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Page 1
Infectious acute hemicerebellitis.
García-Cazorla A, Oliván JA, Pancho C, Sans A, Boix C, Campistol J. García-Cazorla A, et al. Among authors: campistol j. J Child Neurol. 2004 May;19(5):390-2. doi: 10.1177/088307380401900514. J Child Neurol. 2004. PMID: 15224713 Review.
White matter alterations associated with chromosomal disorders.
García-Cazorla A, Sans A, Baquero M, García-Bargo MD, Arellano M, Poo P, Gean E, Campistol J. García-Cazorla A, et al. Among authors: campistol j. Dev Med Child Neurol. 2004 Mar;46(3):148-53. doi: 10.1017/s0012162204000271. Dev Med Child Neurol. 2004. PMID: 14995083 Free article.
[Usefulness of analysis of cerebrospinal fluid for the diagnosis of neurotransmitters and pterin defects and glucose and folate transport deficiencies across blood brain barrier].
Ormazabal A, García Cazorla A, Pérez Dueñas B, Pineda M, Ruiz A, López Laso E, García Silva M, Carilho I, Barbot C, Cormand B, Ribases M, Moller L, Fernández Alvarez E, Campistol J, Artuch R. Ormazabal A, et al. Among authors: campistol j. Med Clin (Barc). 2006 Jun 17;127(3):81-5. doi: 10.1157/13090262. Med Clin (Barc). 2006. PMID: 16827996 Spanish.
A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy: clinical, biochemical and genetic analysis.
Ribasés M, Serrano M, Fernández-Alvarez E, Pahisa S, Ormazabal A, García-Cazorla A, Pérez-Dueñas B, Campistol J, Artuch R, Cormand B. Ribasés M, et al. Among authors: campistol j. Mol Genet Metab. 2007 Nov;92(3):274-7. doi: 10.1016/j.ymgme.2007.07.004. Epub 2007 Aug 14. Mol Genet Metab. 2007. PMID: 17698383
Cranial ultrasound and chronological changes in molybdenum cofactor deficiency.
Serrano M, Lizarraga I, Reiss J, Dias AP, Pérez-Dueñas B, Vilaseca MA, Artuch R, Campistol J, García-Cazorla A. Serrano M, et al. Among authors: campistol j. Pediatr Radiol. 2007 Oct;37(10):1043-6. doi: 10.1007/s00247-007-0558-2. Epub 2007 Aug 18. Pediatr Radiol. 2007. PMID: 17704913
838 results