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Results: 1-12 |
Results: 12

Authors: PETIOT P VIAL C DESAINTVICTOR JF CHARLES N CARRIER H DEPIERRE P BADY B
Citation: P. Petiot et al., DROPPED HEAD SYNDROME - DISCUSSION ABOUT 3 CASES, Revue neurologique, 153(4), 1997, pp. 251-255

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: BADY B VIAL C
Citation: B. Bady et C. Vial, ELECTRODIAGNOSIS OF CARPAL-TUNNEL SYNDROM E - A REVIEW, Neurophysiologie clinique, 26(4), 1996, pp. 183-201

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

Authors: RICHE G TROUILLAS P BADY B
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

Authors: CHAUPLANNAZ G BADY B
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: VIAL C PETIOT P LATOMBE D RUEL JH CONFAVREUX C TRILLET M BADY B
Citation: C. Vial et al., ABDOMINAL-WALL WEAKNESS DUE TO LYME-DISEA SE, Revue neurologique, 149(12), 1993, pp. 810-812

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

Authors: CHABAUD B FLOCARD F DASSE Y RIBOT C BADY B SINDOU M
Citation: B. Chabaud et al., SURGICAL APPLICATIONS OF THE VARIATION OF MEDIAN NERVE ANATOMY AT WRIST, Neuro-chirurgie, 39(2), 1993, pp. 92-100
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