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Results:
1-18
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Results: 18
Authors:
BRAIS B
Citation: B. Brais, SHORT GCG EXPANSIONS IN THE PABP2 GENE CAUSE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (VOL 18, PG 164, 1998), Nature genetics, 19(4), 1998, pp. 404-404
Authors:
BRAIS B
BOUCHARD JP
XIE YG
ROCHEFORT DL
CHRETIEN N
TOME FMS
LAFRENIERE RG
ROMMENS JM
UYAMA E
NOHIRA O
BLUMEN S
KORCYN AD
HEUTINK P
MATHIEU J
DURANCEAU A
CODERE F
FARDEAU M
ROULEAU GA
Citation: B. Brais et al., SHORT GCG EXPANSIONS IN THE PABP2 GENE CAUSE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY, Nature genetics, 18(2), 1998, pp. 164-167
Authors:
XIE YG
ROCHEFORT D
BRAIS B
HOWARD H
HAN FY
GOU LP
MACIEL P
THE BT
LARSSON C
ROULEAU GA
Citation: Yg. Xie et al., RESTRICTION MAP OF A YAC AND COSMID CONTIG ENCOMPASSING THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY CANDIDATE REGION ON CHROMOSOME 14Q11.2-Q13, Genomics (San Diego, Calif.), 52(2), 1998, pp. 201-204
Authors:
BRAIS B
BOUCHARD JP
TOME FMS
FARDEAU M
CODERE F
DURANCEAU A
ROULEAU GA
Citation: B. Brais et al., GENETIC-EVIDENCE FOR THE INVOLVEMENT OF OTHER GENES IN MODULATING THESEVERITY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY, Annals of neurology, 44(3), 1998, pp. 59-59
Authors:
UYAMA E
BRAIS B
NOHIRA O
TOKUNAGA M
CHATEAU D
TOME FMS
ROULEAU GA
UCHINO M
Citation: E. Uyama et al., OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - PHENOTYPE GENOTYPE DIFFERENCE IN2 UNRELATED JAPANESE FAMILIES/, Annals of neurology, 44(3), 1998, pp. 146-146
Authors:
FEIT H
SILBERGLEIT A
SCHNEIDER LB
GUTIERREZ JA
ROULEAU GA
BRAIS B
JACKSON CE
Citation: H. Feit et al., AUTOSOMAL-DOMINANT DISTAL MYOPATHY WITH PHARYNGEAL AND VOCAL CORD WEAKNESS, Neurology, 50(4), 1998, pp. 4011-4011
Authors:
BOUCHARD JP
BRAIS B
BRUNET D
GOULD PV
ROULEAU GA
Citation: Jp. Bouchard et al., RECENT STUDIES ON OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN QUEBEC, Neuromuscular disorders, 7, 1997, pp. 22-29
Authors:
BRAIS B
BOUCHARD JP
GOSSELIN F
XIE YG
FARDEAU M
TOME FMS
ROULEAU GA
Citation: B. Brais et al., USING THE FULL POWER OF LINKAGE ANALYSIS IN 11 FRENCH-CANADIAN FAMILIES TO FINE MAP THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY GENE, Neuromuscular disorders, 7, 1997, pp. 70-74
Authors:
MATHIEU J
LAPOINTE G
BRASSARD A
TREMBLAY C
BRAIS B
ROULEAU GA
BOUCHARD JP
Citation: J. Mathieu et al., A PILOT-STUDY ON UPPER ESOPHAGEAL SPHINCTER DILATATION FOR THE TREATMENT OF DYSPHAGIA IN PATIENTS WITH OCULOPHARYNGEAL MUSCULAR-DYSTROPHY, Neuromuscular disorders, 7, 1997, pp. 100-104
Authors:
NEETENS A
MARTIN JJ
BRAIS B
WEIN B
DREUW B
TIJSSEN CC
CEUTERICK C
Citation: A. Neetens et al., OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD), Neuro-ophthalmology, 17(4), 1997, pp. 189-200
Authors:
KIBAR Z
DERKALOUSTIAN VM
BRAIS B
HANI V
FRASER FC
ROULEAU GA
Citation: Z. Kibar et al., THE GENE RESPONSIBLE FOR CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA MAPS TO THE PERICENTROMERIC REGION OF CHROMOSOME 13Q, Human molecular genetics, 5(4), 1996, pp. 543-547
Authors:
UYAMA E
NOHIRA O
BRAIS B
TOME FMS
TOKUNAGA M
OKABE T
ROULEAU GA
CHATEAU D
UCHINO M
Citation: E. Uyama et al., OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN JAPANESE - CLINICOPATHOLOGICAL AND GENETIC-STUDIES, Annals of neurology, 40(6), 1996, pp. 1-1
Authors:
BRAIS B
TOME FMS
FARDEAU M
XIE YG
ROULEAU GA
BOUCHARD JP
Citation: B. Brais et al., THE NATURAL-HISTORY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY BASED ON THE STUDY OF A LARGE COHORT OF FRENCH-CANADIAN MUTATION CARRIERS, Neurology, 46(2), 1996, pp. 4083-4083
Authors:
BRAIS B
XIE YG
SANSON M
MORGAN K
WEISSENBACH J
KORCZYN AD
BLUMEN SC
FARDEAU M
TOME FMS
BOUCHARD JP
ROULEAU GA
Citation: B. Brais et al., THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY LOCUS MAPS TO THE REGION OF THE CARDIAC ALPHA-MYOSIN AND BETA-MYOSIN HEAVY-CHAIN GENES ON CHROMOSOME14Q11.2-Q13, Human molecular genetics, 4(3), 1995, pp. 429-434
Authors:
BRAIS B
BOUCHARD JP
XIE YG
TOME FMS
FARDEAU M
ROULEAU GA
Citation: B. Brais et al., A MORE SEVERE FORM OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD) IS DOCUMENTED IN A GENETICALLY PROVEN HOMOZYGOUS PATIENT, Neurology, 45(4), 1995, pp. 243-243
Authors:
BRAIS B
MORGAN K
XIE Y
TOME FMS
FARDEAU M
BOUCHARD JP
ROULEAU GA
Citation: B. Brais et al., STRONG LINKAGE DISEQUILIBRIUM SUGGEST ONE FOUNDER MUTATION IS RESPONSIBLE FOR ALL CASES OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD) IN THEFRENCH-CANADIAN POPULATION, American journal of human genetics, 57(4), 1995, pp. 910-910
Authors:
BRAIS B
Citation: B. Brais, CHARCOT,JEAN,MARTIN AND APHASIA - TREADING THE LINE BETWEEN EXPERIMENTAL PHYSIOLOGY AND PATHOLOGICAL ANATOMY, Brain and language, 45(4), 1993, pp. 511-530
Authors:
BRAIS B
ROULEAU GA
SANSON M
GOSSELIN F
BOUCHARD JP
Citation: B. Brais et al., OCULOPHARYNGEAL MUSCULAR-DYSTROPHY REVISITED - DIAGNOSTIC-CRITERIA AND VARIABILITY IN PHENOTYPE, Neurology, 43(4), 1993, pp. 201-201
Risultati:
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