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carrilho i
(29 results)?
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
Orphanet J Rare Dis. 2015 Sep 26;10:123. doi: 10.1186/s13023-015-0335-5.
Orphanet J Rare Dis. 2015.
PMID: 26410222
Free PMC 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: carilho i.
Med Clin (Barc). 2006 Jun 17;127(3):81-5. doi: 10.1157/13090262.
Med Clin (Barc). 2006.
PMID: 16827996
Spanish.
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