Milà M - Search Results

1

Maternal transmission in sporadic Huntington's disease.

Sánchez A, Milà M, Castellví-Bel S, Rosich M, Jiménez D, Badenas C, Estivill X. Sánchez A, et al. Among authors: mila m. J Neurol Neurosurg Psychiatry. 1997 May;62(5):535-7. doi: 10.1136/jnnp.62.5.535. J Neurol Neurosurg Psychiatry. 1997. PMID: 9153618 Free PMC article.

2

Huntington's disease: confirmation of diagnosis and presymptomatic testing in Spanish families by genetic analysis.

Sánchez A, Castellví-Bel S, Milà M, Genis D, Calopa M, Jiménez D, Estivill X. Sánchez A, et al. Among authors: mila m. J Neurol Neurosurg Psychiatry. 1996 Dec;61(6):625-7. doi: 10.1136/jnnp.61.6.625. J Neurol Neurosurg Psychiatry. 1996. PMID: 8971113 Free PMC article.

3

[Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis].

Sánchez A, Milà M, Castellví-Bel S, Calopa M, Genís D, Jiménez D, Estivill X. Sánchez A, et al. Among authors: mila m. Med Clin (Barc). 1997 May 10;108(18):687-90. Med Clin (Barc). 1997. PMID: 9324583 Spanish.

4

Dentatorubropallidoluysian atrophy in a spanish family: a clinical, radiological, pathological, and genetic study.

Muñoz E, Milà M, Sánchez A, Latorre P, Ariza A, Codina M, Ballesta F, Tolosa E. Muñoz E, et al. Among authors: mila m. J Neurol Neurosurg Psychiatry. 1999 Dec;67(6):811-4. doi: 10.1136/jnnp.67.6.811. J Neurol Neurosurg Psychiatry. 1999. PMID: 10567506 Free PMC article.

5

Chemiluminescent detection of blotted PCR products (CB-PCR) of two CAG dynamic mutations (Huntington's disease and spinocerebellar ataxia type 1).

Castellví-Bel S, Matilla T, Banchs MI, Kruyer H, Corral J, Milà M, Estivill X. Castellví-Bel S, et al. Among authors: mila m. J Med Genet. 1994 Aug;31(8):654-5. doi: 10.1136/jmg.31.8.654. J Med Genet. 1994. PMID: 7815428 Free PMC article.

6

Screening for FXTAS in 95 Spanish patients negative for Huntington disease.

Rodriguez-Revenga L, Santos MM, Sánchez A, Pujol M, Gómez-Anson B, Badenas C, Jiménez D, Madrigal I, Milà M. Rodriguez-Revenga L, et al. Among authors: mila m. Genet Test. 2008 Mar;12(1):135-8. doi: 10.1089/gte.2007.0074. Genet Test. 2008. PMID: 18373410

7

Prenatal diagnosis of fragile X syndrome: (CGG)n expansion and methylation of chorionic villus samples.

Castellví-Bel S, Milà M, Soler A, Carrió A, Sánchez A, Villa M, Jiménez MD, Estivill X. Castellví-Bel S, et al. Among authors: mila m. Prenat Diagn. 1995 Sep;15(9):801-7. doi: 10.1002/pd.1970150903. Prenat Diagn. 1995. PMID: 8559749

8

Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene.

Milà M, Castellví-Bel S, Sánchez A, Lázaro C, Villa M, Estivill X. Milà M, et al. J Med Genet. 1996 Apr;33(4):338-40. doi: 10.1136/jmg.33.4.338. J Med Genet. 1996. PMID: 8730293 Free PMC article.

9

A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion.

Milà M, Castellví-Bel S, Giné R, Vazquez C, Badenas C, Sánchez A, Estivill X. Milà M, et al. Hum Genet. 1996 Oct;98(4):419-21. doi: 10.1007/s004390050232. Hum Genet. 1996. PMID: 8792815

10

Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.

Milà M, Sànchez A, Badenas C, Brun C, Jiménez D, Villa MP, Castellví-Bel S, Estivill X. Milà M, et al. Hum Genet. 1997 Oct;100(5-6):503-7. doi: 10.1007/s004390050542. Hum Genet. 1997. PMID: 9341861

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

191 results

Search Page

Filters