Zortea M - Search Results

1

A genetic polymorphism in the human HOXB1 homeobox gene implying a 9bp tandem repeat in the amino-terminal coding region. Mutations in brief no. 200. Online.

Faiella A, Zortea M, Barbaria E, Albani F, Capra V, Cama A, Boncinelli E. Faiella A, et al. Among authors: zortea m. Hum Mutat. 1998;12(5):363. Hum Mutat. 1998. PMID: 10671062

2

Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families.

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. Mostacciuolo ML, et al. Among authors: zortea m. Hum Mutat. 2001;18(1):32-41. doi: 10.1002/humu.1147. Hum Mutat. 2001. PMID: 11438991

3

A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.

Vazza G, Zortea M, Boaretto F, Micaglio GF, Sartori V, Mostacciuolo ML. Vazza G, et al. Among authors: zortea m. Am J Hum Genet. 2000 Aug;67(2):504-9. doi: 10.1086/303017. Epub 2000 Jun 30. Am J Hum Genet. 2000. PMID: 10877981 Free PMC article.

4

Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1.

Zortea M, Vettori A, Trevisan CP, Bellini S, Vazza G, Armani M, Simonati A, Mostacciuolo ML. Zortea M, et al. J Med Genet. 2002 Jun;39(6):387-90. doi: 10.1136/jmg.39.6.387. J Med Genet. 2002. PMID: 12070243 Free PMC article.

5

A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset.

Vazza G, Merlini L, Bertolin C, Zortea M, Mostacciuolo ML. Vazza G, et al. Among authors: zortea m. Neuromuscul Disord. 2006 Dec;16(12):878-81. doi: 10.1016/j.nmd.2006.09.002. Epub 2006 Oct 17. Neuromuscul Disord. 2006. PMID: 17052905

6

Prevalence of inherited ataxias in the province of Padua, Italy.

Zortea M, Armani M, Pastorello E, Nunez GF, Lombardi S, Tonello S, Rigoni MT, Zuliani L, Mostacciuolo ML, Gellera C, Di Donato S, Trevisan CP. Zortea M, et al. Neuroepidemiology. 2004 Nov-Dec;23(6):275-80. doi: 10.1159/000080092. Epub 2004 Aug 5. Neuroepidemiology. 2004. PMID: 15297793

7

Ataxia and congenital muscular dystrophy: the follow-up of a new specific phenotype.

Trevisan CP, Pastorello E, Tonello S, Armani M, Rigoni MT, Tormene AP, Freda MP, Zortea M, Lombardi S. Trevisan CP, et al. Among authors: zortea m. Brain Dev. 2001 Mar;23(2):108-14. doi: 10.1016/s0387-7604(01)00187-5. Brain Dev. 2001. PMID: 11248459

8

Friedreich's ataxia: clinical heterogeneity in two sisters.

Armani M, Zortea M, Pastorello E, Lombardi S, Tonello S, Zuliani L, Rigoni MT, Trevisan CP. Armani M, et al. Among authors: zortea m. Neurol Sci. 2006 Jun;27(2):140-2. doi: 10.1007/s10072-006-0617-8. Neurol Sci. 2006. PMID: 16816915

9

Modulation of neural networks and symptom correlated in fibromyalgia: A randomized double-blind multi-group explanatory clinical trial of home-based transcranial direct current stimulation.

Lopes Alves R, Zortea M, Vicuña Serrano P, Laranjeira VDS, Franceschini Tocchetto B, Ramalho L, Fernanda da Silveira Alves C, Brugnera Tomedi R, Pereira de Almeida R, Machado Bruck S, Medeiros L, R S Sanches P, P Silva D Jr, Torres ILS, Fregni F, Caumo W. Lopes Alves R, et al. Among authors: zortea m. PLoS One. 2024 Nov 13;19(11):e0288830. doi: 10.1371/journal.pone.0288830. eCollection 2024. PLoS One. 2024. PMID: 39536019 Free PMC article. Clinical Trial.

10

A prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts.

NIHR Global Health Research Unit on Global Surgery; STARSurg Collaborative. NIHR Global Health Research Unit on Global Surgery, et al. Lancet Digit Health. 2024 Jul;6(7):e507-e519. doi: 10.1016/S2589-7500(24)00065-7. Lancet Digit Health. 2024. PMID: 38906616 Free article.

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