Vuillaume I - Search Results

1

Pneumatic transport is critical for leukaemic patients with major leukocytosis: what precautions to measure lactate dehydrogenase, potassium and aspartate aminotransferase?

Guiheneuf R, Vuillaume I, Mangalaboyi J, Launay D, Berthon C, Maury JC, Maboudou P, Rousseaux J. Guiheneuf R, et al. Among authors: vuillaume i. Ann Clin Biochem. 2010 Jan;47(Pt 1):94-6. doi: 10.1258/acb.2009.009044. Epub 2009 Nov 25. Ann Clin Biochem. 2010. PMID: 19940199

2

[Interferences by a monoclonal IgM in biochemical analyses: detection and recommendations].

Barbier A, Vuillaume I, Baras A, Coiteux V, Maboudou P, Rousseaux J. Barbier A, et al. Among authors: vuillaume i. Ann Biol Clin (Paris). 2007 Jul-Aug;65(4):411-5. Ann Biol Clin (Paris). 2007. PMID: 17627923 Free article. French.

3

Simple nonisotopic assays for detection of (CAG)n repeats expansions associated with seven neurodegenerative disorders.

Vuillaume I, Schraen S, Rousseaux J, Sablonnière B. Vuillaume I, et al. Diagn Mol Pathol. 1998 Jun;7(3):174-9. doi: 10.1097/00019606-199806000-00009. Diagn Mol Pathol. 1998. PMID: 9836074

4

High concentrations of lithium heparin decrease measured serum sodium in some analyzers.

Vuillaume I, Penet S, Rakza T, Storme L, Kacet N, Lequien P, Rousseaux J. Vuillaume I, et al. Clin Chem. 1999 Oct;45(10):1880-1. Clin Chem. 1999. PMID: 10508144 No abstract available.

5

[Hemolysis interferences on frequently required stat analysis: a French multicentric study].

Poupon C, Lefèvre G, Ngo-François S, Alibeu C, Barbé F, Bourbonneux V, Cartier R, Morin C, Szymanowicz A, Vuillaume I; Groupe de travail du Collège national de biochimie des hôpitaux. Poupon C, et al. Among authors: vuillaume i. Ann Biol Clin (Paris). 2015 Nov-Dec;73(6):705-16. doi: 10.1684/abc.2015.1090. Ann Biol Clin (Paris). 2015. PMID: 26635050 Free article. French.

6

A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1.

Vuillaume I, Devos D, Schraen-Maschke S, Dina C, Lemainque A, Vasseur F, Bocquillon G, Devos P, Kocinski C, Marzys C, Destée A, Sablonnière B. Vuillaume I, et al. Ann Neurol. 2002 Nov;52(5):666-70. doi: 10.1002/ana.10344. Ann Neurol. 2002. PMID: 12402269

7

Absence of unidentified CAG repeat expansion in patients with Huntington's disease-like phenotype.

Vuillaume I, Meynieu P, Schraen-Maschke S, Destée A, Sablonnière B. Vuillaume I, et al. J Neurol Neurosurg Psychiatry. 2000 May;68(5):672-5. doi: 10.1136/jnnp.68.5.672. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766906 Free PMC article.

8

Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease.

Nazé P, Vuillaume I, Destée A, Pasquier F, Sablonnière B. Nazé P, et al. Among authors: vuillaume i. Neurosci Lett. 2002 Aug 2;328(1):1-4. doi: 10.1016/s0304-3940(02)00231-8. Neurosci Lett. 2002. PMID: 12123845

9

Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease.

Vuillaume I, Vermersch P, Destée A, Petit H, Sablonnière B. Vuillaume I, et al. J Neurol Neurosurg Psychiatry. 1998 Jun;64(6):758-62. doi: 10.1136/jnnp.64.6.758. J Neurol Neurosurg Psychiatry. 1998. PMID: 9647305 Free PMC article.

10

[Triplet expansion diseases].

Sablonnière B, Vuillaume I, Schraen-Maschke S. Sablonnière B, et al. Among authors: vuillaume i. Ann Biol Clin (Paris). 2000 May-Jun;58(3):356-60. Ann Biol Clin (Paris). 2000. PMID: 10846241 Free article. Review. French. No abstract available.

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