less specificity than the FVC. These results support the use of HRCT in tandem with PFTs for the screening of ILD in juvenile SSc.

Published
2022
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24. sj-pdf-1-jso-10.1177_23971983221143244 – Supplemental material for Gender differences in juvenile systemic sclerosis patients: Results from the international juvenile scleroderma inception cohort

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Terreri, Maria Teresa, Sakamoto, Ana Paula, Stanevicha, Valda, Anton, Jordi, Feldman, Brian M, Sztajnbok, Flavio, Khubchandani, Raju, Alexeeva, Ekaterina, Katsicas, Maria, Sawhney, Sujata, Smith, Vanessa, Appenzeller, Simone, Avcin, Tadej, Kostik, Mikhail, Lehman, Thomas, Marrani, Edoardo, Schonenberg-Meinema, Dieneke, Sifuentes-Giraldo, Walter-Alberto, Vasquez-Canizares, Natalia, Janarthanan, Mahesh, Moll, Monika, Nemcova, Dana, Patwardhan, Anjali, Santos, Maria Jose, Battagliotti, Cristina, Berntson, Lillemor, Bica, Blanca, Brunner, Jürgen, Cimaz, Rolando, Costa-Reis, Patricia, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Johnson, Sindhu R, Kaiser, Daniela, Kallinich, Tilmann, Lazarevic, Dragana, Minden, Kirsten, Nielsen, Susan, Nuruzzaman, Farzana, Opsahl Hetlevik, Siri, Uziel, Yosef, Helmus, Nicola, and Torok, Kathryn S

Subjects
110322 Rheumatology and Arthritis, FOS: Clinical medicine
Abstract

Supplemental material, sj-pdf-1-jso-10.1177_23971983221143244 for Gender differences in juvenile systemic sclerosis patients: Results from the international juvenile scleroderma inception cohort by Ivan Foeldvari, Jens Klotsche, Ozgur Kasapcopur, Amra Adrovic, Maria Teresa Terreri, Ana Paula Sakamoto, Valda Stanevicha, Jordi Anton, Brian M Feldman, Flavio Sztajnbok, Raju Khubchandani, Ekaterina Alexeeva, Maria Katsicas, Sujata Sawhney, Vanessa Smith, Simone Appenzeller, Tadej Avcin, Mikhail Kostik, Thomas Lehman, Edoardo Marrani, Dieneke Schonenberg-Meinema, Walter-Alberto Sifuentes-Giraldo, Natalia Vasquez-Canizares, Mahesh Janarthanan, Monika Moll, Dana Nemcova, Anjali Patwardhan, Maria Jose Santos, Cristina Battagliotti, Lillemor Berntson, Blanca Bica, Jürgen Brunner, Rolando Cimaz, Patricia Costa-Reis, Despina Eleftheriou, Liora Harel, Gerd Horneff, Sindhu R Johnson, Daniela Kaiser, Tilmann Kallinich, Dragana Lazarevic, Kirsten Minden, Susan Nielsen, Farzana Nuruzzaman, Siri Opsahl Hetlevik, Yosef Uziel, Nicola Helmus and Kathryn S Torok in Journal of Scleroderma and Related Disorders

Published
2022
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25. Underdetection of Interstitial Lung Disease in Juvenile Systemic Sclerosis

Author

Foeldvari, Ivan, primary, Klotsche, Jens, additional, Hinrichs, Bernd, additional, Helmus, Nicola, additional, Kasapcopur, Ozgur, additional, Adrovic, Amra, additional, Sztajnbok, Flavio, additional, Terreri, Maria Teresa, additional, Anton, Jordi, additional, Smith, Vanessa, additional, Katsicas, Maria, additional, Kostik, Mikhail, additional, Vasquez‐Canizares, Natalia, additional, Avcin, Tadej, additional, Feldman, Brian, additional, Janarthanan, Mahesh, additional, Santos, Maria Jose, additional, Sawhney, Sujata, additional, Schonenberg‐Meinema, Dieneke, additional, Sifuentes‐Giraldo, Walter‐Alberto, additional, Alexeeva, Ekaterina, additional, Appenzeller, Simone, additional, Battagliotti, Cristina, additional, Berntson, Lillemor, additional, Bica, Blanca, additional, Costa‐Reis, Patrícia, additional, Eleftheriou, Despina, additional, Kallinich, Tilmann, additional, Lehman, Thomas, additional, Marrani, Edoardo, additional, Minden, Kirsten, additional, Nielsen, Susan, additional, Nuruzzaman, Farzana, additional, Patwardhan, Anjali, additional, Khubchandani, Raju, additional, Stanevicha, Valda, additional, Uziel, Yosef, additional, and Torok, Kathryn S., additional

Published
2022
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29. Familial Blau syndrome:First molecularly confirmed report from India

Author

Janarthanan, Mahesh, Poddar, Chanchal, Sudharshan, S., Seabra, Luis, and Crow, Yanick

Subjects
Genetic disorders -- Diagnosis -- Case studies, Health
Abstract

Byline: Mahesh. Janarthanan, Chanchal. Poddar, S. Sudharshan, Luis. Seabra, Yanick. CrowBlau syndrome (BS) is a rare autoinflammatory disorder characterized by the clinical triad of arthritis, uveitis, and dermatitis due to [...]

Published
2019

36. Proceedings of the 24th Paediatric Rheumatology European Society Congress: Part three

Author

Atsali, Erato, Kassara, Dimitra, Katsimbri, Pelagia, Boiu, Sorina, Boumpas, Dimitrios T., Papaevangelou, Vana, Oshlyanska, Olena A., Omelchenko, Ludmila I., Ljudvik, Tatiana A., Bouchalova, Katerina, Schüller, Marcel, Franova, Jana, Skotakova, Jarmila, Macku, Marie, Fellas, Antoni, Hawke, Fiona, Santos, Derek, Coda, Andrea, Kelempisioti, Anthi, Keskitalo, Paula, Glumoff, Virpi, Kulmala, Petri, Vahasalo, Paula, Mozaffar, Mohammed A., Turkistani, Asraa K., Sangoof, Samaa O., Sevostyanov, Vladislav, Zholobova, Elena, Bountouvi, Evangelia, Theodoropoulos, konstantinos, Moutsiou, Renata, Tsalapaki, Christina, Diaz, Talia, Osorio, Sofia, Braña, Maria Teresa, Ramirez, Yuridiana, Aparicio, Luis, Rodriguez, Andres, Faugier, Enrique, Maldonado, Rocio, Gicchino, Maria Francesca, Granato, Carmela, Macchini, Giulia, Capalbo, Daniela, Olivieri, Alma Nunzia, Hasson, Nathan, Marino, Achille, Narula, Sona, Lerman, Melissa, Calonge, Maria Amelia Muñoz, Loza, Sara Maria Murias, Alcobendas, Rosa Maria, Remesal, Agustin, Núñez-Cuadros, Esmeralda, Zavala, Rocio Galindo, Rego, Gisela Díaz-Cordovés, Fernández, Cristina Antúnez, Molina, Yaiza García, Cardona, Antonio L. Urda, Sahin, Nihal, Durmus, Habibe S., Pinarbasi, Ayse S., Gunduz, Zubeyde, Poyrazoglu, Muammer H., Karaman, Zehra F., Oktem, Turhan, Oner, Mithat, Dusunsel, Ruhan, Susic, Gordana, Krstajic, Tamara, Vujovic, Dragana, Radlovic, Nedeljko, Lekovic, Zoran, Novakovic, Dusica, Lomic, Gordana Milosevski, Mördrup, Karina, Hesselstrand, Gunilla, Sorić, Iva, Lamot, Lovro, Vidovic, Mandica, Lamot, Mirta, Harjacek, Miroslav, Adank, Eva, Schneider, Elvira Cannizzaro, Abdalla, Eiman, Ullah, Irfan, Jeyaseelan, L., Abdwani, Reem, Shaqsi, Laila A. L., Zakwani, Ibrahim A. l., Fanouriakis, Antonis, Janarthanan, Mahesh, Vetrichelvan, Dhanarathnamoorthy, Ramachandran, P., Geminiganesan, Sangeetha, Kumar, Dinesh, Rao, Subba, Papatesta, Eleni-Maria, Maritsi, Despoina, Eleftheriou, Irini, Tsolia, Maria, Vougiouka, Olga, Çakan, Mustafa, Ayaz, Nuray Aktay, Karadağ, Şerife Gül, Keskindemirci, Gonca, Keltsev, Vladimir, Grebenkina, Lyudmila, Kim, Kwang Nam, Ahn, Jong Gyun, Kim, Young Dae, Maggio, Maria Cristina, Cimaz, Rolando, Failla, Maria Concetta, Dones, Piera, Collura, Mirella, Corsello, Giovanni, Rhim, Jung-Woo, Kim, Ki-Hwan, Lee, Soo-Young, Han, Seung-Beom, Kang, Jin-Han, Chung, Jae-Hee, Lee, Soo-Jung, Jeong, Dae-Chul, Santimov, Andrei, Rupp, Regina, Alekseev, Igor, Plutova, Natalya, Moskvina, Ekaterina, Kruchina, Marina, Tarasenko, Aleksandra, Sokolova, Natalya, Saveleva, Ekaterina, Bogdanov, Ilia, Ivanov, Dmitrii, Kandrina, Tatiana, Kopanevich, Olga, Grafskaia, Anastasiia, Ignateva, Natalia, Pulukchu, Daria, Pavlova, Natalia, Kalashnikova, Olga, Kornishina, Tatiana, Dubko, Margarita, Chasnyk, Vyacheslav, Kostik, Mikhail, Sowdagar, Shama, Sankar, Janani, Ramesh, Venkateswari, Szabo, Iulia E., Sirbe, Claudia, Pamfil, Cristina, Damian, Laura, Rednic, Simona, Deac, Maria, Sparchez, Mihaela, Filipescu, Ileana, Parvu, Mirela, Balint, Dumitrita, and Nicoara, Ancuta

Subjects
lcsh:Diseases of the musculoskeletal system, lcsh:RJ1-570, lcsh:Pediatrics, lcsh:RC925-935, Meeting Abstracts
Published
2017

37. Do Raynaud phenomenon negative juvenile systemic scleroderma patients have a different pattern of organ involvement as Raynaud phenomenon positive patients?

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Torok, Kathryn, Stanevicha, Valda, Terreri, M. T., Alexeeva, Ekaterina, Katsicas, Maria, Smith, Vanessa, Sztajnbok, Flavio, Avcin, Tadey, Cimaz, Rolando, Anton, Jordi, Kostik, Mikhail, Lehman, Thomas, Sifuentes-Giraldo, W. Alberto, Appenzeller, Simone, Janarthanan, Mahesh, Moll, Monika, Nemcova, Dana, Jose Santos, Maria, Battagliotti, Cristina, Berntson, Lillemor, Brunner, Jürgen, Costa Reis, Patrícia, Eleftheriou, Despina, Harel, Liora, Kallinich, Tilmann, Minden, Kirsten, Nielsen, Susan, Uziel, Yosef, Stevens, Ann, Pilkington, Clarissa, and Helmus, Nicola

Subjects
integumentary system, ddc: 610, 610 Medical sciences, Medicine, skin and connective tissue diseases
Abstract

Background: Juvenile systemic scleroderma (jSSc) is an orphan disease, with an estimated prevalence of 3 per 1000 000 children. Most jSSc patients primarily present with Raynaud phenomenon (RP). We investigated in our patient of the juvenile scleroderma inception cohort, how fare patients with (RP+)[for full text, please go to the a.m. URL], 46. Kongress der Deutschen Gesellschaft für Rheumatologie (DGRh), 32. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie (DGORh), Wissenschaftliche Herbsttagung der Gesellschaft für Kinder- und Jugendrheumatologie (GKJR)

Published
2019
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38. AB0967 IS THERE A DIFFERENCE IN PRESENTATION OF FEMALE AND MALE PATIENTS WITH JUVENILE SYSTEMIC SCLERODERMA. AN UPDATE FROM THE JUVENILE SYSTEMIC SCLERODERMA INCEPTION COHORT. WWW.JUVENILE-SCLERODERMA.COM

Author

Foeldvari, Ivan, primary, Klotsche, Jens, additional, Kasapcopur, Ozgur, additional, Adrovic, Amra, additional, Torok, Kathryn, additional, Stanevicha, Valda, additional, Sztajnbok, Flávio R., additional, Sakamoto, Ana Paula, additional, Alexeeva, Ekaterina, additional, Anton, Jordi, additional, Katsikas, Maria, additional, Smith, Vanessa, additional, Avcin, Tadej, additional, Cimaz, Rolando, additional, Kostik, Mikhail, additional, Lehman, Thomas, additional, Sifuentes-Giraldo, Walter Alberto, additional, Appenzeller, Simone, additional, Janarthanan, Mahesh, additional, Moll, Monika, additional, Nemcova, Dana, additional, Santos, Maria Jose, additional, Nassar, Amara, additional, Battagliotti, Cristina, additional, Berntson, Lillemor, additional, Bica, Blanca, additional, Brunner, Juergen, additional, Reis, Patricia Costa, additional, Eleftheriou, Despina, additional, Harel, Liora, additional, Horneff, Gerd, additional, Kallinich, Tilmann, additional, Lazarevic, Dragana, additional, Minden, Kirsten, additional, Nielsen, Susan, additional, Nuruzzaman, Farzana, additional, Patwardhan, Anjali, additional, Uziel, Yosef, additional, and Helmus, Nicola, additional

Published
2019
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39. SAT0479 UPDATE FROM THE JUVENILE SCLERODERMA INCEPTION COHORT. WWW.JUVENILE-SCLERODERMA.COM

Author

Foeldvari, Ivan, primary, Klotsche, Jens, additional, Kasapcopur, Ozgur, additional, Adrovic, Amra, additional, Torok, Kathryn, additional, Stanevicha, Valda, additional, Sztajnbok, Flávio R., additional, Tererri, Maria T., additional, Alexeeva, Ekaterina, additional, Anton, Jordi, additional, Katsikas, Maria, additional, Smith, Vanessa, additional, Avcin, Tadej, additional, Cimaz, Rolando, additional, Kostik, Mikhail, additional, Lehman, Thomas, additional, Sifuentes-Giraldo, Walter Alberto, additional, Appenzeller, Simone, additional, Janarthanan, Mahesh, additional, Moll, Monika, additional, Nemcova, Dana, additional, Santos, Maria Jose, additional, Schonenberg, Dieneke, additional, Battagliotti, Cristina, additional, Berntson, Lillemor, additional, Bica, Blanca, additional, Brunner, Juergen, additional, Reis, Patricia Costa, additional, Eleftheriou, Despina, additional, Harel, Liora, additional, Horneff, Gerd, additional, Kallinich, Tilmann, additional, Lazarevic, Dragana, additional, Minden, Kirsten, additional, Nielsen, Susan, additional, Nuruzzaman, Farzana, additional, Patwardhan, Anjali, additional, Uziel, Yosef, additional, and Helmus, Nicola, additional

Published
2019
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43. Update from the Juvenile Scleroderma Inception Cohort

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Torok, Kathryn S., Stanevicha, Valda, Sztajnbok, Flavio, Terreri, Maria Teresa, Alexeeva, Ekaterina, Anton, Jordi, Katsicas, Maria M., Smith, Vanessa, Avcin, Tadey, Cimaz, Rolando, Kostik, Mikhail, Lehman, Thomas J. A., Sifuentes-Giraldo, Walter A., Appenzeller, Simone, Janarthanan, Mahesh, Nemkova, Dana, Santos, Maria Jose, Battagliotti, Cristina, Berntson, Lillemor, Bica, Blanca, Brunner, Juergen, Reis, Patricia Costa, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Kallinich, Tilmann, Lazarevic, Dragana, Minden, Kirsten, Nielsen, Susan Mary, Uziel, Yosef, Helmus, Nicola, Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Torok, Kathryn S., Stanevicha, Valda, Sztajnbok, Flavio, Terreri, Maria Teresa, Alexeeva, Ekaterina, Anton, Jordi, Katsicas, Maria M., Smith, Vanessa, Avcin, Tadey, Cimaz, Rolando, Kostik, Mikhail, Lehman, Thomas J. A., Sifuentes-Giraldo, Walter A., Appenzeller, Simone, Janarthanan, Mahesh, Nemkova, Dana, Santos, Maria Jose, Battagliotti, Cristina, Berntson, Lillemor, Bica, Blanca, Brunner, Juergen, Reis, Patricia Costa, Eleftheriou, Despina, Harel, Liora, Horneff, Gerd, Kallinich, Tilmann, Lazarevic, Dragana, Minden, Kirsten, Nielsen, Susan Mary, Uziel, Yosef, and Helmus, Nicola

Published
2018

44. Is there a Difference in the Presentation of male and female Patients with diffuse subtype of juvenile systemic Sclerosis? Results from the juvenile Scleroderma Inception Cohort www.juvenile-scleroderma.com

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Stanevicha, Valda, Terreri, M. T., Alexeeva, Ekaterina, Katsicas, Maria, Smith, Vanessa, Cimaz, Rolando, Kostik, Mikhail, Lehman, Thomas, Anton, Jordi, Sifuentes-Giraldo, W. Alberto, Sztajnbok, Flavio, Avcin, Tadey, Janarthanan, Mahesh, Jose Santos, Maria, Moll, Monika, Nemcova, Dana, Battagliotti, Cristina, Brunner, Jürgen, Eleftheriou, Despina, Harel, Liora, Kallinich, Tilmann, Minden, Kirsten, Nielsen, Susan, Torok, Kathryn, Uziel, Josef, Stevens, Ann, Pilkington, Clarissa, and Helmus, Nicola

Subjects
ddc: 610, 610 Medical sciences, Medicine
Abstract

Background: Juvenile systemic sclerosis (jSSc) is an orphan autoimmune disease. Several adult publications looked at the differences between the clinical presentation of male and female patients with Systemic Sclerosis. There is a rarity of data regarding this topic in pediatric jSSc. The juvenile scleroderma[for full text, please go to the a.m. URL], 45. Kongress der Deutschen Gesellschaft für Rheumatologie (DGRh), 31. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie (DGORh), 27. Jahrestagung der Gesellschaft für Kinder- und Jugendrheumatologie (GKJR)

Published
2017

45. Update on the juvenile systemic Sclerosis Inception Cohort Project. Characteristics of the first 97 Patients at first Assessment. www.juvenile-scleroderma.com

Author

Foeldvari, Ivan, Klotsche, Jens, Kasapcopur, Ozgur, Adrovic, Amra, Stanevicha, Valda, Torok, Kathryn, Terreri, M. T., Alexeeva, Ekaterina, Katsicas, Maria, Smith, Vanessa, Sztajnbok, Flavio, Avcin, Tadey, Cimaz, Rolando, Anton, Jordi, Kostik, Mikhail, Lehman, Thomas, Sifuentes-Giraldo, W. Alberto, Appenzeller, Simone, Janarthanan, Mahesh, Moll, Monika, Nemcova, Dana, Jose Santos, Maria, Battagliotti, Cristina, Berntson, Lillemor, Brunner, Jürgen, Eleftheriou, Despina, Harel, Liora, Kallinich, Tilmann, Minden, Kirsten, Nielsen, Susan, Uziel, Yosef, Pilkington, Clarissa, Stevens, Ann, and Helmus, Nicola

Subjects
ddc: 610, 610 Medical sciences, Medicine
Abstract

Background: Juvenile systemic sclerosis (jSSc) is an orphan autoimmune disease. Currently just smaller retrospective data exist regarding presentation of organ involvement. In the previous studies assessment of the organ involvement was not standardized. Our project is the first one, where data of jSSc[for full text, please go to the a.m. URL], 45. Kongress der Deutschen Gesellschaft für Rheumatologie (DGRh), 31. Jahrestagung der Deutschen Gesellschaft für Orthopädische Rheumatologie (DGORh), 27. Jahrestagung der Gesellschaft für Kinder- und Jugendrheumatologie (GKJR)

Published
2017

48. Are diffuse and limited juvenile systemic sclerosis different in clinical presentation? Clinical characteristics of a juvenile systemic sclerosis cohort

Author

Foeldvari, Ivan, primary, Klotsche, Jens, additional, Torok, Kathryn S, additional, Kasapcopur, Ozgur, additional, Adrovic, Amra, additional, Stanevicha, Valda, additional, Terreri, Maria Teresa, additional, Alexeeva, Ekaterina, additional, Katsicas, Maria, additional, Cimaz, Rolando, additional, Kostik, Mikhail, additional, Lehman, Thomas, additional, Sifuentes-Giraldo, Walter-Alberto, additional, Smith, Vanessa, additional, Sztajnbok, Flavio, additional, Avcin, Tadej, additional, Jose Santos, Maria, additional, Moll, Monika, additional, Nemcova, Dana, additional, Battagliotti, Cristina, additional, Eleftheriou, Despina, additional, Janarthanan, Mahesh, additional, Kallinich, Tilmann, additional, Anton, Jordi, additional, Minden, Kirsten, additional, Nielsen, Susan, additional, Uziel, Yosef, additional, and Helmus, Nicola, additional

Published
2018
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