Suchergebnisse - "Jain, Minal S"

PubPharm (7)

1

A Cross-Sectional Study of Nemaline Myopathy

enthalten in: Neurology | 2021

von Amburgey, K. | Acker, M. | Saeed, S. | +20

2

Biallelic loss of function variants in SYT2 cause a treatable congenital onset presynaptic myasthenic syndrome

enthalten in: American journal of medical genetics. Part A | 2020

von Donkervoort, S. | Mohassel, P. | Laugwitz, L. | +26

3

6-minute walk test as a measure of disease progression and fatigability in a cohort of individuals with RYR1-related myopathies

enthalten in: Orphanet journal of rare diseases | 2018

von Witherspoon, J. | Vasavada, R. | Waite, M. | +6

4

A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome

enthalten in: Nature communications | 2017

von Di Gioia, S. | Connors, S. | Matsunami, N. | +68

5

Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies

enthalten in: Neuromuscular disorders : NMD | 2015

von Meilleur, K. | Jain, M. | Hynan, L. | +30

6

Novel assessment tools to evaluate clinical and laboratory responses in a subset of patients enrolled in the Rituximab in Myositis trial

enthalten in: Clinical and experimental rheumatology | 2014

von Rider, L. | Yip, A. | Horkayne-Szakaly, I. | +9

7

Damage extent and predictors in adult and juvenile dermatomyositis and polymyositis as determined with the myositis damage index

enthalten in: Arthritis and rheumatism | 2009

von Rider, L. | Lachenbruch, P. | Monroe, J. | +25

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