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Results: 1-23 |
Results: 23
MOLECULAR PATHOLOGY OF FATAL FAMILIAL INSOMNIA
Authors: PARCHI P PETERSEN RB CHEN SG AUTILIOGAMBETTI L CAPELLARI S MONARI L CORTELLI P MONTAGNA P LUGARESI E GAMBETTI P
Citation: P. Parchi et al., MOLECULAR PATHOLOGY OF FATAL FAMILIAL INSOMNIA, Brain pathology, 8(3), 1998, pp. 539-548
CEREBELLAR-ATAXIA, HYPOGONADISM AND CHORIORETINOPATHY - MOLECULAR ANALYSIS OF AN ITALIAN FAMILY
Authors: RIZZI R CARELLI V MONARI L MOCHI M LIGUORI R SENSI M COCOZZA S FILLA A MONTAGNA P
Citation: R. Rizzi et al., CEREBELLAR-ATAXIA, HYPOGONADISM AND CHORIORETINOPATHY - MOLECULAR ANALYSIS OF AN ITALIAN FAMILY, Italian journal of neurological sciences, 19(1), 1998, pp. 41-44
STUDIES ON TRANSMITOCHONDRIAL CYBRIDS UNVEIL BIOENERGETIC DEFECTS IN NON-LEBERS PROGRESSIVE SPORADIC OPTIC ATROPHY
Authors: MARTINUZZI A BUCCHI L MONARI L GHELLI A LUGARESI E MONTAGNA P CARELLI V
Citation: A. Martinuzzi et al., STUDIES ON TRANSMITOCHONDRIAL CYBRIDS UNVEIL BIOENERGETIC DEFECTS IN NON-LEBERS PROGRESSIVE SPORADIC OPTIC ATROPHY, Neurology, 50(4), 1998, pp. 1010-1010
LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) WITH 14484 ND6 MUTATION IN A NORTH-AFRICAN PATIENT/
Authors: CARELLI V BARBONI P ZACCHINI A MANCINI R MONARI L CEVOLI S LIGUORI R SENSI M LUGARESI E MONTAGNA P
Citation: V. Carelli et al., LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) WITH 14484 ND6 MUTATION IN A NORTH-AFRICAN PATIENT/, Journal of the neurological sciences, 160(2), 1998, pp. 183-188
SEARCHING FOR MIGRAINE GENES - EXCLUSION OF 290 CM OUT OF THE WHOLE HUMAN GENOME
Authors: MONARI L MOCHI M VALENTINO ML ARNALDI C CORTELLI P DEMONTE A PIERANGELI G PROLOGO G SCAPOLI C SORIANI S MONTAGNA P
Citation: L. Monari et al., SEARCHING FOR MIGRAINE GENES - EXCLUSION OF 290 CM OUT OF THE WHOLE HUMAN GENOME, Italian journal of neurological sciences, 18(5), 1997, pp. 277-282
DEFECTIVE BRAIN AND MUSCLE ENERGY-METABOLISM SHOWN BY IN-VIVO P-31 MAGNETIC-RESONANCE SPECTROSCOPY IN NONAFFECTED CARRIERS OF 11778-MTDNA MUTATION
Authors: BARBIROLI B MONTAGNA P CORTELLI P IOTTI S LODI R BARBONI P MONARI L LUGARESI E FRASSINETI C ZANIOL P
Citation: B. Barbiroli et al., DEFECTIVE BRAIN AND MUSCLE ENERGY-METABOLISM SHOWN BY IN-VIVO P-31 MAGNETIC-RESONANCE SPECTROSCOPY IN NONAFFECTED CARRIERS OF 11778-MTDNA MUTATION, Neurology, 45(7), 1995, pp. 1364-1369
FAMILIAL PROGRESSIVE SUBCORTICAL GLIOSIS - PRESENCE OF PRIONS AND LINKAGE TO CHROMOSOME-17
Authors: PETERSEN RB TABATON M CHEN SG MONARI L RICHARDSON SL LYNCHES T MANETTO V LANSKA DJ MARKESBERY WR CURRIER RD AUTILIOGAMBETTI L WILHELMSEN KC GAMBETTI P
Citation: Rb. Petersen et al., FAMILIAL PROGRESSIVE SUBCORTICAL GLIOSIS - PRESENCE OF PRIONS AND LINKAGE TO CHROMOSOME-17, Neurology, 45(6), 1995, pp. 1062-1067
A NOVEL MECHANISM OF PHENOTYPIC HETEROGENEITY DEMONSTRATED BY THE EFFECT OF A POLYMORPHISM ON A PATHOGENIC MUTATION IN THE PRNP (PRION PROTEIN GENE)
Authors: PETERSEN RB GOLDFARB LG TABATON M BROWN P MONARI L CORTELLI P MONTAGNA P AUTILIOGAMBETTI L GAJDUSEK DC LUGARESI E GAMBETTI P
Citation: Rb. Petersen et al., A NOVEL MECHANISM OF PHENOTYPIC HETEROGENEITY DEMONSTRATED BY THE EFFECT OF A POLYMORPHISM ON A PATHOGENIC MUTATION IN THE PRNP (PRION PROTEIN GENE), Molecular neurobiology, 8(2-3), 1994, pp. 99-103
ABNORMAL PLATELET MITOCHONDRIAL-FUNCTION IN PATIENTS AFFECTED BY MIGRAINE WITH AND WITHOUT AURA
Authors: SANGIORGI S MOCHI M RIVA R CORTELLI P MONARI L PIERANGELI G MONTAGNA P
Citation: S. Sangiorgi et al., ABNORMAL PLATELET MITOCHONDRIAL-FUNCTION IN PATIENTS AFFECTED BY MIGRAINE WITH AND WITHOUT AURA, Cephalalgia, 14(1), 1994, pp. 21-23
PROTEINASE-RESISTANT PRION PROTEIN IN FATAL FAMILIAL INSOMNIA-REGIONAL DISTRIBUTION AND CORRELATION WITH HISTOPATHOLOGY
Authors: PARCHI P CASTELLANI R CORTELLI P MONTAGNA P CHEN S MONARI L PETERSEN RB LUGARESI E AUTILIOGAMBETTI L GAMBETTI P
Citation: P. Parchi et al., PROTEINASE-RESISTANT PRION PROTEIN IN FATAL FAMILIAL INSOMNIA-REGIONAL DISTRIBUTION AND CORRELATION WITH HISTOPATHOLOGY, Neurobiology of aging, 15, 1994, pp. 190000088-190000089
TRUNCATED FORMS OF PRION PROTEIN IN HUMAN BRAIN AND CELL-LINES
Authors: CHEN SG PETERSEN R PARCHI P MONARI L WANG W GAMBETTI P GAMBETTI L
Citation: Sg. Chen et al., TRUNCATED FORMS OF PRION PROTEIN IN HUMAN BRAIN AND CELL-LINES, Neurobiology of aging, 15, 1994, pp. 190000089-190000089
NUCLEAR-STRUCTURE FUNCTIONS IN CARBON NEAR X = 1
Authors: BENVENUTI AC BOLLINI D CAMPORESI T MONARI L NAVARRIA FL ARGENTO A CVACH J LOHMANN W PIEMONTESE L GENCHEV VI HLADKY J GOLUTVIN IA KIRYUSHIN YT KISELEV VS KRIVOKHIZHIN VG KUKHTIN VV NEMECEK S PESHEKHONOV DV REIMER P SAVIN IA SMIRNOV GI SULTANOV S VOLODKO AG ZACEK J JAMNIK D KOPP R MEYERBERKHOUT U STAUDE A TEICHERT KM TIRLER R VOSS R ZUPANCIC C FELTESSE J MISZTAJN A OURAOU A RICHHENNION P SACQUIN Y SMADJA G VERRECCHIA P VIRCHAUX M
Citation: Ac. Benvenuti et al., NUCLEAR-STRUCTURE FUNCTIONS IN CARBON NEAR X = 1, Zeitschrift fur Physik. C, Particles and fields, 63(1), 1994, pp. 29-36
P-31-MAGNETIC RESONANCE SPECTROSCOPY IN MIGRAINE WITHOUT AURA
Authors: MONTAGNA P CORTELLI P MONARI L PIERANGELI G PARCHI P LODI R IOTTI S FRASSINETI C ZANIOL P LUGARESI E BARBIROLI B
Citation: P. Montagna et al., P-31-MAGNETIC RESONANCE SPECTROSCOPY IN MIGRAINE WITHOUT AURA, Neurology, 44(4), 1994, pp. 666-669
FATAL FAMILIAL INSOMNIA AND FAMILIAL CREUTZFELDT-JAKOB-DISEASE - DIFFERENT PRION PROTEINS DETERMINED BY A DNA POLYMORPHISM
Authors: MONARI L CHEN SG BROWN P PARCHI P PETERSEN RB MIKOL J GRAY F CORTELLI P MONTAGNA P GHETTI B GOLDFARB LG GAJDUSEK DC LUGARESI E GAMBETTI P AUTILIOGAMBETTI L
Citation: L. Monari et al., FATAL FAMILIAL INSOMNIA AND FAMILIAL CREUTZFELDT-JAKOB-DISEASE - DIFFERENT PRION PROTEINS DETERMINED BY A DNA POLYMORPHISM, Proceedings of the National Academy of Sciences of the United Statesof America, 91(7), 1994, pp. 2839-2842
ARYLSULFATASE A PSEUDODEFICIENCY AND LAFORA BODIES IN A PATIENT WITH PROGRESSIVE MYOCLONIC EPILEPSY
Authors: TINUPER P PLAZZI G MONARI L SANGIORGI S PELLISSIER JF CERULLO A PROVINI F CAPELLARI S BARUZZI A LUGARESI E MONTAGNA P
Citation: P. Tinuper et al., ARYLSULFATASE A PSEUDODEFICIENCY AND LAFORA BODIES IN A PATIENT WITH PROGRESSIVE MYOCLONIC EPILEPSY, Epilepsia, 35(2), 1994, pp. 332-335
TESTING MODELS FOR GENETIC DETERMINATION IN MIGRAINE
Authors: MOCHI M SANGIORGI S CORTELLI P CARELLI V SCAPOLI C CRISCI M MONARI L PIERANGELI G MONTAGNA P
Citation: M. Mochi et al., TESTING MODELS FOR GENETIC DETERMINATION IN MIGRAINE, Cephalalgia, 13(6), 1993, pp. 389-394
HIGH PREVALENCE OF LOW PROTEIN-C AND PROTEIN-S LEVELS IN PATIENTS SUFFERING FROM MIGRAINE
Authors: LUDOVICI S LEGNANI C PALARETI G PIERANGELI G MONARI L CORTELLI P COCCHERI S
Citation: S. Ludovici et al., HIGH PREVALENCE OF LOW PROTEIN-C AND PROTEIN-S LEVELS IN PATIENTS SUFFERING FROM MIGRAINE, Thrombosis research, 70, 1993, pp. 106-106
FATAL FAMILIAL INSOMNIA AND ONE SUBTYPE OF FAMILIAL CREUTZFELDT-JAKOBDISEASE - EFFECT OF A POLYMORPHISM IN THE PRION PROTEIN GENE ON A PATHOGENIC MUTATION
Authors: PETERSEN RB GOLDFARB L TABATON M BROWN P LEBLANC A MONTAGNA P CORTELLI P MONARI L AUTILIOGAMBETTI L GAJDUSEK DC LUGARESI E GAMBETTI P
Citation: Rb. Petersen et al., FATAL FAMILIAL INSOMNIA AND ONE SUBTYPE OF FAMILIAL CREUTZFELDT-JAKOBDISEASE - EFFECT OF A POLYMORPHISM IN THE PRION PROTEIN GENE ON A PATHOGENIC MUTATION, Neurology, 43(4), 1993, pp. 192-192
DEFECTIVE MUSCLE AND BRAIN METABOLISM SHOWN BY 31P MAGNETIC-RESONANCESPECTROSCOPY (31P-MRS) IN NON-MANIFESTING CARRIERS OF LEBERS HEREDITARY OPTIC NEUROPATHY (LHON)
Authors: BARBIROLI B MONTAGNA P CORTELLI P MONARI L LUGARESI E FRASSINETI C LODI R IOTTI S ZANIOL P
Citation: B. Barbiroli et al., DEFECTIVE MUSCLE AND BRAIN METABOLISM SHOWN BY 31P MAGNETIC-RESONANCESPECTROSCOPY (31P-MRS) IN NON-MANIFESTING CARRIERS OF LEBERS HEREDITARY OPTIC NEUROPATHY (LHON), Neurology, 43(4), 1993, pp. 221-221
P-31-MAGNETIC RESONANCE SPECTROSCOPY (P-31-MRS) IN MIGRAINE WITHOUT AURA (MWOA)
Authors: MONTAGNA P CORTELLI P MONARI L PIERANGELI G PARCHI P LODI R IOTTI S ZANIOL P LUGARESI E BARBIROLI B
Citation: P. Montagna et al., P-31-MAGNETIC RESONANCE SPECTROSCOPY (P-31-MRS) IN MIGRAINE WITHOUT AURA (MWOA), Neurology, 43(4), 1993, pp. 326-327
DETECTION OF PRION PROTEIN IN FIBROBLASTS FROM 2 FATAL FAMILIAL INSOMNIA KINDRED
Authors: MONARI L PETERSEN RB CHEN SG CORTELLI P MONTAGNA P BERG L JULIEN J LUGARESI E AUTILIOGAMBETTI L GAMBETTI P
Citation: L. Monari et al., DETECTION OF PRION PROTEIN IN FIBROBLASTS FROM 2 FATAL FAMILIAL INSOMNIA KINDRED, Journal of neuropathology and experimental neurology, 52(3), 1993, pp. 293-293
EFFECT OF A POLYMORPHISM ON THE PATHOGENIC 178ASN MUTATION IN THE PRION PROTEIN GENE
Authors: PETERSEN RB GOLDFARB L TABATON M BROWN P LEBLANC A MONTAGNA P CORTELLI P MONARI L AUTILIOGAMBETTI L GAJDUSEK DC LUGARESI E GAMBETTI P
Citation: Rb. Petersen et al., EFFECT OF A POLYMORPHISM ON THE PATHOGENIC 178ASN MUTATION IN THE PRION PROTEIN GENE, Journal of neuropathology and experimental neurology, 52(3), 1993, pp. 293-293
FATAL FAMILIAL INSOMNIA AND THE WIDENING SPECTRUM OF PRION DISEASES
Authors: GAMBETTI P PETERSEN R MONARI L TABATON M AUTILIOGAMBETTI L CORTELLI P MONTAGNA P LUGARESI E
Citation: P. Gambetti et al., FATAL FAMILIAL INSOMNIA AND THE WIDENING SPECTRUM OF PRION DISEASES, British Medical Bulletin, 49(4), 1993, pp. 980-994
Risultati: 1-23 |