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Human Molecular Genetics
|
May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markers
M R Passos-Bueno, C Wijmenga, R E Takata, et al.
Journal of Molecular Neuroscience : MN
|
October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophies
M Vainzof, L V Anderson, E M McNally, et al.
American Journal of Medical Genetics
|
April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Journal of Child Neurology
|
April 11, 2000
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases
U C Reed, S K Marie, M Vainzof, et al.
Nature Genetics
|
February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin
E S Moreira, T J Wiltshire, G Faulkner, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization
C Rosenberg, L Navajas, D F Vagenas, et al.
Cell Transplantation
|
November 22, 2012
Human adipose-derived mesenchymal stromal cells injected systemically into GRMD dogs without immunosuppression are able to reach the host muscle and express human dystrophin
N M Vieira, M Valadares, E Zucconi, et al.
Stem Cell Reviews and Reports
|
June 20, 2014
Human adipose tissue derived pericytes increase life span in Utrn (tm1Ked) Dmd (mdx) /J mice
M C Valadares, J P Gomes, G Castello, et al.
Human Molecular Genetics
|
December 1, 1996
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)
C G Bönnemann, M R Passos-Bueno, E M McNally, et al.
Neuromuscular Disorders : NMD
|
March 16, 2015
A normal life without muscle dystrophin
M Zatz, N M Vieira, E Zucconi, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 85) with videos related to
Sort By:
Page
of 9
Human Molecular Genetics
|
May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markers
M R Passos-Bueno, C Wijmenga, R E Takata, et al.
Journal of Molecular Neuroscience : MN
|
October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophies
M Vainzof, L V Anderson, E M McNally, et al.
American Journal of Medical Genetics
|
April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
M R Passos-Bueno, B C Byth, S Rosenberg, et al.
Journal of Child Neurology
|
April 11, 2000
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases
U C Reed, S K Marie, M Vainzof, et al.
Nature Genetics
|
February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin
E S Moreira, T J Wiltshire, G Faulkner, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization
C Rosenberg, L Navajas, D F Vagenas, et al.
Cell Transplantation
|
November 22, 2012
Human adipose-derived mesenchymal stromal cells injected systemically into GRMD dogs without immunosuppression are able to reach the host muscle and express human dystrophin
N M Vieira, M Valadares, E Zucconi, et al.
Stem Cell Reviews and Reports
|
June 20, 2014
Human adipose tissue derived pericytes increase life span in Utrn (tm1Ked) Dmd (mdx) /J mice
M C Valadares, J P Gomes, G Castello, et al.
Human Molecular Genetics
|
December 1, 1996
Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)
C G Bönnemann, M R Passos-Bueno, E M McNally, et al.
Neuromuscular Disorders : NMD
|
March 16, 2015
A normal life without muscle dystrophin
M Zatz, N M Vieira, E Zucconi, et al.
Page
of 9