Results 151 to 160 of about 484,924 (172)

Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene. [PDF]

open access: yesBrain, 2013
In 2001, we reported linkage of an autosomal dominant form of limb-girdle muscular dystrophy, limb-girdle muscular dystrophy 1F, to chromosome 7q32.1-32.2, but the identity of the mutant gene was elusive.
Josep Gámez   +2 more
exaly   +2 more sources

Prevalence of chronic pain in a national cohort of patients with limb-girdle muscular dystrophy: a cross-sectional study

Disability and Rehabilitation, 2022
Lone Knudsen   +2 more
exaly  

Ayurvedic management in limb girdle muscular dystrophy – A case report

Journal of Ayurveda and Integrative Medicine, 2022
Kshipra Rajoria, Sarvesh Kumar Singh
exaly  

Allosteric Modulation of GSK-3β as a New Therapeutic Approach in Limb Girdle Muscular Dystrophy R1 Calpain 3-Related

International Journal of Molecular Sciences, 2021
Amets Saenz, Valle Palomo, Ana Martínez
exaly  

Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP related

Muscle and Nerve, 2020
Eric M Libell, Bridget M Zimmerman
exaly  

Long-term clinical and MRI follow-up in two POMT2-related limb girdle muscular dystrophy (LGMDR14) patients

Brain and Development, 2023
Federico Zara   +2 more
exaly  

Limb-girdle muscular dystrophy type 2I: two Chinese families and a review in Asian patients

International Journal of Neuroscience, 2018
Dan-Ni Wang, Guo-Rong Xu, Min-Ting Lin
exaly  

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