Baldellou-Vázquez A - Search Results

1

[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. Rev Neurol. 2003 Apr 1-15;36(7):629-32. Rev Neurol. 2003. PMID: 12666042 Free article. Spanish.

2

[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. Rev Neurol. 2002 May 16-31;34(10):946-50. Rev Neurol. 2002. PMID: 12134326 Free article. Review. Spanish.

3

[Hereditary neuromuscular diseases in paediatrics. Our experience over the last 14 years].

López-Pisón J, Rebage V, Baldellou-Vázquez A, Capablo-Liesa JL, Colomer J, Calvo MT, Sáenz de Cabezón A, Alfaro-Torres J, del Agua C, Bestué M, Peña-Segura JL. López-Pisón J, et al. Rev Neurol. 2005 Aug 1-15;41(3):145-50. Rev Neurol. 2005. PMID: 16047297 Free article. Spanish.

4

[Our experience in the diagnosis of peroxisomal diseases with an abnormal fatty acid profile].

López-Pisón J, Pérez-Delgado R, García-Oguiza A, Lafuente-Hidalgo M, García-Jiménez M, Calvo-Ruata ML, Peña-Segura JL, Rebage V, Girós-Blasco M, Coll MJ, Baldellou-Vázquez A. López-Pisón J, et al. Among authors: baldellou vazquez a. Rev Neurol. 2008 Jul 1-15;47(1):1-5. Rev Neurol. 2008. PMID: 18592472 Free article. Spanish.

5

[Rubinstein-Taybi syndrome associated with hypoplasia of an extremity. A report of a neonatal case].

Ruiz Moreno JA, Moros Peña M, Molina Chica I, Rebage Moisés V, López Pisón J, Baldellou Vázquez A, Marco Tello A. Ruiz Moreno JA, et al. An Esp Pediatr. 1998 Mar;48(3):321-4. An Esp Pediatr. 1998. PMID: 9608100 Spanish. No abstract available.

6

[Recommendations for the dietary treatment of phenylketonuria].

Baldellou Vázquez A, Ruiz-Echarri Zalaya MP, Salazar García-Blanco MI. Baldellou Vázquez A, et al. An Esp Pediatr. 1999 Dec;51(6):625-8. An Esp Pediatr. 1999. PMID: 10666895 Spanish. No abstract available.

7

[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. An Esp Pediatr. 2000 Mar;52(3):251-7. An Esp Pediatr. 2000. PMID: 11003903 Spanish.

8

[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. An Esp Pediatr. 2000 Apr;52(4):392-4. An Esp Pediatr. 2000. PMID: 11003935 Spanish.

9

[Neuropaediatrics and primary care. Our experience in the 21st century].

López-Pisón J, Pérez-Delgado R, García-Oguiza A, Lafuente-Hidalgo M, Sebastián-Torres B, Cabrerizo de Diago R, Rebage V, García-Jiménez MC, Baldellou-Vázquez A, Arana-Navarro T, Alonso-Martínez V, Mengual-Gil JM, Bastarós-García JC, Peña-Segura JL. López-Pisón J, et al. Among authors: baldellou vazquez a. Rev Neurol. 2008;47 Suppl 1:S45-53. Rev Neurol. 2008. PMID: 18767016 Free article. Spanish.

10

[Total homocysteine levels in children with diabetes type 1. Conditional factors].

Martínez Laborda S, Salazar García-Blanco MI, Rodríguez Rigual M, Baldellou Vázquez A. Martínez Laborda S, et al. Among authors: baldellou vazquez a. An Pediatr (Barc). 2008 Mar;68(3):264-8. doi: 10.1157/13116707. An Pediatr (Barc). 2008. PMID: 18358138 Free article. Spanish.

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