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Limb-girdle muscular dystrophy type 2F
Known as:
LGMD2F
, Muscular Dystrophy, Limb-Girdle, Type 2F
, Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
National Institutes of Health
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Related topics
Related topics
5 relations
Autosomal recessive inheritance
Muscle Weakness
SGCD gene
Ventricular hypertrophy
Broader (1)
Sarcoglycanopathies
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Chronic oral administration of Ang-(1-7) improves skeletal muscle, autonomic and locomotor phenotypes in muscular dystrophy.
R. Sabharwal
,
M. Cicha
,
R. Sinisterra
,
F. D. de Sousa
,
Robson A S Santos
,
M. Chapleau
Clinical science
2014
Corpus ID: 2901548
Muscular dystrophies are a group of heterogeneous genetic disorders that cause progressive muscle weakness and wasting, dilated…
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2014
2014
Limb-Girdle Muscular Dystrophy Type 2F
C. Angelini
2014
Corpus ID: 73764185
LGMD2F is clinically characterized by limb-girdle weakness, cardiomyopathy, and respiratory impairment. Since it is caused by…
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Review
2004
Review
2004
[Limb-girdle muscular dystrophy; update].
Y. Sunada
Rinshō shinkeigaku Clinical neurology
2004
Corpus ID: 32768701
Sixteen different forms of limb-girdle muscular dystrophies (LGMDs) have emerged from recent molecular genetic studies, six forms…
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2004
2004
Klinik und Genetik der Gliedergürteldystrophien
J. Finsterer
Der Nervenarzt
2004
Corpus ID: 9809532
ZusammenfassungGliedergürteldystrophien (limb girdle muscular dystrophies, LGMD) sind genetisch heterogene, primäre Myopathien…
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Review
2003
Review
2003
Molecular bases of autosomal recessive limb-girdle muscular dystrophies.
V. Nigro
Acta myologica
2003
Corpus ID: 27101127
Limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of genetically determined disorders with a primary or…
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1999
1999
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin–glycoprotein complex
M. Vainzof
,
E. Moreira
,
G. Ferraz
,
M. Passos-Bueno
,
S. Marie
,
M. Zatz
European Journal of Human Genetics
1999
Corpus ID: 19922414
Based on the pattern of distribution of the SG proteins in patients with LGMD2C and 2D, and on the observed decreased abundance…
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Highly Cited
1997
Highly Cited
1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).
A. Carrié
,
F. Piccolo
,
+15 authors
M. Jeanpierre
Journal of Medical Genetics
1997
Corpus ID: 30620069
Sarcoglycanopathies are a genetically heterogeneous group of autosomal recessive muscular dystrophies in which the primary defect…
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Review
1997
Review
1997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey
P. Dincer
,
F. Leturcq
,
+16 authors
Haluk Topaloàlu
Annals of Neurology
1997
Corpus ID: 28524591
Autosomal recessive limb girdle muscular dystrophy (LGMD2) is a clinically and genetically heterogenous group of diseases…
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