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Year Number of Results
1952 1
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1955 2
1956 3
1957 1
1961 1
1962 1
1963 2
1966 2
1968 3
1969 2
1971 3
1972 1
1973 4
1974 6
1975 8
1976 10
1977 11
1978 5
1979 8
1980 6
1981 8
1982 8
1983 12
1984 9
1985 16
1986 6
1987 13
1988 12
1989 21
1990 13
1991 21
1992 19
1993 30
1994 23
1995 39
1996 48
1997 47
1998 59
1999 57
2000 68
2001 62
2002 53
2003 85
2004 80
2005 101
2006 86
2007 98
2008 103
2009 98
2010 113
2011 121
2012 123
2013 147
2014 144
2015 163
2016 153
2017 137
2018 157
2019 155
2020 151
2021 162
2022 173
2023 164
2024 50

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3,180 results

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Page 1
Limb-girdle Muscular Dystrophy and Therapy: Insights into Cell and Gene-based Approaches.
Taheri F, Taghizadeh E, Pour MJR, Rostami D, Renani PG, Rastgar-Moghadam A, Hayat SMG. Taheri F, et al. Curr Gene Ther. 2020;19(6):386-394. doi: 10.2174/1566523220666200218113526. Curr Gene Ther. 2020. PMID: 32067617 Review.
The Limb-Girdle Muscular Dystrophies (LGMD) are genetically heterogeneous disorders, responsible for muscle wasting and severe form of dystrophies. Despite the critical developments in the insight and information of pathomechanisms of limb …
The Limb-Girdle Muscular Dystrophies (LGMD) are genetically heterogeneous disorders, responsible for muscle wast …
Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations.
Lasa-Elgarresta J, Mosqueira-Martín L, Naldaiz-Gastesi N, Sáenz A, López de Munain A, Vallejo-Illarramendi A. Lasa-Elgarresta J, et al. Int J Mol Sci. 2019 Sep 13;20(18):4548. doi: 10.3390/ijms20184548. Int J Mol Sci. 2019. PMID: 31540302 Free PMC article. Review.
Limb-girdle muscular dystrophy recessive 1 (LGMDR1), previously known as LGMD2A, is a rare disease caused by mutations in the CAPN3 gene. ...These novel approaches may be clinically relevant not only for LGMDR1 but also for other muscular dys …
Limb-girdle muscular dystrophy recessive 1 (LGMDR1), previously known as LGMD2A, is a rare disease caused by mut …
Limb-girdle muscular dystrophy type 2I: two Chinese families and a review in Asian patients.
Wang DN, Wang ZQ, Chen YQ, Xu GR, Lin MT, Wang N. Wang DN, et al. Int J Neurosci. 2018 Mar;128(3):199-207. doi: 10.1080/00207454.2017.1380640. Epub 2017 Oct 2. Int J Neurosci. 2018. PMID: 28931339 Review.
BACKGROUND: Limb-girdle muscular dystrophy type 2I (LGMD2I) is an autosomal recessive hereditary disorder caused by mutations in the fukutin-related protein (FKRP) gene. ...
BACKGROUND: Limb-girdle muscular dystrophy type 2I (LGMD2I) is an autosomal recessive hereditary disorder caused …
Limb-Girdle Muscular Dystrophy 2B and Miyoshi Presentations of Dysferlinopathy.
Patel NJ, Van Dyke KW, Espinoza LR. Patel NJ, et al. Am J Med Sci. 2017 May;353(5):484-491. doi: 10.1016/j.amjms.2016.05.024. Epub 2016 May 30. Am J Med Sci. 2017. PMID: 28502335 Review.
We report the following 2 subtypes of progressive limb-girdle dystrophy type 2B: limb-girdle muscular dystrophy type 2B (LGMD2B) and Miyoshi. ...
We report the following 2 subtypes of progressive limb-girdle dystrophy type 2B: limb-girdle muscular …
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients.
Ten Dam L, Frankhuizen WS, Linssen WHJP, Straathof CS, Niks EH, Faber K, Fock A, Kuks JB, Brusse E, de Coo R, Voermans N, Verrips A, Hoogendijk JE, van der Pol L, Westra D, de Visser M, van der Kooi AJ, Ginjaar I. Ten Dam L, et al. Clin Genet. 2019 Aug;96(2):126-133. doi: 10.1111/cge.13544. Epub 2019 May 6. Clin Genet. 2019. PMID: 30919934
In this retrospective study, we conducted a clinico-genetic analysis of patients with autosomal recessive limb-girdle muscular dystrophy (LGMD) and Miyoshi muscular dystrophy (MMD). ...
In this retrospective study, we conducted a clinico-genetic analysis of patients with autosomal recessive limb-girdle muscu …
[Research advances in limb-girdle muscular dystrophy type 2Q].
Zhang M, Lan D. Zhang M, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2019 Aug;21(8):839-844. doi: 10.7499/j.issn.1008-8830.2019.08.019. Zhongguo Dang Dai Er Ke Za Zhi. 2019. PMID: 31416513 Free PMC article. Review. Chinese.
Limb-girdle muscular dystrophy (LGMD) is a group of muscular dystrophies with predominantly proximal muscular weakness, and some genes associated with this disease have been identified at present. ...Major phenotypes of PLEC gene m …
Limb-girdle muscular dystrophy (LGMD) is a group of muscular dystrophies with predominantly proxim …
Muscular Dystrophies.
Carter JC, Sheehan DW, Prochoroff A, Birnkrant DJ. Carter JC, et al. Clin Chest Med. 2018 Jun;39(2):377-389. doi: 10.1016/j.ccm.2018.01.004. Clin Chest Med. 2018. PMID: 29779596 Review.
Muscular dystrophies represent a complex, varied, and important subset of neuromuscular disorders likely to require the care of a pulmonologist. The spectrum of conditions encapsulated by this subset ranges from severe and fatal congenital muscular dystrop …
Muscular dystrophies represent a complex, varied, and important subset of neuromuscular disorders likely to require the care o …
Electroretinogram abnormalities in FKRP-related limb-girdle muscular dystrophy (LGMDR9).
Hagedorn JL, Dunn TM, Bhattarai S, Stephan C, Mathews KD, Pfeifer W, Drack AV. Hagedorn JL, et al. Doc Ophthalmol. 2023 Feb;146(1):7-16. doi: 10.1007/s10633-022-09909-4. Epub 2022 Nov 18. Doc Ophthalmol. 2023. PMID: 36399172
BACKGROUND: Dystroglycanopathies are a heterogeneous group of membrane-related muscular dystrophies. The dystroglycanopathy phenotype includes a spectrum of severity ranging from severe congenital muscular dystrophy to adult-onset limb-girdle …
BACKGROUND: Dystroglycanopathies are a heterogeneous group of membrane-related muscular dystrophies. The dystroglycanopathy ph …
Limb-girdle muscular dystrophy-associated protein diseases.
Broglio L, Tentorio M, Cotelli MS, Mancuso M, Vielmi V, Gregorelli V, Padovani A, Filosto M. Broglio L, et al. Neurologist. 2010 Nov;16(6):340-52. doi: 10.1097/NRL.0b013e3181d35b39. Neurologist. 2010. PMID: 21150381 Review.
The limb-girdle muscular dystrophies are a genetically and clinically heterogeneous group of diseases. Most of these proteinopathies show wide inter- and intrafamilial phenotypic heterogeneity, so that limb-girdle involvement may be often …
The limb-girdle muscular dystrophies are a genetically and clinically heterogeneous group of diseases. Most of t …
Limb-girdle muscular dystrophy due to GMPPB mutations: A case report and comprehensive literature review.
Sun L, Shen D, Xiong T, Zhou Z, Lu X, Cui F. Sun L, et al. Bosn J Basic Med Sci. 2020 May 1;20(2):275-280. doi: 10.17305/bjbms.2019.3992. Bosn J Basic Med Sci. 2020. PMID: 30684953 Free PMC article. Review.
Herein, we reported a case of a 29-year-old Chinese male presenting with limb-girdle muscular dystrophy (LGMD) who was found to have two heterozygous GMPPB mutations. The patient had a progressive limb weakness for 19 years. His parents and elde …
Herein, we reported a case of a 29-year-old Chinese male presenting with limb-girdle muscular dystrophy (LGMD) w …
3,180 results

Searches related to "limb-girdle muscular dystrophy"