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Results: 1-14 |
Results: 14

Authors: COURTOIS FJ GONNAUD PM CHARVIER KF LERICHE A RAYMOND DP
Citation: Fj. Courtois et al., SYMPATHETIC SKIN-RESPONSES AND PSYCHOGENIC ERECTIONS IN SPINAL-CORD INJURED MEN, Spinal cord, 36(2), 1998, pp. 125-131

Authors: KHOUATRA C HONNORAT J BOMBARON P GERINIERE L PINEDE L GONNAUD PM SOUQUET PJ PASQUIER J BERNARD JP
Citation: C. Khouatra et al., PARANEOPLASTIC INTESTINAL PSEUDOOBSTRUCTI ON AND SENSORY NEURONOPATHYREVEALING A SMALL-CELL LUNG-CARCINOMA, La Revue de medecine interne, 18(8), 1997, pp. 652-656

Authors: ZENONE T REVOL A DURIEU I GRANGE C SIBILLE M GONNAUD PM VITALDURAND D LEVRAT R
Citation: T. Zenone et al., CARBON-MONOXIDE POISONING, La Revue de medecine interne, 18, 1997, pp. 308-310

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: 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: 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

Authors: STURTZ F GONNAUD PM BESSE JL CHAZOT G VANDENBERGHE A
Citation: F. Sturtz et al., CHARCOT-MARIE-TOOTH DISEASE, Archives de pediatrie, 2(1), 1995, pp. 70-78

Authors: ROBIN C GONNAUD PM DURIEU I CROISILE B GARASSUS P LEVRAT R CHAZOT G AIMARD G TRILLET M
Citation: C. Robin et al., PROGRESSIVE LUPUS DEMENTIA - 2 CASES WITH OR WITHOUT ANTIPHOSPHOLIPIDANTIBODIES, Revue neurologique, 151(12), 1995, pp. 699-707

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: JARRY O ENRICO MF GONNAUD PM GRAND C PEROL M GUERIN JC
Citation: O. Jarry et al., TUBERCULOUS LYMPHADENOPATHY REVEALED BY A POLYNEUROPATHY - CAUSAL RELATION OR SIMPLE COINCIDENCE, Revue des maladies respiratoires, 11(3), 1994, pp. 294-296

Authors: LEGUERN E 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

Authors: BOST M BONNEBOUCHE C GONNAUD PM COCHAT P GILBERT B DUPONT C CHAZOT G VANDENBERGHE A
Citation: M. Bost et al., NEW ALLELE OF PROBE D17S61 PRESENT IN THE CHARCOT-MARIE-TOOTH 1A DUPLICATION, Clinical genetics, 46(5), 1994, pp. 380-381

Authors: ENRICO MF BROUSSOLLE E GONNAUD PM CHAZOT G
Citation: Mf. Enrico et al., PARTIAL KINESIOGENIC MOTOR SEIZURES IN A 59-YEAR OLD MAN - A RARE CIRCUMSTANCE OF REVELATION OF DIABETES, La Presse medicale, 22(20), 1993, pp. 967-967

Authors: LEGUERN E 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 REGION IN 13 FRENCH FAMILIES AFFECTED BY HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PAISIES (HNPP), American journal of human genetics, 53(3), 1993, pp. 1193-1193
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