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Results: 1-11 |
Results: 11

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: 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: KHURANA TS SPECHT LA BEGGS AH TOME FMS LETUREQ F CHEVALLAY M CHAFEY P KUNKEL LM
Citation: Ts. Khurana et al., THE CONCOMITANT USE OF DYSTROPHIN AND UTROPHIN DYSTROPHIN RELATED PROTEIN ANTIBODIES TO REDUCE MISDIAGNOSIS OF DUCHENNE/BECKER-MUSCULAR-DYSTROPHY/, Biochemical and biophysical research communications, 241(2), 1997, pp. 232-235

Authors: PINI A MERLINI L TOME FMS CHEVALLAY M GOBBI G
Citation: A. Pini et al., MEROSIN-NEGATIVE CONGENITAL MUSCULAR-DYSTROPHY, OCCIPITAL EPILEPSY WITH PERIODIC SPASMS AND FOCAL CORTICAL DYSPLASIA - REPORT OF 3 ITALIAN CASES IN 2 FAMILIES, Brain & development, 18(4), 1996, pp. 316-322

Authors: TREVISAN CP MARTINELLO F FERRUZZA E FANIN M CHEVALLAY M TOME FMS
Citation: Cp. Trevisan et al., BRAIN ALTERATIONS IN THE CLASSICAL FORM OF CONGENITAL MUSCULAR-DYSTROPHY - CLINICAL AND NEUROIMAGING FOLLOW-UP OF 12 CASES AND CORRELATION WITH THE EXPRESSION OF MEROSIN IN MUSCLE, Child's nervous system, 12(10), 1996, pp. 604-610

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: LAFORET P LOMBES A EYMARD B DANAN C CHEVALLAY M ROUCHE A FRACHON P FARDEAU M
Citation: P. Laforet et al., CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH RAGGED-RED FIBERS -CLINICAL, MORPHOLOGICAL AND GENETIC INVESTIGATIONS IN 43 PATIENTS, Neuromuscular disorders, 5(5), 1995, pp. 399-413

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: SEWRY CA CHEVALLAY M TOME FMS
Citation: Ca. Sewry et al., EXPRESSION OF LAMININ SUBUNITS IN HUMAN FETAL SKELETAL-MUSCLE, Histochemical Journal, 27(7), 1995, pp. 497-504

Authors: SAMSON F MESNARD L HEIMBURGER M HANAUER A CHEVALLAY M MERCADIER JJ PELISSIER JF FEINGOLD N JUNIEN C MANDEL JL FARDEAU M
Citation: F. Samson et al., GENETIC-LINKAGE HETEROGENEITY IN MYOTUBULAR MYOPATHY, American journal of human genetics, 57(1), 1995, pp. 120-126

Authors: TOME FMS MATSUMURA K CHEVALLAY M CAMPBELL KP FARDEAU M
Citation: Fms. Tome et al., EXPRESSION OF DYSTROPHIN-ASSOCIATED GLYCOPROTEINS DURING HUMAN FETAL MUSCLE DEVELOPMENT - A PRELIMINARY IMMUNOCYTOCHEMICAL STUDY, Neuromuscular disorders, 4(4), 1994, pp. 343-348
Risultati: 1-11 |