Found: 22
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Association of HLA-DR, DQ genotype with different beta-cell functions at IDDM diagnosis in Japanese children.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Incidence and Characteristics of Adrenal Crisis in Children Younger than 7 Years with 21-Hydroxylase Deficiency: A Nationwide Survey in Japan.
- Published in:
- Hormone Research in Paediatrics, 2018, v. 89, n. 3, p. 166, doi. 10.1159/000486393
- 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
Clinical features at diagnosis and responses to antithyroid drugs in younger children with Graves' disease compared with adolescent patients.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 7/8, p. 677, doi. 10.1515/jpem-2013-0288
- By:
- Publication type:
- Article
Higher dose of methimazole causes frequent adverse effects in the management of Graves' disease in children and adolescents.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 9/10, p. 863, doi. 10.1515/jpem-2012-0138
- By:
- Publication type:
- Article
Comparison of methimazole and propylthiouracil in the management of children and adolescents with Graves' disease: efficacy and adverse reactions during initial treatment and long-term outcome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 257, doi. 10.1515/jpem.2011.194
- By:
- Publication type:
- Article
Comparison of methimazole and propylthiouracil in the management of children and adolescents with Graves' disease: efficacy and adverse reactions during initial treatment and long-term outcome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 257, doi. 10.1515/JPEM.2011.194
- By:
- Publication type:
- Article
Autosomal dominant familial hypoparathyroidism and sensorineural deafness without renal dysplasia.
- Published in:
- European Journal of Endocrinology, 1998, v. 139, n. 6, p. 631, doi. 10.1530/eje.0.1390631
- By:
- Publication type:
- Article
Guidelines for Newborn Screening of Congenital Hypothyroidism (2021 Revision).
- Published in:
- Clinical Pediatric Endocrinology, 2023, v. 32, n. 1, p. 26, doi. 10.1297/cpe.2022-0063
- By:
- Publication type:
- Article
Extra-endocrine phenotypes at infancy in multiple endocrine neoplasia type 2B: A case series of six Japanese patients.
- Published in:
- Clinical Pediatric Endocrinology, 2021, v. 30, n. 4, p. 195, doi. 10.1297/cpe.30.195
- By:
- Publication type:
- Article
Association between AAAG Repeat Polymorphism in the P3 Promoter of the Human Parathyroid Hormone (PTH)/ PTH-Related Peptide Receptor Gene and Adult Height, Urinary Pyridinoline Excretion, and Promoter Activity.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 4, p. 1791, doi. 10.1210/jcem.87.4.8419
- By:
- Publication type:
- Article
Outcome of a Baby Born from a Mother with Acquired Juvenile Hypothyroidism Having Undetectable Thyroid Hormone Concentrations.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 8, p. 2630, doi. 10.1210/jcem.84.8.5907
- By:
- Publication type:
- Article
Newborn Screening for Congenital Hypothyroidism in Japan.
- Published in:
- International Journal of Neonatal Screening (IJNS), 2021, v. 7, n. 3, p. 1, doi. 10.3390/ijns7030034
- By:
- Publication type:
- Article
A case of "asymmetrical" Graves' disease with lateral radioisotope uptake.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Identification of INS and KCNJ11 gene mutations in type 1B diabetes in Japanese children with onset of diabetes before 5 yr of age.
- Published in:
- Pediatric Diabetes, 2013, v. 14, n. 2, p. 112, doi. 10.1111/j.1399-5448.2012.00917.x
- By:
- Publication type:
- Article
HLA-class II and class I genotypes among Japanese children with Type 1A diabetes and their families.
- Published in:
- Pediatric Diabetes, 2012, v. 13, n. 1, p. 33, doi. 10.1111/j.1399-5448.2011.00833.x
- By:
- Publication type:
- Article
Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan.
- Published in:
- Endocrine Journal, 2020, v. 67, n. 8, p. 853, doi. 10.1507/endocrj.ej20-0011
- By:
- Publication type:
- Article
Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in Japan.
- Published in:
- Clinical Pediatric Endocrinology, 2017, v. 26, n. 4, p. 207, doi. 10.1297/cpe.26.207
- By:
- Publication type:
- Article
Guidelines for the treatment of childhood-onset Graves' disease in Japan, 2016.
- Published in:
- Clinical Pediatric Endocrinology, 2017, v. 26, n. 2, p. 29
- By:
- Publication type:
- Article
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision).
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 107
- By:
- Publication type:
- Article
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision).
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 77
- By:
- Publication type:
- Article
A Report of Three Girls with Antithyroid Drug-Induced Agranulocytosis; Retrospective Analysis of 18 Cases Aged 15 Years or Younger Reported between 1995 and 2009.
- Published in:
- 2011
- By:
- Publication type:
- Case Study