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Results: 1-25 | 26-39
Results: 1-25/39
CHARCOT-MARIE-TOOTH-DISEASE - AN INTERMEDIATE FORM
Authors: VILLANOVA M TIMMERMAN V DEJONGHE P MALANDRINI A RIZZUTO N VANBROECKHOVEN C GUAZZI GC ROSSI A
Citation: M. Villanova et al., CHARCOT-MARIE-TOOTH-DISEASE - AN INTERMEDIATE FORM, Neuromuscular disorders, 8(6), 1998, pp. 392-393
NEURONAL INTRANUCLEAR INCLUSION DISEASE - NEUROPATHOLOGIC STUDY OF A CASE
Authors: MALANDRINI A VILLANOVA M TRIPODI S PALMERI S SICURELLI F PARROTTA E BERTI G SALVADORI C CINTORINO M GUAZZI GC
Citation: A. Malandrini et al., NEURONAL INTRANUCLEAR INCLUSION DISEASE - NEUROPATHOLOGIC STUDY OF A CASE, Brain & development, 20(5), 1998, pp. 290-294
JUVENILE LEIGH-SYNDROME WITH PROTRACTED COURSE PRESENTING AS CHRONIC SENSORY-MOTOR NEUROPATHY, ATAXIA, DEAFNESS AND RETINITIS-PIGMENTOSA - A CLINICOPATHOLOGICAL REPORT
Authors: MALANDRINI A PALMERI S FABRIZI GM VILLANOVA M BERTI G SALVADORI C GARDINI G MOTTI L SOLIME F GUAZZI GC
Citation: A. Malandrini et al., JUVENILE LEIGH-SYNDROME WITH PROTRACTED COURSE PRESENTING AS CHRONIC SENSORY-MOTOR NEUROPATHY, ATAXIA, DEAFNESS AND RETINITIS-PIGMENTOSA - A CLINICOPATHOLOGICAL REPORT, Journal of the neurological sciences, 155(2), 1998, pp. 218-221
IMMUNOLOCALIZATION OF SEVERAL LAMININ CHAINS IN THE NORMAL HUMAN CENTRAL AND PERIPHERAL NERVOUS-SYSTEM
Authors: VILLANOVA M SEWRY C MALANDRINI A TOTI P MUNTONI F MERLINI L TORELLI S TOSI P MARALDI NM GUAZZI GC
Citation: M. Villanova et al., IMMUNOLOCALIZATION OF SEVERAL LAMININ CHAINS IN THE NORMAL HUMAN CENTRAL AND PERIPHERAL NERVOUS-SYSTEM, Journal of submicroscopic cytology and pathology, 29(3), 1997, pp. 409-413
INTRACELLULAR DETECTION OF LAMININ ALPHA(2) CHAIN IN SKIN BY ELECTRON-MICROSCOPY IMMUNOCYTOCHEMISTRY - COMPARISON BETWEEN NORMAL AND LAMININ ALPHA(2) CHAIN DEFICIENT SUBJECTS
Authors: SQUARZONI S VILLANOVA M SABATELLI P MALANDRINI A TOTI P PINI A MERLINI L GUAZZI GC MARALDI NM
Citation: S. Squarzoni et al., INTRACELLULAR DETECTION OF LAMININ ALPHA(2) CHAIN IN SKIN BY ELECTRON-MICROSCOPY IMMUNOCYTOCHEMISTRY - COMPARISON BETWEEN NORMAL AND LAMININ ALPHA(2) CHAIN DEFICIENT SUBJECTS, Neuromuscular disorders, 7(2), 1997, pp. 91-98
A SYNDROME OF AUTOSOMAL RECESSIVE PONTOCEREBELLAR HYPOPLASIA WITH WHITE-MATTER ABNORMALITIES AND PROTRACTED COURSE IN 2 BROTHERS
Authors: MALANDRINI A PALMERI S VILLANOVA M PARROTTA E SICURELLI F AMATO D DEFALCO D GUAZZI GC
Citation: A. Malandrini et al., A SYNDROME OF AUTOSOMAL RECESSIVE PONTOCEREBELLAR HYPOPLASIA WITH WHITE-MATTER ABNORMALITIES AND PROTRACTED COURSE IN 2 BROTHERS, Brain & development, 19(3), 1997, pp. 209-211
DETECTION OF BORRELIA-BURGDORFERI DNA AND COMPLEMENT MEMBRANE ATTACK COMPLEX DEPOSITS IN THE SURAL NERVE OF A PATIENT WITH CHRONIC POLYNEUROPATHY AND TERTIARY LYME-DISEASE
Authors: MAIMONE D VILLANOVA M STANTA G BONIN S MALANDRINI A GUAZZI GC ANNUNZIATA P
Citation: D. Maimone et al., DETECTION OF BORRELIA-BURGDORFERI DNA AND COMPLEMENT MEMBRANE ATTACK COMPLEX DEPOSITS IN THE SURAL NERVE OF A PATIENT WITH CHRONIC POLYNEUROPATHY AND TERTIARY LYME-DISEASE, Muscle & nerve, 20(8), 1997, pp. 969-975
UNUSUAL CLINICAL-FEATURES AND EARLY BRAIN MRI LESIONS IN A FAMILY WITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY
Authors: MALANDRINI A CARRERA P CIACCI G GONNELLI S VILLANOVA M PALMERI S VISMARA L BRANCOLINI V SIGNORINI E FERRARI M GUAZZI GC
Citation: A. Malandrini et al., UNUSUAL CLINICAL-FEATURES AND EARLY BRAIN MRI LESIONS IN A FAMILY WITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY, Neurology, 48(5), 1997, pp. 1200-1203
IL-6 DETECTION IN MULTIPLE-SCLEROSIS BRAIN
Authors: MAIMONE D GUAZZI GC ANNUNZIATA P
Citation: D. Maimone et al., IL-6 DETECTION IN MULTIPLE-SCLEROSIS BRAIN, Journal of the neurological sciences, 146(1), 1997, pp. 59-65
THE POTENTIAL ROLE OF HEPATITIS-C VIRUS IN THE PATHOGENESIS OF THE NEUROLOGICAL SYNDROME IN CHRONIC HEPATITIS-C
Authors: CAUDAI C MAIMONE D ALMI P ANNUNZIATA P BASTIANONI I BOGGIANO CA GUAZZI GC PADULA M VALENSIN PE
Citation: C. Caudai et al., THE POTENTIAL ROLE OF HEPATITIS-C VIRUS IN THE PATHOGENESIS OF THE NEUROLOGICAL SYNDROME IN CHRONIC HEPATITIS-C, Gut, 41(3), 1997, pp. 411-412
LOCALIZATION OF LAMININ ALPHA-2 CHAIN IN NORMAL HUMAN CENTRAL-NERVOUS-SYSTEM - AN IMMUNOFLUORESCENCE AND ULTRASTRUCTURAL-STUDY
Authors: VILLANOVA M MALANDRINI A SABATELLI P SEWRY CA TOTI P TORELLI S SIX J SCARFO G PALMA L MUNTONI F SQUARZONI S TOSI P MARALDI NM GUAZZI GC
Citation: M. Villanova et al., LOCALIZATION OF LAMININ ALPHA-2 CHAIN IN NORMAL HUMAN CENTRAL-NERVOUS-SYSTEM - AN IMMUNOFLUORESCENCE AND ULTRASTRUCTURAL-STUDY, Acta Neuropathologica, 94(6), 1997, pp. 567-571
LOCALIZATION OF MEROSIN IN THE NORMAL HUMAN BRAIN - IMPLICATIONS FOR CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSIN DEFICIENCY
Authors: VILLANOVA M MALANDRINI A TOTI P SALVESTRONI R SIX J MARTIN JJ GUAZZI GC
Citation: M. Villanova et al., LOCALIZATION OF MEROSIN IN THE NORMAL HUMAN BRAIN - IMPLICATIONS FOR CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSIN DEFICIENCY, Journal of submicroscopic cytology and pathology, 28(1), 1996, pp. 1-4
PALATAL MYOCLONUS AND UNUSUAL MRI FINDINGS IN A PATIENT WITH MEMBRANOUS LIPODYSTROPHY
Authors: MALANDRINI A SCARPINI C PALMERI S VILLANOVA M PARROTTA E TRIPODI S GIANI S DEFALCO D GUAZZI GC
Citation: A. Malandrini et al., PALATAL MYOCLONUS AND UNUSUAL MRI FINDINGS IN A PATIENT WITH MEMBRANOUS LIPODYSTROPHY, Brain & development, 18(1), 1996, pp. 59-63
CLINICOPATHOLOGICAL STUDY OF FAMILIAL LATE INFANTILE HALLERVORDEN-SPATZ DISEASE - A PARTICULAR FORM OF NEUROACANTHOCYTOSIS
Authors: MALANDRINI A FABRIZI GM BARTALUCCI P SALVADORI C BERTI G SABO C GUAZZI GC
Citation: A. Malandrini et al., CLINICOPATHOLOGICAL STUDY OF FAMILIAL LATE INFANTILE HALLERVORDEN-SPATZ DISEASE - A PARTICULAR FORM OF NEUROACANTHOCYTOSIS, Child's nervous system, 12(3), 1996, pp. 155-160
ACANTHOCYTOSIS, RETINITIS-PIGMENTOSA, PALLIDAL DEGENERATION - REPORT OF 2 CASES WITHOUT SERUM-LIPID ABNORMALITIES
Authors: MALANDRINI A CESARETTI S MULINARI M PALMERI S FABRIZI GM VILLANOVA M PARROTTA E MONTAGNANI A MONTAGNANI M ANICHINI M GUAZZI GC
Citation: A. Malandrini et al., ACANTHOCYTOSIS, RETINITIS-PIGMENTOSA, PALLIDAL DEGENERATION - REPORT OF 2 CASES WITHOUT SERUM-LIPID ABNORMALITIES, Journal of the neurological sciences, 140(1-2), 1996, pp. 129-131
ATAXIA-TELANGIECTASIA - SOMATOSENSORY, BRAIN-STEM AUDITORY AND MOTOR EVOKED-POTENTIALS IN 6 PATIENTS
Authors: SCARPINI C MONDELLI M GUAZZI GC FEDERICO A
Citation: C. Scarpini et al., ATAXIA-TELANGIECTASIA - SOMATOSENSORY, BRAIN-STEM AUDITORY AND MOTOR EVOKED-POTENTIALS IN 6 PATIENTS, Developmental Medicine and Child Neurology, 38(1), 1996, pp. 65-73
AN UNUSUAL TYPE OF PRIMARY CEREBRAL HEMIHYPOTROPHY WITH SIGNS OF DYSFUNCTIONAL NEURONAL MIGRATION
Authors: MALANDRINI A LORUSSO F VILLANOVA M SALVESTRONI R SICURELLI F SALVADORI C PAOLOZZI C GUAZZI GC
Citation: A. Malandrini et al., AN UNUSUAL TYPE OF PRIMARY CEREBRAL HEMIHYPOTROPHY WITH SIGNS OF DYSFUNCTIONAL NEURONAL MIGRATION, Acta Neuropathologica, 92(6), 1996, pp. 631-634
CLINICOPATHOLOGICAL AND GENETIC-STUDIES OF 2 FURTHER ITALIAN FAMILIESWITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY
Authors: MALANDRINI A CARRERA P PALMERI S CAVALLARO T FABRIZI GM VILLANOVA M FATTAPPOSTA M VISMARA L BRANCOLINI V TANGANELLI P CALI A MOROCUTTI C ZEVIANI M FERRARI M GUAZZI GC
Citation: A. Malandrini et al., CLINICOPATHOLOGICAL AND GENETIC-STUDIES OF 2 FURTHER ITALIAN FAMILIESWITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY, Acta Neuropathologica, 92(2), 1996, pp. 115-122
NEURONAL INTRANUCLEAR INCLUSION DISEASE - POLYMERASE CHAIN-REACTION AND ULTRASTRUCTURAL-STUDY OF RECTAL BIOPSY SPECIMEN IN A NEW CASE
Authors: MALANDRINI A FABRIZI GM CAVALLARO T ZAZZI M PARROTTA E ROMANO L BERTI G VILLANOVA M GUAZZI GC
Citation: A. Malandrini et al., NEURONAL INTRANUCLEAR INCLUSION DISEASE - POLYMERASE CHAIN-REACTION AND ULTRASTRUCTURAL-STUDY OF RECTAL BIOPSY SPECIMEN IN A NEW CASE, Acta Neuropathologica, 91(2), 1996, pp. 215-218
AUTOSOMAL RECESSIVE PARAPARESIS WITH AMYOTROPHY OF HANDS AND FEET ANDWHITE-MATTER LESIONS
Authors: MALANDRINI A SCARPINI C VILLANOVA M SICURELLI F PARROTTA E DEFALCO D GUAZZI GC
Citation: A. Malandrini et al., AUTOSOMAL RECESSIVE PARAPARESIS WITH AMYOTROPHY OF HANDS AND FEET ANDWHITE-MATTER LESIONS, Acta neurologica Scandinavica, 94(1), 1996, pp. 60-62
ULTRASTRUCTURE AND IMMUNOREACTIVITY OF DYSTROPHIC AXONS INDICATE A DIFFERENT PATHOGENESIS OF HALLERVORDEN-SPATZ DISEASE AND INFANTILE NEUROAXONAL DYSTROPHY
Authors: MALANDRINI A CAVALLARO T FABRIZI GM BERTI G SALVESTRONI R SALVADORI C GUAZZI GC
Citation: A. Malandrini et al., ULTRASTRUCTURE AND IMMUNOREACTIVITY OF DYSTROPHIC AXONS INDICATE A DIFFERENT PATHOGENESIS OF HALLERVORDEN-SPATZ DISEASE AND INFANTILE NEUROAXONAL DYSTROPHY, Virchows Archiv, 427(4), 1995, pp. 415-421
MYOPATHIC INVOLVEMENT IN 2 CASES OF HALLERVORDEN-SPATZ DISEASE
Authors: MALANDRINI A BONUCCELLI U PARROTTA E CERAVOLO R BERTI G GUAZZI GC
Citation: A. Malandrini et al., MYOPATHIC INVOLVEMENT IN 2 CASES OF HALLERVORDEN-SPATZ DISEASE, Brain & development, 17(4), 1995, pp. 286-290
SEQUENCE-ANALYSIS OF MITOCHONDRIAL-DNA IN A NEW MATERNALLY INHERITED ENCEPHALOMYOPATHY
Authors: FABRIZI GM TIRANTI V MARIOTTI C GUAZZI GC MALANDRINI A DIDONATO S ZEVIANI M
Citation: Gm. Fabrizi et al., SEQUENCE-ANALYSIS OF MITOCHONDRIAL-DNA IN A NEW MATERNALLY INHERITED ENCEPHALOMYOPATHY, Journal of neurology, 242(8), 1995, pp. 490-496
EARLY-ONSET BENIGN LIMB-GIRDLE MYOPATHY WITH CONTRACTURES AND FACIAL INVOLVEMENT AFFECTING A FATHER AND DAUGHTER
Authors: MALANDRINI A SCARPINI C FABRIZI GM PARROTTA E SALVADORI C GUAZZI GC
Citation: A. Malandrini et al., EARLY-ONSET BENIGN LIMB-GIRDLE MYOPATHY WITH CONTRACTURES AND FACIAL INVOLVEMENT AFFECTING A FATHER AND DAUGHTER, Journal of the neurological sciences, 132(2), 1995, pp. 195-200
SERUM ANTIBRAIN ENDOTHELIUM ANTIBODIES AND COGNITIVE ASSESSMENT IN PATIENTS WITH BINSWANGERS ENCEPHALOPATHY
Authors: ANNUNZIATA P CIONI C MOSCHINI F RICCUCCI A GUAZZI GC
Citation: P. Annunziata et al., SERUM ANTIBRAIN ENDOTHELIUM ANTIBODIES AND COGNITIVE ASSESSMENT IN PATIENTS WITH BINSWANGERS ENCEPHALOPATHY, Journal of the neurological sciences, 128(1), 1995, pp. 96-102
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