Authors:
RICHARD I
BRENGUIER L
DINCER P
ROUDAUT C
BADY B
BURGUNDER JM
CHEMALY R
GARCIA CA
HALABY G
JACKSON CE
KURNIT DM
LEFRANC G
LEGUM C
LOISELET J
MERLINI L
NIVELONCHEVALLIER A
OLLAGNONROMAN E
RESTAGNO G
TOPALOGLU H
BECKMANN JS
Citation: I. Richard et al., MULTIPLE INDEPENDENT MOLECULAR ETIOLOGY FOR LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A PATIENTS FROM VARIOUS GEOGRAPHICAL ORIGINS, American journal of human genetics, 60(5), 1997, pp. 1128-1138
Authors:
STURTZ FG
CHAUVIN F
OLLAGNONROMAN E
BOST M
LATOUR P
BONNEBOUCHE C
GONNAUD PM
BADY B
CHAZOT G
VANDENBERGHE A
BEAUVAIS P
CHAPON F
CLAVELOU P
FLOCARD F
MATHIEU M
POUGET J
RENDU M
Citation: Fg. Sturtz et al., MODELIZATION OF MOTOR-NERVE CONDUCTION VELOCITIES FOR CHARCOT-MARIE-TOOTH (TYPE-1) PATIENTS, European neurology, 36(4), 1996, pp. 224-228
Authors:
VILLEFERLIN T
DUMOULIN R
STEPIEN G
MATHA V
BADY B
FLOCARD F
CARRIER H
MATHIEU M
MOUSSON B
Citation: T. Villeferlin et al., FINE MAPPING OF RANDOMLY DISTRIBUTED MULTIPLE DELETIONS OF MITOCHONDRIAL-DNA IN A CASE OF CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, Molecular and cellular probes, 9(3), 1995, pp. 207-214
Citation: G. Riche et al., IMPROVEMENT OF ISAACS-SYNDROME AFTER TREATMENT WITH AZATHIOPRINE, Journal of Neurology, Neurosurgery and Psychiatry, 59(4), 1995, pp. 448-448
Authors:
ELBAZ A
VALESANTOS J
JURKATROTT K
LAPIE P
OPHOFF RA
BADY B
LINKS TP
PIUSSAN C
VILA A
MONNIER N
PADBERG GW
ABE K
FEINGOLD N
GUIMARAES J
WINTZEN AR
VANDERHOEVEN JH
SAUDUBRAY JM
GRUNFELD JP
LENOIR G
NIVET H
ECHENNE B
FRANTS RR
FARDEAU M
LEHMANNHORN F
FONTAINE B
Citation: A. Elbaz et al., HYPOKALEMIC PERIODIC PARALYSIS AND THE DIHYDROPYRIDINE RECEPTOR (CACNLIA3) - GENOTYPE-PHENOTYPE CORRELATIONS FOR 2 PREDOMINANT MUTATIONS AND EVIDENCE FOR THE ABSENCE OF A FOUNDER EFFECT IN 16 CAUCASIAN FAMILIES, American journal of human genetics, 56(2), 1995, pp. 374-380
Authors:
GONNAUD PM
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
Citation: G. Chauplannaz et B. Bady, HEREDITARY MYASTHENIC SYNDROMES WITH LATE -ONSET - USEFULNESS OF ELECTROPHYSIOLOGIC TESTS, Revue neurologique, 150(2), 1994, pp. 142-148
Authors:
PETIOT P
CHARLES N
VIAL C
MCGREGOR B
AIMARD G
TRILLET M
BADY B
Citation: P. Petiot et al., NEUROLOGICAL COMPLICATIONS OF GOLD THERAP Y - NOSOLOGICAL DISCUSSION ABOUT ONE CASE, Revue neurologique, 149(10), 1993, pp. 562-565