Found: 21
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Surgical management of hypospadias in cases with concomitant disorders of sex development.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Staged segmental urethroplasty for scrotal/perineal hypospadias: a new concept.
- Published in:
- 2016
- By:
- Publication type:
- journal article
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.
- Published in:
- PLoS ONE, 2018, v. 13, n. 11, p. 1, doi. 10.1371/journal.pone.0206184
- By:
- Publication type:
- Article
Left atrial dysfunction and stiffness in pediatric and adult patients with Type 1 diabetes mellitus assessed with speckle tracking echocardiography.
- Published in:
- Pediatric Diabetes, 2021, v. 22, n. 2, p. 303, doi. 10.1111/pedi.13141
- By:
- Publication type:
- Article
Assessment of Growth Disturbance in Japanese Children with IBD.
- Published in:
- International Journal of Pediatrics, 2010, p. 1, doi. 10.1155/2010/958915
- By:
- Publication type:
- Article
Gallstone formation due to rapid weight loss through hyperthyroidism.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 12, p. 1395, doi. 10.1515/jpem-2019-0149
- By:
- Publication type:
- Article
Present status of prophylactic thyroidectomy in pediatric multiple endocrine neoplasia 2: a nationwide survey in Japan 1997–2017.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 6, p. 585, doi. 10.1515/jpem-2018-0444
- By:
- Publication type:
- Article
A case of 46,XY complete gonadal dysgenesis with a novel missense variant in SRY.
- Published in:
- Clinical Pediatric Endocrinology, 2023, v. 32, n. 4, p. 235, doi. 10.1297/cpe.2023-0032
- By:
- Publication type:
- Article
Effects of Lactobacillus gasseri OLL 2716 (LG21) on Helicobacter pylori infection in children.
- Published in:
- 2002
- By:
- Publication type:
- letter
A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorder.
- Published in:
- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00178-2
- By:
- Publication type:
- Article
Cytochrome P450 Oxidoreductase Deficiency: Identification and Characterization of Biallelic Mutations and Genotype-Phenotype Correlations in 35 Japanese Patients.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 5, p. 1723, doi. 10.1210/jc.2008-2816
- By:
- Publication type:
- Article
Cytomegalovirus as a potential trigger for systemic lupus erythematosus: a case report.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Immunological investigation of the hepatic tissue from infants with biliary atresia.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Phenotypic Variability and Newly Identified Mutations of the IVD Gene in Japanese Patients with Isovaleric Acidemia.
- Published in:
- Tohoku Journal of Experimental Medicine, 2015, v. 236, n. 2, p. 103, doi. 10.1620/tjem.236.103
- By:
- Publication type:
- Article
Pulse steroids as induction therapy for children with ulcerative colitis.
- Published in:
- Pediatrics International, 2011, v. 53, n. 6, p. 974, doi. 10.1111/j.1442-200X.2011.03405.x
- By:
- Publication type:
- Article
Laboratory evaluation of blood plasma separation device in children.
- Published in:
- Pediatrics International, 2010, v. 52, n. 6, p. 891, doi. 10.1111/j.1442-200X.2010.03278.x
- By:
- Publication type:
- Article
Studies of anti-inflammatory effects of Rooibos tea in rats.
- Published in:
- Pediatrics International, 2009, v. 51, n. 5, p. 700, doi. 10.1111/j.1442-200X.2009.02835.x
- By:
- Publication type:
- Article
Changes in the presence of urine Helicobacter pylori antibody in Japanese children in three different age groups.
- Published in:
- Pediatrics International, 2008, v. 50, n. 3, p. 291, doi. 10.1111/j.1442-200X.2008.02587.x
- By:
- Publication type:
- Article
Expression of COX-1, COX-2, and PPAR-γ in the gastric mucosa of children with Helicobacter pylori infection.
- Published in:
- Pediatrics International, 2008, v. 50, n. 1, p. 1, doi. 10.1111/j.1442-200X.2007.02504.x
- By:
- Publication type:
- Article
A report of two novel NR5A1 mutation families: possible clinical phenotype of psychiatric symptoms of anxiety and/or depression.
- Published in:
- Clinical Endocrinology, 2013, v. 78, n. 6, p. 957, doi. 10.1111/cen.12054
- By:
- Publication type:
- Article
Isolated growth hormone deficiency in two siblings because of paternal mosaicism for a mutation in the GH1 gene.
- Published in:
- Clinical Endocrinology, 2012, v. 76, n. 3, p. 420, doi. 10.1111/j.1365-2265.2011.04224.x
- By:
- Publication type:
- Article