Sarrazin AM - Search Results

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Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.

Roddier K, Thomas T, Marleau G, Gagnon AM, Dicaire MJ, St-Denis A, Gosselin I, Sarrazin AM, Larbrisseau A, Lambert M, Vanasse M, Gaudet D, Rouleau GA, Brais B. Roddier K, et al. Among authors: sarrazin am. Neurology. 2005 May 24;64(10):1762-7. doi: 10.1212/01.WNL.0000161849.29944.43. Neurology. 2005. PMID: 15911806

Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12s rRNA gene: evidence of heteroplasmy.

el-Schahawi M, López de Munain A, Sarrazin AM, Shanske AL, Basirico M, Shanske S, DiMauro S. el-Schahawi M, et al. Among authors: sarrazin am. Neurology. 1997 Feb;48(2):453-6. doi: 10.1212/wnl.48.2.453. Neurology. 1997. PMID: 9040738

Sudden infant death syndrome (SIDS) in a family with myophosphorylase deficiency.

el-Schahawi M, Bruno C, Tsujino S, Sarrazin AM, Shanske S, LeRoux MG, DiMauro S. el-Schahawi M, et al. Among authors: sarrazin am. Neuromuscul Disord. 1997 Mar;7(2):81-3. doi: 10.1016/s0960-8966(97)00424-0. Neuromuscul Disord. 1997. PMID: 9131647

Efficient biostimulation of native and introduced quorum-quenching Rhodococcus erythropolis populations is revealed by a combination of analytical chemistry, microbiology, and pyrosequencing.

Cirou A, Mondy S, An S, Charrier A, Sarrazin A, Thoison O, DuBow M, Faure D. Cirou A, et al. Appl Environ Microbiol. 2012 Jan;78(2):481-92. doi: 10.1128/AEM.06159-11. Epub 2011 Nov 11. Appl Environ Microbiol. 2012. PMID: 22081576 Free PMC article.

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