AAAAAA

   
Results: 1-11 |
Results: 11
CAG REPEAT EXPANSION IN AN ITALIAN FAMILY WITH SPINOCEREBELLAR ATAXIATYPE-2 (SCA2) - A CLINICAL AND GENETIC-STUDY
Authors: MALANDRINI A GALLI L VILLANOVA M PALMERI S PARROTTA E DEFALCO D CAPPELLI M GRIECO GS RENIERI A GUAZZI G
Citation: A. Malandrini et al., CAG REPEAT EXPANSION IN AN ITALIAN FAMILY WITH SPINOCEREBELLAR ATAXIATYPE-2 (SCA2) - A CLINICAL AND GENETIC-STUDY, European neurology, 40(3), 1998, pp. 164-168
HIGH-LEVELS OF CEREBROSPINAL-FLUID IGM BINDING TO MYELIN BASIC-PROTEIN ARE ASSOCIATED WITH EARLY BENIGN COURSE IN MULTIPLE-SCLEROSIS
Authors: ANNUNZIATA P PLUCHINO S MARTINO T GUAZZI G
Citation: P. Annunziata et al., HIGH-LEVELS OF CEREBROSPINAL-FLUID IGM BINDING TO MYELIN BASIC-PROTEIN ARE ASSOCIATED WITH EARLY BENIGN COURSE IN MULTIPLE-SCLEROSIS, Journal of neuroimmunology, 77(1), 1997, pp. 128-133
SELECTIVE BILATERAL AMYOTROPHY OF THE ANTERIOR TIBIAL MUSCLE - A CASE-REPORT
Authors: VILLANOVA M MALANDRINI A LOUBOUTIN JP PALMERI S GINANNESCHI F SIX J VOLTERRANI L GUAZZI G
Citation: M. Villanova et al., SELECTIVE BILATERAL AMYOTROPHY OF THE ANTERIOR TIBIAL MUSCLE - A CASE-REPORT, Muscle & nerve, 20(10), 1997, pp. 1335-1336
LOCALIZATION OF THE LAMININ ALPHA-2 CHAIN IN NORMAL HUMAN SKELETAL-MUSCLE AND PERIPHERAL-NERVE - AN ULTRASTRUCTURAL IMMUNOLABELING STUDY
Authors: MALANDRINI A VILLANOVA M SABATELLI P SQUARZONI S SIX J TOTI P GUAZZI G MARALDI NM
Citation: A. Malandrini et al., LOCALIZATION OF THE LAMININ ALPHA-2 CHAIN IN NORMAL HUMAN SKELETAL-MUSCLE AND PERIPHERAL-NERVE - AN ULTRASTRUCTURAL IMMUNOLABELING STUDY, Acta Neuropathologica, 93(2), 1997, pp. 166-172
MUSCULAR-DYSTROPHY, MENTAL-RETARDATION AND CARDIOMYOPATHY NOT ASSOCIATED WITH DYSTROPHIN DEFICIENCY
Authors: VILLANOVA M MALANDRINI A BIANCOTTI R LOFGREN A MONGINI T SIX J SALVESTRONI R PARROTTA E VANBROECKHOVEN C PAOLOZZI C GUAZZI G
Citation: M. Villanova et al., MUSCULAR-DYSTROPHY, MENTAL-RETARDATION AND CARDIOMYOPATHY NOT ASSOCIATED WITH DYSTROPHIN DEFICIENCY, Neuromuscular disorders, 6(3), 1996, pp. 167-172
AUTOSOMAL-DOMINANT LIMB-GIRDLE MYOPATHY WITH RAGGED-RED FIBERS AND CARDIOMYOPATHY - A PEDIGREE STUDY BY IN-VIVO P-31-MR SPECTROSCOPY INDICATING A MULTISYSTEM MITOCHONDRIAL DEFECT
Authors: FABRIZI GM LODI R DETTORRE M MALANDRINI A CAVALLARO T RIMOLDI M ZANIOL P BARBIROLI B GUAZZI G
Citation: Gm. Fabrizi et al., AUTOSOMAL-DOMINANT LIMB-GIRDLE MYOPATHY WITH RAGGED-RED FIBERS AND CARDIOMYOPATHY - A PEDIGREE STUDY BY IN-VIVO P-31-MR SPECTROSCOPY INDICATING A MULTISYSTEM MITOCHONDRIAL DEFECT, Journal of the neurological sciences, 137(1), 1996, pp. 20-27
THE A-TRANSITION TO G-TRANSITION AT NT-3243 OF THE MITOCHONDRIAL TRNA(LEU)(UUR) MAY CAUSE AN MERRF SYNDROME
Authors: FABRIZI GM CARDAIOLI E GRIECO GS CAVALLARO T MALANDRINI A MANNESCHI L DOTTI MT FEDERICO A GUAZZI G
Citation: Gm. Fabrizi et al., THE A-TRANSITION TO G-TRANSITION AT NT-3243 OF THE MITOCHONDRIAL TRNA(LEU)(UUR) MAY CAUSE AN MERRF SYNDROME, Journal of Neurology, Neurosurgery and Psychiatry, 61(1), 1996, pp. 47-51
ATAXIA, MENTAL DETERIORATION, EPILEPSY IN A FAMILY WITH DOMINANT ENAMEL HYPOPLASIA - A VARIANT OF KOHLSCHUTTER-TONZ SYNDROME
Authors: GUAZZI G PALMERI S MALANDRINI A CIACCI G DIPERRI R MANCINI G MESSINA C SALVADORI C
Citation: G. Guazzi et al., ATAXIA, MENTAL DETERIORATION, EPILEPSY IN A FAMILY WITH DOMINANT ENAMEL HYPOPLASIA - A VARIANT OF KOHLSCHUTTER-TONZ SYNDROME, American journal of medical genetics, 50(1), 1994, pp. 79-83
ATYPICAL MCLEOD SYNDROME MANIFESTED AS X-LINKED CHOREA-ACANTHOCYTOSIS, NEUROMYOPATHY AND DILATED CARDIOMYOPATHY - REPORT OF A FAMILY
Authors: MALANDRINI A FABRIZI GM TRUSCHI F DIPIETRO G MOSCHINI F BARTALUCCI P BERTI G SALVADORI C BUCALOSSI A GUAZZI G
Citation: A. Malandrini et al., ATYPICAL MCLEOD SYNDROME MANIFESTED AS X-LINKED CHOREA-ACANTHOCYTOSIS, NEUROMYOPATHY AND DILATED CARDIOMYOPATHY - REPORT OF A FAMILY, Journal of the neurological sciences, 124(1), 1994, pp. 89-94
TEACHER-TRAINING AND PERMANENT EDUCATION
Authors: GUAZZI G
Citation: G. Guazzi, TEACHER-TRAINING AND PERMANENT EDUCATION, Italian journal of neurological sciences, 14(8), 1993, pp. 591-592
A 9-BP MICRODUPLICATION IN THE MITOCHONDRIAL-DNA ASSOCIATED WITH A NEW MATERNALLY INHERITED ENCEPHALOMYOPATHY
Authors: FABRIZI GM GUAZZI G DIDONATO S TIRANTI V MALANDRINI A FEDERICO A MARIOTTI C CARRARA F ZEVIANI M
Citation: Gm. Fabrizi et al., A 9-BP MICRODUPLICATION IN THE MITOCHONDRIAL-DNA ASSOCIATED WITH A NEW MATERNALLY INHERITED ENCEPHALOMYOPATHY, Neurology, 43(4), 1993, pp. 401-402
Risultati: 1-11 |