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A VERBAL SCALE FOR THE INTERPRETATION OF EVIDENCE
Authors: AITKEN CGG TARONI F
Citation: Cgg. Aitken et F. Taroni, A VERBAL SCALE FOR THE INTERPRETATION OF EVIDENCE, Science & justice, 38(4), 1998, pp. 279-281
PROBABILISTIC REASONING IN THE LAW - PART 1 - ASSESSMENT OF PROBABILITIES AND EXPLANATION OF THE VALUE OF DNA EVIDENCE (VOL 38, PG, 165, 1998)
Authors: TARONI F AITKEN CGG
Citation: F. Taroni et Cgg. Aitken, PROBABILISTIC REASONING IN THE LAW - PART 1 - ASSESSMENT OF PROBABILITIES AND EXPLANATION OF THE VALUE OF DNA EVIDENCE (VOL 38, PG, 165, 1998), Science & justice, 38(4), 1998, pp. 283-283
PROBABILISTIC REASONING IN THE LAW - PART-1 - ASSESSMENT OF PROBABILITIES AND EXPLANATION OF THE VALUE OF DNA EVIDENCE
Authors: TARONI F AITKEN CGG
Citation: F. Taroni et Cgg. Aitken, PROBABILISTIC REASONING IN THE LAW - PART-1 - ASSESSMENT OF PROBABILITIES AND EXPLANATION OF THE VALUE OF DNA EVIDENCE, Science & justice, 38(3), 1998, pp. 165-177
PROBABILISTIC REASONING IN THE LAW - PART-2 - ASSESSMENT OF PROBABILITIES AND EXPLANATION OF THE VALUE OF TRACE EVIDENCE OTHER THAN DNA
Authors: TARONI F AITKEN CGG
Citation: F. Taroni et Cgg. Aitken, PROBABILISTIC REASONING IN THE LAW - PART-2 - ASSESSMENT OF PROBABILITIES AND EXPLANATION OF THE VALUE OF TRACE EVIDENCE OTHER THAN DNA, Science & justice, 38(3), 1998, pp. 179-188
2 CPT2 MUTATIONS IN 3 JAPANESE PATIENTS WITH CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY - FUNCTIONAL-ANALYSIS AND ASSOCIATION WITH POLYMORPHIC HAPLOTYPES AND 2 CLINICAL PHENOTYPES
Authors: WATAYA K AKANUMA J CAVADINI P AOKI Y KURE S INVERNIZZI F YOSHIDA I KIRA J TARONI F MATSUBARA Y NARISAWA K
Citation: K. Wataya et al., 2 CPT2 MUTATIONS IN 3 JAPANESE PATIENTS WITH CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY - FUNCTIONAL-ANALYSIS AND ASSOCIATION WITH POLYMORPHIC HAPLOTYPES AND 2 CLINICAL PHENOTYPES, Human mutation, 11(5), 1998, pp. 377-386
VERY-LONG-CHAIN ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY IN A CHILD WITH RECURRENT MYOGLOBINURIA
Authors: MINETTI C GARAVAGLIA B BADO M INVERNIZZI F BRUNO C RIMOLDI M PONS R TARONI F CORDONE G
Citation: C. Minetti et al., VERY-LONG-CHAIN ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY IN A CHILD WITH RECURRENT MYOGLOBINURIA, Neuromuscular disorders, 8(1), 1998, pp. 3-6
EXPRESSION OF FRATAXIN GENE AND GENE-PRODUCT IN THE MAMMALIAN CENTRAL-NERVOUS-SYSTEM
Authors: GIAVAZZI A PRINCIVALLE A CAVADINI P TARONI F BATTAGLIA G
Citation: A. Giavazzi et al., EXPRESSION OF FRATAXIN GENE AND GENE-PRODUCT IN THE MAMMALIAN CENTRAL-NERVOUS-SYSTEM, European journal of neuroscience, 10, 1998, pp. 12215-12215
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
FUMARATE HYDRATASE DEFICIENCY
Authors: BONIOLI E DISTEFANO A PERI V CARUSO U CERONE R LAMANTEA E TARONI F BELLINI C
Citation: E. Bonioli et al., FUMARATE HYDRATASE DEFICIENCY, Journal of inherited metabolic disease, 21(4), 1998, pp. 435-436
FACIAL-NERVE IS LIABLE TO PRESSURE PALSY
Authors: POLONI TE MERLO IM ALFONSI E MARINOUAKTIPI K BOTTI S ARRIGO A TARONI F CERONI M
Citation: Te. Poloni et al., FACIAL-NERVE IS LIABLE TO PRESSURE PALSY, Neurology, 51(1), 1998, pp. 320-322
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
FRATAXIN GENE-MUTATIONS IN FRIEDREICHS ATAXIA ALLELES NOT CARRYING THE GAA EXPANSION
Authors: GELLERA C BOTTI S CASTELLOTTI B RIGGIO MC MAZZUCCHELLI F DIDONATO S TARONI F
Citation: C. Gellera et al., FRATAXIN GENE-MUTATIONS IN FRIEDREICHS ATAXIA ALLELES NOT CARRYING THE GAA EXPANSION, Neurology, 50(4), 1998, pp. 53001-53001
MUTATIONS IN THE FRATAXIN GENE OF FRIEDREICHS ATAXIA CONFER SENSITIVITY TO OXIDANT STRESS
Authors: WONG A TARONI F GELLERA C CORTOPASSI G
Citation: A. Wong et al., MUTATIONS IN THE FRATAXIN GENE OF FRIEDREICHS ATAXIA CONFER SENSITIVITY TO OXIDANT STRESS, Neurology, 50(4), 1998, pp. 53002-53002
BAYESIAN FRAMEWORK FOR THE EVALUATION OF FIBER TRANSFER EVIDENCE
Authors: CHAMPOD C TARONI F
Citation: C. Champod et F. Taroni, BAYESIAN FRAMEWORK FOR THE EVALUATION OF FIBER TRANSFER EVIDENCE, Science & justice, 37(2), 1997, pp. 75-83
INTERPRETATION OF SCIENTIFIC EVIDENCE .2.
Authors: AITKEN C TARONI F
Citation: C. Aitken et F. Taroni, INTERPRETATION OF SCIENTIFIC EVIDENCE .2., Science & justice, 37(1), 1997, pp. 65-65
BAYESIAN-ANALYSIS OF DNA PROFILING DATA IN FORENSIC IDENTIFICATION APPLICATIONS - DISCUSSION
Authors: AITKEN CGG TARONI F
Citation: Cgg. Aitken et F. Taroni, BAYESIAN-ANALYSIS OF DNA PROFILING DATA IN FORENSIC IDENTIFICATION APPLICATIONS - DISCUSSION, Journal of the Royal Statistical Society. Series A. Statistics in society, 160, 1997, pp. 463-463
FACTORS ASSOCIATED WITH GALLSTONE DISEASE IN THE MICOL EXPERIENCE
Authors: ATTILI AF CAPOCACCIA R CARULLI N FESTI D RODA E BARBARA L CAPOCACCIA L MENOTTI A OKOLICSANYI L RICCI G LALLONI L MARIOTTI S SAMA C SCAFATO E MUNTONI S TARONI F MORISI G VALENTE F
Citation: Af. Attili et al., FACTORS ASSOCIATED WITH GALLSTONE DISEASE IN THE MICOL EXPERIENCE, Hepatology, 26(4), 1997, pp. 809-818
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
FRIEDREICHS ATAXIA IN NORTHERN ITALY - DNA EXPANSION AND GENOTYPE-PHENOTYPE CORRELATIONS
Authors: PAREYSON D GELLERA C CASTELLOTTI B ZAPPACOSTA B MAZZUCCHELLI F RIGGIO MC TARONI F PANDOLFO M DIDONATO S
Citation: D. Pareyson et al., FRIEDREICHS ATAXIA IN NORTHERN ITALY - DNA EXPANSION AND GENOTYPE-PHENOTYPE CORRELATIONS, Neurology, 48(3), 1997, pp. 26004-26004
CHARACTERIZATION OF CARNITINE PALMITOYLTRANSFERASES IN PATIENTS WITH A CARNITINE PALMITOYLTRANSFERASE DEFICIENCY - IMPLICATIONS FOR DIAGNOSIS AND THERAPY
Authors: SCHAEFER J JACKSON S TARONI F SWIFT P TURNBULL DM
Citation: J. Schaefer et al., CHARACTERIZATION OF CARNITINE PALMITOYLTRANSFERASES IN PATIENTS WITH A CARNITINE PALMITOYLTRANSFERASE DEFICIENCY - IMPLICATIONS FOR DIAGNOSIS AND THERAPY, Journal of Neurology, Neurosurgery and Psychiatry, 62(2), 1997, pp. 169-176
EVIDENCES THAT HUMAN FRATAXIN LOCALIZES IN THE MITOCHONDRIA AND IS EXPRESSED IN NEURAL TISSUES SELECTIVELY AFFECTED IN FRIEDREICHS ATAXIA
Authors: CAVADINI P DIBLASI C PRINCIVALLE A BARATTA S DIDONATO S BATTAGLIA G MORA M TARONI F
Citation: P. Cavadini et al., EVIDENCES THAT HUMAN FRATAXIN LOCALIZES IN THE MITOCHONDRIA AND IS EXPRESSED IN NEURAL TISSUES SELECTIVELY AFFECTED IN FRIEDREICHS ATAXIA, American journal of human genetics, 61(4), 1997, pp. 219-219
GENE MICROMUTATIONS IN FRIEDREICHS ATAXIA ALLELES NOT CARRYING THE GAA EXPANSION
Authors: BOTTI S CASTELLOTTI B RIGGIO MC BARATTA S DIDONATO S CAVADINI P GELLERA C TARONI F
Citation: S. Botti et al., GENE MICROMUTATIONS IN FRIEDREICHS ATAXIA ALLELES NOT CARRYING THE GAA EXPANSION, American journal of human genetics, 61(4), 1997, pp. 1912-1912
INTERPRETATION OF SCIENTIFIC EVIDENCE
Authors: TARONI F AITKEN C
Citation: F. Taroni et C. Aitken, INTERPRETATION OF SCIENTIFIC EVIDENCE, Science & justice, 36(4), 1996, pp. 290-292
FATTY-ACID MITOCHONDRIAL BETA-OXIDATION AND HYPOGLYCEMIA IN CHILDREN
Authors: TARONI F UZIEL G
Citation: F. Taroni et G. Uziel, FATTY-ACID MITOCHONDRIAL BETA-OXIDATION AND HYPOGLYCEMIA IN CHILDREN, Current opinion in neurology, 9(6), 1996, pp. 477-485
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