Results 221 to 230 of about 12,800 (285)

Muscle MRI in patients with dysferlinopathy: Pattern recognition and implications for clinical trialP [PDF]

, 2018
et al,, Harms, Matthew, Pestronk, Alan
core   +1 more source

A Clinical Study on the Utility of Muscle Biopsy in Patients with Suspected Myopathy. [PDF]

Ann Indian Acad Neurol
Karunakaran S, Kuruvilla A, Nair M, Nair SS, Narasimhaiah D.   +4 more
europepmc   +1 more source

Genetic and Structural Variations in Czech Patients With Congenital Myopathies. [PDF]

Clin Genet
Zídková J, Lauerová B, Mensová L, Kramářová T, Kopčilová J, Réblová K, Soukup Vodičková M, Hujňáková M, Haberlová J, Rohlenová M, Mazanec R, Šoukalová J, Gaillyová R, Vyhnálková E, Balaščaková M, Danhofer P, Juříková L, Grečmalová D, Gřegořová A, Plevová P, Langová M, Honzík T, Magner M, Klincová M, Solařová P, Šenkeříková M, Fajkusová L.   +26 more
europepmc   +1 more source

Dysferlinopathy as cause of long-term hyperCKemia with preserved strength. [PDF]

Orphanet J Rare Dis
Cheema I, Goodwin J, Liewluck T, Bucelli RC, Pestronk A, Milone M.   +5 more
europepmc   +1 more source

Multimodal Evaluation of Bethlem Myopathy with the c.788G > A Variant in the COL6A1 Gene: a case report with genetic, ultrasonographic, and structural-functional discordance correlations. [PDF]

Acta Myol
Herrera Malpica WS, Gómez JC, Ortiz-Corredor F, Hernández PVM, Correa-Arrieta C.   +4 more
europepmc   +1 more source