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S K Marie

Showing results (31-40 of 45) with videos related to

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Brain & Development|July 7, 1999
Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardationU C Reed, A M Tsanaclis, M Vainzof, et al.
Genomics|May 1, 1995
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionM R Passos-Bueno, R Bashir, E S Moreira, et al.
Human Molecular Genetics|July 1, 1995
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyM R Bueno, E S Moreira, M Vainzof, et al.
Revista Do Hospital Das Clinicas|May 2, 2000
Primary biliary cirrhosis and myopathy: an uncommon associationB C Migueletto, A E Neto, E Z Domingues, et al.
Japanese Journal of Cancer Research : Gann|November 21, 2001
Helicobacter pylori seropositivity among 963 Japanese Brazilians according to sex, age, generation, and lifestyle factorsL S Ito, S M Oba, N Hamajima, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
A Caucasian family with the 3271 mutation in mitochondrial DNAS K Marie, Y Goto, M R Passos-Bueno, et al.
Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, 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 casesU C Reed, S K Marie, M Vainzof, 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.
Journal of Medical Genetics|February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian familiesM R Passos-Bueno, E S Moreira, S K Marie, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Brain & Development|July 7, 1999
Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardationU C Reed, A M Tsanaclis, M Vainzof, et al.
Genomics|May 1, 1995
Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionM R Passos-Bueno, R Bashir, E S Moreira, et al.
Human Molecular Genetics|July 1, 1995
A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyM R Bueno, E S Moreira, M Vainzof, et al.
Revista Do Hospital Das Clinicas|May 2, 2000
Primary biliary cirrhosis and myopathy: an uncommon associationB C Migueletto, A E Neto, E Z Domingues, et al.
Japanese Journal of Cancer Research : Gann|November 21, 2001
Helicobacter pylori seropositivity among 963 Japanese Brazilians according to sex, age, generation, and lifestyle factorsL S Ito, S M Oba, N Hamajima, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
A Caucasian family with the 3271 mutation in mitochondrial DNAS K Marie, Y Goto, M R Passos-Bueno, et al.
Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, 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 casesU C Reed, S K Marie, M Vainzof, 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.
Journal of Medical Genetics|February 1, 1996
Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian familiesM R Passos-Bueno, E S Moreira, S K Marie, et al.
Pageof 5