Found: 7
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Clinical Presentation of Severe Viral Encephalitis With Known Causative Agents in Children: A Retrospective Study on 16 Patients Hospitalized in a Pediatric Intensive Care Unit (2008-2011).
- Published in:
- Journal of Child Neurology, 2014, v. 29, n. 11, p. 1508, doi. 10.1177/0883073813513330
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- Article
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-80
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- Article
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2.
- Published in:
- 2013
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- Publication type:
- journal article
Mosaic 18q21.2 deletions including the TCF4 gene: A clinical report.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 12, p. 3174, doi. 10.1002/ajmg.a.35588
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- Publication type:
- Article
Pre- and postnatal imaging of early cerebral damage in Sturge-Weber syndrome.
- Published in:
- Pediatric Radiology, 2013, v. 43, n. 11, p. 1536, doi. 10.1007/s00247-013-2743-9
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- Article
Familial Nephrogenic Syndrome of Inappropriate Antidiuresis: Dissociation between Aquaporin-2 and Vasopressin Excretion.
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- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 9, p. E37, doi. 10.1210/jc.2009-2524
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- Publication type:
- Article
Agenesis of the Corpus Callosum with Facial Dysmorphism and Intellectual Disability in Sibs Associated with Compound Heterozygous KDM5B Variants.
- Published in:
- Genes, 2021, v. 12, n. 9, p. 1397, doi. 10.3390/genes12091397
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- Article