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LOPES J
LEGUERN E
GOUIDER R
TARDIEU S
ABBAS N
BIROUK N
GUGENHEIM M
BOUCHE P
AGID Y
BRICE A
ARNEBES MC
BRICHET B
CHAPON F
CHAZOT G
CLAVELOU P
DESNUELLE C
DIRAISON P
DUBAS F
GONNAUD PM
HURTEVENT JF
KUNTZER T
LAGUENY A
MABIN D
MAYER M
OCHSNER F
OLLAGNONROMAN E
POUGET J
TABARAUD F
VALLAT JM
VANDENBERGHE A
Citation: J. Lopes et al., RECOMBINATION HOT-SPOT IN A 3.2-KB REGION OF THE CHARCOT-MARIE-TOOTH TYPE 1A REPEAT SEQUENCES - NEW TOOLS FOR MOLECULAR DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES AND OF CHARCOT-MARIE-TOOTH TYPE 1A, American journal of human genetics, 58(6), 1996, pp. 1223-1230
Authors:
LATOUR P
BLANQUET F
NELIS E
BONNEBOUCHE C
CHAPON F
DIRAISON P
OLLAGNON E
DAUTIGNY A
PHAMDINH D
CHAZOT G
BOUCHERAT M
VANBROECKHOVEN C
VANDENBERGHE A
Citation: P. Latour et al., MUTATIONS IN THE MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 1B, Human mutation, 6(1), 1995, pp. 50-54
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LEGUERN E
GOUIDER R
LOPES J
ABBAS N
GUGENHEIM M
TARDIEU S
RAVISE N
LEGER JM
VALLAT JM
BOUCHE P
AGID Y
BRICE A
ARNEBES MC
BRICHET B
BIROUK N
CHAPON F
CHAZOT G
CLAVELOU P
DESNUELLE C
DIRAISON P
DUBAS F
GONNAUD PM
HURTEVENT JF
KUNTZER T
LAGUENY A
MABIN D
OSHSNER F
OLLAGNONROMAN E
POUGET J
TABERAUD F
VANDENBERGHE A
Citation: E. Leguern et al., CONSTANT REARRANGEMENT OF THE CMT1A-REP SEQUENCES IN HNPP PATIENTS WITH A DELETION IN CHROMOSOME 17P11.2 - A STUDY OF 30 UNRELATED CASES, Human molecular genetics, 4(9), 1995, pp. 1673-1674
Citation: V. Zumbo et al., AR-40 AR-39 CHRONOLOGY OF TERTIARY MAGMATIC ACTIVITY IN SOUTHERN YEMEN DURING THE EARLY RED SEA-ADEN RIFTING/, Journal of volcanology and geothermal research, 65(3-4), 1995, pp. 265-279
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TFELTHANSEN P
HENRY P
MULDER LJ
SCHELDEWAERT RG
SCHOENEN E
CHAZOT G
Citation: P. Tfelthansen et al., THE EFFECTIVENESS OF COMBINED ORAL LYSINE ACETYLSALICYLATE AND METOCLOPRAMIDE COMPARED WITH ORAL SUMATRIPTAN FOR MIGRAINE, Lancet, 346(8980), 1995, pp. 923-926
Authors:
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GONNAUD PM
DURIEU I
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GARASSUS P
LEVRAT R
CHAZOT G
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Citation: C. Robin et al., PROGRESSIVE LUPUS DEMENTIA - 2 CASES WITH OR WITHOUT ANTIPHOSPHOLIPIDANTIBODIES, Revue neurologique, 151(12), 1995, pp. 699-707
Authors:
DOMINEY P
DECETY J
BROUSSOLLE E
CHAZOT G
JEANNEROD M
Citation: P. Dominey et al., MOTOR IMAGERY OF A LATERALIZED SEQUENTIAL TASK IS ASYMMETRICALLY SLOWED IN HEMI-PARKINSONS PATIENTS, Neuropsychologia, 33(6), 1995, pp. 727-741
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CHAZOT G
EMILE J
BERTIN L
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DUCLOS H
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GIRARD D
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GRANJON YM
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LEJEUNNE C
MALLECOURT J
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MIHOUT B
NEUSCHWANDER P
TAPIE P
RASCOL A
REIS J
ROGEZ R
SAVET JF
SERRATRICE G
TOURNILHAC M
TRISCHLER JL
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Citation: F. Boureau et al., COMPARISON OF SUBCUTANEOUS SUMATRIPTAN WITH USUAL ACUTE TREATMENTS FOR MIGRAINE, European neurology, 35(5), 1995, pp. 264-269
Authors:
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PHAMDINH D
DAUTIGNY A
LATOUR P
BONNEBOUCHE C
CORBILLON E
CHAZOT G
VANDENBERGHE A
Citation: F. Blanquetgrossard et al., CHARCOT-MARIE-TOOTH TYPE 1B NEUROPATHY - 3RD MUTATION OF SERINE-63 CODON IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN P0 GENE, Clinical genetics, 48(6), 1995, pp. 281-283
Authors:
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BROUSSOLLE E
PIOLLET H
VIALLET F
KHALFALLAH Y
CHAZOT G
Citation: P. Ryvlin et al., MAGNETIC-RESONANCE-IMAGING EVIDENCE OF DECREASED PUTAMENAL IRON CONTENT IN IDIOPATHIC PARKINSONS-DISEASE, Archives of neurology, 52(6), 1995, pp. 583-588
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DUTHEL S
BOST M
BONNEBOUCHE C
BOUCHERAT M
CHAZOT G
LATOUR P
Citation: A. Vandenberghe et al., DUPLICATIONS AND DELETIONS IN CHARCOT-MARIE-TOOTH (CMT) DISEASE AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) - A REFINED MUTATION MODEL, American journal of human genetics, 57(4), 1995, pp. 1335-1335
Authors:
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STURTZ F
FOURBIL Y
BONNEBOUCHE C
TRANCHANT C
WARTER JM
CHAZOT G
BADY B
VIAL C
BRECHARD AS
VANDENBERGHE A
Citation: Pm. Gonnaud et al., DNA ANALYSIS AS A TOOL TO CONFIRM THE DIAGNOSIS OF ASYMPTOMATIC HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) WITH FURTHER EVIDENCE FOR THE OCCURRENCE OF DE-NOVO MUTATIONS, Acta neurologica Scandinavica, 92(4), 1995, pp. 313-318
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RICHARD A
BERTIN L
BOUREAU F
CHAZOT G
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Citation: H. Dallens et al., RESPONSIVENESS ASSESSMENT OF A SPECIFIC QUALITY-OF-LIFE QUESTIONNAIREFOR MIGRAINEURS (QVM), Quality of life research, 3(1), 1994, pp. 72-72
Authors:
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STURTZ F
GUGENHEIM M
GOUIDER R
BONNEBOUCHE C
RAVISE N
GONNAUD PM
TARDIEU S
BOUCHE P
CHAZOT G
AGID Y
VANDENBERGHE A
BRICE A
Citation: E. Leguern et al., DETECTION OF DELETION WITHIN 17P11.2 IN 7 FRENCH FAMILIES WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP), Cytogenetics and cell genetics, 65(4), 1994, pp. 261-264
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GEOFFRIAU M
BRUN J
TAILLARD J
BUREAU C
CHAZOT G
CLAUSTRAT B
Citation: R. Zaidan et al., MELATONIN IS ABLE TO INFLUENCE ITS SECRETION IN HUMANS - DESCRIPTION OF A PHASE-RESPONSE CURVE, Neuroendocrinology, 60(1), 1994, pp. 105-112
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FOURBIL Y
BLANQUET F
MATTEI MG
ROECKEL N
LATOUR P
CHAZOT G
VANDENBERGHE A
DAUTIGNY A
Citation: D. Phamdinh et al., THE MAJOR PERIPHERAL MYELIN PROTEIN ZERO GENE - STRUCTURE AND LOCALIZATION IN THE CLUSTER OF FC-GAMMA RECEPTOR GENES ON HUMAN-CHROMOSOME 1Q21.3-Q23, Human molecular genetics, 2(12), 1993, pp. 2051-2054