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Results:
1-18
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Results: 18
Authors:
LAMER S
CARLIER RY
PINARD JM
MOMPOINT D
BAGARD C
BURDAIRON E
ESTOURNET B
BAROIS A
VALLEE C
Citation: S. Lamer et al., CONGENITAL MUSCULAR-DYSTROPHY - USE OF BRAIN MR-IMAGING FINDINGS TO PREDICT MEROSIN DEFICIENCY, Radiology, 206(3), 1998, pp. 811-816
Authors:
MERLINI L
BAROIS A
DEMONTE A
ECHENNE B
GALLANO P
JARRE L
KALAYDJIEVA L
LEVYGOMES A
NAVARRO C
TOUTAIN A
TURNEV I
URTIZBEREA A
VALLAT JM
VOIT T
WARTER JM
KAPLAN JC
Citation: L. Merlini et al., LIMB-GIRDLE MUSCULAR-DYSTROPHY 2C WITH C283Y MUTATION IN GYPSIES - CHARACTERIZATION OF THE CLINICAL PHENOTYPE, Neurology, 50(4), 1998, pp. 3020-3020
Authors:
TOME FMS
HE Y
CHEVALLAY M
NICOLAS V
CRUAUD C
HORI H
MIZUTA T
ESTOURNET B
BAROIS A
FARDEAU M
GUICHENEY P
Citation: Fms. Tome et al., CONGENITAL MUSCULAR-DYSTROPHY WITH PARTIAL LAMININ ALPHA-2 CHAIN (MEROSIN) DEFICIENCY - IMMUNOCYTOCHEMICAL AND MOLECULAR STUDIES, Neurology, 50(4), 1998, pp. 15004-15004
Authors:
GUICHENEY P
VIGNIER N
ZHANG X
HE Y
CRUAUD C
FREY V
HELBLINGLECLERC A
RICHARD P
ESTOURNET B
MERLINI L
TOPALOGLU H
MORA M
HARPEY JP
HAENGGELI CA
BAROIS A
HAINQUE B
SCHWARTZ K
TOME FMS
FARDEAU M
TRYGGVASON K
Citation: P. Guicheney et al., PCR BASED MUTATION SCREENING OF THE LAMININ ALPHA-2 CHAIN GENE (LAMA2) - APPLICATION TO PRENATAL-DIAGNOSIS AND SEARCH FOR FOUNDER EFFECTS IN CONGENITAL MUSCULAR-DYSTROPHY, Journal of Medical Genetics, 35(3), 1998, pp. 211-217
Authors:
BAROIS A
ESTOURNETMATHIAUD B
Citation: A. Barois et B. Estournetmathiaud, RESPIRATORY-PROBLEMS IN SPINAL MUSCULAR ATROPHIES, Pediatric pulmonology, 1997, pp. 140-141
Authors:
GUICHENEY P
VIGNIER N
HELBLINGLECLERC A
NISSINEN M
ZHANG X
CRUAUD C
LAMBERT JC
RICHELME C
TOPALOGLU H
MERLINI L
BAROIS A
SCHWARTZ K
TOME FMS
TRYGGVASON K
FARDEAU M
Citation: P. Guicheney et al., GENETICS OF LAMININ ALPHA-2 CHAIN (OR MEROSIN) DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY - FROM IDENTIFICATION OF MUTATIONS TO PRENATAL-DIAGNOSIS, Neuromuscular disorders, 7(3), 1997, pp. 180-186
Authors:
HATTON F
BOUVIERCOLLE MH
JOUGLA E
BAROIS A
Citation: F. Hatton et al., AUTOPSIES OF SUDDEN-INFANT-DEATH-SYNDROME - CLASSIFICATION AND EPIDEMIOLOGY, Acta paediatrica, 85(12), 1996, pp. 1515-1515
Authors:
FARDEAU M
TOME FMS
HELBLINGLECLERC A
EVANGELISTA T
OTTOLINI A
CHEVALLAY M
BAROIS A
ESTOURNET B
HARPEY JP
FAURE S
GUICHENEY P
HILLAIRE D
Citation: M. Fardeau et al., CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSI N DEFICIENCY - CLINICAL, HISTOPATHOLOGICAL, IMMUNOCYTOCHEMICAL AND GENETIC-STUDY, Revue neurologique, 152(1), 1996, pp. 11-19
Authors:
PEREZ A
MULOT R
VARDON G
BAROIS A
GALLEGO J
Citation: A. Perez et al., THORACOABDOMINAL PATTERN OF BREATHING IN NEUROMUSCULAR DISORDERS, Chest, 110(2), 1996, pp. 454-461
Authors:
HATTON F
BOUVIERCOLLE MH
BAROIS A
IMBERT MC
LEROYER A
BOUVIER S
JOUGLA E
Citation: F. Hatton et al., AUTOPSIES OF SUDDEN-INFANT-DEATH-SYNDROME - CLASSIFICATION AND EPIDEMIOLOGY, Acta paediatrica, 84(12), 1995, pp. 1366-1371
Authors:
HELBLINGLECLERC A
TOPALOGLU H
TOME FMS
SEWRY C
GYAPAY G
NOAM I
MUNTONI F
DUBOWITZ V
BAROIS A
ESTOURNET B
URTIZBEREA JA
WEISSENBACH J
SCHWARTZ K
FARDEAU M
GUICHENEY P
Citation: A. Helblingleclerc et al., READJUSTING THE LOCALIZATION OF MEROSIN ( LAMININ ALPHA-2-CHAIN) DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY LOCUS ON CHROMOSOME 6Q2, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 318(12), 1995, pp. 1245-1252
Authors:
TOME FMS
LECLERC A
GUICHENEY P
CHEVALLAY M
HILLAIRE D
ESTOURNET B
BAROIS A
FARDEAU M
Citation: Fms. Tome et al., MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHIES, Neurology, 45(4), 1995, pp. 407-407
Authors:
COMMARE MC
KURSTJENS SP
BAROIS A
Citation: Mc. Commare et al., DIAPHRAGMATIC PARALYSIS IN CHILDREN - A REVIEW OF 11 CASES, Pediatric pulmonology, 18(3), 1994, pp. 187-193
Authors:
NORDMANN P
COMMARE MC
RONCO E
BAROIS A
NAUCIEL H
Citation: P. Nordmann et al., MEDIASTINITIS DUE TO NONTYPHI SALMONELLA, Clinical infectious diseases, 18(2), 1994, pp. 255-256
Authors:
HILLAIRE D
LECLERC A
FAURE S
TOPALOGLU H
CHIANNILKULCHAI N
GUICHENEY P
GRINAS L
LEGOS P
PHILPOT J
EVANGELISTA T
ROUTON MC
MAYER M
PELLISSIER JF
ESTOURNET B
BAROIS A
HENTATI F
FEINGOLD N
BECKMANN JS
DUBOWITZ V
TOME FMS
FARDEAU M
Citation: D. Hillaire et al., LOCALIZATION OF MEROSIN-NEGATIVE CONGENITAL MUSCULAR-DYSTROPHY TO CHROMOSOME 6Q2 BY HOMOZYGOSITY MAPPING, Human molecular genetics, 3(9), 1994, pp. 1657-1661
Authors:
TOME FMS
EVANGELISTA T
LECLERC A
SUNADA Y
MANOLE E
ESTOURNET B
BAROIS A
CAMPBELL KP
FARDEAU M
Citation: Fms. Tome et al., CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSIN DEFICIENCY, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 317(4), 1994, pp. 351-357
Authors:
COMMARE MC
FRANCOIS B
ESTOURNET B
BAROIS A
Citation: Mc. Commare et al., ONDINES CURSE - A DISCUSSION OF 5 CASES, Neuropediatrics, 24(6), 1993, pp. 313-318
Authors:
HACHFISOUSSI F
COUDERT V
BIRON R
BAROIS A
Citation: F. Hachfisoussi et al., QUININE INTOXICATION TREATED BY HIGH-DOSE OF DIAZEPAM, Archives francaises de pediatrie, 50(6), 1993, pp. 485-488
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