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Start Over Author "Shahram Attarian" Journal neuromuscular disorders
7 results on '"Shahram Attarian"'

1. 254th ENMC international workshop. Formation of a European network to initiate a European data collection, along with development and sharing of treatment guidelines for adult SMA patients. Virtual meeting 28 – 30 January 2022

Author

Maggie C. Walter, Pascal Laforêt, W. Ludo van der Pol, Elena Pegoraro, Shahram Attarian, Bart Bartels, Ksenija Gorni, Nathalie Goemans, Nicole Gusset, Victoria Hodgkinson, Tim Hagenacker, Janbernd Kirschner, Andrea Klein, Anna Kostera-Pruszczyk, Hanns Lochmüller, Chiara Marini-Bettolo, Eugenio Mercuri, Robert Muni-Lofra, Laetitia Ouillade, Rosaline Quinlivan, Constantinos Papadopoulos, Hélène Prigent, Emmanuelle Salort-Campana, Valeria A Sansone, Rivka Smit, Piera Smeriglio, Simone Thiele, Ben Tichler, Peter Van den Bergh, Juan F Vazquez-Costa, and John Vissing

Subjects
Neurology, Pediatrics, Perinatology and Child Health, Medizin, Neurology (clinical), Genetics (clinical)
Published
2023

2. 265th ENMC International Workshop: Muscle imaging in Facioscapulohumeral Muscular Dystrophy (FSHD): relevance for clinical trials. 22-24 April 2022, Hoofddorp, The Netherlands

Author

Mauro Monforte, Shahram Attarian, John Vissing, Jordi Diaz-Manera, Giorgio Tasca, Raj Badiani, David Bendahan, Pierre Carlier, Robert-Yves Carlier, Olof Dahlqvist Leinhard, Roberto Fernandez-Torron, Teresa Gerhalter, Linda Heskamp, Hermien Kan, Doris Leung, Aurea Martins-Bach, Kisten Meiburger, Anna Pichiecchio, Michal Rataj, Sabrina Sacconi, Francesco Santini, Nens van Alfen, Sanne Vincenten, and Nicol Voermans

Subjects
Neurology, Pediatrics, Perinatology and Child Health, Neurology (clinical), Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Genetics (clinical)
Abstract

Item does not contain fulltext

Published
2023

3. Expanding importance of HMERF titinopathy: new mutations and clinical aspects

Author

A. Semmler, B. Udd, Wolfram Kress, Shahram Attarian, Ricardo Reisin, Sabrina Sacconi, Andoni Urtizberea, T. Stojkovic, Marco Savarese, Peter Hackman, Tahseen Mozaffar, A. Berardo, Johanna Palmio, Maggie C. Walter, J.E. Bach, T. Lai, S. Leonard, Farzad Fatehi, and Benedikt Schoser

Subjects
0301 basic medicine, business.industry, Computational biology, 030105 genetics & heredity, Bioinformatics, 03 medical and health sciences, 0302 clinical medicine, Neurology, Pediatrics, Perinatology and Child Health, Medicine, Neurology (clinical), business, 030217 neurology & neurosurgery, Genetics (clinical)
Published
2017

4. ActiMyo home monitoring in adult patients with limb girdle muscular dystrophy type 2B and facioscapulohumeral muscular dystrophy in study ATYR 1940-C-004

Author

Kathryn R. Wagner, Tahseen Mozaffar, A. Richiardi, Amélie Moraux, Shahram Attarian, L. Servais, G. Walker, Stanley Iyadurai, S. Shukla, M. Grelet, John Vissing, David Vissiere, M. Villeret, M. Annoussamy, Teresa Gidaro, and E. Gasnier

Subjects
Neurology, Adult patients, business.industry, Pediatrics, Perinatology and Child Health, Medicine, Facioscapulohumeral muscular dystrophy, Neurology (clinical), Anatomy, business, medicine.disease, Genetics (clinical), Limb-girdle muscular dystrophy
Published
2017

5. A randomized, double-blinded, placebo-controlled, multiple ascending dose study to evaluate the safety, tolerability, pharmacokinetics, immunogenicity, and biological activity of ATYR1940 in adult patients with facioscapulohumeral muscular dystrophy (FSHD)

Author

Arend Heerschap, E. Campana-Salort, A. Gershman, C. Audebert, M. Ashlock, Hermien E. Kan, K. Chiang, M. Do, L. Carey, V. Harbers, Stanley Iyadurai, Linda Heskamp, J. Mendlein, E. Abbink, Mauro Monforte, K. Blackburn, Shahram Attarian, Enzo Ricci, and John T. Kissel

Subjects
0301 basic medicine, medicine.medical_specialty, Adult patients, Double blinded, business.industry, Immunogenicity, Biological activity, Safety tolerability, 030105 genetics & heredity, medicine.disease, Placebo, 03 medical and health sciences, 0302 clinical medicine, Neurology, Pharmacokinetics, Internal medicine, Pediatrics, Perinatology and Child Health, medicine, Physical therapy, Facioscapulohumeral muscular dystrophy, Neurology (clinical), business, 030217 neurology & neurosurgery, Genetics (clinical)
Published
2016

6. M.P.2.13 The French Pompe registry: A prospective clinical survey of patients with late onset Pompe disease in France

Author

Shahram Attarian, T. Stojkovic, Claude Desnuelle, Jean Pouget, V. Doppler, Bruno Eymard, David Orlikowski, Pierre Labauge, Léonard Féasson, C. Vincitorio, N. Pellegrini, P. Laforêt, M. Minot-Myhe, C. Payant, Isabelle Pénisson-Besnier, Sabrina Sacconi, and Fabien Zagnoli

Subjects
Pediatrics, medicine.medical_specialty, Neurology, business.industry, Pediatrics, Perinatology and Child Health, Medicine, Late onset, Neurology (clinical), Disease, business, Genetics (clinical)
Published
2007

7. G.P.7.07 Efficacy and safety of salbutamol in the treatment of facioscapulohumeral muscular dystrophy

Author

P. Laforêt, J.Y. Hogrel, Jean Pouget, Claude Desnuelle, V. Doppler, Gwenn Ollivier, Bruno Eymard, C. Payant, and Shahram Attarian

Subjects
medicine.medical_specialty, business.industry, medicine.disease, Gastroenterology, Neurology, Internal medicine, Pediatrics, Perinatology and Child Health, medicine, Salbutamol, Facioscapulohumeral muscular dystrophy, Neurology (clinical), business, Genetics (clinical), medicine.drug
Published
2007

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