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39 results

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Page 1
[Severe neonatal mitochondrial cytopathy caused by isolated COX defect].
Ruiz Escusol S, Ferreras Ames A, Rubio Morales L, Medrano Marina P, López Pisón J, Baldellóu Vázquez A, Marco Tello A, Rebage Moisés V. Ruiz Escusol S, et al. Among authors: baldellou vazquez a. An Esp Pediatr. 2000 Apr;52(4):392-4. An Esp Pediatr. 2000. PMID: 11003935 Spanish.
[Non-ketotic hyperglycinemia: clinical and therapeutic course in three patients].
Rite Gracia S, Guallarte Alias MP, Martínez Moral M, Baldellou Vázquez A, Rite Montañés S, Ruiz-Echarri Zalaya MP, Marco Tello A, Rebage Moisés V. Rite Gracia S, et al. Among authors: baldellou vazquez a. An Esp Pediatr. 1999 Apr;50(4):408-10. An Esp Pediatr. 1999. PMID: 10356838 Spanish. No abstract available.
[Oxidative phosphorylation defects with neonatal presentation: review of our caseload].
Rebage Moisés V, Rite Gracia S, López-Pisón J, Muñoz Albillos M, Aisa Pardo E, Giménez Más JA, Arenas Barbero J, Montoya Vilarroya J, Marco Telloa A, Salazar García-Blanco MI, Baldellou Vázquez A. Rebage Moisés V, et al. Among authors: baldellou vazquez a. An Esp Pediatr. 2000 Mar;52(3):251-7. An Esp Pediatr. 2000. PMID: 11003903 Spanish.
[Smith Lemli Opitz Syndrome type II of neonatal diagnosis and review of the most interesting clinical features].
Ramírez-Gómara A, Castejón-Ponce E, Martínez-Martínez M, García-Bodega O, Rite-Gracia S, Segura- Arazuri D, López-Pisón J, Baldellou-Vázquez A, Marco-Tello A, López-López A, Rebage-Moisés V. Ramírez-Gómara A, et al. Among authors: baldellou vazquez a. Rev Neurol. 2002 May 16-31;34(10):946-50. Rev Neurol. 2002. PMID: 12134326 Free article. Review. Spanish.
[Leigh syndrome caused by cytochrome-C oxidase deficiency: a clinical case].
Soria Aznar J, Valle Traid AJ, Campos Calleja C, Jiménez Más JA, Baldellou Vázquez A, López-Pisón J. Soria Aznar J, et al. Among authors: baldellou vazquez a. An Esp Pediatr. 1996 Sep;45(3):286-8. An Esp Pediatr. 1996. PMID: 9019971 Spanish. No abstract available.
[Monosomy r(13), a new observation].
Rebage Moisés V, Baldellou Vázquez A. Rebage Moisés V, et al. Among authors: baldellou vazquez a. An Esp Pediatr. 2001 Jul;55(1):95-6. An Esp Pediatr. 2001. PMID: 11412483 Spanish. No abstract available.
[Severe fulminant form of neonatal citrullinemia. Report of a case].
Lalaguna-Mallada P, García-Romero R, Alonso-del Val B, Rite-Gracia S, Lopez-Pisón J, Baldellou-Vázquez A, Salazar García-Blanco MI, Yus-Gotor C, Briones-Godino P, Marco-Tello A, Rebage V. Lalaguna-Mallada P, et al. Among authors: baldellou vazquez a. Rev Neurol. 2003 Apr 1-15;36(7):629-32. Rev Neurol. 2003. PMID: 12666042 Free article. Spanish.
[Hereditary juvenile cobalamin deficiency due to mutations in GIF gene].
García Jiménez MC, Baldellou Vázquez A, Calvo Martín MT, Pérez-Lungmus G, López Pisón J. García Jiménez MC, et al. Among authors: baldellou vazquez a. An Pediatr (Barc). 2008 Jul;69(1):56-8. doi: 10.1157/13124221. An Pediatr (Barc). 2008. PMID: 18620679 Free article. Spanish.
39 results