Zobrazeno 1 - 10
of 83
pro vyhledávání: '"I, Vuillaume"'
Autor:
V. Danel-Brunaud, Luc Defebvre, B. Halleumieux, Arnaud Delval, I. Vuillaume, Céline Tard, A.-S. Lia
Publikováno v:
Pratique Neurologique - FMC. 12:69-71
Autor:
S, Penet, I, Vuillaume, T, Nicolas, A, Szymanowicz, C, Houlbert, P, Pernet, Isabelle, Vuillaume
Publikováno v:
Annales de biologie clinique. 70:261-272
For point-of-care-testing (POCT), the French regulation on medical biology states allows a unique situation where a delayed validation of results is possible. This paper proposes guidelines to organize POCT post-analytical phase in agreement with the
Publikováno v:
Annales d'Endocrinologie. 66:545-551
Cet article rapporte le cas d’un homme presentant une ataxie cerebelleuse d’evolution progressive depuis l’enfance associee a un hypogonadisme hypogonadotrope partiel decouvert au decours d’un bilan d’infecondite. L’association de ces deu
Autor:
Alain Destée, A. Kwiatkowski, P. Jissendi Tchofo, Luc Defebvre, Gilles Ryckewaert, Patrick F. Chinnery, Caroline Moreau, David Devos, I Vuillaume
Publikováno v:
Parkinsonism & Related Disorders. 18:110-112
Autor:
P, Pernet, M C, Guimont, I, Vuillaume, S, Penet, A, Szymanowicz, C, Houlbert, V, Annaix, M, Vaubourdolle, Isabelle, Vuillaume
Publikováno v:
Annales de biologie clinique.
Implementation is the main step of the point-of-care testing (POCT) device installation process to comply with EN ISO 22870. The multidisciplinary POCT management group is in charge to align that process with the standards but also with the French re
Autor:
S Batey, I Vuillaume, Ann Curtis, A Curtis, Patrick F. Chinnery, David Devos, John Burn, Alain Destée, Anne Lombès
Publikováno v:
Journal of medical genetics. 47(1)
In 2003 we re-investigated a French family with a progressive adult onset movement disorder and cystic cavitation of the basal ganglia on brain magnetic resonance imaging (MRI).1 The clinical picture was strikingly similar to that which we described
Autor:
I Vuillaume, JB True, Philippe Tarroux, Y Decroix, BJ Paniel, Pierre Vincens, P Poitout, Régis Calvayrac
Publikováno v:
Biomedicine & Pharmacotherapy. 45:435-444
We report that an internal and non-UV-dependent type of neoplasia, the human cervical intraepithelial neoplasia (SIL), is also deficient in catalase activity, like the UV-induced tumors in the autosomal recessive human epithelial disease, xeroderma p
Publikováno v:
Annales de biologie clinique. 65(4)
We present a case of analytical interference on three parameters (lactate dehydrogenase, uric acid and alkalin phosphatase), caused by a monoclonal IgM, evidenced in a patient with Waldenström disease. Mechanism of interference was probably related
Publikováno v:
Brain
Neuroferritinopathy is a progressive potentially treatable adult-onset movement disorder caused by mutations in the ferritin light chain gene (FTL1). Features overlap with common extrapyramidal disorders: idiopathic torsion dystonia, idiopathic Parki
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