Valles-Ayoub Y - Search Results

1

MTHFR C677T genotype frequency in patients of Middle Eastern descent as determined by real-time PCR and melting curve analysis.

Haghighatgoo A, Valles-Ayoub Y, Saechao C, Esfandiarifard S, Martinez SL, Pietruszka M, Darvish D. Haghighatgoo A, et al. Among authors: valles ayoub y. Genet Test Mol Biomarkers. 2009 Aug;13(4):471-6. doi: 10.1089/gtmb.2009.0008. Genet Test Mol Biomarkers. 2009. PMID: 19594372

2

Validation of GNE:p.M712T identification by melting curve analysis.

Valles-Ayoub Y, Saechao C, Haghighatgoo A, Neshat MS, Esfandiarifard S, Pietruszka M, Darvish D. Valles-Ayoub Y, et al. Genet Test. 2008 Mar;12(1):101-9. doi: 10.1089/gte.2007.0034. Genet Test. 2008. PMID: 18373408

3

Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descent.

Saechao C, Valles-Ayoub Y, Esfandiarifard S, Haghighatgoo A, No D, Shook S, Mendell JR, Rosales-Quintero X, Felice KJ, Morel CF, Pietruska M, Darvish D. Saechao C, et al. Among authors: valles ayoub y. Genet Test Mol Biomarkers. 2010 Apr;14(2):157-62. doi: 10.1089/gtmb.2009.0157. Genet Test Mol Biomarkers. 2010. PMID: 20059379

4

Wolman disease (LIPA p.G87V) genotype frequency in people of Iranian-Jewish ancestry.

Valles-Ayoub Y, Esfandiarifard S, No D, Sinai P, Khokher Z, Kohan M, Kahen T, Darvish D. Valles-Ayoub Y, et al. Genet Test Mol Biomarkers. 2011 Jun;15(6):395-8. doi: 10.1089/gtmb.2010.0203. Epub 2011 Feb 3. Genet Test Mol Biomarkers. 2011. PMID: 21291321

5

Serum neural cell adhesion molecule is hyposialylated in hereditary inclusion body myopathy.

Valles-Ayoub Y, Esfandiarifard S, Sinai P, Carbajo R, Khokher Z, No D, Pietruszka M, Darvish B, Kakkis E, Darvish D. Valles-Ayoub Y, et al. Genet Test Mol Biomarkers. 2012 May;16(5):313-7. doi: 10.1089/gtmb.2011.0146. Epub 2011 Nov 15. Genet Test Mol Biomarkers. 2012. PMID: 22085395

6

Novel GNE mutations in autosomal recessive hereditary inclusion body myopathy patients.

No D, Valles-Ayoub Y, Carbajo R, Khokher Z, Sandoval L, Stein B, Tarnopolsky MA, Mozaffar T, Darvish B, Pietruszka M, Darvish D. No D, et al. Among authors: valles ayoub y. Genet Test Mol Biomarkers. 2013 May;17(5):376-82. doi: 10.1089/gtmb.2012.0408. Epub 2013 Feb 25. Genet Test Mol Biomarkers. 2013. PMID: 23437777

7

Prevalence of GNE p.M712T and hereditary inclusion body myopathy (HIBM) in Sangesar population of Northern Iran.

Khademian H, Mehravar E, Urtizberea J, Sagoo S, Sandoval L, Carbajo R, Darvish B, Valles-Ayoub Y, Darvish D. Khademian H, et al. Among authors: valles ayoub y. Clin Genet. 2013 Dec;84(6):589-92. doi: 10.1111/cge.12086. Epub 2013 Feb 21. Clin Genet. 2013. PMID: 23278550

8

Non-GNE Quadriceps Sparing Distal Myopathy in an Iranian Jewish Patient.

Mishra SK, Valles-Ayoub Y, Darvish D, Khosa S, Moheb N, Trikamji B, Rafiei N, Freundlich R. Mishra SK, et al. Among authors: valles ayoub y. J Clin Neuromuscul Dis. 2019 Jun;20(4):210-213. doi: 10.1097/CND.0000000000000231. J Clin Neuromuscul Dis. 2019. PMID: 31135625

9

Targeting GNE Myopathy: A Dual Prodrug Approach for the Delivery of N-Acetylmannosamine 6-Phosphate.

Morozzi C, Sedláková J, Serpi M, Avigliano M, Carbajo R, Sandoval L, Valles-Ayoub Y, Crutcher P, Thomas S, Pertusati F. Morozzi C, et al. Among authors: valles ayoub y. J Med Chem. 2019 Sep 12;62(17):8178-8193. doi: 10.1021/acs.jmedchem.9b00833. Epub 2019 Aug 20. J Med Chem. 2019. PMID: 31386361

10

A DNA repair abnormality specific for rearranged immunoglobulin variable genes in germinal center B cells.

Fairhurst RM, Valles-Ayoub Y, Neshat M, Braun J. Fairhurst RM, et al. Mol Immunol. 1996 Feb;33(3):231-44. doi: 10.1016/0161-5890(95)00145-x. Mol Immunol. 1996. PMID: 8649444

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