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Items: 1 to 50 of 343

1.

Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literature.

Benzoni C, Aquino D, Di Bella D, Sarto E, Moscatelli M, Pareyson D, Taroni F, Salsano E.

J Clin Neurosci. 2020 Mar 26. pii: S0967-5868(20)30092-8. doi: 10.1016/j.jocn.2020.03.033. [Epub ahead of print]

PMID:
32223977
2.

ATPase domain AFG3L2 mutations alter OPA1 processing and cause Optic Neuropathy.

Caporali L, Magri S, Legati A, Del Dotto V, Tagliavini F, Balistreri F, Nasca A, La Morgia C, Carbonelli M, Valentino ML, Lamantea E, Baratta S, Schöls L, Schüle R, Barboni P, Cascavilla ML, Maresca A, Capristo M, Ardissone A, Pareyson D, Cammarata G, Melzi L, Zeviani M, Peverelli L, Lamperti C, Bianchi Marzoli S, Fang M, Synofzik M, Ghezzi D, Carelli V, Taroni F.

Ann Neurol. 2020 Mar 26. doi: 10.1002/ana.25723. [Epub ahead of print]

PMID:
32219868
3.

Born with a solitary kidney: at risk of hypertension.

La Scola C, Marra G, Ammenti A, Pasini A, Taroni F, Bertulli C, Morello W, Ceccoli M, Mencarelli F, Guarino S, Puccio G, Montini G.

Pediatr Nephrol. 2020 Mar 24. doi: 10.1007/s00467-020-04535-1. [Epub ahead of print]

PMID:
32211991
4.

Estimating the quantity of transferred DNA in primary and secondary transfers.

Samie L, Taroni F, Champod C.

Sci Justice. 2020 Mar;60(2):128-135. doi: 10.1016/j.scijus.2019.09.008. Epub 2019 Oct 23. No abstract available.

PMID:
32111285
5.

Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms.

Pensato V, Magri S, Bella ED, Tannorella P, Bersano E, Sorarù G, Gatti M, Ticozzi N, Taroni F, Lauria G, Mariotti C, Gellera C.

J Clin Med. 2020 Feb 3;9(2). pii: E412. doi: 10.3390/jcm9020412.

6.

Glutamine Synthetase 1 Increases Autophagy Lysosomal Degradation of Mutant Huntingtin Aggregates in Neurons, Ameliorating Motility in a Drosophila Model for Huntington's Disease.

Vernizzi L, Paiardi C, Licata G, Vitali T, Santarelli S, Raneli M, Manelli V, Rizzetto M, Gioria M, Pasini ME, Grifoni D, Vanoni MA, Gellera C, Taroni F, Bellosta P.

Cells. 2020 Jan 13;9(1). pii: E196. doi: 10.3390/cells9010196.

7.

Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian population.

Mongelli A, Magri S, Salvatore E, Rizzo E, De Rosa A, Fico T, Gatti M, Gellera C, Taroni F, Mariotti C, Nanetti L.

Neurol Sci. 2020 Jan 15. doi: 10.1007/s10072-019-04233-3. [Epub ahead of print]

PMID:
31940111
8.

RARS1-related hypomyelinating leukodystrophy: Expanding the spectrum.

Mendes MI, Green LMC, Bertini E, Tonduti D, Aiello C, Smith D, Salsano E, Beerepoot S, Hertecant J, von Spiczak S, Livingston JH, Emrick L, Fraser J, Russell L, Bernard G, Magri S, Di Bella D, Taroni F, Koenig MK, Moroni I, Cappuccio G, Brunetti-Pierri N, Rhee J, Mendelsohn BA, Helbig I, Helbig K, Muhle H, Ismayl O, Vanderver AL, Salomons GS, van der Knaap MS, Wolf NI.

Ann Clin Transl Neurol. 2020 Jan;7(1):83-93. doi: 10.1002/acn3.50960. Epub 2019 Dec 8.

9.

A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects.

D'Arrigo S, Tessarollo V, Taroni F, Baratta S, Pantaleoni C, Schiaffi E, Ciano C.

Neuropediatrics. 2019 Nov 29. doi: 10.1055/s-0039-3400985. [Epub ahead of print]

PMID:
31784971
10.

Bayesian networks and dissonant items of evidence: A case study.

De March I, Taroni F.

Forensic Sci Int Genet. 2020 Jan;44:102172. doi: 10.1016/j.fsigen.2019.102172. Epub 2019 Oct 10.

PMID:
31629186
11.

From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations.

Gatti M, Magri S, Nanetti L, Sarto E, Di Bella D, Salsano E, Pantaleoni C, Mariotti C, Taroni F.

Am J Med Genet A. 2019 Nov;179(11):2277-2283. doi: 10.1002/ajmg.a.61339. Epub 2019 Aug 22.

PMID:
31436889
12.

Saposin B deficiency as a cause of adult-onset metachromatic leukodystrophy.

Fenu S, Castellotti B, Farina L, Cavallaro T, Di Bella D, Benzoni C, Gellera C, Pareyson D, Taroni F, Salsano E.

Neurology. 2019 Aug 13;93(7):310-312. doi: 10.1212/WNL.0000000000007951. Epub 2019 Jul 9. No abstract available.

PMID:
31289144
13.

Voiding cystourethrography and 99MTC-MAG3 renal scintigraphy in pediatric vesicoureteral reflux: what is the role of indirect cystography?

Capone V, Taroni F, Pavesi MA, Castellani M, Consonni D, Berrettini A, Crapella B, Marra G, De Palma D, Zucchetta P, Manzoni GA, Montini G.

J Pediatr Urol. 2019 Oct;15(5):514.e1-514.e6. doi: 10.1016/j.jpurol.2019.06.004. Epub 2019 Jun 17.

PMID:
31285138
14.

The efficiency of DNA extraction kit and the efficiency of recovery techniques to release DNA using flow cytometry.

Samie L, Champod C, Glutz V, Garcia M, Castella V, Taroni F.

Sci Justice. 2019 Jul;59(4):405-410. doi: 10.1016/j.scijus.2019.02.003. Epub 2019 Feb 21. No abstract available.

PMID:
31256811
15.

Natural history, dynamics, and ecology of human papillomaviruses in genital infections of young women: protocol of the PAPCLEAR cohort study.

Murall CL, Rahmoun M, Selinger C, Baldellou M, Bernat C, Bonneau M, Boué V, Buisson M, Christophe G, D'Auria G, Taroni F, Foulongne V, Froissart R, Graf C, Grasset S, Groc S, Hirtz C, Jaussent A, Lajoie J, Lorcy F, Picot E, Picot MC, Ravel J, Reynes J, Rousset T, Seddiki A, Teirlinck M, Tribout V, Tuaillon É, Waterboer T, Jacobs N, Bravo IG, Segondy M, Boulle N, Alizon S.

BMJ Open. 2019 Jun 11;9(6):e025129. doi: 10.1136/bmjopen-2018-025129.

16.

More on the question 'When does absence of evidence constitute evidence of absence?' How Bayesian confirmation theory can logically support the answer.

Taroni F, Bozza S, Hicks T, Garbolino P.

Forensic Sci Int. 2019 Aug;301:e59-e63. doi: 10.1016/j.forsciint.2019.05.044. Epub 2019 May 29.

PMID:
31178229
17.

Expanding the spectrum of genes responsible for hereditary motor neuropathies.

Previtali SC, Zhao E, Lazarevic D, Pipitone GB, Fabrizi GM, Manganelli F, Mazzeo A, Pareyson D, Schenone A, Taroni F, Vita G, Bellone E, Ferrarini M, Garibaldi M, Magri S, Padua L, Pennisi E, Pisciotta C, Riva N, Scaioli V, Scarlato M, Tozza S, Geroldi A, Jordanova A, Ferrari M, Molineris I, Reilly MM, Comi G, Carrera P, Devoto M, Bolino A.

J Neurol Neurosurg Psychiatry. 2019 Oct;90(10):1171-1179. doi: 10.1136/jnnp-2019-320717. Epub 2019 Jun 5.

PMID:
31167812
18.

Neuropsychological features of adult form of Alexander disease.

Draghi L, Salsano E, Farina L, Di Bella D, Fenu S, Pareyson D, Taroni F, Piacentini SHMJ.

J Neurol Sci. 2019 Jun 15;401:87-89. doi: 10.1016/j.jns.2019.04.030. Epub 2019 Apr 23. No abstract available.

PMID:
31039531
19.

A Case of Hypotonia-Cystinuria Syndrome With Genito-Urinary Malformations and Extrarenal Involvement.

Taroni F, Capone V, Berrettini A, De Marco EA, Manzoni GA, Montini G.

Front Pediatr. 2019 Apr 9;7:127. doi: 10.3389/fped.2019.00127. eCollection 2019.

20.

HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature.

DiFrancesco JC, Castellotti B, Milanesi R, Ragona F, Freri E, Canafoglia L, Franceschetti S, Ferrarese C, Magri S, Taroni F, Costa C, Labate A, Gambardella A, Solazzi R, Binda A, Rivolta I, Di Gennaro G, Casciato S, D'Incerti L, Barbuti A, DiFrancesco D, Granata T, Gellera C.

Epilepsy Res. 2019 Jul;153:49-58. doi: 10.1016/j.eplepsyres.2019.04.004. Epub 2019 Apr 8. Review.

PMID:
30986657
21.

Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.

Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, Day JW, Sumner CJ, Lloyd TE, Li J, Yum SW, Taroni F, Baas F, Choi BO, Pareyson D, Scherer SS, Reilly MM, Shy ME, Züchner S; Inherited Neuropathy Consortium.

J Neuromuscul Dis. 2019;6(2):201-211. doi: 10.3233/JND-190377.

22.

Are Inconclusive Decisions in Forensic Science as Deficient as They Are Said to Be?

Biedermann A, Bozza S, Taroni F, Vuille J.

Front Psychol. 2019 Mar 19;10:520. doi: 10.3389/fpsyg.2019.00520. eCollection 2019.

23.

A novel family with axonal Charcot-Marie-Tooth disease caused by a mutation in the EGR2 gene.

Tozza S, Magri S, Pennisi EM, Schirinzi E, Pisciotta C, Balistreri F, Severi D, Ricci G, Siciliano G, Taroni F, Santoro L, Manganelli F.

J Peripher Nerv Syst. 2019 Jun;24(2):219-223. doi: 10.1111/jns.12314. Epub 2019 Mar 28.

PMID:
30843326
24.

Treatment and long-term outcome in primary distal renal tubular acidosis.

Lopez-Garcia SC, Emma F, Walsh SB, Fila M, Hooman N, Zaniew M, Bertholet-Thomas A, Colussi G, Burgmaier K, Levtchenko E, Sharma J, Singhal J, Soliman NA, Ariceta G, Basu B, Murer L, Tasic V, Tsygin A, Decramer S, Gil-Peña H, Koster-Kamphuis L, La Scola C, Gellermann J, Konrad M, Lilien M, Francisco T, Tramma D, Trnka P, Yüksel S, Caruso MR, Chromek M, Ekinci Z, Gambaro G, Kari JA, König J, Taroni F, Thumfart J, Trepiccione F, Winding L, Wühl E, Ağbaş A, Belkevich A, Vargas-Poussou R, Blanchard A, Conti G, Boyer O, Dursun I, Pınarbaşı AS, Melek E, Miglinas M, Novo R, Mallett A, Milosevic D, Szczepanska M, Wente S, Cheong HI, Sinha R, Gucev Z, Dufek S, Iancu D; European dRTA Consortium, Kleta R, Schaefer F, Bockenhauer D.

Nephrol Dial Transplant. 2019 Jun 1;34(6):981-991. doi: 10.1093/ndt/gfy409.

PMID:
30773598
25.

Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A.

Tao F, Beecham GW, Rebelo AP, Svaren J, Blanton SH, Moran JJ, Lopez-Anido C, Morrow JM, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, Day JW, Sumner CJ, Lloyd TE, Li J, Yum SW, Taroni F, Baas F, Choi BO, Pareyson D, Scherer SS, Reilly MM, Shy ME, Züchner S; Inherited Neuropathy Consortium.

Ann Neurol. 2019 Mar;85(3):316-330. doi: 10.1002/ana.25426.

PMID:
30706531
26.

Late-onset and fast progressive neuropathy and cardiomyopathy in Val32Ala transthyretin gene mutation.

Cazzato D, Dalla Bella E, Saveri P, Taroni F, Marucci G, Lauria G.

Neurol Sci. 2019 Jun;40(6):1267-1269. doi: 10.1007/s10072-019-3716-z. Epub 2019 Jan 26.

PMID:
30685801
28.

ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype.

Nanetti L, Sarto E, Castaldo A, Magri S, Mongelli A, Rossi Sebastiano D, Canafoglia L, Grisoli M, Malaguti C, Rivieri F, D'Amico MC, Di Bella D, Franceschetti S, Mariotti C, Taroni F.

J Neurol. 2019 Feb;266(2):378-385. doi: 10.1007/s00415-018-9141-z. Epub 2018 Dec 4.

PMID:
30515630
29.

The role of clinical and neuroimaging features in the diagnosis of CADASIL.

Bersano A, Bedini G, Markus HS, Vitali P, Colli-Tibaldi E, Taroni F, Gellera C, Baratta S, Mosca L, Carrera P, Ferrari M, Cereda C, Grieco G, Lanfranconi S, Mazucchelli F, Zarcone D, De Lodovici ML, Bono G, Boncoraglio GB, Parati EA, Calloni MV, Perrone P, Bordo BM, Motto C, Agostoni E, Pezzini A, Padovani A, Micieli G, Cavallini A, Molini G, Sasanelli F, Sessa M, Comi G, Checcarelli N, Carmerlingo M, Corato M, Marcheselli S, Fusi L, Grampa G, Uccellini D, Beretta S, Ferrarese C, Incorvaia B, Tadeo CS, Adobbati L, Silani V, Faragò G, Trobia N, Grond-Ginsbach C, Candelise L; Lombardia GENS-group.

J Neurol. 2018 Dec;265(12):2934-2943. doi: 10.1007/s00415-018-9072-8. Epub 2018 Oct 11.

PMID:
30311053
30.

Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation.

Magri S, Fracasso V, Plumari M, Alfei E, Ghezzi D, Gellera C, Rusmini P, Poletti A, Di Bella D, Elia AE, Pantaleoni C, Taroni F.

Hum Mutat. 2018 Dec;39(12):2060-2071. doi: 10.1002/humu.23658. Epub 2018 Oct 10.

31.

Dynamic signatures: A review of dynamic feature variation and forensic methodology.

Linden J, Marquis R, Bozza S, Taroni F.

Forensic Sci Int. 2018 Oct;291:216-229. doi: 10.1016/j.forsciint.2018.08.021. Epub 2018 Aug 29. Review.

PMID:
30241096
32.

Commentary: Likelihood Ratio as Weight of Forensic Evidence: A Closer Look.

Aitken C, Nordgaard A, Taroni F, Biedermann A.

Front Genet. 2018 Jun 22;9:224. doi: 10.3389/fgene.2018.00224. eCollection 2018. No abstract available.

33.

Primary brain calcification: an international study reporting novel variants and associated phenotypes.

Ramos EM, Carecchio M, Lemos R, Ferreira J, Legati A, Sears RL, Hsu SC, Panteghini C, Magistrelli L, Salsano E, Esposito S, Taroni F, Richard AC, Tranchant C, Anheim M, Ayrignac X, Goizet C, Vidailhet M, Maltete D, Wallon D, Frebourg T, Pimentel L, Geschwind DH, Vanakker O, Galasko D, Fogel BL, Innes AM, Ross A, Dobyns WB, Alcantara D, O'Driscoll M, Hannequin D, Campion D; French PFBC study group, Oliveira JR, Garavaglia B, Coppola G, Nicolas G.

Eur J Hum Genet. 2018 Oct;26(10):1462-1477. doi: 10.1038/s41431-018-0185-4. Epub 2018 Jun 28.

34.

Critical analysis of forensic cut-offs and legal thresholds: A coherent approach to inference and decision.

Biedermann A, Taroni F, Bozza S, Augsburger M, Aitken CGG.

Forensic Sci Int. 2018 Jul;288:72-80. doi: 10.1016/j.forsciint.2018.04.030. Epub 2018 Apr 25.

PMID:
29734052
35.

Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patients.

Mongelli A, Sarro L, Rizzo E, Nanetti L, Meucci N, Pezzoli G, Goldwurm S, Taroni F, Mariotti C, Gellera C.

Neurosci Lett. 2018 Jun 21;678:37-42. doi: 10.1016/j.neulet.2018.04.044. Epub 2018 Apr 30.

PMID:
29715545
36.

Pediatric nephrolithiasis: a systematic approach from diagnosis to treatment.

Marra G, Taroni F, Berrettini A, Montanari E, Manzoni G, Montini G.

J Nephrol. 2019 Apr;32(2):199-210. doi: 10.1007/s40620-018-0487-1. Epub 2018 Apr 21. Review.

PMID:
29680873
37.

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

Nicolas A, Kenna KP, Renton AE, Ticozzi N, Faghri F, Chia R, Dominov JA, Kenna BJ, Nalls MA, Keagle P, Rivera AM, van Rheenen W, Murphy NA, van Vugt JJFA, Geiger JT, Van der Spek RA, Pliner HA, Shankaracharya, Smith BN, Marangi G, Topp SD, Abramzon Y, Gkazi AS, Eicher JD, Kenna A; ITALSGEN Consortium, Mora G, Calvo A, Mazzini L, Riva N, Mandrioli J, Caponnetto C, Battistini S, Volanti P, La Bella V, Conforti FL, Borghero G, Messina S, Simone IL, Trojsi F, Salvi F, Logullo FO, D'Alfonso S, Corrado L, Capasso M, Ferrucci L; Genomic Translation for ALS Care (GTAC) Consortium, Moreno CAM, Kamalakaran S, Goldstein DB; ALS Sequencing Consortium, Gitler AD, Harris T, Myers RM; NYGC ALS Consortium, Phatnani H, Musunuri RL, Evani US, Abhyankar A, Zody MC; Answer ALS Foundation, Kaye J, Finkbeiner S, Wyman SK, LeNail A, Lima L, Fraenkel E, Svendsen CN, Thompson LM, Van Eyk JE, Berry JD, Miller TM, Kolb SJ, Cudkowicz M, Baxi E; Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium, Benatar M, Taylor JP, Rampersaud E, Wu G, Wuu J; SLAGEN Consortium, Lauria G, Verde F, Fogh I, Tiloca C, Comi GP, Sorarù G, Cereda C; French ALS Consortium, Corcia P, Laaksovirta H, Myllykangas L, Jansson L, Valori M, Ealing J, Hamdalla H, Rollinson S, Pickering-Brown S, Orrell RW, Sidle KC, Malaspina A, Hardy J, Singleton AB, Johnson JO, Arepalli S, Sapp PC, McKenna-Yasek D, Polak M, Asress S, Al-Sarraj S, King A, Troakes C, Vance C, de Belleroche J, Baas F, Ten Asbroek ALMA, Muñoz-Blanco JL, Hernandez DG, Ding J, Gibbs JR, Scholz SW, Floeter MK, Campbell RH, Landi F, Bowser R, Pulst SM, Ravits JM, MacGowan DJL, Kirby J, Pioro EP, Pamphlett R, Broach J, Gerhard G, Dunckley TL, Brady CB, Kowall NW, Troncoso JC, Le Ber I, Mouzat K, Lumbroso S, Heiman-Patterson TD, Kamel F, Van Den Bosch L, Baloh RH, Strom TM, Meitinger T, Shatunov A, Van Eijk KR, de Carvalho M, Kooyman M, Middelkoop B, Moisse M, McLaughlin RL, Van Es MA, Weber M, Boylan KB, Van Blitterswijk M, Rademakers R, Morrison KE, Basak AN, Mora JS, Drory VE, Shaw PJ, Turner MR, Talbot K, Hardiman O, Williams KL, Fifita JA, Nicholson GA, Blair IP, Rouleau GA, Esteban-Pérez J, García-Redondo A, Al-Chalabi A; Project MinE ALS Sequencing Consortium, Rogaeva E, Zinman L, Ostrow LW, Maragakis NJ, Rothstein JD, Simmons Z, Cooper-Knock J, Brice A, Goutman SA, Feldman EL, Gibson SB, Taroni F, Ratti A, Gellera C, Van Damme P, Robberecht W, Fratta P, Sabatelli M, Lunetta C, Ludolph AC, Andersen PM, Weishaupt JH, Camu W, Trojanowski JQ, Van Deerlin VM, Brown RH Jr, van den Berg LH, Veldink JH, Harms MB, Glass JD, Stone DJ, Tienari P, Silani V, Chiò A, Shaw CE, Traynor BJ, Landers JE.

Neuron. 2018 Mar 21;97(6):1268-1283.e6. doi: 10.1016/j.neuron.2018.02.027.

38.

Analysing and exemplifying forensic conclusion criteria in terms of Bayesian decision theory.

Biedermann A, Bozza S, Taroni F.

Sci Justice. 2018 Mar;58(2):159-165. doi: 10.1016/j.scijus.2017.07.002. Epub 2017 Jul 21.

39.

Cortical thickness, stance control, and arithmetic skill: An exploratory study in premanifest Huntington disease.

Nanetti L, Contarino VE, Castaldo A, Sarro L, Bachoud-Levi AC, Giavazzi M, Frittoli S, Ciammola A, Rizzo E, Gellera C, Bruzzone MG, Taroni F, Grisoli M, Mariotti C.

Parkinsonism Relat Disord. 2018 Jun;51:17-23. doi: 10.1016/j.parkreldis.2018.02.033. Epub 2018 Feb 23.

PMID:
29496355
40.

Bayesian networks of age estimation and classification based on dental evidence: A study on the third molar mineralization.

Sironi E, Pinchi V, Pradella F, Focardi M, Bozza S, Taroni F.

J Forensic Leg Med. 2018 Apr;55:23-32. doi: 10.1016/j.jflm.2018.02.005. Epub 2018 Feb 9.

PMID:
29455020
41.

A solution for the rare type match problem when using the DIP-STR marker system.

Cereda G, Gill RD, Taroni F.

Forensic Sci Int Genet. 2018 May;34:88-96. doi: 10.1016/j.fsigen.2017.07.010. Epub 2017 Aug 24.

PMID:
29433057
42.

Effect of diazoxide on Friedreich ataxia models.

Santoro A, Anjomani Virmouni S, Paradies E, Villalobos Coa VL, Al-Mahdawi S, Khoo M, Porcelli V, Vozza A, Perrone M, Denora N, Taroni F, Merla G, Palmieri L, Pook MA, Marobbio CMT.

Hum Mol Genet. 2018 Mar 15;27(6):992-1001. doi: 10.1093/hmg/ddy016.

PMID:
29325032
43.

The meaning of justified subjectivism and its role in the reconciliation of recent disagreements over forensic probabilism.

Biedermann A, Bozza S, Taroni F, Aitken C.

Sci Justice. 2017 Nov;57(6):477-483. doi: 10.1016/j.scijus.2017.08.005. Epub 2017 Sep 22.

44.

On the Bayesian approach to forensic age estimation of living individuals.

Sironi E, Vuille J, Morling N, Taroni F.

Forensic Sci Int. 2017 Dec;281:e24-e29. doi: 10.1016/j.forsciint.2017.11.007. Epub 2017 Nov 11.

PMID:
29162298
45.

Age estimation by assessment of pulp chamber volume: a Bayesian network for the evaluation of dental evidence.

Sironi E, Taroni F, Baldinotti C, Nardi C, Norelli GA, Gallidabino M, Pinchi V.

Int J Legal Med. 2018 Jul;132(4):1125-1138. doi: 10.1007/s00414-017-1733-0. Epub 2017 Nov 14.

PMID:
29138952
46.

Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.

Cortese A, Laurà M, Casali C, Nishino I, Hayashi YK, Magri S, Taroni F, Stuani C, Saveri P, Moggio M, Ripolone M, Prelle A, Pisciotta C, Sagnelli A, Pichiecchio A, Reilly MM, Buratti E, Pareyson D.

Eur J Neurol. 2018 Jan;25(1):154-163. doi: 10.1111/ene.13478. Epub 2017 Dec 2.

PMID:
29029362
47.

Reply to Morrison et al. (2016) Refining the relevant population in forensic voice comparison - A response to Hicks et alii (2015) The importance of distinguishing information from evidence/observations when formulating propositions.

Hicks T, Biedermann A, de Koeijer JA, Taroni F, Champod C, Evett IW.

Sci Justice. 2017 Sep;57(5):401-402. doi: 10.1016/j.scijus.2017.04.005. Epub 2017 Apr 11. No abstract available.

PMID:
28889871
48.

CADASIL: Treatment and Management Options.

Bersano A, Bedini G, Oskam J, Mariotti C, Taroni F, Baratta S, Parati EA.

Curr Treat Options Neurol. 2017 Sep;19(9):31. doi: 10.1007/s11940-017-0468-z. Review.

PMID:
28741120
49.

Towards a Bayesian evaluation of features in questioned handwritten signatures.

Gaborini L, Biedermann A, Taroni F.

Sci Justice. 2017 May;57(3):209-220. doi: 10.1016/j.scijus.2017.01.004. Epub 2017 Jan 31.

50.

Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.

Capone VP, Morello W, Taroni F, Montini G.

Int J Mol Sci. 2017 Apr 11;18(4). pii: E796. doi: 10.3390/ijms18040796. Review.

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