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Results: 1-15 |
Results: 15
TRANSDUCED FIBROBLASTS AND METACHROMATIC LEUKODYSTROPHY LYMPHOCYTES TRANSFER ARYLSULFATASE A TO MYELINATING GLIA AND DEFICIENT CELLS IN-VITRO
Authors: SANGALLI A TAVEGGIA C SALVIATI A WRABETZ L BORDIGNON C SEVERINI GM
Citation: A. Sangalli et al., TRANSDUCED FIBROBLASTS AND METACHROMATIC LEUKODYSTROPHY LYMPHOCYTES TRANSFER ARYLSULFATASE A TO MYELINATING GLIA AND DEFICIENT CELLS IN-VITRO, Human gene therapy, 9(14), 1998, pp. 2111-2119
FREQUENCY OF LEWY BODY PATHOLOGY IN A COMMUNITY-BASED INCIDENCE STUDYOF DEMENTIA
Authors: SALVIATI A DICKSON DW PARISI JE JOHNSON KA ROCCA WA PETERSEN RC KOKMEN E
Citation: A. Salviati et al., FREQUENCY OF LEWY BODY PATHOLOGY IN A COMMUNITY-BASED INCIDENCE STUDYOF DEMENTIA, Annals of neurology, 44(3), 1998, pp. 25-25
MOLECULAR-GENETIC CHARACTERIZATION OF 2 METACHROMATIC LEUKODYSTROPHY PATIENTS WHO CARRY THE T799G MUTATION AND SHOW DIFFERENT PHENOTYPES - DESCRIPTION OF A NOVEL NULL-TYPE MUTATION (VOL 102, PG 459, 1998)
Authors: GOMEZLIRA M PERUSI C MOTTES M PIGNATTI PF MANFREDI M RIZZUTO N SALVIATI A
Citation: M. Gomezlira et al., MOLECULAR-GENETIC CHARACTERIZATION OF 2 METACHROMATIC LEUKODYSTROPHY PATIENTS WHO CARRY THE T799G MUTATION AND SHOW DIFFERENT PHENOTYPES - DESCRIPTION OF A NOVEL NULL-TYPE MUTATION (VOL 102, PG 459, 1998), Human genetics, 102(5), 1998, pp. 602-602
MOLECULAR-GENETIC CHARACTERIZATION OF 2 METACHROMATIC LEUKODYSTROPHY PATIENTS WHO CARRY THE T799G MUTATION AND SHOW DIFFERENT PHENOTYPES - DESCRIPTION OF A NOVEL NULL-TYPE MUTATION
Authors: GOMEZLIRA M PERUSI C MOTTES M PIGNATTI PF MANFREDI M RIZZUTO N SALVIATI A
Citation: M. Gomezlira et al., MOLECULAR-GENETIC CHARACTERIZATION OF 2 METACHROMATIC LEUKODYSTROPHY PATIENTS WHO CARRY THE T799G MUTATION AND SHOW DIFFERENT PHENOTYPES - DESCRIPTION OF A NOVEL NULL-TYPE MUTATION, Human genetics, 102(4), 1998, pp. 459-463
SPLICING MUTATION CAUSES INFANTILE SANDHOFF-DISEASE
Authors: GOMEZLIRA M PERUSI C MOTTES M PIGNATTI PF RIZZUTO N GATTI R SALVIATI A
Citation: M. Gomezlira et al., SPLICING MUTATION CAUSES INFANTILE SANDHOFF-DISEASE, American journal of medical genetics, 75(3), 1998, pp. 330-333
PREVALENCE OF ALZHEIMERS-DISEASE AND OTHER DEMENTING DISORDERS IN AN ITALIAN POPULATION AGED 75 YEARS AND OLDER
Authors: BENEDETTI MD DETOGNI L MANFREDI M DANTI G SALVIATI A FILIPPONI S STENTA G FINCATI E PAMPANIN M RIZZUTO N
Citation: Md. Benedetti et al., PREVALENCE OF ALZHEIMERS-DISEASE AND OTHER DEMENTING DISORDERS IN AN ITALIAN POPULATION AGED 75 YEARS AND OLDER, Neurology, 50(4), 1998, pp. 1004-1004
NEUROPATHOLOGY OF COGNITIVELY NORMAL ELDERLY INDIVIDUALS
Authors: SALVIATI A MCDONALD WC JOHNSON KA BOHAC DL PETERSEN LE BOEVE BF WARING SC PARISI JE
Citation: A. Salviati et al., NEUROPATHOLOGY OF COGNITIVELY NORMAL ELDERLY INDIVIDUALS, Neurology, 50(4), 1998, pp. 3005-3005
MEMORY FUNCTION AND NEUROFIBRILLARY DEGENERATION IN THE MEDIAL TEMPORAL-LOBE
Authors: BOEVE BF BRAAK H PARISI JE SALVIATI A IVNIK RJ WARING SC KOKMEN E PETERSEN RC
Citation: Bf. Boeve et al., MEMORY FUNCTION AND NEUROFIBRILLARY DEGENERATION IN THE MEDIAL TEMPORAL-LOBE, Neurology, 50(4), 1998, pp. 3008-3008
NEUROPATHOLOGIC FEATURES OF VERY OLD COGNITIVELY INTACT AND DEMENTED SUBJECTS
Authors: SALVIATI A PARISI JE PETERSEN RC JOHNSON K PETERSEN LE WARING SC KOKMEN E
Citation: A. Salviati et al., NEUROPATHOLOGIC FEATURES OF VERY OLD COGNITIVELY INTACT AND DEMENTED SUBJECTS, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 8-8
A NOVEL MUTATION WHICH REPRESENTS THE 5TH NONPATHOGENIC POLYMORPHISM IN THE CODING SEQUENCE OF THE ARYLSULFATASE-A GENE
Authors: PERUSI C GOMEZLIRA M MOTTES M PIGNATTI PF RIZZUTO N SALVIATI A
Citation: C. Perusi et al., A NOVEL MUTATION WHICH REPRESENTS THE 5TH NONPATHOGENIC POLYMORPHISM IN THE CODING SEQUENCE OF THE ARYLSULFATASE-A GENE, Molecular and cellular probes, 11(6), 1997, pp. 449-451
FAMILIAL CAVERNOUS HEMANGIOMA WITH ATYPICAL NEUROIMAGING
Authors: PASSARIN MG SALVIATI A GAMBINA G TEZZON F TOMELLERI G DEOTTO L ZANONI T BOVI P GEROSA M NICOLATO A MAZZA C IUZZOLINO P GHIMENTON C FERRARI G
Citation: Mg. Passarin et al., FAMILIAL CAVERNOUS HEMANGIOMA WITH ATYPICAL NEUROIMAGING, Italian journal of neurological sciences, 17(4), 1996, pp. 295-300
SENSORY INVOLVEMENT IN X-LINKED SPINE-BULBAR MUSCULAR-ATROPHY (KENNEDYS-SYNDROME) - AN ELECTROPHYSIOLOGICAL STUDY
Authors: POLO A TEATINI F DANNA S MANGANOTTI P SALVIATI A DALLAPICCOLA B ZANETTE G RIZZUTO N
Citation: A. Polo et al., SENSORY INVOLVEMENT IN X-LINKED SPINE-BULBAR MUSCULAR-ATROPHY (KENNEDYS-SYNDROME) - AN ELECTROPHYSIOLOGICAL STUDY, Journal of neurology, 243(5), 1996, pp. 388-392
EFFECTS OF LONG-TERM CONDUCTION BLOCK ON MEMBRANE-PROPERTIES OF REINNERVATED AND NORMALLY INNERVATED RAT SKELETAL-MUSCLE
Authors: PASINO E BUFFELLI M ARANCIO O BUSETTO G SALVIATI A CANGIANO A
Citation: E. Pasino et al., EFFECTS OF LONG-TERM CONDUCTION BLOCK ON MEMBRANE-PROPERTIES OF REINNERVATED AND NORMALLY INNERVATED RAT SKELETAL-MUSCLE, Journal of physiology, 497(2), 1996, pp. 457-472
A 48-BP INSERTION BETWEEN EXON-13 AND EXON-14 OF THE HEXB GENE CAUSESINFANTILE-ONSET SANDHOFF DISEASE
Authors: GOMEZLIRA M PERUSI C BRUTTI N FARNETANI MA MARGOLLICCI MA RIZZUTO N PIGNATTI PF SALVIATI A
Citation: M. Gomezlira et al., A 48-BP INSERTION BETWEEN EXON-13 AND EXON-14 OF THE HEXB GENE CAUSESINFANTILE-ONSET SANDHOFF DISEASE, Human mutation, 6(3), 1995, pp. 260-262
A COMMON BETA-HEXOSAMINIDASE GENE MUTATION IN ADULT SANDHOFF DISEASE PATIENTS
Authors: GOMEZLIRA M SANGALLI A MOTTES M PERUSI C PIGNATTI PF RIZZUTO N SALVIATI A
Citation: M. Gomezlira et al., A COMMON BETA-HEXOSAMINIDASE GENE MUTATION IN ADULT SANDHOFF DISEASE PATIENTS, Human genetics, 96(4), 1995, pp. 417-422
Risultati: 1-15 |