Found: 12
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A case of osteopathia striata with cranial sclerosis with facial nerve palsies.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Hemorrhagic duodenal ulcer as a rare complication prior to antiplatelet therapy for Kawasaki disease.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
LIN7A Depletion Disrupts Cerebral Cortex Development, Contributing to Intellectual Disability in 12q21-Deletion Syndrome.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092695
- By:
- Publication type:
- Article
Successful treatment with pulse cyclophosphamide of a steroid-refractory hepatitic variant of liver acute graft-vs.-host disease in a child.
- Published in:
- Pediatric Transplantation, 2012, v. 16, n. 7, p. E315, doi. 10.1111/j.1399-3046.2012.01664.x
- By:
- Publication type:
- Article
Novel algorithm for automated genotyping of microsatellites.
- Published in:
- Nucleic Acids Research, 2004, v. 32, n. 20, p. 6069, doi. 10.1093/nar/gkh946
- By:
- Publication type:
- Article
Human herpesvirus 6 infection mimicking measles: two pediatric cases.
- Published in:
- Turkish Journal of Pediatrics, 2015, v. 57, n. 1, p. 74
- By:
- Publication type:
- Article
Absence of allelic loss in cytomegalic neurons of cortical tuber in the Eker rat model of tuberous sclerosis.
- Published in:
- Acta Neuropathologica, 2004, v. 107, n. 1, p. 47, doi. 10.1007/s00401-003-0778-y
- By:
- Publication type:
- Article
Efficacy and safety associated with the infusion speed of intravenous immunoglobulin for the treatment of Kawasaki disease: a randomized controlled trial.
- Published in:
- Pediatric Rheumatology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12969-021-00601-6
- By:
- Publication type:
- Article
Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Two New XPD Patients Compound Heterozygous for the Same Mutation Demonstrate Diverse Clinical Features.
- Published in:
- Journal of Investigative Dermatology, 2005, v. 125, n. 1, p. 86, doi. 10.1111/j.0022-202X.2005.23745.x
- By:
- Publication type:
- Article
A TUBB4A Met363Thr variant in pediatric hypomyelination without atrophy of the basal ganglia.
- Published in:
- Human Genome Variation, 2022, v. 9, n. 1, p. 1, doi. 10.1038/s41439-022-00198-6
- By:
- Publication type:
- Article
Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 16, p. 2305, doi. 10.1093/hmg/ddi234
- By:
- Publication type:
- Article