Found: 13
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Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a rare cause of parainfectious rhabdomyolysis.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Tuberous sclerosis and congenital lymphedema.
- Published in:
- Pediatric Dermatology, 2003, v. 20, n. 4, p. 371, doi. 10.1046/j.1525-1470.2003.20326_3.x
- By:
- Publication type:
- Article
Moya Moya Syndrome in a Child With Pyruvate Kinase Deficiency and Combined Prothrombotic Factors.
- Published in:
- Journal of Child Neurology, 2007, v. 22, n. 4, p. 474, doi. 10.1177/0883073807301934
- By:
- Publication type:
- Article
Different Additional Risk Factors for Cerebral Infarctions Associated With the Factor V Leiden Mutation in a Family.
- Published in:
- Journal of Child Neurology, 2006, v. 21, n. 10, p. 903, doi. 10.1177/08830738060210100601
- By:
- Publication type:
- Article
Acute Necrotizing Encephalopathy of Childhood in Non-Asian Patients: Report of Three Cases and Literature Review.
- Published in:
- Journal of Child Neurology, 2006, v. 21, n. 10, p. 872, doi. 10.1177/08830738060210101401
- By:
- Publication type:
- Article
Early Alteration in Bone Metabolism in Epileptic Children Receiving Carbamazepine Monotherapy Owing to the Induction of Hepatic Drug-Metabolizing Enzymes.
- Published in:
- Journal of Child Neurology, 2005, v. 20, n. 6, p. 513, doi. 10.1177/08830738050200060801
- By:
- Publication type:
- Article
Infantile Spasms in an Infant With Cytomegalovirus Infection Treated With Ganciclovir.
- Published in:
- Journal of Child Neurology, 2004, v. 19, n. 1, p. 50, doi. 10.1177/08830738040190010705
- By:
- Publication type:
- Article
Acute Necrotizing Encephalopathy Associated With Parainfluenza Virus in a Caucasian Child.
- Published in:
- Journal of Child Neurology, 2003, v. 18, n. 8, p. 570, doi. 10.1177/08830738030180081301
- By:
- Publication type:
- Article
Congenital Microcephaly in Two Infants With the Factor V Leiden Mutation.
- Published in:
- Journal of Child Neurology, 2002, v. 17, n. 12, p. 904, doi. 10.1177/08830738020170123001
- By:
- Publication type:
- Article
Correspondence.
- Published in:
- 2002
- By:
- Publication type:
- Letter
Bcl-2 and caspase-9 serum levels in children and adolescents with idiopathic epilepsy and active seizures.
- Published in:
- Minerva Pediatrics, 2022, v. 74, n. 1, p. 40, doi. 10.23736/S2724-5276.17.04787-9
- By:
- Publication type:
- Article
Metachromatic leukodystrophy in Greece: observations on 4 cases.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 1, p. 30, doi. 10.1111/j.1399-0004.1990.tb03387.x
- By:
- Publication type:
- Article
Brain Hamartoma in an Infant with Bannayan-Riley-Ruvalcaba Syndrome: Patient Report and Review of the Literature.
- Published in:
- International Journal on Disability & Human Development (De Gruyter), 2000, v. 1, n. 4, p. 243, doi. 10.1515/ijdhd.2000.1.4.243
- By:
- Publication type:
- Article