Found: 35
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Bilateral ovarian teratomas successfully treated by ovary-conserving technique.
- Published in:
- Pediatrics International, 2006, v. 48, n. 2, p. 181, doi. 10.1111/j.1442-200X.2006.02190.x
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- Publication type:
- Article
A sex reversal infant with XX karyotype and complete male external genitalia.
- Published in:
- Pediatrics International, 1995, v. 37, n. 6, p. 706, doi. 10.1111/j.1442-200X.1995.tb03410.x
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- Publication type:
- Article
Allelic variations of the D2 dopamine receptor gene in children with idiopathic short stature.
- Published in:
- Journal of Human Genetics, 1999, v. 44, n. 1, p. 26, doi. 10.1007/s100380050101
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- Publication type:
- Article
Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.
- Published in:
- 2012
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- Publication type:
- journal article
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.
- Published in:
- 2008
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- Publication type:
- journal article
Identification of Novel Human GH-1 Gene Polymorphisms that Are Associated with Growth Hormone Secretion and Height.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 3, p. 1290, doi. 10.1210/jcem.85.3.6468
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- Publication type:
- Article
A new compound heterozygous mutation (W17X, 436 + 5G --> T) in the cytochrome P450c17 gene causes 17 alpha-hydroxylase/17,20-lyase deficiency.
- Published in:
- 1998
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- Publication type:
- journal article
Cognitive Bias and Diagnostic Errors among Physicians in Japan: A Self-Reflection Survey.
- Published in:
- International Journal of Environmental Research & Public Health, 2022, v. 19, n. 8, p. 4645, doi. 10.3390/ijerph19084645
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- Publication type:
- Article
Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2–H19 domain in bodies and placentas.
- Published in:
- Journal of Molecular Medicine, 2008, v. 86, n. 10, p. 1171, doi. 10.1007/s00109-008-0377-4
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- Publication type:
- Article
Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency.
- Published in:
- Human Genetics, 2000, v. 107, n. 4, p. 320, doi. 10.1007/s004390000363
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- Publication type:
- Article
Novel compound heterozygous mutations in the SBP2 gene: characteristic clinical manifestations and the implications of GH and triiodothyronine in longitudinal bone growth and maturation.
- Published in:
- European Journal of Endocrinology, 2012, v. 166, n. 4, p. 757, doi. 10.1530/EJE-11-0812
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- Publication type:
- Article
Factors and impact of physicians' diagnostic errors in malpractice claims in Japan.
- Published in:
- PLoS ONE, 2020, v. 15, n. 8, p. 1, doi. 10.1371/journal.pone.0237145
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- Publication type:
- Article
Association of the CTLA-4 Gene 49 A/G Polymorphism With Type 1 Diabetes and Autoimmune Thyroid Disease in Japanese Children.
- Published in:
- Diabetes Care, 2003, v. 26, n. 3, p. 843, doi. 10.2337/diacare.26.3.843
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- Publication type:
- Article
Relationship Between Serum Levels of Methylguanidine and Glycemic Control in IDDM Children.
- Published in:
- Diabetes Care, 1993, v. 16, n. 8, p. 1196, doi. 10.2337/diacare.16.8.1196
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- Publication type:
- Article
Lipoprotein(a) Levels in Japanese Children With IDDM.
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- Diabetes Care, 1993, v. 16, n. 5, p. 846, doi. 10.2337/diacare.16.5.846
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- Publication type:
- Article
Reversible secondary pseudohypoaldosteronism due to pyelonephritis.
- Published in:
- Pediatric Nephrology, 2002, v. 17, n. 12, p. 1069
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- Publication type:
- Article
Distal renal tubular acidosis associated with hypercalcemia and nephrocalcinosis in an infant.
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- Pediatric Nephrology, 2002, v. 17, n. 11, p. 977, doi. 10.1007/s00467-002-0987-y
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- Publication type:
- Article
November 2002.
- Published in:
- Pediatric Nephrology, 2002, v. 17, n. 11, p. 979
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- Publication type:
- Article
Identification of mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteins.
- Published in:
- 1999
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- Publication type:
- journal article
Identification of mutations in the hepatocyte nuclear factor (HNF)-1 alpha gene in Japanese subjects with IDDM.
- Published in:
- 1997
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- Publication type:
- journal article
The Utility of Virtual Patient Simulations for Clinical Reasoning Education.
- Published in:
- International Journal of Environmental Research & Public Health, 2020, v. 17, n. 15, p. 5325, doi. 10.3390/ijerph17155325
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- Publication type:
- Article
Long-Term 3,5,3′-Triiodothyroacetic Acid Therapy in a Child with Hyperthyroidism Caused by Thyroid Hormone Resistance: Pharmacological Study and Therapeutic Recommendations.
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- Thyroid, 2012, v. 22, n. 10, p. 1069, doi. 10.1089/thy.2011.0450
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- Publication type:
- Article
Identification and Functional Analysis of Novel Inactivating Thyrotropin Receptor Mutations in Patients with Thyrotropin Resistance.
- Published in:
- Thyroid, 2006, v. 16, n. 5, p. 471
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- Publication type:
- Article
Novel Inactivating Missense Mutations in the Thyrotropin Receptor Gene in Japanese Children with Resistance to Thyrotropin.
- Published in:
- Thyroid, 2001, v. 11, n. 6, p. 551, doi. 10.1089/105072501750302859
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- Publication type:
- Article
A Novel Point Mutation of Thyroid Hormone Receptor β Gene in a Family with Resistance to Thyroid Hormone.
- Published in:
- Thyroid, 1997, v. 7, n. 5, p. 771, doi. 10.1089/thy.1997.7.771
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- Publication type:
- Article
A Novel Point Mutation (R243Q) in Exon 7 of the c-erbAβ Thyroid Hormone Receptor Gene in a Family with Resistance to Thyroid Hormone.
- Published in:
- Thyroid, 1995, v. 5, n. 5, p. 355, doi. 10.1089/thy.1995.5.355
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- Publication type:
- Article
Survey of potentially inappropriate prescriptions for common cold symptoms in Japan: A cross-sectional study.
- Published in:
- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0265874
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- Publication type:
- Article
A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy.
- Published in:
- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 251, doi. 10.1297/cpe.26.251
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- Publication type:
- Article
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision).
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- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 107
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- Publication type:
- Article
Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan.
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- Clinical Pediatric Endocrinology, 2015, v. 24, n. 4, p. 167, doi. 10.1297/cpe.24.167
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- Publication type:
- Article
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision).
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- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 77
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- Publication type:
- Article
Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome.
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- Clinical Pediatric Endocrinology, 2012, v. 21, n. 2, p. 29, doi. 10.1297/cpe.21.29
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- Publication type:
- Article
Background factors associated with academic motivation for attending medical school immediately after admission in Japan: A single‐center study.
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- Journal of General & Family Medicine, 2022, v. 23, n. 3, p. 164, doi. 10.1002/jgf2.528
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- Publication type:
- Article
Primary care doctor fostering and clinical research training in Sweden: Implications for Japan.
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- Journal of General & Family Medicine, 2019, v. 20, n. 1, p. 4, doi. 10.1002/jgf2.211
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- Publication type:
- Article
Japan can learn from the Swedish primary care doctor fostering system.
- Published in:
- Journal of General & Family Medicine, 2018, v. 19, n. 5, p. 183, doi. 10.1002/jgf2.197
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- Publication type:
- Article