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365 results

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Page 1
Management of 35 critically ill hyperammonemic neonates: Role of early administration of metabolite scavengers and continuous hemodialysis.
Abily-Donval L, Dupic L, Joffre C, Brassier A, Arnoux JB, Grimaud M, Lesage F, de Saint Blanquat L, Bekri S, Marret S, Pontoizeau C, Renolleau S, Ottolenghi C, de Lonlay P, Oualha M. Abily-Donval L, et al. Among authors: de saint blanquat l, de lonlay p. Arch Pediatr. 2020 Jul;27(5):250-256. doi: 10.1016/j.arcped.2020.05.002. Epub 2020 May 14. Arch Pediatr. 2020. PMID: 32418642
[Metabolic emergencies: diagnostic algorithm of lactic acidosis].
Valayannopoulos V, Arnoux JB, Rio M, de Lonlay P. Valayannopoulos V, et al. Among authors: de lonlay p. Arch Pediatr. 2009 Jun;16(6):637-9. doi: 10.1016/S0929-693X(09)74095-3. Arch Pediatr. 2009. PMID: 19541113 French. No abstract available.
[Enzyme replacement therapy for lysosomal storage disorders].
Valayannopoulos V, Brassier A, Chabli A, Caillaud C, Lemoine M, Odent T, Arnoux JB, de Lonlay P. Valayannopoulos V, et al. Among authors: de lonlay p. Arch Pediatr. 2011 Oct;18(10):1119-23. doi: 10.1016/j.arcped.2011.07.002. Epub 2011 Aug 27. Arch Pediatr. 2011. PMID: 21873040 Review. French.
[Diagnosing an inborn metabolic error with consciousness disorders].
Arnoux JB, Brassier A, Guemann AS, Grisel C, de Lonlay P. Arnoux JB, et al. Among authors: de lonlay p. Arch Pediatr. 2015 May;22(5 Suppl 1):50-1. doi: 10.1016/S0929-693X(15)30026-9. Arch Pediatr. 2015. PMID: 26112517 French. No abstract available.
[Prenatal symptoms and diagnosis of inherited metabolic diseases].
Brassier A, Ottolenghi C, Boddaert N, Sonigo P, Attié-Bitach T, Millischer-Bellaiche AE, Baujat G, Cormier-Daire V, Valayannopoulos V, Seta N, Piraud M, Chadefaux-Vekemans B, Vianey-Saban C, Froissart R, de Lonlay P. Brassier A, et al. Among authors: de lonlay p. Arch Pediatr. 2012 Sep;19(9):959-69. doi: 10.1016/j.arcped.2012.06.002. Epub 2012 Aug 9. Arch Pediatr. 2012. PMID: 22884749 French.
Renal transplantation in 4 patients with methylmalonic aciduria: a cell therapy for metabolic disease.
Brassier A, Boyer O, Valayannopoulos V, Ottolenghi C, Krug P, Cosson MA, Touati G, Arnoux JB, Barbier V, Bahi-Buisson N, Desguerre I, Charbit M, Benoist JF, Dupic L, Aigrain Y, Blanc T, Salomon R, Rabier D, Guest G, de Lonlay P, Niaudet P. Brassier A, et al. Among authors: de lonlay p. Mol Genet Metab. 2013 Sep-Oct;110(1-2):106-10. doi: 10.1016/j.ymgme.2013.05.001. Epub 2013 May 14. Mol Genet Metab. 2013. PMID: 23751327
Acute psychosis in propionic acidemia: 2 case reports.
Dejean de la Bâtie C, Barbier V, Valayannopoulos V, Touati G, Maltret A, Brassier A, Arnoux JB, Grévent D, Chadefaux B, Ottolenghi C, Canouï P, de Lonlay P. Dejean de la Bâtie C, et al. Among authors: de lonlay p. J Child Neurol. 2014 Feb;29(2):274-9. doi: 10.1177/0883073813508812. Epub 2013 Dec 11. J Child Neurol. 2014. PMID: 24334345
Two new cases of serine deficiency disorders treated with l-serine.
Brassier A, Valayannopoulos V, Bahi-Buisson N, Wiame E, Hubert L, Boddaert N, Kaminska A, Habarou F, Desguerre I, Van Schaftingen E, Ottolenghi C, de Lonlay P. Brassier A, et al. Among authors: de lonlay p. Eur J Paediatr Neurol. 2016 Jan;20(1):53-60. doi: 10.1016/j.ejpn.2015.10.007. Epub 2015 Nov 5. Eur J Paediatr Neurol. 2016. PMID: 26610677
365 results