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Retinoic acid receptor beta and angiopoietin-like protein 1 are involved in the regulation of human androgen biosynthesis.
- Published in:
- Scientific Reports, 2015, p. 10132, doi. 10.1038/srep10132
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- Publication type:
- Article
Increased enzymuria in diabetic children without persistent minimal albuminuria.
- Published in:
- Nephrology, 1997, v. 3, n. 6, p. 487, doi. 10.1111/j.1440-1797.1997.tb00273.x
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- Publication type:
- Article
Suprasellar Germinomas in Childhood and Adolescence: Diagnostic Pitfalls.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 1998, v. 11, n. 6, p. 693, doi. 10.1515/jpem.1998.11.6.693
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- Publication type:
- Article
Genetics of the Growth Hormone Axis.
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- Journal of Pediatric Endocrinology & Metabolism, 1997, v. 10, n. 2, p. 161, doi. 10.1515/jpem.1997.10.2.161
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- Publication type:
- Article
LRH-1 May Rescue SF-1 Deficiency for Steroidogenesis: An in vitroand in vivoStudy.
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- Sexual Development, 2015, v. 9, n. 3, p. 144, doi. 10.1159/000381575
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- Publication type:
- Article
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
- Published in:
- Nature Genetics, 2015, v. 47, n. 4, p. 393, doi. 10.1038/ng.3239
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- Publication type:
- Article
Human 3Ś-hydroxysteroid dehydrogenase deficiency seems to affect fertility but may not harbor a tumor risk: lesson from an experiment of nature.
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- European Journal of Endocrinology, 2015, v. 173, n. 5, p. K1, doi. 10.1530/EJE-15-0599
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- Publication type:
- Article
Short stature in two siblings heterozygous for a novel bioinactive GH mutant (GH-P59S) suggesting that the mutant also affects secretion of the wild-type GH.
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- European Journal of Endocrinology, 2013, v. 168, n. 3, p. K35, doi. 10.1530/EJE-12-0847
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- Publication type:
- Article
GH mutant (R77C) in a pedigree presenting with the delay of growth and pubertal development: structural analysis of the mutant and evaluation of the biological activity.
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- European Journal of Endocrinology, 2007, v. 157, p. S67, doi. 10.1530/EJE-07-0339
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- Publication type:
- Article
Clinical and biochemical description of a novel CYP21A2 gene mutation 962_963insA using a new 3D model for the P450c21 protein.
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- European Journal of Endocrinology, 2006, v. 155, n. 1, p. 143, doi. 10.1530/eje.1.02172
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- Publication type:
- Article
Genetic control of growth.
- Published in:
- European Journal of Endocrinology, 2005, v. 152, n. 1, p. 11, doi. 10.1530/eje.1.01797
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- Publication type:
- Article
Primary GH insensitivity `(Laron syndrome) caused by a novel 4 kb deletion encompassing exon 5 of the GH receptor gene: effect of intermittent long-term treatment with recombinant human IGF-I.
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- European Journal of Endocrinology, 2004, v. 150, n. 5, p. 0635
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- Publication type:
- Article
Description of the SAGhE Cohort: A Large European Study of Mortality and Cancer Incidence Risks after Childhood Treatment with Recombinant Growth Hormone.
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- Hormone Research in Paediatrics, 2015, v. 84, n. 3, p. 172, doi. 10.1159/000435856
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- Publication type:
- Article
Natural History of Growth Hormone Deficiency in a Pediatric Cohort.
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- Hormone Research in Paediatrics, 2015, v. 83, n. 4, p. 252, doi. 10.1159/000369392
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- Publication type:
- Article
Alteration of ZnT5-Mediated Zinc Import into the Early Secretory Pathway Affects the Secretion of Growth Hormone from Rat Pituitary Cells.
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- Hormone Research in Paediatrics, 2014, v. 82, n. 4, p. 245, doi. 10.1159/000365924
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- Publication type:
- Article
Genetics of Growth.
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- Hormone Research in Paediatrics, 2014, v. 80, n. 6, p. 379, doi. 10.1159/000355402
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- Publication type:
- Article
The Role of Zinc Dynamics in Growth Hormone Secretion.
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- Hormone Research in Paediatrics, 2014, v. 80, n. 6, p. 381, doi. 10.1159/000355408
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- Publication type:
- Article
Acute Encephalopathy with Unilateral Cortical-Subcortical Lesions in Two Unrelated Kindreds Treated with Glucocorticoids Prenatally for Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Established Facts and Novel Insight.
- Published in:
- Hormone Research in Paediatrics, 2013, v. 80, n. 1, p. 57, doi. 10.1159/000348515
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- Publication type:
- Article
Towards Optimal Treatment with Growth Hormone in Short Children and Adolescents: Evidence and Theses.
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- Hormone Research in Paediatrics, 2013, v. 79, n. 2, p. 51, doi. 10.1159/000347121
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- Publication type:
- Article
Impact of Estrogen Replacement throughout Childhood on Growth, Pituitary-Gonadal Axis and Bone in a 46,XX Patient with CYP19A1 Deficiency.
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- Hormone Research in Paediatrics, 2012, v. 78, n. 4, p. 261, doi. 10.1159/000341585
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- Publication type:
- Article
RNA Interference in Mammalian Cell Systems.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 75, n. 1, p. 63, doi. 10.1159/000322817
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- Publication type:
- Article
Use of Combined Liothyronine and Thyroxine Therapy for Consumptive Hypothyroidism Associated with Hepatic Haemangiomas in Infancy.
- Published in:
- 2010
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- Publication type:
- Case Study
Growth Hormone Concentration and Disappearance Rate, Insulin-Like Growth Factors I and II and Insulin Levels in Iron-Deficient Veal Calves.
- Published in:
- Annals of Nutrition & Metabolism, 1994, v. 38, n. 5, p. 281, doi. 10.1159/000177822
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- Publication type:
- Article
Heterozygous GHR gene mutation in a child with idiopathic short stature.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 3/4, p. 329, doi. 10.1515/jpem-2013-0359
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- Publication type:
- 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).
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- European Journal of Endocrinology, 2001, v. 145, n. 4, p. 439
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- Publication type:
- Article
Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls.
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- European Journal of Endocrinology, 1997, v. 137, n. 5, p. 474, doi. 10.1530/eje.0.1370474
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- Publication type:
- Article
Children's and adolescent's self - assessment of metabolic control versus professional judgment: a cross-sectional retrospective and prospective cohort study.
- Published in:
- International Journal of Pediatric Endocrinology, 2013, v. 2013, n. 1, p. 1, doi. 10.1186/1687-9856-2013-21
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- Publication type:
- Article
Butyrate Increases Intracellular Calcium Levels and Enhances Growth Hormone Release from Rat Anterior Pituitary Cells via the G-Protein-Coupled Receptors GPR41 and 43.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0107388
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- Publication type:
- Article
Differential Regulation of Human 3β-Hydroxysteroid Dehydrogenase Type 2 for Steroid Hormone Biosynthesis by Starvation and Cyclic Amp Stimulation: Studies in the Human Adrenal NCI-H295R Cell Model.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068691
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- Publication type:
- Article
Role of AMP-Activated Protein Kinase on Steroid Hormone Biosynthesis in Adrenal NCI-H295R Cells.
- Published in:
- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0030956
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- Publication type:
- Article
Characterization of Novel SCAR (Steroidogenic Acute Regulatory Protein) Mutations Causing Non-Classic Lipoid Adrenal Hyperplasia.
- Published in:
- PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0020178
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- Publication type:
- Article
Doping mit Anabolika - auch ein Thema für den Hausarzt!
- Published in:
- Therapeutische Umschau, 2014, v. 71, n. 4, p. 245, doi. 10.1024/0040-5930/a000508
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- Publication type:
- Article
Mutation analysis of the muscarinic cholinergic receptor genes in isolated growth hormone deficiency type IB.
- Published in:
- 2009
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- Publication type:
- journal article
Influence of Growth Hormone (GH) Receptor Deletion of Exon 3 and Full-Length Isoforms on GH Response and Final Height in Patients with Severe GH Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 3, p. 974, doi. 10.1210/jc.2007-1382
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- Publication type:
- Article
Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency.
- Published in:
- 2007
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- Publication type:
- journal article
Evaluation of the Biological Activity of a Growth Hormone (GH) Mutant (R77C) and Its Impact on GH Responsiveness and Stature.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 8, p. 2893, doi. 10.1210/jc.2006-2238
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- Publication type:
- Article
A novel mutation L260P of the steroidogenic acute regulatory protein gene in three unrelated patients of Swiss ancestry with congenital lipoid adrenal hyperplasia.
- Published in:
- 2005
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- Publication type:
- journal 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
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- Publication type:
- Article
Isolated Autosomal Dominant Growth Hormone Deficiency: An Evolving Pituitary Deficit? A Multicenter Follow-Up Study.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 4, p. 2089, doi. 10.1210/jc.2004-1280
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- Publication type:
- Article
Obesity Due to Proopiomelanocortin Deficiency: Three New Cases and Treatment Trials with Thyroid Hormone and ACTH4 –10.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 10, p. 4633, doi. 10.1210/jc.2003-030502
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- Publication type:
- Article
Obesity due to proopiomelanocortin deficiency: three new cases and treatment trials with thyroid hormone and ACTH4-10.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Reduced Longevity in Untreated Patients with Isolated Growth Hormone Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 8, p. 3664, doi. 10.1210/jc.2002-021938
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- Publication type:
- Article
An Exon Splice Enhancer Mutation Causes Autosomal Dominant GH Deficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 2, p. 847, doi. 10.1210/jcem.87.2.8236
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- 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
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- Publication type:
- Article
Autosomal Dominant GH Deficiency Due to an Arg183His GH-1 Gene Mutation: Clinical and Molecular Evidence of Impaired Regulated GH Secretion.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 8, p. 3941, doi. 10.1210/jcem.86.8.7723
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- 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
Phenotypic Variability in Familial Combined Pituitary Hormone Deficiency Caused by a PROP1 Gene Mutation Resulting in the Substitution of Arg3Cys at Codon 120 (R120C)
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 10, p. 3727, doi. 10.1210/jcem.83.10.5172
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- Publication type:
- Article
Half-life of exogenous growth hormone following suppression of endogenous growth hormone secretion with somatostatin in type I (insulin-dependent) diabetes mellitus.
- Published in:
- Clinical Endocrinology, 1992, v. 36, n. 3, p. 255, doi. 10.1111/j.1365-2265.1992.tb01441.x
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- Publication type:
- Article
Cancer Risks in Patients Treated With Growth Hormone in Childhood: The SAGhE European Cohort Study.
- Published in:
- 2017
- By:
- Publication type:
- journal article