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
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
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
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
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
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
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
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
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
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