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144 results

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Page 1
Clinical course of 63 patients with neonatal onset urea cycle disorders in the years 2001-2013.
Unsinn C, Das A, Valayannopoulos V, Thimm E, Beblo S, Burlina A, Konstantopoulou V, Mayorandan S, de Lonlay P, Rennecke J, Derbinski J, Hoffmann GF, Häberle J. Unsinn C, et al. Among authors: valayannopoulos v. Orphanet J Rare Dis. 2016 Aug 19;11(1):116. doi: 10.1186/s13023-016-0493-0. Orphanet J Rare Dis. 2016. PMID: 27538463 Free PMC article.
Coexistence in the same family of both focal and diffuse forms of hyperinsulinism.
Valayannopoulos V, Vaxillaire M, Aigrain Y, Jaubert F, Bellanné-Chantelot C, Ribeiro MJ, Brunelle F, Froguel P, Robert JJ, Polak M, Nihoul-Fékété C, de Lonlay P. Valayannopoulos V, et al. Diabetes Care. 2007 Jun;30(6):1590-2. doi: 10.2337/dc06-2327. Epub 2007 Mar 23. Diabetes Care. 2007. PMID: 17384337 No abstract available.
Development of liver disease despite mannose treatment in two patients with CDG-Ib.
Mention K, Lacaille F, Valayannopoulos V, Romano S, Kuster A, Cretz M, Zaidan H, Galmiche L, Jaubert F, de Keyzer Y, Seta N, de Lonlay P. Mention K, et al. Among authors: valayannopoulos v. Mol Genet Metab. 2008 Jan;93(1):40-3. doi: 10.1016/j.ymgme.2007.08.126. Epub 2007 Oct 22. Mol Genet Metab. 2008. PMID: 17945525
Variable outcome of growth hormone administration in respiratory chain deficiency.
Romano S, Samara D, Crosnier H, Valayannopoulos V, Polak M, Chrétien D, Rötig A, Munnich A, Brauner R, de Lonlay P. Romano S, et al. Among authors: valayannopoulos v. Mol Genet Metab. 2008 Feb;93(2):195-9. doi: 10.1016/j.ymgme.2007.09.007. Epub 2007 Oct 22. Mol Genet Metab. 2008. PMID: 17951089
Risk assessment of acute vascular events in congenital disorder of glycosylation type Ia.
Arnoux JB, Boddaert N, Valayannopoulos V, Romano S, Bahi-Buisson N, Desguerre I, de Keyzer Y, Munnich A, Brunelle F, Seta N, Dautzenberg MD, de Lonlay P. Arnoux JB, et al. Among authors: valayannopoulos v. Mol Genet Metab. 2008 Apr;93(4):444-9. doi: 10.1016/j.ymgme.2007.11.006. Epub 2008 Feb 21. Mol Genet Metab. 2008. PMID: 18093857
[Congenital Disorders of Glycosylation (CDG)].
de Lonlay P, Valayannopoulos V, Dupré T, Vuillaumier-Barrot S, Seta N. de Lonlay P, et al. Among authors: valayannopoulos v. Arch Pediatr. 2008 Jun;15(5):602-5. doi: 10.1016/S0929-693X(08)71847-5. Arch Pediatr. 2008. PMID: 18582686 French. No abstract available.
Neurological aspects of hyperinsulinism-hyperammonaemia syndrome.
Bahi-Buisson N, Roze E, Dionisi C, Escande F, Valayannopoulos V, Feillet F, Heinrichs C, Chadefaux-Vekemans B, Dan B, de Lonlay P. Bahi-Buisson N, et al. Among authors: valayannopoulos v. Dev Med Child Neurol. 2008 Dec;50(12):945-9. doi: 10.1111/j.1469-8749.2008.03114.x. Dev Med Child Neurol. 2008. PMID: 19046187 Free article.
144 results