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Results:
1-11
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Results: 11
Authors:
LALIOTI MD
SCOTT HS
GENTON P
GRID D
OUAZZANI R
MRABET A
IBRAHIM S
GOUIDER R
DRAVET C
CHKILI T
BOTTANI A
BURESI C
MALAFOSSE A
ANTONARAKIS SE
Citation: Md. Lalioti et al., A PCR AMPLIFICATION METHOD REVEALS INSTABILITY OF THE DODECAMER REPEAT IN PROGRESSIVE MYOCLONUS EPILEPSY (EPM1) AND NO CORRELATION BETWEEN THE SIZE OF THE REPEAT AND AGE AT ONSET, American journal of human genetics, 62(4), 1998, pp. 842-847
Authors:
LALIOTI MD
SCOTT HS
GENTON P
GRID D
OUAZZANI R
MRABET A
IBRAHIM S
GOUIDER R
DRAVET C
CHKILI T
BOTTANI A
BURESI C
MALAFOSSE A
ANTONARAKIS SE
Citation: Md. Lalioti et al., THE EXPANDED DODECAMER REPEAT IN PROGRESSIVE MYOCLONUS EPILEPSY (EPM1) IS UNSTABLE, SHOWS NO CORRELATION WITH AGE-OF-ONSET, AND RESULTS IN REDUCED EXPRESSION OF REPORTER GENES IN-VITRO, European journal of human genetics, 6, 1998, pp. 4166-4166
Authors:
GOMEZGARRE P
ANTA B
CASTROGAGO M
LINDHOUT D
TASSINARI CA
MICHELUCCI R
MALAFOSSE A
TOPCU M
GRID D
DRAVET C
SERRATOSA J
Citation: P. Gomezgarre et al., REDUCTION OF THE LAFORA-DISEASE CANDIDATE GENE REGION TO A 2 CM INTERVAL IN CHROMOSOME 6Q24 AND EVIDENCE FOR GENETIC-HETEROGENEITY, European journal of human genetics, 6, 1998, pp. 4198-4198
Authors:
DAVID G
DURR A
STEVANIN G
CANCEL G
ABBAS N
BENOMAR A
BELAL S
LEBRE AS
ABADABENDIB M
GRID D
HOLMBERG M
YAHYAOUI M
HENTATI F
CHKILI T
AGID Y
BRICE A
Citation: G. David et al., MOLECULAR AND CLINICAL CORRELATIONS IN AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA WITH PROGRESSIVE MACULAR DYSTROPHY (SCA7), Human molecular genetics, 7(2), 1998, pp. 165-170
UNVERRICHT-LUNDBORG-DISEASE - CLINICAL AND ELECTROPHYSIOLOGICAL ASPECTS IN 19 NORTH-AFRICAN FAMILIES
Authors:
GOUIDER R
IBRAHIM S
FREDJ M
GARGOURI A
SAIDI H
OUEZZANI R
MALAFOSSE A
YAHIAOUI M
GRID D
MRABET A
Citation: R. Gouider et al., UNVERRICHT-LUNDBORG-DISEASE - CLINICAL AND ELECTROPHYSIOLOGICAL ASPECTS IN 19 NORTH-AFRICAN FAMILIES, Revue neurologique, 154(6-7), 1998, pp. 503-507
Authors:
LABAUGE P
OUAZZANI R
MRABET A
GRID D
GENTON P
DRAVET C
CHKILI T
BECK C
BURESI C
BALDYMOULINIER M
MALAFOSSE A
Citation: P. Labauge et al., ALLELIC HETEROGENEITY OF MEDITERRANEAN MYOCLONUS AND THE CYSTATIN-B GENE, Annals of neurology, 41(5), 1997, pp. 686-689
Authors:
KESSALI M
ZEMMOURI R
GUILBOT A
MAISONOBE T
BRICE A
LEGUERN E
GRID D
Citation: M. Kessali et al., A CLINICAL, ELECTROPHYSIOLOGIC, NEUROPATHOLOGIC, AND GENETIC-STUDY OF2 LARGE ALGERIAN FAMILIES WITH AN AUTOSOMAL RECESSIVE DEMYELINATING FORM OF CHARCOT-MARIE-TOOTH-DISEASE, Neurology, 48(4), 1997, pp. 867-873
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
Authors:
STEVANIN G
TROTTIER Y
CANCEL G
DURR A
DAVID G
DIDIERJEAN O
BURK K
IMBERT G
SAUDOU F
ABADABENDIB M
GOURFINKELAN I
BENOMAR A
ABBAS N
KLOCKGETHER T
GRID D
AGID Y
MANDEL JL
BRICE A
Citation: G. Stevanin et al., SCREENING FOR PROTEINS WITH POLYGLUTAMINE EXPANSIONS IN AUTOSOMAL-DOMINANT CEREBELLAR ATAXIAS, Human molecular genetics, 5(12), 1996, pp. 1887-1892
Authors:
LEGUERN E
GUILBOT A
KESSALI M
RAVISE N
TASSIN J
MAISONOBE T
GRID D
BRICE A
Citation: E. Leguern et al., HOMOZYGOSITY MAPPING OF AN AUTOSOMAL RECESSIVE FORM OF DEMYELINATING CHARCOT-MARIE-TOOTH DISEASE TO CHROMOSOME 5Q23-Q33, Human molecular genetics, 5(10), 1996, pp. 1685-1688
Authors:
MALAFOSSE A
BECK C
BELLET H
OUAZZANI R
GRID D
MRABET A
GENTON P
DRAVET C
BALDYMOULINIER M
Citation: A. Malafosse et al., MOLECULAR-GENETIC STUDY OF UNVERRICHT-LUNDBORG-DISEASE IN MAGHREBI (NORTH-AFRICAN) PEDIGREES, Epilepsia, 36, 1995, pp. 6-6
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