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Results: 1-25 | 26-28
Results: 1-25/28
A MISSENSE MUTATION IN THE ALPHA-B-CRYSTALLIN CHAPERONE GENE CAUSES ADESMIN-RELATED MYOPATHY
Authors: VICART P CARON A GUICHENEY P LI ZL PREVOST MC FAURE A CHATEAU D CHAPON F TOME F DUPRET JM PAULIN D FARDEAU M
Citation: P. Vicart et al., A MISSENSE MUTATION IN THE ALPHA-B-CRYSTALLIN CHAPERONE GENE CAUSES ADESMIN-RELATED MYOPATHY, Nature genetics, 20(1), 1998, pp. 92-95
A MUTATION IN MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH-DISEASE TYPE-II
Authors: BESANCON R CHAPON F LATOUR P DIRAISON P SCHAEFFER S BOUCHERAT M CHAMBA G VANDENBERGHE A
Citation: R. Besancon et al., A MUTATION IN MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH-DISEASE TYPE-II, European journal of human genetics, 6, 1998, pp. 1029-1029
A MUTATION IN MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE-II
Authors: BESANCON R CHAPON F LATOUR P DIRAISON P SCHAEFFER S BOUCHERAT M CHAMBA G VANDENBERGHE A
Citation: R. Besancon et al., A MUTATION IN MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE-II, European journal of neuroscience, 10, 1998, pp. 2102-2102
EFFECTS OF DAMAGE TO THE BASAL FOREBRAIN ON BRAIN GLUCOSE-UTILIZATION- A REEVALUATION USING POSITRON-EMISSION-TOMOGRAPHY IN BABOONS WITH EXTENSIVE UNILATERAL EXCITOTOXIC LESION
Authors: LEMESTRIC C CHAVOIX C CHAPON F MEZENGE F EPELBAUM J BARON JC
Citation: C. Lemestric et al., EFFECTS OF DAMAGE TO THE BASAL FOREBRAIN ON BRAIN GLUCOSE-UTILIZATION- A REEVALUATION USING POSITRON-EMISSION-TOMOGRAPHY IN BABOONS WITH EXTENSIVE UNILATERAL EXCITOTOXIC LESION, Journal of cerebral blood flow and metabolism, 18(5), 1998, pp. 476-490
AN UNUSUAL TYPE OF A FAMILIAL SENSORY NEUROPATHY WITH DYSAUTONOMIA
Authors: DUBUC L LEPORRIER N QUESNEY A MALLET JF BERTHELIN C VIDAUD M LECHEVALIER B CHAPON F
Citation: L. Dubuc et al., AN UNUSUAL TYPE OF A FAMILIAL SENSORY NEUROPATHY WITH DYSAUTONOMIA, Brain pathology, 7(4), 1997, pp. 1383-1383
PITUITARY APOPLEXY OF A GONADOTROPH ADENOMA FOLLOWING GONADOTROPIN-RELEASING-HORMONE AGONIST THERAPY FOR PROSTATIC-CANCER
Authors: REZNIK Y CHAPON F LAHLOU N DEBOUCHER N MAHOUDEAU J
Citation: Y. Reznik et al., PITUITARY APOPLEXY OF A GONADOTROPH ADENOMA FOLLOWING GONADOTROPIN-RELEASING-HORMONE AGONIST THERAPY FOR PROSTATIC-CANCER, Journal of endocrinological investigation, 20(9), 1997, pp. 566-568
THE IN-VIVO METABOLIC PATTERN OF LOW-GRADE BRAIN GLIOMAS - A POSITRONEMISSION TOMOGRAPHIC STUDY USING F-18 FLUORODEOXYGLUCOSE AND C-11 L-METHYLMETHIONINE
Authors: DERLON JM PETITTABOUE MC CHAPON F BEAUDOUIN V NOEL MH CREVEUIL C COURTHEOUX P HOUTTEVILLE JP
Citation: Jm. Derlon et al., THE IN-VIVO METABOLIC PATTERN OF LOW-GRADE BRAIN GLIOMAS - A POSITRONEMISSION TOMOGRAPHIC STUDY USING F-18 FLUORODEOXYGLUCOSE AND C-11 L-METHYLMETHIONINE, Neurosurgery, 40(2), 1997, pp. 276-287
PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA) IN CEREBRAL CAVERNOMAS - ANIMMUNOCYTOCHEMICAL STUDY OF 42 CASES
Authors: NOTELET L HOUTTEVILLE JP KHOURY S LECHEVALIER B CHAPON F
Citation: L. Notelet et al., PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA) IN CEREBRAL CAVERNOMAS - ANIMMUNOCYTOCHEMICAL STUDY OF 42 CASES, Surgical neurology, 47(4), 1997, pp. 364-370
DISTAL MUSCULAR WEAKNESS INVOLVING THE FO RELIMBS AND RUNNING FROM 3 YEARS IN A 61-YEAR-OLD MAN
Authors: GHERARDI R BERTRAN F CHAPON F
Citation: R. Gherardi et al., DISTAL MUSCULAR WEAKNESS INVOLVING THE FO RELIMBS AND RUNNING FROM 3 YEARS IN A 61-YEAR-OLD MAN, Revue neurologique, 153(5), 1997, pp. 360-366
THE LIFE AND WORK OF TERIADE, ART PUBLISH ER OF ILLUSTRATED BOOKS BY MATISSE, PICASSO, MIRO, AND CHAGALL
Authors: CHAPON F
Citation: F. Chapon, THE LIFE AND WORK OF TERIADE, ART PUBLISH ER OF ILLUSTRATED BOOKS BY MATISSE, PICASSO, MIRO, AND CHAGALL, L'Oeil, (486), 1997, pp. 88
FAMILIAL CAVERNOUS MALFORMATIONS IN A LARGE FRENCH KINDRED - MAPPING OF THE GENE TO THE CCM1 LOCUS ON CHROMOSOME 7Q
Authors: NOTELET L CHAPON F KHOURY S VAHEDI K CHODKIEWICZ JP COURTHEOUX P IBAZIZEN M CABANIS EA LECHEVALIER B TOURNIERLASSERVE E HOUTTEVILLE JP
Citation: L. Notelet et al., FAMILIAL CAVERNOUS MALFORMATIONS IN A LARGE FRENCH KINDRED - MAPPING OF THE GENE TO THE CCM1 LOCUS ON CHROMOSOME 7Q, Journal of Neurology, Neurosurgery and Psychiatry, 63(1), 1997, pp. 40-45
NEW MUTATIONS IN THE X-LINKED FORM OF CHARCOT-MARIE-TOOTH DISEASE
Authors: LATOUR P FABREGUETTE A RESSOT C BLANQUETGROSSARD F ANTOINE JC CALVAS P CHAPON F CORBILLON E OLLAGNON E STURTZ F BOUCHERAT M CHAZOT G DAUTIGNY A PHAMDINH D VANDENBERGHE A
Citation: P. Latour et al., NEW MUTATIONS IN THE X-LINKED FORM OF CHARCOT-MARIE-TOOTH DISEASE, European neurology, 37(1), 1997, pp. 38-42
CHARCOT-MARIE-TOOTH TYPE-1B NEUROPATHY - A MUTATION AT THE SINGLE GLYCOSYLATION SITE IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN-P0
Authors: BLANQUETGROSSARD E PHAMDINH D DAUTIGNY A LATOUR P BONNEBOUCHE C DIRAISON P CHAPON F CHAZOT G VANDENBERGHE A
Citation: E. Blanquetgrossard et al., CHARCOT-MARIE-TOOTH TYPE-1B NEUROPATHY - A MUTATION AT THE SINGLE GLYCOSYLATION SITE IN THE MAJOR PERIPHERAL MYELIN GLYCOPROTEIN-P0, Human mutation, 8(2), 1996, pp. 185-186
AKINETIC MUTISM WITH RIGHT HEMIPLEGIA DUE TO AN INFARCT IN THE TERRITORY OF THE LEFT ANTERIOR CEREBRAL-ARTERY
Authors: LECHEVALIER B BERTRAN F BUSSON P CHAPON F RAOUL G DELASAYETTE V
Citation: B. Lechevalier et al., AKINETIC MUTISM WITH RIGHT HEMIPLEGIA DUE TO AN INFARCT IN THE TERRITORY OF THE LEFT ANTERIOR CEREBRAL-ARTERY, Revue neurologique, 152(3), 1996, pp. 181-189
HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES WITH A PARTIAL DELETION OF THE REGION OFTEN DUPLICATED IN CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A
Authors: CHAPON F DIRAISON P LECHEVALIER B CHAZOT G VIADER F BONNEBOUCHE C VANDENBERGHE A TIMMERMAN V VANBROECKHOVEN C VANDENBERGHE A
Citation: F. Chapon et al., HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES WITH A PARTIAL DELETION OF THE REGION OFTEN DUPLICATED IN CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, Journal of Neurology, Neurosurgery and Psychiatry, 61(5), 1996, pp. 535-536
MODELIZATION OF MOTOR-NERVE CONDUCTION VELOCITIES FOR CHARCOT-MARIE-TOOTH (TYPE-1) PATIENTS
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
MOLECULAR DIAGNOSIS OF CHARCOT-MARIE-TOOTH IA DISEASE AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES BY QUANTIFYING CMTIA-REPSEQUENCES - CONSEQUENCES OF RECOMBINATIONS AT VARIANT SITES ON CHROMOSOME 17P11.2-12
Authors: VANDENBERGHE A LATOUR P CHAUPLANNAZ G CHAPON F POUGET J DUMAS R LAGUENAY A OLLAGNON E BOST M DUTHEL S CHAZOT G BOUCHERAT M
Citation: A. Vandenberghe et al., MOLECULAR DIAGNOSIS OF CHARCOT-MARIE-TOOTH IA DISEASE AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES BY QUANTIFYING CMTIA-REPSEQUENCES - CONSEQUENCES OF RECOMBINATIONS AT VARIANT SITES ON CHROMOSOME 17P11.2-12, Clinical chemistry, 42(7), 1996, pp. 1021-1025
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
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
CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, GENETIC HOMOGENEITY, AND MAPPING OF THE LOCUS WITHIN A 2-CM INTERVAL
Authors: DUCROS A NAGY T ALAMOWITCH S NIBBIO A JOUTEL A VAHEDI K CHABRIAT H IBAZIZEN MT JULIEN J DAVOUS P GOAS JY LYONCAEN O DUBOIS B DUCROCQ X SALSA F RAGNO M BURKHARD P BASSETTI C HUTCHINSON M VERIN M VIADER F CHAPON F LEVASSEUR M MAS JL DELRIEU O MACIAZEK J PRIEUR M MOHRENWEISER H BACH JF BOUSSER MG TOURNIERLASSERVE E
Citation: A. Ducros et al., CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, GENETIC HOMOGENEITY, AND MAPPING OF THE LOCUS WITHIN A 2-CM INTERVAL, American journal of human genetics, 58(1), 1996, pp. 171-181
MUTATIONS IN THE MYELIN PROTEIN ZERO GENE ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE 1B
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
CONSTANT REARRANGEMENT OF THE CMT1A-REP SEQUENCES IN HNPP PATIENTS WITH A DELETION IN CHROMOSOME 17P11.2 - A STUDY OF 30 UNRELATED CASES
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
MYOSITIS-OSSIFICANS PROGRESSIVA
Authors: PENNIELLO MJ CHAPON F OLIVIER D LEROY F GUILLOIS B LECHEVALIER B
Citation: Mj. Penniello et al., MYOSITIS-OSSIFICANS PROGRESSIVA, Archives de pediatrie, 2(1), 1995, pp. 34-38
DEMONSTRATION OF A SPECIFIC PROFILE OF PA THOLOGICAL TAU-PROTEINS IN FRONTOTEMPORAL DEMENTIA CASES
Authors: VERMERSCH P BORDET R LEDOZE F RUCHOUX MM CHAPON F THOMAS P DESTEE A LECHEVALLIER B DELACOURTE A
Citation: P. Vermersch et al., DEMONSTRATION OF A SPECIFIC PROFILE OF PA THOLOGICAL TAU-PROTEINS IN FRONTOTEMPORAL DEMENTIA CASES, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 318(4), 1995, pp. 439-445
ADULT CELIAC-DISEASE REVEALED BY A SENSOR Y-MOTOR NEUROPATHY
Authors: VIADER F CHAPON F DAO T RIVRAIN Y LECHEVALIER B
Citation: F. Viader et al., ADULT CELIAC-DISEASE REVEALED BY A SENSOR Y-MOTOR NEUROPATHY, La Presse medicale, 24(4), 1995, pp. 222-224
ACUTE NECROTIZING VASCULITIS (POLYARTERITIS-NODOSA) CONFINED TO THE NERVE WITH SPONTANEOUS-RECOVERY
Authors: DELASAYETTE V MACRO M DIRAISON P BERTRAN F LECHEVALIER B CHAPON F
Citation: V. Delasayette et al., ACUTE NECROTIZING VASCULITIS (POLYARTERITIS-NODOSA) CONFINED TO THE NERVE WITH SPONTANEOUS-RECOVERY, British journal of rheumatology, 34(7), 1995, pp. 694-695
Risultati: 1-25 | 26-28