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Results: 1-22 |
Results: 22
De Finetti's subjectivism, the assessment of probabilities and the evaluation of evidence: a commentary for forensic scientists
Authors: Taroni, F Aitken, CGG Garbolino, P
Citation: F. Taroni et al., De Finetti's subjectivism, the assessment of probabilities and the evaluation of evidence: a commentary for forensic scientists, SCI JUSTICE, 41(3), 2001, pp. 145-150
Healthcare reform and disease management in Italy - Promoting the effectiveness and appropriateness of health service use
Authors: Grilli, R Donatini, A Taroni, F
Citation: R. Grilli et al., Healthcare reform and disease management in Italy - Promoting the effectiveness and appropriateness of health service use, DIS MANAG H, 9(8), 2001, pp. 441-449
Comparative and cross-cultural health research: a practical guide.
Authors: Taroni, F
Citation: F. Taroni, Comparative and cross-cultural health research: a practical guide., EUR J PUB H, 11(3), 2001, pp. 354-354
Phenotype and genotype variation in primary carnitine deficiency
Authors: Wang, YH Korman, SH Ye, J Gargus, JJ Gutman, A Taroni, F Garavaglia, B Longo, N
Citation: Yh. Wang et al., Phenotype and genotype variation in primary carnitine deficiency, GENET MED, 3(6), 2001, pp. 387-392
Charcot-Marie-Tooth disease type I and related demyelinating neuropathies:Mutation analysis in a large cohort of Italian families
Authors: Mostacciuolo, ML Righetti, E Zortea, M Bosello, V Schiavon, F Vallo, L Merlini, L Siciliano, G Fabrizi, GM Rizzuto, N Milani, M Baratta, S Taroni, F
Citation: Ml. Mostacciuolo et al., Charcot-Marie-Tooth disease type I and related demyelinating neuropathies:Mutation analysis in a large cohort of Italian families, HUM MUTAT, 18(1), 2001, pp. 32-41
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations
Authors: Gellera, C Castellotti, B Riggio, MC Silani, V Morandi, L Testa, D Casali, C Taroni, F Di Donato, S Zeviani, M Mariotti, C
Citation: C. Gellera et al., Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations, NEUROMUSC D, 11(4), 2001, pp. 404-410
Detection of nandrolone metabolites in urine after a football game in professional and amateur players: a Bayesian comparison
Authors: Robinson, N Taroni, F Saugy, M Ayotte, C Mangin, P Dvorak, J
Citation: N. Robinson et al., Detection of nandrolone metabolites in urine after a football game in professional and amateur players: a Bayesian comparison, FOREN SCI I, 122(2-3), 2001, pp. 130-135
Triplet repeat diseases: From basic to clinical aspects - Foreword
Authors: Poletti, A Servadio, A Taroni, F
Citation: A. Poletti et al., Triplet repeat diseases: From basic to clinical aspects - Foreword, BRAIN RES B, 56(3-4), 2001, pp. 159-159
Lethal neonatal presentation of carnitine palmitoyltransferase I deficiency
Authors: Invernizzi, F Burlina, AB Donadio, A Giordano, G Taroni, F Garavaglia, B
Citation: F. Invernizzi et al., Lethal neonatal presentation of carnitine palmitoyltransferase I deficiency, J INH MET D, 24(5), 2001, pp. 601-602
Fingerprint evidence evaluation: Is it really so different to other evidence types?
Authors: Taroni, F Margot, P
Citation: F. Taroni et P. Margot, Fingerprint evidence evaluation: Is it really so different to other evidence types?, SCI JUSTICE, 40(4), 2000, pp. 277-278
Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: Lack of genotype-phenotype correlation
Authors: Wang, YH Taroni, F Garavagalia, B Longo, N
Citation: Yh. Wang et al., Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: Lack of genotype-phenotype correlation, HUM MUTAT, 16(5), 2000, pp. 401-407
Forensic evaluation of mtDNA in a population from south west Switzerland
Authors: Dimo-Simonin, N Grange, F Taroni, F Brandt-Casadevall, C Mangin, P
Citation: N. Dimo-simonin et al., Forensic evaluation of mtDNA in a population from south west Switzerland, INT J LEGAL, 113(2), 2000, pp. 89-97
Clinical and molecular heterogeneity in very-long-chain acyl-coenzyme A dehydrogenase deficiency
Authors: Pons, R Cavadini, P Baratta, S Invernizzi, F Lamantea, E Garavaglia, B Taroni, F
Citation: R. Pons et al., Clinical and molecular heterogeneity in very-long-chain acyl-coenzyme A dehydrogenase deficiency, PED NEUROL, 22(2), 2000, pp. 98-105
Fibres evidence, probabilistic evaluation and collaborative test
Authors: Taroni, F Aitken, CGG
Citation: F. Taroni et Cgg. Aitken, Fibres evidence, probabilistic evaluation and collaborative test, FOREN SCI I, 114(1), 2000, pp. 45-47
DNA evidence, probabilistic evaluation and collaborative tests
Authors: Taroni, F Aitken, CGG
Citation: F. Taroni et Cgg. Aitken, DNA evidence, probabilistic evaluation and collaborative tests, FOREN SCI I, 108(2), 2000, pp. 121-143
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation
Authors: Pareyson, D Taroni, F Botti, S Morbin, M Baratta, S Lauria, G Ciano, C Sghirlanzoni, A
Citation: D. Pareyson et al., Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation, NEUROLOGY, 54(8), 2000, pp. 1696-1698
Two-step processing of human frataxin by mitochondrial processing peptidase - Precursor and intermediate forms are cleaved at different rates
Authors: Cavadini, P Adamec, J Taroni, F Gakh, O Isaya, G
Citation: P. Cavadini et al., Two-step processing of human frataxin by mitochondrial processing peptidase - Precursor and intermediate forms are cleaved at different rates, J BIOL CHEM, 275(52), 2000, pp. 41469-41475
The likelihood approach to compare populations: a study on DNA evidence and pitfalls of intuitions
Authors: Taroni, F Aitken, CGG
Citation: F. Taroni et Cgg. Aitken, The likelihood approach to compare populations: a study on DNA evidence and pitfalls of intuitions, SCI JUSTICE, 39(4), 1999, pp. 213-222
The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis
Authors: Wong, A Yang, J Cavadini, P Gellera, C Lonnerdal, B Taroni, F Cortepassi, G
Citation: A. Wong et al., The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis, HUM MOL GEN, 8(3), 1999, pp. 425-430
Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: Insights on treatment
Authors: Parini, R Invernizzi, F Menni, F Garavaglia, B Melotti, D Rimoldi, M Salera, S Tosetto, C Taroni, F
Citation: R. Parini et al., Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: Insights on treatment, J INH MET D, 22(6), 1999, pp. 733-739
Charcot-Marie-Tooth disease type 2 and P0 gene mutations
Authors: Pareyson, D Sghirlanzoni, A Bolti, S Ciano, C Fallica, E Mora, M Taroni, F
Citation: D. Pareyson et al., Charcot-Marie-Tooth disease type 2 and P0 gene mutations, NEUROLOGY, 52(5), 1999, pp. 1110-1111
Yeast and human frataxin are processed to mature form in two sequential steps by the mitochondrial processing peptidase
Authors: Branda, SS Cavadini, P Adamec, J Kalousek, F Taroni, F Isaya, G
Citation: Ss. Branda et al., Yeast and human frataxin are processed to mature form in two sequential steps by the mitochondrial processing peptidase, J BIOL CHEM, 274(32), 1999, pp. 22763-22769
Risultati: 1-22 |