AAAAAA

   
Results: 1-25 | 26-26
Results: 1-25/26
SEGREGATION OF A MISSENSE MUTATION IN THE MICROTUBULE-ASSOCIATED PROTEIN-TAU GENE WITH FAMILIAL FRONTOTEMPORAL DEMENTIA AND PARKINSONISM
Authors: DUMANCHIN C CAMUZAT A CAMPION D VERPILLAT P HANNEQUIN D DUBOIS B SAUGIERVEBER P MARTIN C PENET C CHARBONNIER F AGID Y FREBOURG T BRICE A
Citation: C. Dumanchin et al., SEGREGATION OF A MISSENSE MUTATION IN THE MICROTUBULE-ASSOCIATED PROTEIN-TAU GENE WITH FAMILIAL FRONTOTEMPORAL DEMENTIA AND PARKINSONISM, Human molecular genetics (Print), 7(11), 1998, pp. 1825-1829
APOLIPOPROTEIN-E GENOTYPE IN FAMILIAL PARKINSONS-DISEASE
Authors: DURR A MEDJBEUR S DIDIERJEAN O VIDAILHET M BONNET AM GRID D PENET C BRICE A AGID Y MARTINEZ M FEINGOLD J AMOUYEL P BORG M BROUSSOLLE E DESTEE A DURIF F FENELON G FEVE JR POLLAK P RASCOL O TISON F TRANCHANT C WARTER JM VERIN M VIALLET F
Citation: A. Durr et al., APOLIPOPROTEIN-E GENOTYPE IN FAMILIAL PARKINSONS-DISEASE, Journal of Neurology, Neurosurgery and Psychiatry, 63(3), 1997, pp. 394-395
NO EFFECT OF THE ALPHA-1-ANTICHYMOTRYPSIN-A ALLELE IN ALZHEIMERS-DISEASE
Authors: DIDIERJEAN O MARTINEZ M CAMPION D HANNEQUIN D DUBOIS B MARTIN C PUEL M ANTERION CT PASQUIER F MOREAU O BABRON MC PENET C AGID Y CLERGETDARPOUX F FREBOURG T BRICE A
Citation: O. Didierjean et al., NO EFFECT OF THE ALPHA-1-ANTICHYMOTRYPSIN-A ALLELE IN ALZHEIMERS-DISEASE, Journal of Neurology, Neurosurgery and Psychiatry, 63(1), 1997, pp. 103-105
APOLIPOPROTEIN-E AND ALZHEIMER-DISEASE - GENOTYPE-SPECIFIC RISKS BY AGE AND SEX
Authors: BICKEBOLLER H CAMPION D BRICE A AMOUYEL P HANNEQUIN D DIDIERJEAN O PENET C MARTIN C PEREZTUR J MICHON A DUBOIS B LEDOZE F THOMASANTERION C PASQUIER F PUEL M DEMONET JF MOREAUD O BABRON MC MEULIEN D GUEZ D CHARTIERHARLIN MC FREBOURG T AGID Y MARTINEZ M CLERGETDARPOUX F
Citation: H. Bickeboller et al., APOLIPOPROTEIN-E AND ALZHEIMER-DISEASE - GENOTYPE-SPECIFIC RISKS BY AGE AND SEX, American journal of human genetics, 60(2), 1997, pp. 439-446
A NOVEL PRESENILIN-1 MUTATION RESULTING IN FAMILIAL ALZHEIMERS-DISEASE WITH AN ONSET AGE OF 29 YEARS
Authors: CAMPION D BRICE A DUMANCHIN C PUEL M BAULAC M DELASAYETTE V HANNEQUIN D DUYCKAERTS C MICHON A MARTIN C MOREAU V PENET C MARTINEZ M CLERGETDARPOUX F AGID Y FREBOURG T
Citation: D. Campion et al., A NOVEL PRESENILIN-1 MUTATION RESULTING IN FAMILIAL ALZHEIMERS-DISEASE WITH AN ONSET AGE OF 29 YEARS, NeuroReport, 7(10), 1996, pp. 1582-1584
SPINOCEREBELLAR ATAXIA-3 AND MACHADO-JOSEPH DISEASE - CLINICAL, MOLECULAR, AND NEUROPATHOLOGICAL FEATURES
Authors: DURR A STEVANIN G CANCEL G DUYCKAERTS C ABBAS N DIDIERJEAN O CHNEIWEISS H BENOMAR A LYONCAEN O JULIEN J SERDARU M PENET C AGID Y BRICE A
Citation: A. Durr et al., SPINOCEREBELLAR ATAXIA-3 AND MACHADO-JOSEPH DISEASE - CLINICAL, MOLECULAR, AND NEUROPATHOLOGICAL FEATURES, Annals of neurology, 39(4), 1996, pp. 490-499
CLINICAL AND GENETIC ABNORMALITIES IN PATIENTS WITH FRIEDREICHS ATAXIA
Authors: DURR A COSSEE M AGID Y CAMPUZANO V MIGNARD C PENET C MANDEL JL BRICE A KOENIG M
Citation: A. Durr et al., CLINICAL AND GENETIC ABNORMALITIES IN PATIENTS WITH FRIEDREICHS ATAXIA, The New England journal of medicine, 335(16), 1996, pp. 1169-1175
NO FOUNDER EFFECT IN 3 NOVEL ALZHEIMERS-DISEASE FAMILIES WITH APP-717VAL-]ILE MUTATION
Authors: CAMPION D BRICE A HANNEQUIN D CHARBONNIER F DUBOIS B MARTIN C MICHON A PENET C BELLIS M CALENDA A MARTINEZ M AGID Y CLERGETDARPOUX F FREBOURG T
Citation: D. Campion et al., NO FOUNDER EFFECT IN 3 NOVEL ALZHEIMERS-DISEASE FAMILIES WITH APP-717VAL-]ILE MUTATION, Journal of Medical Genetics, 33(8), 1996, pp. 661-664
APOLIPOPROTEIN-E GENOTYPE DOES NOT AFFECT AGE AT ONSET IN PATIENTS WITH CHROMOSOME-14 ENCODED ALZHEIMERS-DISEASE
Authors: BRICE A TARDIEU S DIDIERJEAN O LEGUERN E MICHON A PILLON B HAHN V DUBOIS B PENET C AGID Y CAMPION D MARTINEZ M BABRON MC CLERGETDARPOUX F BELLIS M CALANDA A HEILIG R WEISSENBACH J MALLET J FREBOURG T HANNEQUIN D PUEL M LEDOZE F PASQUIER F ZIMMERMANN MA THOMASANTERION C MOREAU O
Citation: A. Brice et al., APOLIPOPROTEIN-E GENOTYPE DOES NOT AFFECT AGE AT ONSET IN PATIENTS WITH CHROMOSOME-14 ENCODED ALZHEIMERS-DISEASE, Journal of Medical Genetics, 33(2), 1996, pp. 174-175
PHENOTYPE OF AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA LINKED TO CHROMOSOME-2
Authors: DURR A DAVOINE CS PATERNOTTE C VONFELLENBERG J COGILNICEAN S COUTINHO P LAMY C BOURGEOIS S PRUDHOMME JF PENET C MAS JL BURGUNDER JM HAZAN J WEISSENBACH J BRICE A FONTAINE B
Citation: A. Durr et al., PHENOTYPE OF AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA LINKED TO CHROMOSOME-2, Brain, 119, 1996, pp. 1487-1496
THE GENE FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA WITH PIGMENTARY MACULAR DYSTROPHY MAPS TO CHROMOSOME 3P12-P21.1
Authors: BENOMAR A KROLS L STEVANIN G CANCEL G LEGUERN E DAVID G OUHABI H MARTIN JJ DURR A ZAIM A RAVISE N BUSQUE C PENET C VANREGEMORTER N WEISSENBACH J YAHYAOUI M CHKILI T AGID Y VANBROECKHOVEN C BRICE A
Citation: A. Benomar et al., THE GENE FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA WITH PIGMENTARY MACULAR DYSTROPHY MAPS TO CHROMOSOME 3P12-P21.1, Nature genetics, 10(1), 1995, pp. 84-88
MUTATIONS OF THE PRESENILIN-I GENE IN FAMILIES WITH EARLY-ONSET ALZHEIMERS-DISEASE
Authors: CAMPION D FLAMAN JM BRICE A HANNEQUIN D DUBOIS B MARTIN C MOREAU V CHARBONNIER F DIDIERJEAN O TARDIEU S PENET C PUEL M PASQUIER F LEDOZE F BELLIS G CALENDA A HEILIG R MARTINEZ M MALLET J BELLIS M CLERGETDARPOUX F AGID Y FREBOURG T
Citation: D. Campion et al., MUTATIONS OF THE PRESENILIN-I GENE IN FAMILIES WITH EARLY-ONSET ALZHEIMERS-DISEASE, Human molecular genetics, 4(12), 1995, pp. 2373-2377
EXCLUSION OF THE CANDIDATE LOCUS FSP1 IN 6 FAMILIES WITH LATE-ONSET AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA
Authors: FONTAINE B RIME CS HAZAN J DURR A STEVANIN G PENET C REBOUL J AGID Y LYONCAEN O BAUMANN N WEISSENBACH J BRICE A
Citation: B. Fontaine et al., EXCLUSION OF THE CANDIDATE LOCUS FSP1 IN 6 FAMILIES WITH LATE-ONSET AUTOSOMAL-DOMINANT SPASTIC PARAPLEGIA, Neuromuscular disorders, 5(1), 1995, pp. 11-17
ANALYSIS OF THE SCA1 CAG REPEAT IN A LARGE NUMBER OF FAMILIES WITH DOMINANT ATAXIA - CLINICAL AND MOLECULAR CORRELATIONS
Authors: DUBOURG O DURR A CANCEL G STEVANIN G CHNEIWEISS H PENET C AGID Y BRICE A
Citation: O. Dubourg et al., ANALYSIS OF THE SCA1 CAG REPEAT IN A LARGE NUMBER OF FAMILIES WITH DOMINANT ATAXIA - CLINICAL AND MOLECULAR CORRELATIONS, Annals of neurology, 37(2), 1995, pp. 176-180
SCA2 IS NOT A MAJOR LOCUS FOR ADCA TYPE-I IN FRENCH FAMILIES
Authors: CANCEL G STEVANIN G DURR A CHNEIWEISS H PENET C POTHIN Y AGID Y BRICE A
Citation: G. Cancel et al., SCA2 IS NOT A MAJOR LOCUS FOR ADCA TYPE-I IN FRENCH FAMILIES, American journal of medical genetics, 60(5), 1995, pp. 382-385
ALLELIC ASSOCIATION AT THE D14S43 LOCUS IN EARLY-ONSET ALZHEIMERS-DISEASE
Authors: BRICE A TARDIEU S CAMPION D LEGUERN E MARTINEZ M CARPENTIER A PENET C DUBOIS B BELLIS M MALLET J HANNEQUIN D CLERGETDARPOUX F AGID Y MICHON A PILLON B BABRON MC CALANDA A PUEL M LEDOZE F PASQUIER F ZIMMERMANN MA DESI M VERCELETTO M THOMASANTERION C LEMAITRE MH JAILLARDSERRADT A TOUCHON J
Citation: A. Brice et al., ALLELIC ASSOCIATION AT THE D14S43 LOCUS IN EARLY-ONSET ALZHEIMERS-DISEASE, American journal of medical genetics, 60(2), 1995, pp. 91-93
DOES THE ATAXO-CHOREIC FORM OF DRPLA EXIS T IN EUROPE - SCREENING FORTHE MUTATION IN 120 FAMILIES
Authors: DUBOURG O DURR A CHNEIWEISS H STEVANIN G CANCEL G PENET C AGID Y BRICE A
Citation: O. Dubourg et al., DOES THE ATAXO-CHOREIC FORM OF DRPLA EXIS T IN EUROPE - SCREENING FORTHE MUTATION IN 120 FAMILIES, Revue neurologique, 151(11), 1995, pp. 657-660
ANALYSIS OF THE SCA1 CAG REPEAT IN 90 FAMILIES WITH AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I - CLINICAL AND MOLECULAR CORRELATIONS
Authors: DUBOURG O DURR A CANCEL G STEVANNIN G CHNEIWEISS H PENET C AGID Y BRICE A
Citation: O. Dubourg et al., ANALYSIS OF THE SCA1 CAG REPEAT IN 90 FAMILIES WITH AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I - CLINICAL AND MOLECULAR CORRELATIONS, Neurology, 45(4), 1995, pp. 422-422
A LARGE PEDIGREE WITH EARLY-ONSET ALZHEIMERS-DISEASE - CLINICAL, NEUROPATHOLOGIC, AND GENETIC-CHARACTERIZATION
Authors: CAMPION D BRICE A HANNEQUIN D TARDIEU S DUBOIS B CALENDA A BRUN E PENET C TAYOR J MARTINEZ M BELLIS M MALLET J AGID Y CLERGETDARPOUX F
Citation: D. Campion et al., A LARGE PEDIGREE WITH EARLY-ONSET ALZHEIMERS-DISEASE - CLINICAL, NEUROPATHOLOGIC, AND GENETIC-CHARACTERIZATION, Neurology, 45(1), 1995, pp. 80-85
MARKED PHENOTYPIC HETEROGENEITY ASSOCIATED WITH EXPANSION OF A CAG REPEAT SEQUENCE AT THE SPINOCEREBELLAR ATAXIA-3 MACHADO-JOSEPH DISEASE LOCUS
Authors: CANCEL G ABBAS N STEVANIN G DURR A CHNEIWEISS H NERI C DUYCKAERTS C PENET C CANN HM AGID Y BRICE A
Citation: G. Cancel et al., MARKED PHENOTYPIC HETEROGENEITY ASSOCIATED WITH EXPANSION OF A CAG REPEAT SEQUENCE AT THE SPINOCEREBELLAR ATAXIA-3 MACHADO-JOSEPH DISEASE LOCUS, American journal of human genetics, 57(4), 1995, pp. 809-816
LINKAGE ANALYSES BETWEEN DOMINANT X-LINKED CHARCOT-MARIE-TOOTH-DISEASE, AND 15 XQ11-XQ21 MICROSATELLITES IN A NEW LARGE FAMILY - 3 NEW MARKERS ARE CLOSELY LINKED TO THE GENE
Authors: LEGUERN E RAVISE N GUGENHEIM M VIGNAL A PENET C BOUCHE P WEISSENBACH J AGID Y BRICE A
Citation: E. Leguern et al., LINKAGE ANALYSES BETWEEN DOMINANT X-LINKED CHARCOT-MARIE-TOOTH-DISEASE, AND 15 XQ11-XQ21 MICROSATELLITES IN A NEW LARGE FAMILY - 3 NEW MARKERS ARE CLOSELY LINKED TO THE GENE, Neuromuscular disorders, 4(5-6), 1994, pp. 463-469
AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I - MAPPING OF A 3RD LOCUS (SCA3) AND ABSENCE OF GENOTYPE-PHENOTYPE CORRELATION
Authors: DURR A CHNEIWEISS H STEVANIN G CANCEL G PENET C AGID Y BRICE A
Citation: A. Durr et al., AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I - MAPPING OF A 3RD LOCUS (SCA3) AND ABSENCE OF GENOTYPE-PHENOTYPE CORRELATION, Neurology, 44(4), 1994, pp. 10000294-10000294
A 3RD LOCUS FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I MAPS TO CHROMOSOME 14Q24.3-QTER - EVIDENCE FOR THE EXISTENCE OF A 4TH LOCUS
Authors: STEVANIN G LEGUERN E RAVISE N CHNEIWEISS H DURR A CANCEL G VIGNAL A BOCH AL RUBERG M PENET C POTHIN Y LAGROUA I HAGUENAU M RANCUREL G WEISSENBACH J AGID Y BRICE A
Citation: G. Stevanin et al., A 3RD LOCUS FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I MAPS TO CHROMOSOME 14Q24.3-QTER - EVIDENCE FOR THE EXISTENCE OF A 4TH LOCUS, American journal of human genetics, 54(1), 1994, pp. 11-20
GENETIC-HETEROGENEITY OF AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I - EVIDENCE FOR THE EXISTENCE OF A 3RD LOCUS
Authors: STEVANIN G CHNEIWEISS H LEGUERN E RAVISE N DURR A PENET C AGID Y BRICE A
Citation: G. Stevanin et al., GENETIC-HETEROGENEITY OF AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-I - EVIDENCE FOR THE EXISTENCE OF A 3RD LOCUS, Human molecular genetics, 2(9), 1993, pp. 1483-1485
FAMILIAL ESSENTIAL TREMOR AND IDIOPATHIC TORSION DYSTONIA ARE DIFFERENT GENETIC ENTITIES
Authors: DURR A STEVANIN G JEDYNAK CP PENET C AGID Y BRICE A
Citation: A. Durr et al., FAMILIAL ESSENTIAL TREMOR AND IDIOPATHIC TORSION DYSTONIA ARE DIFFERENT GENETIC ENTITIES, Neurology, 43(11), 1993, pp. 2212-2214
Risultati: 1-25 | 26-26