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Results: 1-17 |
Results: 17
CYTOCHROME-C-OXIDASE SUBUNIT-I MICRODELETION IN A PATIENT WITH MOTOR-NEURON DISEASE
Authors: COMI GP BORDONI A SALANI S FRANCESCHINA L SCIACCO M PRELLE A FORTUNATO F ZEVIANI M NAPOLI L BRESOLIN N MOGGIO M AUSENDA CD TAANMAN JW SCARLATO G
Citation: Gp. Comi et al., CYTOCHROME-C-OXIDASE SUBUNIT-I MICRODELETION IN A PATIENT WITH MOTOR-NEURON DISEASE, Annals of neurology, 43(1), 1998, pp. 110-116
A NOVEL MITOCHONDRIAL TRNA(ILE) POINT MUTATION IN CHRONIC PROGRESSIVEEXTERNAL OPHTHALMOPLEGIA
Authors: FRANCESCHINA L SALANI S BORDONI A SCIACCO M NAPOLI L COMI GP PRELLE A FORTUNATO F HADJIGEORGIOU GM FARINA E BRESOLIN N DANGELO MG SCARLATO G
Citation: L. Franceschina et al., A NOVEL MITOCHONDRIAL TRNA(ILE) POINT MUTATION IN CHRONIC PROGRESSIVEEXTERNAL OPHTHALMOPLEGIA, Journal of neurology, 245(11), 1998, pp. 755-758
MODULATION OF CASPASE-3 ACTIVITY AND FAS LIGAND MESSENGER-RNA EXPRESSION IN RAT-LIVER CELLS IN-VIVO BY ALCOHOL AND LIPOPOLYSACCHARIDE
Authors: DEACIUC IV FORTUNATO F DSOUZA NB HILL DH SCHMIDT J LEE EY MCCLAIN CJ
Citation: Iv. Deaciuc et al., MODULATION OF CASPASE-3 ACTIVITY AND FAS LIGAND MESSENGER-RNA EXPRESSION IN RAT-LIVER CELLS IN-VIVO BY ALCOHOL AND LIPOPOLYSACCHARIDE, Hepatology, 28(4), 1998, pp. 81-81
FIBROBLASTS MEDIATED GENE-TRANSFER TO SKELETAL-MUSCLE - IN-VIVO INDUCTION OF MYOGENESIS BY A TETRACYCLINE CONTROLLED PROMOTER SYSTEM
Authors: COLUCCI M AUSENDA CD TORRENTE Y DELISO A DANGELO MG GIORDA R PARINI B CORTI S FORTUNATO F COMI GP BRESOLIN N SCARLATO G
Citation: M. Colucci et al., FIBROBLASTS MEDIATED GENE-TRANSFER TO SKELETAL-MUSCLE - IN-VIVO INDUCTION OF MYOGENESIS BY A TETRACYCLINE CONTROLLED PROMOTER SYSTEM, Neurology, 50(4), 1998, pp. 38003-38003
THE PROTEOSOME INHIBITOR MG132 SENSITIZES MIAPACA-2 PANCREATIC TUMOR-CELLS TO TUMOR-NECROSIS-FACTOR (TNF)-INDUCED APOPTOSIS THROUGH STABILIZATION OF THE NF-KAPPA-B-I-KAPPA-B COMPLEX
Authors: FORTUNATO F BARVE S JOSHIBARVE S GATES LK
Citation: F. Fortunato et al., THE PROTEOSOME INHIBITOR MG132 SENSITIZES MIAPACA-2 PANCREATIC TUMOR-CELLS TO TUMOR-NECROSIS-FACTOR (TNF)-INDUCED APOPTOSIS THROUGH STABILIZATION OF THE NF-KAPPA-B-I-KAPPA-B COMPLEX, Gastroenterology, 114(4), 1998, pp. 2449-2449
SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS
Authors: PRELLE A COMI GP TANCREDI L RIGOLETTO C CISCATO P FORTUNATO F NESTI S SCIACCO M ROBOTTI M BAZZI P FELISARI G MOGGIO M SCARLATO G
Citation: A. Prelle et al., SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS, Acta Neuropathologica, 96(5), 1998, pp. 509-514
AN ATYPICAL CASE OF PARTIAL MEROSIN DEFICIENCY CONGENITAL MUSCULAR-DYSTROPHY
Authors: PRELLE A COMI GP RIGOLETTO C TURCONI A FELISARI G CISCATO P FORTUNATO F MESSINA S BRESOLIN N MORA M MOGGIO M SCARLATO G
Citation: A. Prelle et al., AN ATYPICAL CASE OF PARTIAL MEROSIN DEFICIENCY CONGENITAL MUSCULAR-DYSTROPHY, Journal of neurology, 244(6), 1997, pp. 391-395
FREQUENCY OF ALPHA-SARCOGLYCAN AND GAMMA-SARCOGLYCAN DEFICIENCY IN A LARGE POPULATION OF MYOPATHIC PATIENTS
Authors: PRELLE A TANCREDI L COMI GP RIGOLETTO C CISCATO P FORTUNATO F FELISARI G MOGGIO M SCARLATO G
Citation: A. Prelle et al., FREQUENCY OF ALPHA-SARCOGLYCAN AND GAMMA-SARCOGLYCAN DEFICIENCY IN A LARGE POPULATION OF MYOPATHIC PATIENTS, Neurology, 48(3), 1997, pp. 3131-3131
A G(-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT (VOL 4, PG 2171, 1995)(1))
Authors: COMI GP CIAFALONI E DESILVA HAR PRELLE A BARDONI A RIGOLETTO C ROBOTTI M BRESOLIN N MOGGIO M FORTUNATO F CISCATO P TURCONI A ROSES AD SCARLATO G
Citation: Gp. Comi et al., A G(-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT (VOL 4, PG 2171, 1995)(1)), Human molecular genetics, 5(4), 1996, pp. 562-562
A G(-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT(1))
Authors: COMI GP CIAFALONI E DESILVA HAR PRELLE A BARDONI A RIGOLETTO C ROBOTTI M BRESOLIN N MOGGIO M FORTUNATO F CISCATO P TURCONI A ROSE AD SCARLATO G
Citation: Gp. Comi et al., A G(-]A TRANSVERSION AT THE 5'-SPLICE-SITE OF INTRON-69 OF THE DYSTROPHIN GENE CAUSING THE ABSENCE OF PERIPHERAL-NERVE DP116 AND SEVERE CLINICAL INVOLVEMENT IN A DMD PATIENT(1)), Human molecular genetics, 4(11), 1995, pp. 2171-2174
DUPLICATION OF DYSTROPHIN GENE AND DISSIMILAR CLINICAL PHENOTYPE IN THE SAME FAMILY
Authors: TOSCANO A VITIELLO L COMI GP GALVAGNI F MIORIN M PRELLE A FORTUNATO F BARDONI A MORA M FIUMARA A FALSAPERLA R TOMELLERI G TONIN P DANIELI GA VITA G
Citation: A. Toscano et al., DUPLICATION OF DYSTROPHIN GENE AND DISSIMILAR CLINICAL PHENOTYPE IN THE SAME FAMILY, Neuromuscular disorders, 5(6), 1995, pp. 475-481
UTROPHIN EXPRESSION DURING HUMAN FETAL DEVELOPMENT
Authors: RIGOLETTO C PRELLE A CISCATO P MOGGIO M COMI G FORTUNATO F SCARLATO G
Citation: C. Rigoletto et al., UTROPHIN EXPRESSION DURING HUMAN FETAL DEVELOPMENT, International journal of developmental neuroscience, 13(6), 1995, pp. 585-593
MUSCLE PHOSPHOGLYCERATE MUTASE (PGAM) DEFICIENCY IN THE 1ST CAUCASIANPATIENT - BIOCHEMISTRY, MUSCLE CULTURE AND P-31-MR SPECTROSCOPY
Authors: VITA G TOSCANO A BRESOLIN N MEOLA G FORTUNATO F BARADELLO A BARBIROLI B FRASSINETI C ZANIOL P MESSINA C
Citation: G. Vita et al., MUSCLE PHOSPHOGLYCERATE MUTASE (PGAM) DEFICIENCY IN THE 1ST CAUCASIANPATIENT - BIOCHEMISTRY, MUSCLE CULTURE AND P-31-MR SPECTROSCOPY, Journal of neurology, 241(5), 1994, pp. 289-294
CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA - A CORRELATIVE STUDY OFQUANTITATIVE MOLECULAR-DATA AND HISTOCHEMICAL AND BIOCHEMICAL PROFILE
Authors: FASSATI A BORDONI A AMBONI P FORTUNATO F FAGIOLARI G BRESOLIN N PRELLE A COMI G SCARLATO G
Citation: A. Fassati et al., CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA - A CORRELATIVE STUDY OFQUANTITATIVE MOLECULAR-DATA AND HISTOCHEMICAL AND BIOCHEMICAL PROFILE, Journal of the neurological sciences, 123(1-2), 1994, pp. 140-146
CLINICAL VARIABILITY IN BECKER MUSCULAR-DYSTROPHY - GENETIC, BIOCHEMICAL AND IMMUNOHISTOCHEMICAL CORRELATES
Authors: COMI GP PRELLE A BRESOLIN N MOGGIO M BARDONI A GALLANTI A VITA G TOSCANO A FERRO MT BORDONI A FORTUNATO F CISCATO P FELISARI G TEDESCHI S CASTELLI E GARGHENTINO R TURCONI A FRASCHINI P MARCHI E NEGRETTO GG ADOBBATI L MEOLA G TONIN P PAPADIMITRIOU A SCARLATO G
Citation: Gp. Comi et al., CLINICAL VARIABILITY IN BECKER MUSCULAR-DYSTROPHY - GENETIC, BIOCHEMICAL AND IMMUNOHISTOCHEMICAL CORRELATES, Brain, 117, 1994, pp. 1-14
CLINICAL AND BIOCHEMICAL-EVIDENCE OF SKELETAL-MUSCLE INVOLVEMENT IN GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE DEFICIENCY
Authors: BRESOLIN N COMI GP FORTUNATO F MEOLA G GALLANTI A TAJANA A VELICOGNA M GONANO EF NINFALI P PIFFERI S SCARLATO G
Citation: N. Bresolin et al., CLINICAL AND BIOCHEMICAL-EVIDENCE OF SKELETAL-MUSCLE INVOLVEMENT IN GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE DEFICIENCY, Journal of neurology, 240(5), 1993, pp. 272-277
ABSENCE OF MENTAL-RETARDATION IN A LARGE DMD GENE DELETION INVOLVING BRAIN DYSTROPHIN PROMOTER
Authors: COMI GP BRESOLIN N BARDONI A CASTELLI E PRELLE A FORTUNATO F SCARLATO G
Citation: Gp. Comi et al., ABSENCE OF MENTAL-RETARDATION IN A LARGE DMD GENE DELETION INVOLVING BRAIN DYSTROPHIN PROMOTER, Neurology, 43(4), 1993, pp. 313-313
Risultati: 1-17 |