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Your search keyword '"Barp, A."' showing total 13 results
Start Over Author "Barp, A." Journal neuromuscular disorders
13 results on '"Barp, A."'

1. Functional outcome measures in young, steroid-naïve boys with Duchenne muscular dystrophy

Author

Mayhew, Anna G, Moat, Dionne, McDermott, Michael P., Eagle, Michelle, Griggs, Robert C., King, Wendy M., James, Meredith K., Muni-Lofra, Robert, Shillington, Alison, Gregson, Sarah, Pallant, Lindsey, Skura, Christy, Staudt, Loretta A., Eichinger, Katy, McMurchie, Heather, Rabb, Rosanna, Di Marco, Marina, Brown, Sarah, Zanin, Riccardo, Arnoldi, Maria Teresa, McIntyre, Melissa, Wilson, Amelia, Alfano, Lindsay N., Lowes, Linda P., Blomgren, Colleen, Milev, Evelin, Iodice, Mario, Pasternak, Amy, Chiu, Angela, Lehnert, Ilka, Claus, Nicole, Dieruf, Kathy A., Rolle, Enrica, Nicorici, Alina, Andres, Barbara, Hobbiebrunken, Elke, Roetmann, Gerda, Kern, Victoria, Civitello, Matthew, Vogt, Sibylle, Hayes, Melissa J., Scholtes, Cheryl, Lacroix, Catherine, Gunn, Tara, Warner, Sinead, Newman, Jennifer, Barp, Andrea, Kundrat, Katherine, Kovelman, Staci, Powers, Penny J., and Guglieri, Michela

Published
2022
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3. Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test

Author

Pane, Marika, Fanelli, Lavinia, Mazzone, Elena Stacy, Olivieri, Giorgia, D'Amico, Adele, Messina, Sonia, Scutifero, Marianna, Battini, Roberta, Petillo, Roberta, Frosini, Silvia, Sivo, Serena, Vita, Gian Luca, Bruno, Claudio, Mongini, Tiziana, Pegoraro, Elena, De Sanctis, Roberto, Gardani, Alice, Berardinelli, Angela, Lanzillotta, Valentina, Carlesi, Adelina, Viggiano, Emanuela, Cavallaro, Filippo, Sframeli, Maria, Bello, Luca, Barp, Andrea, Bianco, Flaviana, Bonfiglio, Serena, Rolle, Enrica, Palermo, Concetta, D'Angelo, Grazia, Pini, Antonella, Iotti, Elena, Gorni, Ksenija, Baranello, Giovanni, Bertini, Enrico, Politano, Luisa, Sormani, Maria Pia, and Mercuri, Eugenio

Published
2015
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4. Reliability of the Performance of Upper Limb assessment in Duchenne muscular dystrophy

Author

Pane, Marika, Mazzone, Elena S., Fanelli, Lavinia, De Sanctis, Roberto, Bianco, Flaviana, Sivo, Serena, D’Amico, Adele, Messina, Sonia, Battini, Roberta, Scutifero, Marianna, Petillo, Roberta, Frosini, Silvia, Scalise, Roberta, Vita, Gianluca, Bruno, Claudio, Pedemonte, Marina, Mongini, Tiziana, Pegoraro, Elena, Brustia, Francesca, Gardani, Alice, Berardinelli, Angela, Lanzillotta, Valentina, Viggiano, Emanuela, Cavallaro, Filippo, Sframeli, Maria, Bello, Luca, Barp, Andrea, Bonfiglio, Serena, Rolle, Enrica, Colia, Giulia, Catteruccia, Michela, Palermo, Concetta, D’Angelo, Grazia, Pini, Antonella, Iotti, Elena, Gorni, Ksenija, Baranello, Giovanni, Morandi, Lucia, Bertini, Enrico, Politano, Luisa, Sormani, MariaPia, and Mercuri, Eugenio

Published
2014
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5. COVID-19 AND NEUROMUSCULAR DISEASES

Author

Fortunato, F., primary, Farnè, M., additional, Bianchi, F., additional, Neri, M., additional, Siciliano, G., additional, Sansone, V., additional, Barp, A., additional, Albamonte, E., additional, Vita, G., additional, Atalaia, A., additional, Evangelista, T., additional, Gualandi, F., additional, and Ferlini, A., additional

Published
2021
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6. COVID-19 AND NEUROMUSCULAR DISEASES

Author

Marcella Neri, F. Fortunato, Emilio Albamonte, F. Bianchi, Gianluca Vita, Marianna Farnè, Francesca Gualandi, Alessandra Ferlini, Andrea Barp, A. Atalaia, Teresinha Evangelista, Valeria A. Sansone, and Gabriele Siciliano

Subjects
medicine.medical_specialty, 2019-20 coronavirus outbreak, Telemedicine, Coronavirus disease 2019 (COVID-19), business.industry, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Patient management, Neurology, Pediatrics, Perinatology and Child Health, Medicine, Neurology (clinical), business, Intensive care medicine, Genetics (clinical)
Published
2021

8. Late onset multiple acyl-CoA dehydrogenase deficiency (MADD) myopathy misdiagnosed as polymyositis

Author

Cécile Acquaviva-Bourdain, P. Laforêt, Andrea Barp, Rémi Bellance, and Odile Rigal

Subjects
medicine.medical_specialty, business.industry, Late onset, medicine.disease, Polymyositis, Endocrinology, Neurology, Internal medicine, Pediatrics, Perinatology and Child Health, medicine, Neurology (clinical), medicine.symptom, business, Myopathy, Multiple Acyl-CoA Dehydrogenase Deficiency, Genetics (clinical)
Published
2017

11. Longitudinal functional measures in Becker muscular dystrophy: Implications for clinical trials and Duchenne exon skipping outcomes

Author

Andrea Barp, Paola Campadello, Luca Bello, Claudio Semplicini, Elena Pegoraro, C. Angelini, and Gianni Sorarù

Subjects
Oncology, medicine.medical_specialty, business.industry, medicine.disease, Exon skipping, Clinical trial, Neurology, Internal medicine, Pediatrics, Perinatology and Child Health, medicine, Neurology (clinical), Muscular dystrophy, business, Genetics (clinical)
Published
2015

13. 555P Assessment of IBM-FRS total score and specific domains in a large cohort of inclusion body myositis patients.

Author

Vicino, A., Lauletta, A., Barbaccia, A., Valentino, L., Cheli, M., Saccani, E., Grandis, M., Coccia, M., Barp, A., Ravaglia, S., Bortolani, S., Ruggiero, L., Mongini, T., Verriello, L., Vattemi, G., Filosto, M., Liguori, R., Rodolico, C., Garibaldi, M., and Maggi, L.

Subjects
*INCLUSION body myositis, *OLDER people, *FLEXOR muscles, *MUSCLE diseases, *DISEASE duration
Abstract

Inclusion body myositis (IBM) is among the most frequent acquired muscle diseases in the adult and elderly population, with onset typically > 45 years old. IBM is characterized by initially selective weakness of the quadriceps and deep finger flexors muscles, with a slow generalization and progression of weakness over the patient's lifespan. Disease monitoring may be assessed through the validated "Inclusion body myositis functional rating scale" (IBM-FRS), assessing symptoms and functional limitations in a given moment. However, poor data have been reported on IBM-FRS and its correlation with clinical features in large cohorts of IBM patients. In this cross-sectional study, we investigated the correlation of IBM-FRS specific functional domains with demographic and clinical variables in a large group of IBM patients. The following domains were considered: 1. dysphagia (item 1); 2. arm function (items 2-4); 3. independence (items 5-7); 4. leg function (items 8-10). Overall, 123 patients were included, 41 females (33%), with median age at onset of 64 (range 28 – 83), with onset in 6 patients younger than 45 years old. Walking ability was lost in 13 (10.5%), non-invasive ventilation (NIV) was needed in 13 (10.5%) and percutaneous gastrostomy (PEG) in 7 (5.6%). At IBM-FRS scoring, median age was 74 (range 44-90) and median disease duration was 8 years (range 1-42). Median IBM-FRS total score was 25 (range 3-40). When analyzing specific domains, longer disease duration significantly correlated with domains 2 (p=0.038), 3 (p=0.031) and 4 (p<0.001); age at baseline correlated with groups 2 (p=0.029), 3 (p=0.05) and 4 (p=0.008). Domain 1 correlated with female gender (p=0.001), onset with dysphagia (p=0.025) and PEG (p<0.001). Loss of walking ability correlated with domains 2, 3 and 4 (all p<0.001). No correlation was found between specific domains and age at onset or NIV. Preliminary analysis identified correlations between specific domains of IBM-FRS and clinical variables with implications for patients' stratification. Further studies are needed to investigate longitudinal changes of IBM-FRS and its domains over time. [ABSTRACT FROM AUTHOR]

Published
2024
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