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Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patients
Okhovat AA, Nilipour Y, Boostani R, et al.
Neuromuscular disorders : NMD, 2021, 31, 1, p 29
Adult-onset Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD)
Fatehi F, Okhovat AA, Nilipour Y, et al.
European journal of neurology, 2020
Type 1 FSHD with 6-10 Repeated Units: Factors Underlying Severity in Index Cases and Disease Penetrance in Their Relatives Attention
Salort-Campana E, Fatehi F, Beloribi-Djefaflia S, et al.
International Journal of molecular sciences, 2020, 21, 6
Expanding the importance of HMERF titinopathy: new mutations and clinical aspects
Palmio J, Leonard-Louis S, Sacconi S, et al.
Journal of neurology, 2019, 266, 3, p 680
Hereditary neuropathy with liability to pressure palsies
Attarian S, Fatehi F, Rajabally YA, et al.
Journal of neurology, 2019
The utility of motor unit number index: A systematic review
Fatehi F, Fatehi F, Grapperon AM, et al.
Neurophysiologie clinique = Clinical neurophysiology, 2018, 48, 5, p 251
The third Iranian and the second joint French-Iranian neuromuscular meeting
Sinaei F, Fatehi F
Iranian journal of neurology, 2017, 16, 2, p 105
Late-onset Pompe disease in Iran, a clinical and genetic report
Nazari F, Sinaei F, Nilipour Y, et al.
Muscle & Nerve, 2017, 55, 6, p 835
Long-term follow-up of MRI changes in thigh muscles of patients with Facioscapulohumeral dystrophy: A quantitative study
Fatehi F, Salort-Campana E, Le Troter A, et al.
PLoS ONE, 2017, 12, 8
An international clinimetric evaluation of the MG-QOL15, resulting in slight revision and subsequent validation of the MG-QOL15r
Burns TM, Sadjadi R, Utsugisawa K, et al.
Muscle & Nerve, 2016, 54, 6, p 1015
Muscle MRI of facioscapulohumeral dystrophy (FSHD): A growing demand and a promising approach
Fatehi F, Salort-Campana E, Le Troter A, et al.
Revue neurologique, 2016, 172, 10, p 566
The Schwartz-Jampel syndrome: Case report and review of literature
Basiri K, Fatehi F, Katirij B
Adv Biomed Res, 2015, 4
Dysferlinopathy in Iran: Clinical and genetic report
Fatehi F, Nafissi S, Urtizberea JA, et al.
Journal of the neurological sciences, 2015, 359, 1-2, p 256
Myologie en Iran : des échanges privilégiés avec la France
Urtizberea JA, Fatehi F
Les Cahiers de Myologie, 2014, 10, p. 39-41
