Found: 30
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Similar age-dependent levothyroxine requirements of schoolchildren with congenital or acquired hypothyroidism.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Effect of different growth hormone (GH) mutants on the regulation of GH-receptor gene transcription in a human hepatoma cell line.
- Published in:
- European Journal of Endocrinology, 2002, v. 146, n. 4, p. 573, doi. 10.1530/eje.0.1460573
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- Publication type:
- Article
Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59D/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II).
- Published in:
- European Journal of Endocrinology, 2001, v. 145, n. 4, p. 439
- By:
- Publication type:
- Article
Role for tissue-dependent methylation differences in the expression of FOXE1 in nontumoral thyroid glands.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Linear association between household income and metabolic control in children with insulin-dependent diabetes mellitus despite free access to health care.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
A high prevalence of dual thyroid ectopy in congenital hypothyroidism: evidence for insufficient signaling gradients during embryonic thyroid migration or for the polyclonal nature of the thyroid gland?
- Published in:
- 2012
- By:
- Publication type:
- journal article
Is the Incidence of Congenital Hypothyroidism Really Increasing? A 20-Year Retrospective Population-Based Study in Québec.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 8, p. 2422, doi. 10.1210/jc.2011-1073
- By:
- Publication type:
- Article
Transcriptome, Methylome and Genomic Variations Analysis of Ectopic Thyroid Glands.
- Published in:
- PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013420
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- Publication type:
- Article
Ectopic thyroid gland causing dysphonia: imaging and molecular studies.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 10, p. 4509, doi. 10.1210/jc.2010-0882
- By:
- Publication type:
- Article
Lethal Respiratory Failure and Mild Primary Hypothyroidism in a Term Girl with a de Novo Heterozygous Mutation in the TITF1/NKX2.1 Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 1, p. 197, doi. 10.1210/jc.2008-1402
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- Publication type:
- Article
Random Variability in Congenital Hypothyroidism from Thyroid Dysgenesis over 16 Years in Québec.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 8, p. 3158, doi. 10.1210/jc.2007-0527
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- Publication type:
- Article
Short Stature Caused by a Biologically Inactive Mutant Growth Hormone (GH-C53S).
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 5, p. 2493, doi. 10.1210/jc.2004-1838
- By:
- Publication type:
- Article
New Autosomal Recessive Mutation of the TSH-β Subunit Gene Causing Central Isolated Hypothyroidism.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 9, p. 4468, doi. 10.1210/jcem.86.9.7876
- By:
- Publication type:
- Article
Aromatase Deficiency Caused by a Novel P450arom Gene Mutation: Impact of Absent Estrogen Production on Serum Gonadotropin Concentration in a Boy.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 11, p. 4050, doi. 10.1210/jc.84.11.4050
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- Publication type:
- Article
Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention.
- Published in:
- Journal of the Endocrine Society, 2021, v. 5, n. 3, p. 1, doi. 10.1210/jendso/bvaa183
- By:
- Publication type:
- Article
Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism.
- Published in:
- Thyroid, 2019, v. 29, n. 7, p. 1018, doi. 10.1089/thy.2018.0461
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- Publication type:
- Article
Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing.
- Published in:
- Thyroid, 2016, v. 26, n. 6, p. 852, doi. 10.1089/thy.2016.0009
- By:
- Publication type:
- Article
Association of adrenal insufficiency with insulin-dependent diabetes mellitus in a patient with inactivating mutations in nicotinamide nucleotide transhydrogenase: a phenocopy of the animal model.
- Published in:
- 2017
- By:
- Publication type:
- Opinion
Influence of Adiposity, Physical Activity, Fitness, and Screen Time on Insulin Dynamics Over 2 Years in Children.
- Published in:
- JAMA Pediatrics, 2016, v. 170, n. 3, p. 227, doi. 10.1001/jamapediatrics.2015.3909
- By:
- Publication type:
- Article
Early-Onset Central Diabetes Insipidus due to Compound Heterozygosity for AVP Mutations.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Has Triiodothyronine Treatment of Children after Cardiopulmonary Bypass Surgery Any Long-Term Effects?
- Published in:
- Hormone Research in Paediatrics, 2015, v. 84, n. 2, p. 137, doi. 10.1159/000380782
- By:
- Publication type:
- Article
Somatic Mutations Are Not Observed by Exome Sequencing of Lymphocyte DNA from Monozygotic Twins Discordant for Congenital Hypothyroidism due to Thyroid Dysgenesis.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 83, n. 2, p. 79, doi. 10.1159/000365393
- By:
- Publication type:
- Article
Autonomous Adenomas Caused by Somatic Mutations of the Thyroid-Stimulating Hormone Receptor in Children.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 81, n. 2, p. 73, doi. 10.1159/000357143
- By:
- Publication type:
- Article
Is Ultrasonography Useful in Predicting Thyroid Cancer in Children with Thyroid Nodules and Apparently Benign Cytopathologic Features?
- Published in:
- Hormone Research in Paediatrics, 2011, v. 75, n. 4, p. 269, doi. 10.1159/000322877
- By:
- Publication type:
- Article
Conserved Telomere Length in Human Ectopic Thyroids: An Argument Against Premature Differentiation Causing Arrested Migration.
- Published in:
- Thyroid, 2015, v. 25, n. 9, p. 1050, doi. 10.1089/thy.2015.0204
- By:
- Publication type:
- Article
Discovery of a Fetal Goiter on Prenatal Ultrasound in Women Treated for Graves' Disease: First, Do No Harm.
- Published in:
- Thyroid, 2011, v. 21, n. 8, p. 931, doi. 10.1089/thy.2011.0066
- By:
- Publication type:
- Article
Variation by Ethnicity in the Prevalence of Congenital Hypothyroidism Due to Thyroid Dysgenesis.
- Published in:
- Thyroid, 2011, v. 21, n. 1, p. 13, doi. 10.1089/thy.2010.0205
- By:
- Publication type:
- Article
Congenital Secondary Hypothyroidism Due to a Mutation C105Vfs114X Thyrotropin-β Mutation: Genetic Study of Five Unrelated Families from Switzerland and Argentina.
- Published in:
- Thyroid, 2003, v. 13, n. 6, p. 553
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- Publication type:
- Article
Continuous Subcutaneous Insulin Infusion in Children: A Pilot Study Validating a Protocol to Avoid Hypoglycemia at Initiation.
- Published in:
- Frontiers in Endocrinology, 2017, v. 8, p. 1, doi. 10.3389/fendo.2017.00084
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- Publication type:
- Article
From Bioinactive ACTH to ACTH Antagonist: The Clinical Perspective.
- Published in:
- Frontiers in Endocrinology, 2017, v. 7/8, p. 1, doi. 10.3389/fendo.2017.00017
- By:
- Publication type:
- Article