Publications by authors named "P Divry"

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Seventeen novel mutations that cause profound biotinidase deficiency.
B Wolf, K Jensen, G Hüner, M Demirkol, T Baykal, P Divry

Mol Genet Metab· May 2003

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Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy.
Anne-Marie Lamhonwah, Simon E Olpin, Rodney J Pollitt, Christine Vianey-Saban, Priscille Divry

Am J Med Genet· August 2002

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Mevalonic aciduria and hyper-IgD syndrome: two sides of the same coin?
M Tsimaratos, I Kone-Paut, P Divry, N Philip, B Chabrol

J Inherit Metab Dis· June 2001

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A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency.
E H Touma, M S Rashed, C Vianey-Saban, A Sakr, P Divry

Arch Dis Child· January 2001

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Antenatal expression of multiple acyl-CoA dehydrogenase deficiency.
C Vianey-Saban, R Bouvier, P Cochat, A Buenerd, P Divry

J Inherit Metab Dis· June 2000

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