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Results: 1-25 | 26-26
Results: 1-25/26
DETECTION OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIESAMONG PATIENTS WITH ACUTE PAINLESS MONONEUROPATHY OR PLEXOPATHY
Authors: PAREYSON D SOLARI A TARONI F BOTTI S FALLICA E SCAIOLI V CIANO C SGHIRLANZONI A
Citation: D. Pareyson et al., DETECTION OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIESAMONG PATIENTS WITH ACUTE PAINLESS MONONEUROPATHY OR PLEXOPATHY, Muscle & nerve, 21(12), 1998, pp. 1686-1691
VERY MILD CHARCOT-MARIE-TOOTH-DISEASE IN PATIENTS HETEROZYGOUS FOR A LOSS-OF-FUNCTION MUTATION IN THE P-0 GENE
Authors: PAREYSON D MENICHELLA D BOTTI S SGHIRLANZONI A FALLICA E MORA M CIANO C SHY ME TARONI F
Citation: D. Pareyson et al., VERY MILD CHARCOT-MARIE-TOOTH-DISEASE IN PATIENTS HETEROZYGOUS FOR A LOSS-OF-FUNCTION MUTATION IN THE P-0 GENE, Neurology, 50(4), 1998, pp. 8003-8003
LA TOCCATINA - POLYGLOTTAL APHASIA IN PIRANDELLO
Authors: SGHIRLANZONI A PAREYSON D
Citation: A. Sghirlanzoni et D. Pareyson, LA TOCCATINA - POLYGLOTTAL APHASIA IN PIRANDELLO, Italian journal of neurological sciences, 18(1), 1997, pp. 55-57
NEUROLOGIC COMPLICATIONS OF EPIDURAL-ANESTHESIA
Authors: SGHIRLANZONI A PAREYSON D
Citation: A. Sghirlanzoni et D. Pareyson, NEUROLOGIC COMPLICATIONS OF EPIDURAL-ANESTHESIA, Italian journal of neurological sciences, 18(1), 1997, pp. 63-63
GENE DOSAGE EFFECTS IN HEREDITARY PERIPHERAL NEUROPATHY - EXPRESSION OF PERIPHERAL MYELIN PROTEIN-22 IN CHARCOT-MARIE-TOOTH-DISEASE TYPE 1AAND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES NERVE BIOPSIES
Authors: GABRIEL JM ERNE B PAREYSON D SGHIRLANZONI A TARONI F STECK AJ
Citation: Jm. Gabriel et al., GENE DOSAGE EFFECTS IN HEREDITARY PERIPHERAL NEUROPATHY - EXPRESSION OF PERIPHERAL MYELIN PROTEIN-22 IN CHARCOT-MARIE-TOOTH-DISEASE TYPE 1AAND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES NERVE BIOPSIES, Neurology, 49(6), 1997, pp. 1635-1640
PMP22 FRAMESHIFT MUTATION AND HEREDITARY NEUROPATHY WITH LIABILITY TOPRESSURE PALSIES
Authors: PAREYSON D BOTTI S SGHIRLANZONI A TARONI F
Citation: D. Pareyson et al., PMP22 FRAMESHIFT MUTATION AND HEREDITARY NEUROPATHY WITH LIABILITY TOPRESSURE PALSIES, Neurology, 49(5), 1997, pp. 1478-1478
EPIDURAL-ANESTHESIA
Authors: SGHIRLANZONI A PAREYSON D
Citation: A. Sghirlanzoni et D. Pareyson, EPIDURAL-ANESTHESIA, Neurology, 48(1), 1997, pp. 293-294
PHENOTYPIC HETEROGENEITY IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES ASSOCIATED WITH CHROMOSOME 17P11.2-12 DELETION
Authors: PAREYSON D SCAIOLI V TARONI F BOTTI S LORENZETTI D SOLARI A CIANO C SGHIRLANZONI A
Citation: D. Pareyson et al., PHENOTYPIC HETEROGENEITY IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES ASSOCIATED WITH CHROMOSOME 17P11.2-12 DELETION, Neurology, 46(4), 1996, pp. 1133-1137
HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - A NONSENSEMUTATION IN THE PMP22 GENE IN A FAMILY NOT CARRYING THE COMMON 17P11.2-12 DELETION
Authors: TARONI F BOTTI S SGHIRLANZONI A SCAIOLI V DIDONATO S PAREYSON D
Citation: F. Taroni et al., HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - A NONSENSEMUTATION IN THE PMP22 GENE IN A FAMILY NOT CARRYING THE COMMON 17P11.2-12 DELETION, Neurology, 46(2), 1996, pp. 21002-21002
TOMACULOUS NEUROPATHY IN PATIENTS WITH ACUTE PAINLESS MONONEUROPATHY PLEXOPATHY/
Authors: PAREYSON D SOLARI A SCAIOLI V CIANO C BOTTI S TARONI F SGHIRLANZONI A
Citation: D. Pareyson et al., TOMACULOUS NEUROPATHY IN PATIENTS WITH ACUTE PAINLESS MONONEUROPATHY PLEXOPATHY/, Neurology, 46(2), 1996, pp. 35003-35003
KENNEDYS-DISEASE - CLINICAL AND MOLECULAR STUDY OF 2 ITALIAN FAMILIES
Authors: PAREYSON D CASTELLOTTI B BOTTI S DEFANTI CA GELLERA C TARONI F SGHIRLANZONI A
Citation: D. Pareyson et al., KENNEDYS-DISEASE - CLINICAL AND MOLECULAR STUDY OF 2 ITALIAN FAMILIES, Italian journal of neurological sciences, 16(7), 1995, pp. 467-471
SPINAL EPIDURAL ABSCESS COMPLICATING TUBERCULOUS SPONDYLITIS
Authors: PAREYSON D SAVOIARDO M DINCERTI L SGHIRLANZONI A
Citation: D. Pareyson et al., SPINAL EPIDURAL ABSCESS COMPLICATING TUBERCULOUS SPONDYLITIS, Italian journal of neurological sciences, 16(5), 1995, pp. 321-325
THE LAST DAYS OF MANZONI,ALESSANDRO
Authors: SGHIRLANZONI A
Citation: A. Sghirlanzoni, THE LAST DAYS OF MANZONI,ALESSANDRO, Italian journal of neurological sciences, 16(3), 1995, pp. 199-202
PHENOTYPIC HETEROGENEITY IN HNPP PATIENTS WITH THE 17P11.2-12 DELETION
Authors: PAREYSON D SCAIOLI V LORENZETTI D BOTTI S SOLARI A LUPSKI JR DIDONATO S TARONI F SGHIRLANZONI A
Citation: D. Pareyson et al., PHENOTYPIC HETEROGENEITY IN HNPP PATIENTS WITH THE 17P11.2-12 DELETION, Neurology, 45(4), 1995, pp. 397-397
UNRECOGNIZED CHARCOT-MARIE-TOOTH DISEASE - DIAGNOSTIC DIFFICULTIES INTHE ASSESSMENT OF RECOVERY FROM PARALYSIS
Authors: FIACCHINO F GRANDI L CIANO C SGHIRLANZONI A
Citation: F. Fiacchino et al., UNRECOGNIZED CHARCOT-MARIE-TOOTH DISEASE - DIAGNOSTIC DIFFICULTIES INTHE ASSESSMENT OF RECOVERY FROM PARALYSIS, Anesthesia and analgesia, 81(1), 1995, pp. 199-201
A NONSENSE MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) NOT ASSOCIATED WITH THE 17P11.2 DELETION
Authors: TARONI F BOTTI S SGHIRLANZONI A BOTTEON G DIDONATO S PAREYSON D
Citation: F. Taroni et al., A NONSENSE MUTATION IN THE PMP22 GENE IN HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES (HNPP) NOT ASSOCIATED WITH THE 17P11.2 DELETION, American journal of human genetics, 57(4), 1995, pp. 1327-1327
A 1.5-MB DELETION IN 17P11.2-P12 IS FREQUENTLY OBSERVED IN ITALIAN FAMILIES WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
Authors: LORENZETTI D PAREYSON D SGHIRLANZONI A ROA BB ABBAS NE PANDOLFO M DIDONATO S LUPSKI JR
Citation: D. Lorenzetti et al., A 1.5-MB DELETION IN 17P11.2-P12 IS FREQUENTLY OBSERVED IN ITALIAN FAMILIES WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, American journal of human genetics, 56(1), 1995, pp. 91-98
THE POEMS-SYNDROME - REPORT OF 6 CASES
Authors: PAREYSON D MARAZZI R CONFALONIERI P MANCARDI GL SCHENONE A SGHIRLANZONI A
Citation: D. Pareyson et al., THE POEMS-SYNDROME - REPORT OF 6 CASES, Italian journal of neurological sciences, 15(7), 1994, pp. 353-358
HOMOZYGOUS HYPERTROPHIC HEREDITARY MOTOR AND SENSORY NEUROPATHIES
Authors: SGHIRLANZONI A PAREYSON D MARAZZI R CAVALETTI G BELLONE E MANDICH P BALESTRINI MR RIVA D
Citation: A. Sghirlanzoni et al., HOMOZYGOUS HYPERTROPHIC HEREDITARY MOTOR AND SENSORY NEUROPATHIES, Italian journal of neurological sciences, 15(1), 1994, pp. 5-14
SUBMICROSCOPIC DELETION IN 17P11.2-P12 IN ITALIAN HNPP FAMILIES
Authors: PAREYSON D SGHIRLANZONI A SCAIOLI V CASTELLOTTI B DIDONATO S PANDOLFO M LORENZETTI D LUPSKI JR
Citation: D. Pareyson et al., SUBMICROSCOPIC DELETION IN 17P11.2-P12 IN ITALIAN HNPP FAMILIES, Neurology, 44(4), 1994, pp. 10000306-10000306
CONDUCTION VELOCITIES IN CHARCOT-MARIE-TOOTH POLYNEUROPATHY TYPE-1
Authors: PAREYSON D SGHIRLANZONI A
Citation: D. Pareyson et A. Sghirlanzoni, CONDUCTION VELOCITIES IN CHARCOT-MARIE-TOOTH POLYNEUROPATHY TYPE-1, Neurology, 44(11), 1994, pp. 2216-2216
17P11.2 DUPLICATION IS A COMMON FINDING IN SPORADIC CASES OF CHARCOT-MARIE-TOOTH TYPE-1
Authors: MANCARDI GL UCCELLI A BELLONE E SGHIRLANZONI A MANDICH P PAREYSON D SCHENONE A ABBRUZZESE M AJMAR F
Citation: Gl. Mancardi et al., 17P11.2 DUPLICATION IS A COMMON FINDING IN SPORADIC CASES OF CHARCOT-MARIE-TOOTH TYPE-1, European neurology, 34(3), 1994, pp. 135-139
NEUROLOGIC SYMPTOMS AFTER EPIDURAL-ANESTHESIA - REPORT OF 3 CASES
Authors: GEMMA M BRICCHI M GRISOLI M VISINTINI S PAREYSON D SGHIRLANZONI A
Citation: M. Gemma et al., NEUROLOGIC SYMPTOMS AFTER EPIDURAL-ANESTHESIA - REPORT OF 3 CASES, Acta anaesthesiologica Scandinavica, 38(7), 1994, pp. 742-743
ANTIMYELOPEROXIDASE ANTIBODIES IN CHURG-STRAUSS-SYNDROME - REPLY
Authors: MARAZZI R PAREYSON D BOIARDI A CORBO M SCAIOLI V SGHIRLANZONI A
Citation: R. Marazzi et al., ANTIMYELOPEROXIDASE ANTIBODIES IN CHURG-STRAUSS-SYNDROME - REPLY, Journal of neurology, 240(7), 1993, pp. 450-450
ABSENCE OF 17P11.2 DUPLICATION IN AUTOSOMAL RECESSIVE HYPERTROPHIC HMSN
Authors: SGHIRLANZONI A PAREYSON D BELLONE E MARAZZI R SCAIOLI V
Citation: A. Sghirlanzoni et al., ABSENCE OF 17P11.2 DUPLICATION IN AUTOSOMAL RECESSIVE HYPERTROPHIC HMSN, Neurology, 43(4), 1993, pp. 214-214
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