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Results: 1-25/52
Authors:
JEHENSON P
DUBOC D
LAFORET P
EYMARD B
LOMBES A
FARDEAU M
BRUNET P
SYROTA A
Citation: P. Jehenson et al., C-13 AND P-31 NMR FOR THE DIAGNOSIS OF MUSCULAR PHOSPHORYLASE-KINASE DEFICIENCY, Journal de chimie physique et de physico-chimie biologique, 95(2), 1998, pp. 260-263
Authors:
ANNANE D
FIORELLI M
MAZOYER B
PAPPATA S
EYMARD B
RADVANYI H
JUNIEN C
FARDEAU M
MERLET P
GAJDOS P
SYROTA A
SANSOM Y
DUBOC D
Citation: D. Annane et al., IMPAIRED CEREBRAL GLUCOSE-METABOLISM IN MYOTONIC-DYSTROPHY - A TRIPLET-SIZE DEPENDENT PHENOMENON, Neuromuscular disorders, 8(1), 1998, pp. 39-45
Authors:
DELAPORTE S
CHAUBOURT E
FABRE F
POULAS K
CHAPRON J
EYMARD B
TZARTOS S
KOENIG J
Citation: S. Delaporte et al., ACCUMULATION OF ACETYLCHOLINE-RECEPTORS IS A NECESSARY CONDITION FOR NORMAL ACCUMULATION OF ACETYLCHOLINESTERASE DURING IN-VITRO NEUROMUSCULAR SYNAPTOGENESIS, European journal of neuroscience, 10(5), 1998, pp. 1631-1643
Authors:
LAFORET P
DETOMA C
EYMARD B
BECANE HM
JEANPIERRE M
FARDEAU M
DUBOC D
Citation: P. Laforet et al., CARDIAC INVOLVEMENT IN GENETICALLY CONFIRMED FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, Neurology, 51(5), 1998, pp. 1454-1456
Authors:
PLASSARTSCHIESS E
GERVAIS A
EYMARD B
LAGUENY A
POUGET J
WARTER JM
FARDEAU M
JENTSCH TJ
FONTAINE B
Citation: E. Plassartschiess et al., NOVEL MUSCLE CHLORIDE CHANNEL (CLCN1) MUTATIONS IN MYOTONIA-CONGENITAWITH VARIOUS MODES OF INHERITANCE INCLUDING INCOMPLETE DOMINANCE AND PENETRANCE, Neurology, 50(4), 1998, pp. 1176-1179
Authors:
DUBOC D
ANNANE D
LAFORET P
BECANNE HM
EYMARD B
GAJDOS P
JUNIEN C
WEBER S
MERLET P
JOLIOT F
Citation: D. Duboc et al., QUANTIFICATION OF CORONARY FLOW RESERVE BY POSITRON-EMISSION-TOMOGRAPHY IS A RELIABLE PREDICTOR OF CARDIAC EVENTS IN MYOTONIC-DYSTROPHY, Circulation, 98(17), 1998, pp. 1148-1148
Authors:
CHERIN P
EYMARD B
LAFORET P
GENEREAU T
COUTELLIER A
FAIDEAU M
HERSON S
Citation: P. Cherin et al., TREATMENT OF INCLUSION-BODY MYOSITIS WITH THE ASSOCIATION OF CORTICOSTEROIDS AND INTRAVENOUS IMMUNOGLOBULIN, Arthritis and rheumatism, 41(9), 1998, pp. 412-412
Authors:
CHERIN P
GHERARDI RK
EYMARD B
LAFORET P
COQUET M
MUSSINI JM
FELISSIER JP
DARRASJOLY C
FARDEAU M
HERSON S
Citation: P. Cherin et al., FOCAL INFILTRATIVE MACROPHAGIC MYOFASCIITIS - AN EMERGING ENTITY, Arthritis and rheumatism, 41(9), 1998, pp. 1245-1245
Authors:
DONGER C
KREJCI E
SERRADELL AP
EYMARD B
BON S
NICOLE S
CHATEAU D
GARY F
FARDEAU M
MASSOULIE J
GUICHENEY P
Citation: C. Donger et al., MUTATION IN THE HUMAN ACETYLCHOLINESTERASE-ASSOCIATED COLLAGEN GENE, COLQ, IS RESPONSIBLE FOR CONGENITAL MYASTHENIC SYNDROME WITH END-PLATEACETYLCHOLINESTERASE DEFICIENCY (TYPE IC), American journal of human genetics, 63(4), 1998, pp. 967-975
Authors:
BRUNET G
TOME FMS
EYMARD B
ROBERT JM
Citation: G. Brunet et al., GENEALOGICAL STUDY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN FRANCE, Neuromuscular disorders, 7, 1997, pp. 34-37
Authors:
PERIE S
EYMARD B
LACCOURREYE L
CHAUSSADE S
FARDEAU M
STGUILY JL
Citation: S. Perie et al., DYSPHAGIA IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - A SERIES OF 22 FRENCH CASES, Neuromuscular disorders, 7, 1997, pp. 96-99
Authors:
EYMARD B
CHILLET P
Citation: B. Eymard et P. Chillet, MYASTHENIA-GRAVIS - RECENT PATHOPHYSIOLOG ICAL DATA, La Presse medicale, 26(18), 1997, pp. 872-879
Authors:
DJABIRI F
GAJDOS P
EYMARD B
GOMEZ L
BACH JF
GARCHON HJ
Citation: F. Djabiri et al., NO EVIDENCE FOR AN ASSOCIATION OF ACHR BETA-SUBUNIT GENE (CHRNB1) WITH MYASTHENIA-GRAVIS, Journal of neuroimmunology, 78(1-2), 1997, pp. 86-89
Authors:
RONDOT P
NAVON R
EYMARD B
FARDEAU M
TURPIN JC
LEFEVRE M
BATHIEN N
WU Y
BAUMANN N
Citation: P. Rondot et al., JUVENILE GM2 GANGLIOSIDOSIS WITH PROGRESS IVE SPINAL MUSCULAR-ATROPHYONSET, Revue neurologique, 153(2), 1997, pp. 120-123
Authors:
LAFORET P
EYMARD B
DANAN C
CHEVALLAY M
ROUCHE A
FRACHON P
FARDEAU M
LOMBES A
Citation: P. Laforet et al., PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA OF M ITOCHONDRIAL ORIGIN CONTRIBUTION OF MORPHOLOGICAL AND MOLECULAR EXPLORATIONS, Revue neurologique, 153(1), 1997, pp. 51-58
Authors:
MIAUX Y
CHIRAS J
EYMARD B
LAURIOTPREVOST MC
RADVANYI H
MARTINDUVERNEUIL N
DELAPORTE C
Citation: Y. Miaux et al., CRANIAL MRI FINDINGS IN MYOTONIC-DYSTROPHY, Neuroradiology, 39(3), 1997, pp. 166-170
Authors:
EYMARD B
ROMERO NB
LETURCQ F
PICCOLO F
CARRIE A
JEANPIERRE M
COLLIN H
DEBURGRAVE N
AZIBI K
CHAOUCH M
MERLINI L
THEMARNOEL C
PENISSON I
MAYER M
TANGUY O
CAMPBELL KP
KAPLAN JC
TOME FMS
FARDEAU M
Citation: B. Eymard et al., PRIMARY ADHALINOPATHY (ALPHA-SARCOGLYCANOPATHY) - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATION IN 20 PATIENTS WITH AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY, Neurology, 48(5), 1997, pp. 1227-1234
Authors:
LAFORET P
NICOLINO M
EYMARD B
PUECH JP
CAILLAUD C
POENARU L
FARDEAU M
Citation: P. Laforet et al., GENOTYPE-PHENOTYPE CORRELATION IN JUVENILE AND ADULT-ONSET ACID MALTASE DEFICIENCY, Neurology, 48(3), 1997, pp. 5114-5114
Authors:
FARDEAU M
EYMARD B
MIGNARD C
TOME FMS
RICHARD I
BECKMANN JS
Citation: M. Fardeau et al., CHROMOSOME 15-LINKED LIMB-GIRDLE MUSCULAR-DYSTROPHY - COMPARISON OF THE CLINICAL PHENOTYPES IN REUNION ISLAND AND FRENCH METROPOLITAN COMMUNITIES, Neurology, 48(3), 1997, pp. 21004-21004
Authors:
GARDNEROVA M
EYMARD B
MOREL E
FALTIN M
ZAJAC J
SADOVSKY O
TRIPON P
DOMERGUE M
VERNTDERGARABEDIAN B
BACH JF
Citation: M. Gardnerova et al., THE FETAL ADULT ACETYLCHOLINE-RECEPTOR ANTIBODY RATIO IN MOTHERS WITHMYASTHENIA-GRAVIS AS A MARKER FOR TRANSFER OF THE DISEASE TO THE NEWBORN/, Neurology, 48(1), 1997, pp. 50-54
Authors:
TOURBAH A
STIEVENART JL
IBAZIZEN MT
LUBETZKI C
BAUMANN N
EYMARD B
MOSER HW
LYONCAEN O
CABANIS EA
Citation: A. Tourbah et al., LOCALIZED PROTON MAGNETIC-RESONANCE SPECTROSCOPY IN PATIENTS WITH ADULT ADRENOLEUKODYSTROPHY - INCREASE OF CHOLINE COMPOUNDS IN NORMAL-APPEARING WHITE-MATTER, Archives of neurology, 54(5), 1997, pp. 586-592
Authors:
PICCOLO F
DETOMA C
CHIRON S
LAFORET P
URTIZBEREA JA
EYMARD B
FARDEAU M
KAPLAN JC
JEANPIERRE M
Citation: F. Piccolo et al., PENETRANCE OF THE FSHD MUTATION DIFFERS ACCORDING TO THE D4Z4 REPEAT NUMBER, American journal of human genetics, 61(4), 1997, pp. 1856-1856
Authors:
FARDEAU M
EYMARD B
MIGNARD C
TOME FMS
RICHARD I
BECKMANN JS
Citation: M. Fardeau et al., CHROMOSOME 15-LINKED LIMB-GIRDLE MUSCULAR-DYSTROPHY - CLINICAL PHENOTYPES IN REUNION ISLAND AND FRENCH METROPOLITAN COMMUNITIES, Neuromuscular disorders, 6(6), 1996, pp. 447-453
Authors:
DEKERVILER E
LEROYWILLIG A
DUBOC D
EYMARD B
SYROTA A
Citation: E. Dekerviler et al., MR QUANTIFICATION OF MUSCLE FATTY REPLACEMENT IN MCARDLES-DISEASE, Magnetic resonance imaging, 14(10), 1996, pp. 1137-1141
Authors:
VIGNES S
SAINTGUILY JL
COLIN JY
EYMARD B
WECHSLER B
GODEAU P
Citation: S. Vignes et al., OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - USEF ULNESS OF UPPER ESOPHAGEAL SPHINCTER MYOTOMY - ABOUT ONE CASE, La Revue de medecine interne, 17(12), 1996, pp. 1017-1019