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4. The Changing Landscape of Neonatal Diabetes Mellitus in Italy Between 2003 and 2022.

Author

Rapini, Novella, Delvecchio, Maurizio, Mucciolo, Mafalda, Ruta, Rosario, Rabbone, Ivana, Cherubini, Valentino, Zucchini, Stefano, Cianfarani, Stefano, Prandi, Elena, Schiaffini, Riccardo, Bizzarri, Carla, Piccini, Barbara, Maltoni, Giulio, Predieri, Barbara, Minuto, Nicola, Paola, Rossella Di, Giordano, Mara, Tinto, Nadia, Grasso, Valeria, and Russo, Lucia

Subjects
PANCREATIC enzymes, MOLECULAR genetics, INSULIN resistance, DIABETES, NUCLEOTIDE sequencing
Abstract

Context In the last decade the Sanger method of DNA sequencing has been replaced by next-generation sequencing (NGS). NGS is valuable in conditions characterized by high genetic heterogeneity such as neonatal diabetes mellitus (NDM). Objective To compare results of genetic analysis of patients with NDM and congenital severe insulin resistance (c.SIR) identified in Italy in 2003-2012 (Sanger) vs 2013-2022 (NGS). Methods We reviewed clinical and genetic records of 104 cases with diabetes onset before 6 months of age (NDM + c.SIR) of the Italian dataset. Results Fifty-five patients (50 NDM + 5 c.SIR) were identified during 2003-2012 and 49 (46 NDM + 3 c.SIR) in 2013-2022. Twenty-year incidence was 1:103 340 (NDM) and 1:1 240 082 (c.SIR) live births. Frequent NDM/c.SIR genetic defects (KCNJ11 , INS , ABCC8 , 6q24, INSR) were detected in 41 and 34 probands during 2003-2012 and 2013-2022, respectively. We identified a pathogenic variant in rare genes in a single proband (GATA4) (1/42 or 2.4%) during 2003-2012 and in 8 infants (RFX6 , PDX1 , GATA6 , HNF1B , FOXP3 , IL2RA , LRBA , BSCL2) during 2013-2022 (8/42 or 19%, P =.034 vs 2003-2012). Notably, among rare genes 5 were recessive. Swift and accurate genetic diagnosis led to appropriate treatment: patients with autoimmune NDM (FOXP3 , IL2RA , LRBA) were subjected to bone marrow transplant; patients with pancreas agenesis/hypoplasia (RFX6 , PDX1) were supplemented with pancreatic enzymes, and the individual with lipodystrophy caused by BSCL2 was started on metreleptin. Conclusion NGS substantially improved diagnosis and precision therapy of monogenic forms of neonatal diabetes and c.SIR in Italy. [ABSTRACT FROM AUTHOR]

Published
2024
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5. Pelvic ultrasound and pubertal attainment in girls with sexual precocity: the pivotal role of uterine volume in predicting the timing of menarche

Author

Cattoni, A, Russo, G, Capitoli, G, Rodari, G, Nicolosi, M, Molinari, S, Tondelli, D, Pelliccia, C, Radaelli, S, Arosio, A, Fontana, K, Tattesi, G, Passoni, P, Boneschi, A, Giavoli, C, Meroni, S, Stancampiano, M, Garuti, E, Biondi, A, Balduzzi, A, Bizzarri, C, Cattoni, Alessandro, Russo, Gianni, Capitoli, Giulia, Rodari, Giulia, Nicolosi, Maria Laura, Molinari, Silvia, Tondelli, Daniele, Pelliccia, Ciretta, Radaelli, Silvia, Arosio, Andrea Mario Luciano, Fontana, Katia, Tattesi, Giulia, Passoni, Paolo, Boneschi, Annalisa, Giavoli, Claudia, Meroni, Silvia Laura Carla, Stancampiano, Marianna Rita, Garuti, Elda, Biondi, Andrea, Balduzzi, Adriana, Bizzarri, Carla, Cattoni, A, Russo, G, Capitoli, G, Rodari, G, Nicolosi, M, Molinari, S, Tondelli, D, Pelliccia, C, Radaelli, S, Arosio, A, Fontana, K, Tattesi, G, Passoni, P, Boneschi, A, Giavoli, C, Meroni, S, Stancampiano, M, Garuti, E, Biondi, A, Balduzzi, A, Bizzarri, C, Cattoni, Alessandro, Russo, Gianni, Capitoli, Giulia, Rodari, Giulia, Nicolosi, Maria Laura, Molinari, Silvia, Tondelli, Daniele, Pelliccia, Ciretta, Radaelli, Silvia, Arosio, Andrea Mario Luciano, Fontana, Katia, Tattesi, Giulia, Passoni, Paolo, Boneschi, Annalisa, Giavoli, Claudia, Meroni, Silvia Laura Carla, Stancampiano, Marianna Rita, Garuti, Elda, Biondi, Andrea, Balduzzi, Adriana, and Bizzarri, Carla

Abstract

Introduction: Among girls assessed for pubertal precocity, pelvic ultrasound (pUS) may represent a pivotal tool to predict the time expected to elapse between sonographic assessment and the onset of menarche (TUS-M). Accordingly, the present analysis is meant to define the statistical relationship between sonographic parameters and TUS-M, in order to identify the most reliable predictor of the timing of menarche. Methods: Retrospective, multicenter analysis. Girls assessed for sexual precocity and showing sonographic and clinical findings consistent with pubertal onset upon referral were considered eligible. Patients treated with GnRH analogues were excluded and only those who had subsequently achieved complete and spontaneous pubertal attainment and for whom the exact date of menarche was available were included. Overall, we enrolled 184 girls from five tertiary care Italian Centers. Results: The time elapsed (months) between baseline endocrine assessment and spontaneous achievement of menarche showed a negative statistically significant correlation (p<0.0001) with LH (r:-0.61), FSH (r:-0.59), estradiol (r:-0.52) and stimulated LH values (r:-0.58). Among pUS parameters, ovarian volume (r:-0.17 left, -0.30 right) and uterine body-to-cervix ratio (r:-0.18) poorly correlated with TUS-M, while uterine diameters (r:-0.61 longitudinal, -0.64 anteroposterior) and volume (r:-0.70) achieved a highly statistical significance (p<0.0001). Uterine volume (UV) showed a negative logarithmic relationship with TUS-M and represented the most reliable predictor of the timing of menarche in uni- and multivariable analyses (p <0.001). ROC analyses identified the UV thresholds that best predict the onset of menarche within 18, 12 and 6 months, respectively: 3.76, 6.02 and 8.80 ml. Conclusion: The logarithm of UV shows the best statistical performance in predicting the timing of menarche in girls assessed for pubertal precocity. Accordingly, we developed a user-friendly online a

Published
2024

7. Chronic Kidney Disease and Growth Failure in Children.

Author

Todisco, Tommaso, Ubertini, Grazia Maria, Bizzarri, Carla, Loche, Sandro, and Cappa, Marco

Subjects
CHRONIC kidney failure complications, KIDNEY transplantation, CONSENSUS (Social sciences), MEDICAL protocols, HYPERPARATHYROIDISM, VITAMIN D deficiency, PROTEINURIA, ANEMIA, METABOLIC disorders, REPRODUCTIVE health, DISEASE management, BONE growth, HYPERPHOSPHATEMIA, SEVERITY of illness index, TREATMENT effectiveness, STATURE, HYPOCALCEMIA, CHILD development, QUALITY of life, GROWTH disorders, HUMAN growth hormone, COMORBIDITY, CHILDREN
Abstract

Chronic kidney disease (CKD) is a significant challenge for pediatric endocrinologists, as children with CKD may present a variety of endocrine complications. Growth failure is common in CKD, and its severity is correlated with the degree of renal insufficiency. Management strategies include addressing reversible comorbidities, optimizing nutrition, and ensuring metabolic control. Kidney replacement therapy, including transplantation, determines a significant improvement in growth. According to a recent Consensus Statement, children with CKD stage 3—or on dialysis older >6 months—are eligible for treatment with recombinant growth hormone (rGH) in the case of persistent growth failure. Treatment with rGH may be considered for those with height between the 3rd and 10th percentile and persistent growth deceleration. In children who received kidney transplantation but continue to experience growth failure, initiation of GH therapy is recommended one year post-transplantation if spontaneous catch-up growth does not occur and steroid-free immunosuppression is not an option. In children with CKD, due to nephropathic cystinosis and persistent growth failure, GH therapy should be considered at all stages of CKD. Potential adverse effects and benefits must be regularly assessed during therapy. Treatment with GH is safe in children with CKD. However, its general efficacy is still controversial. All possible problems with a negative impact on growth should be timely addressed and resolved, whenever possible with a personalized approach to the patient. GH therapy may be useful in promoting catch-up growth in children with residual growth potential. Future research should focus on refining effective therapeutic strategies and establishing consensus guidelines to optimize growth outcomes in this population. [ABSTRACT FROM AUTHOR]

Published
2024
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9. Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

Author

Aisenberg, Javier, Akkurt, Ilker, Abdul-Latif, Hussein, Al-Abdullah, Anees, Barak, Lubomir, Van Den Bergh, Joop, Bertrand, Anne-Marie, Bizzarri, Carla, Bonfanti, Riccardo, Bruel, Henri, Burrows, Anthony, Cadario, Francesco, Cameron, Fergus J., Carson, Dennis, Cartigny, Maryse, Cauvin, Vittoria, Cave, Helene, Chakera, Ali, Chetan, Ravi, Chiari, Giovanni, Couch, Bob, Coutant, Régis, Cummings, Elizabeth, Dankovcikova, Adriana, Davis, Liz, Deiss, Dorothee, Delvecchio, Maurizio, Faleschini, Elena, Fauret, Anne-Laure, Finn, Roisin, Ford, Tamsin, Franco, Elisa De, Gallen, Bastian De, Gasperíková, Daniela, Guntamukkala, Padma, Hakeem, Vaseem, Hasegawa, Shinji, Hathout, Eba H., Heffernan, Emmeline, Hill, David, Ho, Josephine, Hoarau, Marie, Holl, Reinhard, Hoddinott, Rebecca, Houghton, Jane, Howard, Neville, Hughes, Natalie, Hunter, Ian, Høgåsen, Anne Kirsti, Kuulasmaa, Helena, Ioacara, Sorin, Iotova, Violeta, Irgens, Henrik, Jaap, Alan, Jones, Kenneth, Kapellen, Thomas, Kaufman, Ellen, Klinge, Andreas, Klupa, Tomasz, Krishnaswamy, Ramaiyer, Lafferty, Tony, LeGault, Laurent, Lambert, Paul, Malecki, Maciej T, Malievsky, Olag, Mathew, Revi, Mathews, Frances, McVie, Robert, Menzel, Ulrike, Metz, Chantale, Meulen, John Van Der, Modgil, Gita, Mul, Dick, Muther, Silvia, Nuboer, Roos, O'Connell, Susan M., O'Riordan, Stephen, Palko, Miroslav, Patel, Kashyap Amratlal, Pesavento, Roberta, Piccinno, Elvira, Pillai, Janani Kumaraguru, Pruhova, Stephanka, Punthakee, Zubin, Rabbone, Ivana, Raile, Klemens, Rincon, Marielisa, Rose, Danette, Sanchez, Janine, Sandereson, Susan, Saxena, Vinay, Schebek, Martin, Schmidt, Dorothee, Shehadeh, Naim, Shiels, Julian P.H., Silva, Jose M. C. L, Stanik, Juraj, Tinklin, Tracy, Tjora, Erling, Tumini, Stefano, Tuomi, Tiinamaija, Uehara, Akiko, Velde, Robert Van der, Vermeulen, Guido, Visser, Uma, Voorhoeve, Paul, Walker, Jan, Weill, Jaques, Weisner, Tobias, Werner, Andrea, Williams, Toni, Woodhead, Helen, øddegård, Rønnaug, Bowman, Pamela, Sulen, Åsta, Barbetti, Fabrizio, Beltrand, Jacques, Svalastoga, Pernille, Codner, Ethel, Tessmann, Ellen H, Juliusson, Petur B, Skrivarhaug, Torild, Pearson, Ewan R, Flanagan, Sarah E, Babiker, Tarig, Thomas, Nicholas J, Shepherd, Maggie H, Ellard, Sian, Klimes, Iwar, Szopa, Magdalena, Polak, Michel, Iafusco, Dario, Hattersley, Andrew T, and Njølstad, Pål R

Published
2018
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10. Insulin Clearance at the Pubertal Transition in Youth with Obesity and Steatosis Liver Disease

Author

Franceschi, Roberto, primary, Fintini, Danilo, additional, Ravà, Lucilla, additional, Mariani, Michela, additional, Aureli, Alessia, additional, Inzaghi, Elena, additional, Pedicelli, Stefania, additional, Deodati, Annalisa, additional, Bizzarri, Carla, additional, Cappa, Marco, additional, Cianfarani, Stefano, additional, and Manco, Melania, additional

Published
2023
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13. Ipertiroidismo e tiroidite autoimmune in età evolutiva

Author

Pellegrin, Maria Chiara, Occhipinti, Alessandro, Bossini, Benedetta, Norbedo, Stefania, Faleschini, Elena, Barbi, Egidio, Bizzarri, Carla, Tornese, Gianluca, Pellegrin, Maria Chiara, Occhipinti, Alessandro, Bossini, Benedetta, Norbedo, Stefania, Faleschini, Elena, Barbi, Egidio, Bizzarri, Carla, and Tornese, Gianluca

Subjects
Radioiodine ablation, endocrine system, endocrine system diseases, Down syndrome, Antithyroid agents, Antithyroid agent, Pediatrics, Perinatology and Child Health, Thyroidectomy, Graves’ disease, Hyperthyroidism
Abstract

Hyperthyroidism is a rare clinical entity in paediatric age. In most cases the etiology is autoimmune and goiter represents the typical presentation. Ophthalmopathy is rare and can precede the diagnosis of autoimmune hyperthyroidism. Thyrotoxicosis caused by the hyperthyroid phase of Hashimoto’s thyroiditis must be carefully distinguished from Graves’ disease (GD), since the first condition has a better prognosis for spontaneous remission. Three treatment options are currently available for the management of paediatric GD. First-line therapy is antithyroid drugs, while thyroidectomy and radioiodine are considered on relapse. A lower remission rate and a higher risk of adverse events are observed after the first course of methimazole in childhood with respect to adulthood. Children and adolescents may require a prolonged antithyroid treatment, but an overall consensus regarding the optimal regimen is lacking.

Published
2021
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15. Glycated haemoglobin in the first year after diagnosis of type 1 diabetes is an independent risk factor for diabetic retinopathy: The IMDIAB 25 years follow‐up study.

Author

Maddaloni, Ernesto, Carlone, Angela, Pitocco, Dario, Leanza, Giulia, Suraci, Concetta, Altomare, Maria, Cavallo, Maria G., Barchetta, Ilaria, Morano, Susanna, Moretti, Chiara, Coraggio, Lucia, Visalli, Natalia, Tramontana, Flavia, Schiaffini, Riccardo, Crinò, Antonino, Buzzetti, Raffaella, Pozzilli, Paolo, Baroni, Marco G, Bizzarri, Carla, and Bodini, Sara

Subjects
TYPE 1 diabetes, DIABETIC retinopathy, INSULIN, GLYCOSYLATED hemoglobin, HEMOGLOBINS, GLYCEMIC control, AUTOANTIBODIES
Abstract

Glycated haemoglobin in the first year after diagnosis of type 1 diabetes is an independent risk factor for diabetic retinopathy: The IMDIAB 25 years follow-up study Effect of intensive diabetes therapy on the progression of diabetic retinopathy in patients with type 1 diabetes: 18 years of follow-up in the DCCT/EDIC. Keywords: HbA1c; metabolic memory; retinopathy; type 1 diabetes EN HbA1c metabolic memory retinopathy type 1 diabetes 3415 3419 5 10/05/23 20231101 NES 231101 BACKGROUND Intensive glycaemic control lowers the risk of microvascular complications.[1] This effect has been shown to persist for up to 18 years of follow-up.[[2], [4]] Whether the glycaemic control obtained during the first months after type 1 diabetes (T1D) onset has an impact on the future risk of chronic complications has not been clarified. Linear regression models were used to test the presence of any association between HbA1c at diabetes onset, mean-first-year HbA1c and HbA1c measured at last follow-up and to test baseline features associated with first-year HbA1c. [Extracted from the article]

Published
2023
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22. Proposal of an Algorithm to Early Detect Attenuated Type I Mucopolysaccharidosis (MPS Ia) among Children with Growth Abnormalities

Author

Baronio, F, Zucchini, S, Zulian, F, Salerno, M, Parini, R, Cattoni, A, Deodato, F, Gaeta, A, Bizzarri, C, Gasperini, S, Pession, A, Baronio, Federico, Zucchini, Stefano, Zulian, Francesco, Salerno, Mariacarolina, Parini, Rossella, Cattoni, Alessandro, Deodato, Federica, Gaeta, Alberto, Bizzarri, Carla, Gasperini, Serena, Pession, Andrea, Baronio, F, Zucchini, S, Zulian, F, Salerno, M, Parini, R, Cattoni, A, Deodato, F, Gaeta, A, Bizzarri, C, Gasperini, S, Pession, A, Baronio, Federico, Zucchini, Stefano, Zulian, Francesco, Salerno, Mariacarolina, Parini, Rossella, Cattoni, Alessandro, Deodato, Federica, Gaeta, Alberto, Bizzarri, Carla, Gasperini, Serena, and Pession, Andrea

Abstract

Background and Objectives: Diagnostic delay is common in attenuated Mucopolysaccharidosis Type I (MPS Ia) due to the rarity of the disease and the variability of clinical presentation. Short stature and impaired growth velocity are frequent findings in MPS Ia, but they rarely raise suspicion as paediatric endocrinologists are generally poorly trained to detect earlier and milder clinical signs of this condition. Materials and Methods: Following a consensus-based methodology, a multidisciplinary panel including paediatric endocrinologists, paediatricians with expertise in metabolic disorders, radiologists, and rheumatologists shared their experience on a possible clinical approach to the diagnosis of MPS Ia in children with short stature or stunted growth. Results: The result was the formation of an algorithm that illustrates how to raise the suspicion of MPS Ia in a patient older than 5 years with short stature and suggestive clinical signs. Conclusion: The proposed algorithm may represent a useful tool to improve the awareness of paediatric endocrinologists and reduce the diagnostic delay for patients with MPS Ia.

Published
2022

25. Prevalence of prediabetes in children and adolescents by class of obesity

Author

Pedicelli, Stefania, primary, Fintini, Danilo, additional, Ravà, Lucilla, additional, Inzaghi, Elena, additional, Deodati, Annalisa, additional, Spreghini, Maria Rita, additional, Bizzarri, Carla, additional, Mariani, Michela, additional, Cianfarani, Stefano, additional, Cappa, Marco, additional, and Manco, Melania, additional

Published
2022
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26. Sedentary lifestyle and precocious puberty in girls during the COVID-19 pandemic: an Italian experience

Author

Chioma, Laura, primary, Bizzarri, Carla, additional, Verzani, Martina, additional, Fava, Daniela, additional, Salerno, Mariacarolina, additional, Capalbo, Donatella, additional, Guzzetti, Chiara, additional, Penta, Laura, additional, Di Luigi, Luigi, additional, di Iorgi, Natascia, additional, Maghnie, Mohamad, additional, Loche, Sandro, additional, and Cappa, Marco, additional

Published
2022
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28. Proposal of an Algorithm to Early Detect Attenuated Type I Mucopolysaccharidosis (MPS Ia) among Children with Growth Abnormalities

Author

Baronio, Federico, primary, Zucchini, Stefano, additional, Zulian, Francesco, additional, Salerno, Mariacarolina, additional, Parini, Rossella, additional, Cattoni, Alessandro, additional, Deodato, Federica, additional, Gaeta, Alberto, additional, Bizzarri, Carla, additional, Gasperini, Serena, additional, and Pession, Andrea, additional

Published
2022
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31. Sulfonylurea-Insensitive Permanent Neonatal Diabetes Caused by a Severe Gain-of-Function Tyr330His Substitution in Kir6.2

Author

McClenaghan, Conor, primary, Rapini, Novella, additional, De Rose, Domenico Umberto, additional, Gao, Jian, additional, Roeglin, Jacob, additional, Bizzarri, Carla, additional, Schiaffini, Riccardo, additional, Tiberi, Eloisa, additional, Mucciolo, Mafalda, additional, Deodati, Annalisa, additional, Perri, Alessandro, additional, Vento, Giovanni, additional, Barbetti, Fabrizio, additional, Nichols, Colin G., additional, and Cianfarani, Stefano, additional

Published
2022
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35. Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin

Author

Bizzarri, Carla, primary, Giannone, Germana Antonella, additional, Gervasoni, Jacopo, additional, Benedetti, Sabina, additional, Albanese, Federica, additional, Strologo, Luca Dello, additional, Guzzo, Isabella, additional, Mucciolo, Mafalda, additional, Camassei, Francesca Diomedi, additional, Emma, Francesco, additional, Cappa, Marco, additional, and Porzio, Ottavia, additional

Published
2021
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41. Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy

Author

Bonfanti, Riccardo, primary, Iafusco, Dario, additional, Rabbone, Ivana, additional, Diedenhofen, Giacomo, additional, Bizzarri, Carla, additional, Patera, Patrizia Ippolita, additional, Reinstadler, Petra, additional, Costantino, Francesco, additional, Calcaterra, Valeria, additional, Iughetti, Lorenzo, additional, Savastio, Silvia, additional, Favia, Anna, additional, Cardella, Francesca, additional, Lo Presti, Donatella, additional, Girtler, Ylenia, additional, Rabbiosi, Sarah, additional, D’Annunzio, Giuseppe, additional, Zanfardino, Angela, additional, Piscopo, Alessia, additional, Casaburo, Francesca, additional, Pintomalli, Letizia, additional, Russo, Lucia, additional, Grasso, Valeria, additional, Minuto, Nicola, additional, Mucciolo, Mafalda, additional, Novelli, Antonio, additional, Marucci, Antonella, additional, Piccini, Barbara, additional, Toni, Sonia, additional, Silvestri, Francesca, additional, Carrera, Paola, additional, Rigamonti, Andrea, additional, Frontino, Giulio, additional, Trada, Michela, additional, Tinti, Davide, additional, Delvecchio, Maurizio, additional, Rapini, Novella, additional, Schiaffini, Riccardo, additional, Mammì, Corrado, additional, Barbetti, Fabrizio, additional, _, _, additional, Aloe, Monica, additional, Amadeo, Simona, additional, Arnaldi, Claudia, additional, Bassi, Marta, additional, Beccaria, Luciano, additional, Benelli, Marzia, additional, Maria Berioloi, Giulia, additional, Bertelli, Enrica, additional, Biagioni, Martina, additional, Bobbio, Adriana, additional, Boccato, Stefano, additional, Bologna, Oriana, additional, Bontempi, Franco, additional, Bonura, Clara, additional, Bracciolini, Giulia, additional, Brufani, Claudia, additional, Bruzzi, Patrizia, additional, Buono, Pietro, additional, Cardani, Roberta, additional, Cardinale, Giuliana, additional, Casertano, Alberto, additional, Cristina Castiglione, Maria, additional, Cauvin, Vittoria, additional, Cherubini, Valentino, additional, Chiarelli, Franco, additional, Chiari, Giovanni, additional, Cianfarani, Stefano, additional, Cirillo, Dante, additional, Citriniti, Felice, additional, Coccioli, Susanna, additional, Cogliardi, Anna, additional, Confetto, Santino, additional, Contreas, Giovanna, additional, Corò, Anna, additional, Corsini, Elisa, additional, Cresta, Nicoletta, additional, De Berardinis, Fiorella, additional, De Donno, Valeria, additional, De Filippo, Giampaolo, additional, De Marco, Rosaria, additional, Deodati, Annalisa, additional, Faleschini, Elena, additional, Fattorusso, Valentina, additional, Favalli, Valeria, additional, Felappi, Barbara, additional, Ferrito, Lucia, additional, Fichera, Graziella, additional, Fontana, Franco, additional, Fornari, Elena, additional, Franceschi, Roberto, additional, Franco, Francesca, additional, Franzese, Adriana, additional, Paola Frongia, Anna, additional, Gaiero, Alberto, additional, Gallo, Francesco, additional, Gargantini, Luigi, additional, Giani, Elisa, additional, Giorgetti, Chiara, additional, Bianchi, Giulia, additional, Graziani, Vanna, additional, Gualtieri, Antonella, additional, Guasti, Monica, additional, Iannicelli, Gennaro, additional, Iannilli, Antonio, additional, Giovanna, Ignaccolo, additional, Ingletto, Dario, additional, Innaurato, Stefania, additional, Inzaghi, Elena, additional, Iovane, Brunella, additional, Kaufmann, Peter, additional, La Loggia, Alfonso, additional, Lapolla, Rosa, additional, Lasagni, Anna, additional, Lazzaro, Nicola, additional, Lenzi, Lorenzo, additional, Lera, Riccardo, additional, Levantini, Gabriella, additional, Lombardo, Fortunato, additional, Lonero, Antonella, additional, Longhi, Silvia, additional, Lucchesi, Sonia, additional, Paola Guerraggio, Lucia, additional, Lucieri, Sergio, additional, Macellaro, Patrizia, additional, Maffeis, Claudio, additional, Mainetti, Bendetta, additional, Maltoni, Giulio, additional, Mameli, Chiara, additional, Mammì, Francesco, additional, Luisa Manca-Bitti, Maria, additional, Manco, Melania, additional, Marino, Monica, additional, Mariano, Matteo, additional, Marigliano, Marco, additional, Marsciani, Alberto, additional, Mastrangelo, Costanzo, additional, Cristina Matteoli, Maria, additional, Mazzali, Elena, additional, Meschi, Franco, additional, MIgliaccio, Antonella, additional, Morandi, Anita, additional, Morganti, Gianfranco, additional, Mozzillo, Enza, additional, Musolino, Gianluca, additional, Nugnes, Rosa, additional, Ortolani, Federica, additional, Pardi, Daniela, additional, Pascarella, Filomena, additional, Passanisi, Stefano, additional, Pedini, Annalisa, additional, Pennati, Cristina, additional, Perrotta, Angelo, additional, Peruzzi, Sonia, additional, Peverelli, Paola, additional, Pezzino, Giulia, additional, Claudia Piona, Anita, additional, Piredda, Gavina, additional, Pistone, Carmelo, additional, Prandi, Elena, additional, Pedieri, Barbara, additional, Di Bonito, Procolo, additional, Pulcina, Anna, additional, Quinci, Maria, additional, Randazzo, Emioli, additional, Ricciardi, Rossella, additional, Ripoli, Carlo, additional, Roppolo, Rosanna, additional, Rutigliano, Irene, additional, Sabbio, Alberto, additional, salardi, Silvana, additional, Salvatoni, Alessandro, additional, Saporiti, Anna, additional, Sardi, Rita, additional, Scanu, Mariapiera, additional, Scaramuzza, Andrea, additional, Eleonardo Schiven, ,, additional, Secco, Andrea, additional, Sessa, Linda, additional, Sogno Valin, Paola, additional, Sordelli, Silvia, additional, Spallino, Luisa, additional, Stagi, Stefano, additional, Stamati, Filomena, additional, Suprani, Tosca, additional, Talarico, Valentina, additional, Timapanaro, Tiziana, additional, Tirendi, Antonella, additional, Tomaselli, Letizia, additional, Tornese, Gianluca, additional, Andrea Trettene, Adolfo, additional, Tumini, Stefano, additional, Valerio, Giuliana, additional, Ventrici, Claudia, additional, Viscardi, Matteo, additional, Zaffani, Silvana, additional, Zampolli, Maria, additional, Zanette, Giorgio, additional, Zecchino, Clara, additional, Antonietta Zedda, Maria, additional, Zonca, Silvia, additional, and Zucchini, Stefano, additional

Published
2021
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46. Adrenoleukodystrophy

Author

Cappa, Marco, primary, Bizzarri, Carla, additional, Vollono, Catello, additional, Petroni, Anna, additional, and Banni, Sebastiano, additional

Published
2010
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50. Blue eyes as a risk factor for type 1 diabetes

Author

Di Stasio, Enrico, Maggi, Daria, Berardesca, Enzo, Marulli, Georgiana Clare, Bizzarri, Carla, Lauria, Angelo, Portuesi, Rosalba, Cavallo, Maria Gisella, Costantino, Francesco, Buzzetti, Raffaella, Astorri, Elisa, Pitocco, Dario, Songini, Marco, and Pozzilli, Paolo

Published
2011
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