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Long-term Effect of Aromatase Inhibition in Aromatase Excess Syndrome.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Congenital Hypothyroidism Due to Truncating PAX8 Mutations: A Case Series and Molecular Function Studies.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Frontispiz: Entropy‐Driven Diastereoselectivity Improvement in the Paternò–Büchi Reaction of 1‐Naphthyl Aryl Ethenes with a Chiral Cyanobenzoate through Remote Alkylation.
- Published in:
- 2018
- By:
- Publication type:
- Cover Art
Entropy‐Driven Diastereoselectivity Improvement in the Paternò–Büchi Reaction of 1‐Naphthyl Aryl Ethenes with a Chiral Cyanobenzoate through Remote Alkylation.
- Published in:
- Angewandte Chemie, 2018, v. 130, n. 18, p. 4974, doi. 10.1002/ange.201801330
- By:
- Publication type:
- Article
Polysomnography as an indicator for cervicomedullary decompression to treat foramen magnum stenosis in achondroplasia.
- Published in:
- Child's Nervous System, 2018, v. 34, n. 11, p. 2275, doi. 10.1007/s00381-018-3880-0
- By:
- Publication type:
- Article
Silver-Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 2, p. 91, doi. 10.1038/jhg.2014.100
- By:
- Publication type:
- Article
Growth Hormone Injection Log Analysis with Electronic Injection Device for Qualifying Adherence to Low-Irritant Formulation and Exploring Influential Factors on Adherence.
- Published in:
- Patient Preference & Adherence, 2023, v. 17, p. 1885, doi. 10.2147/PPA.S417142
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- Publication type:
- Article
Thyroid-stimulating hormone (thyrotropin)-secretion pituitary adenoma in an 8-year-old boy: case report.
- Published in:
- 2012
- By:
- Publication type:
- Report
A case of adolescent trichorhinophalangeal syndrome undergoing pelvic osteotomy for bilateral acetabular dysplasia.
- Published in:
- Journal of Orthopaedic Science, 2023, v. 28, n. 6, p. 1501, doi. 10.1016/j.jos.2021.07.021
- By:
- Publication type:
- Article
Foetal virilisation caused by overproduction of non-aromatisable 11-oxygenated C19 steroids in maternal adrenal tumour.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Chiroptical properties of dithia[3.3]cyclophanes composed of anthracene and pyridine/pyridinium moieties: A combined experimental and theoretical study.
- Published in:
- Chirality, 2017, v. 29, n. 11, p. 677, doi. 10.1002/chir.22740
- By:
- Publication type:
- Article
Entropy-Driven Diastereoselectivity Improvement in the Paternò–Büchi Reaction of 1-Naphthyl Aryl Ethenes with a Chiral Cyanobenzoate through Remote Alkylation.
- Published in:
- Angewandte Chemie International Edition, 2018, v. 57, n. 18, p. 4880, doi. 10.1002/anie.201801330
- By:
- Publication type:
- Article
Association between monoallelic TSHR mutations and congenital hypothyroidism: a statistical approach.
- Published in:
- European Journal of Endocrinology, 2018, v. 178, n. 2, p. 137, doi. 10.1530/EJE-16-1049
- By:
- Publication type:
- Article
Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty.
- Published in:
- European Journal of Endocrinology, 2016, v. 174, n. 4, p. 453, doi. 10.1530/EJE-15-0959
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- Publication type:
- Article
Heterozygous defects in PAX6 gene and congenital hypopituitarism.
- Published in:
- European Journal of Endocrinology, 2015, v. 172, n. 1, p. 37, doi. 10.1530/EJE-14-0255
- By:
- Publication type:
- Article
A Japanese Family with DICER1 Syndrome Found in Childhood-Onset Multinodular Goitre.
- Published in:
- Hormone Research in Paediatrics, 2020, v. 93, n. 7/8, p. 477, doi. 10.1159/000511140
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- Publication type:
- Article
Levothyroxine Dosage as Predictor of Permanent and Transient Congenital Hypothyroidism: A Multicenter Retrospective Study in Japan.
- Published in:
- Hormone Research in Paediatrics, 2019, v. 92, n. 1, p. 45, doi. 10.1159/000502418
- By:
- Publication type:
- 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
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- Publication type:
- Article
Association between Compound Heterozygous Mutations of SLC34A3 and Hypercalciuria.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 82, n. 1, p. 65, doi. 10.1159/000360291
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- Publication type:
- Article
Evaluation of Parathyroid Gland Function Using Sodium Bicarbonate Infusion Test for 22q11.2 Deletion Syndrome.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 75, n. 1, p. 14, doi. 10.1159/000315904
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- Publication type:
- Article
Robust growth hormone responses to GH-releasing peptide 2 in adolescents.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2024, v. 37, n. 8, p. 730, doi. 10.1515/jpem-2024-0115
- By:
- Publication type:
- Article
A 7-year-old boy with central diabetes insipidus presenting with thickened pituitary stalk and anti-rabphilin-3A antibody positivity.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 5, p. 687, doi. 10.1515/jpem-2021-0674
- 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
Two cases of 22q11.2 deletion syndrome with anorectal anomalies and growth retardation.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 7/8, p. 585, doi. 10.1515/jpem.2011.030
- By:
- Publication type:
- Article
Formulation for Effective Screening and Management of Nonalcoholic Steatohepatitis: Noninvasive NAFLD Management Strategy.
- Published in:
- Gastroenterology Research & Practice, 2016, p. 1, doi. 10.1155/2016/6343656
- By:
- Publication type:
- Article
Incidence and Risk Factors for Adrenal Crisis in Pediatric-onset Adrenal Insufficiency: A Prospective Study.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 8, p. e1602, doi. 10.1210/clinem/dgad753
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- 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
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- Publication type:
- Article
Knowns and unknowns about congenital hypothyroidism: 2022 update.
- Published in:
- Clinical Pediatric Endocrinology, 2023, v. 32, n. 1, p. 11, doi. 10.1297/cpe.2022-0016
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- Publication type:
- Article
Letter to the Editor: Testosterone priming increased growth hormone peak levels in the stimulation test and suppressed gonadotropin secretion in three Japanese adolescent boys.
- Published in:
- Clinical Pediatric Endocrinology, 2020, v. 29, n. 4, p. 201, doi. 10.1297/cpe.29.201
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- Publication type:
- Article
Timing of hyponatremia development in patients with salt-wasting-type 21-hydroxylase deficiency.
- Published in:
- Clinical Pediatric Endocrinology, 2020, v. 29, n. 3, p. 105, doi. 10.1297/cpe.29.105
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- Publication type:
- Article
A nationwide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in childhood, adolescent, and young adult cancer survivors.
- Published in:
- Clinical Pediatric Endocrinology, 2020, v. 29, n. 2, p. 55, doi. 10.1297/cpe.29.55
- By:
- Publication type:
- Article
A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant.
- Published in:
- Human Genome Variation, 2024, v. 11, n. 1, p. 1, doi. 10.1038/s41439-024-00265-0
- By:
- Publication type:
- Article
Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-67715-x
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- Publication type:
- Article
Contrasting Behaviour of Exciplex Ensembles in the Diastereodifferentiating Paternò–Büchi Reaction of Chiral Cyanobenzoate with Naphthyl- and Phenylethenes on Direct or Charge-Transfer Excitation.
- Published in:
- Australian Journal of Chemistry, 2015, v. 68, n. 11, p. 1693, doi. 10.1071/CH15404
- By:
- Publication type:
- Article
A study of the etiology of transient congenital hypothyroidism in Niigata Prefecture, Japan.
- Published in:
- 2013
- By:
- Publication type:
- Abstract
Criteria for radiologic diagnosis of hypochondroplasia in neonates.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Re-Evaluation of the Prevalence of Permanent Congenital Hypothyroidism in Niigata, Japan: A Retrospective Study.
- Published in:
- International Journal of Neonatal Screening (IJNS), 2021, v. 7, n. 2, p. 1, doi. 10.3390/ijns7020027
- By:
- Publication type:
- Article
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1-PPP1CB complexes.
- Published in:
- Human Genetics, 2019, v. 138, n. 1, p. 21, doi. 10.1007/s00439-018-1951-7
- By:
- Publication type:
- Article
PTEN mutation in a Japanese boy with autonomously functioning thyroid nodule.
- Published in:
- Pediatrics International, 2017, v. 59, n. 11, p. 1223, doi. 10.1111/ped.13427
- By:
- Publication type:
- Article
Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1b.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Comprehensive Next-Generation Sequencing Analyses of Hypoparathyroidism: Identification of Novel GCM2 Mutations.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Nonclassic TSH Resistance: TSHR Mutation Carriers with Discrepantly High Thyroidal Iodine Uptake.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 8, p. E1340, doi. 10.1210/jc.2011-0070
- By:
- Publication type:
- Article
Lower Birth Weight Associated with Current Overweight Status Is Related with the Metabolic Syndrome in Obese Japanese Children.
- Published in:
- Hypertension Research, 2007, v. 30, n. 7, p. 627, doi. 10.1291/hypres.30.627
- By:
- Publication type:
- Article
Lower Birth Weight and Visceral Fat Accumulation Are Related to Hyperinsulinemia and Insulin Resistance in Obese Japanese Children.
- Published in:
- Hypertension Research, 2005, v. 28, n. 6, p. 529, doi. 10.1291/hypres.28.529
- By:
- Publication type:
- Article
Usefulness of Serum Adiponectin Level as a Diagnostic Marker of Metabolic Syndrome in Obese Japanese Children.
- Published in:
- Hypertension Research, 2005, v. 28, n. 1, p. 51, doi. 10.1291/hypres.28.51
- By:
- Publication type:
- Article
A Study of Maternal Patients Diagnosed with Inborn Errors of Metabolism Due to Positive Newborn Mass Screening in Their Newborns.
- Published in:
- Children, 2023, v. 10, n. 8, p. 1341, doi. 10.3390/children10081341
- By:
- Publication type:
- Article
Infantile-Onset Isolated Neurohypophyseal Langerhans Cell Histiocytosis with Central Diabetes Insipidus: A Case Report.
- Published in:
- Children, 2022, v. 9, n. 5, p. 716, doi. 10.3390/children9050716
- By:
- Publication type:
- Article
Regulation of Serum Sodium Levels during Chemotherapy Using Selective Arginine Vasopressin V2-Receptor Antagonist Tolvaptan in a Four-Year-Old Girl with a Suprasellar Germ Cell Tumor.
- Published in:
- Children, 2021, v. 8, n. 4, p. 1, doi. 10.3390/children8040293
- By:
- Publication type:
- Article
Radiological clues to the early diagnosis of hypochondroplasia in the neonatal period: Report of two patients.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 3, p. 630, doi. 10.1002/ajmg.a.34424
- By:
- Publication type:
- Article
A family of pseudohypoparathyroidism type Ia with an 850-kb submicroscopic deletion encompassing the whole GNAS locus.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 1, p. 261, doi. 10.1002/ajmg.a.34393
- By:
- Publication type:
- Article