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Pregnancy-Associated Plasma Protein (PAPP)-A2 in Physiology and Disease.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 12, p. 3576, doi. 10.3390/cells10123576
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- Publication type:
- Article
Diagnosis of intra-amniotic infection by proteomic profiling and identification of novel biomarkers.
- Published in:
- 2004
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- Publication type:
- journal article
Insulin Resistance Is Associated With Increased Serum Concentration of IGF-Binding Protein--Related Protein 1 (IGFBP-rP1/MAC25).
- Published in:
- Diabetes, 2006, v. 55, n. 8, p. 2333, doi. 10.2337/db05-1627
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- Publication type:
- Article
Insulin-like growth factor I/somatomedin-C (IGF-I/SM-C) and glucocorticoids synergistically regulate mitosis in competent human fibroblasts.
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- Journal of Cellular Physiology, 1983, v. 116, n. 2, p. 191, doi. 10.1002/jcp.1041160210
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- Publication type:
- Article
Structural Characterization and Immunohistochemical Localization of Receptors for Insulin-Like Growth Factor II in the Rat Pituitary Gland.
- Published in:
- Neuroendocrinology, 1989, v. 49, n. 3, p. 248, doi. 10.1159/000125124
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- Publication type:
- Article
Sex Chromosome Fragment in a Phenotypically Normal Female.
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- Clinical Pediatrics, 1986, v. 25, n. 1, p. 36, doi. 10.1177/000992288602500106
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- Publication type:
- Article
Mutations in pregnancy-associated plasma protein A2 cause short stature due to low IGF-I availability.
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- EMBO Molecular Medicine, 2016, v. 8, n. 4, p. 363, doi. 10.15252/emmm.201506106
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- Publication type:
- Article
Results from the First 2 Years of a Clinical Trial with Recombinant DNA-derived Human Growth Hormone (Somatrem) in Turner's Syndrome.
- Published in:
- Acta Paediatrica, 1987, v. 76, n. s331, p. 59, doi. 10.1111/j.1651-2227.1987.tb17100.x
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- Publication type:
- Article
Testicular tumors with Peutz-Jeghers syndrome.
- Published in:
- 1986
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- Publication type:
- journal article
Insulin-Like Growth Factors are Mitogenic for Human Keratinocytes and a Squamous Cell Carcinoma.
- Published in:
- Journal of Investigative Dermatology, 1991, v. 96, n. 1, p. 104, doi. 10.1111/1523-1747.ep12515914
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- Publication type:
- Article
Characterization of Insulin-Like Growth Factor-I/Somatomedin-C Receptors on Human Keratinocyte Monolayers.
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- Journal of Investigative Dermatology, 1986, v. 87, n. 2, p. 264, doi. 10.1111/1523-1747.ep12696645
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- Publication type:
- Article
STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability.
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- European Journal of Endocrinology, 2015, v. 173, n. 3, p. 291, doi. 10.1530/EJE-15-0398
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- Publication type:
- Article
Development of additional pituitary hormone deficiencies in pediatric patients originally diagnosed with idiopathic isolated GH deficiency.
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- European Journal of Endocrinology, 2014, v. 170, n. 1, p. 13, doi. 10.1530/EJE-13-0643
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- Publication type:
- Article
Intrauterine and postnatal growth failure with normal GH/IGF1 axis and insulin-resistant diabetes in a consanguineous kinship.
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- European Journal of Endocrinology, 2012, v. 166, n. 3, p. 521, doi. 10.1530/EJE-11-0769
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- Publication type:
- Article
IGF-I therapy in growth disorders.
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- European Journal of Endocrinology, 2007, v. 157, p. S57, doi. 10.1530/EJE-07-0187
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- Publication type:
- Article
Idiopathic short stature: will genetics influence the choice between GH and IGF-I therapy?
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- European Journal of Endocrinology, 2007, v. 157, p. S33, doi. 10.1530/EJE-07-0292
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- Publication type:
- Article
Pharmacogenomics and pharmacoproteomics in the evaluation and management of short stature.
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- European Journal of Endocrinology, 2007, v. 157, p. S27, doi. 10.1530/EJE-07-0186
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- Publication type:
- Article
New molecular mechanisms of GH resistance.
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- European Journal of Endocrinology, 2004, p. S11, doi. 10.1530/eje.0.151s011
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- Publication type:
- Article
Identification of the first patient with a confirmed mutation of the JAK-STAT system.
- Published in:
- Pediatric Nephrology, 2005, v. 20, n. 3, p. 303, doi. 10.1007/s00467-004-1678-7
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- Publication type:
- Article
Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04521-0
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- Publication type:
- Article
A Novel, Heterozygous, de novo Splicing Variant Affecting the Intracellular Domain of the Growth Hormone Receptor, and Causing a Mild Short Stature.
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- Hormone Research in Paediatrics, 2024, v. 97, n. 4, p. 397, doi. 10.1159/000534183
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- Publication type:
- Article
The History of the Insulin-Like Growth Factor System.
- Published in:
- Hormone Research in Paediatrics, 2022, v. 95, n. 6, p. 619, doi. 10.1159/000527123
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- Publication type:
- Article
When Is a Positive Test for Pediatric Growth Hormone Deficiency a True-Positive Test?
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- Hormone Research in Paediatrics, 2022, v. 94, n. 11/12, p. 399, doi. 10.1159/000521281
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- Publication type:
- Article
Efficacy and Safety of Once-Weekly Somatrogon Compared with Once-Daily Somatropin (Genotropin®) in Japanese Children with Pediatric Growth Hormone Deficiency: Results from a Randomized Phase 3 Study.
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- Hormone Research in Paediatrics, 2022, v. 95, n. 3, p. 275, doi. 10.1159/000524600
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- Publication type:
- Article
A Novel Mutation in Insulin-Like Growth Factor 1 Receptor (c.641-2A>G) Is Associated with Impaired Growth, Hypoglycemia, and Modified Immune Phenotypes.
- Published in:
- Hormone Research in Paediatrics, 2020, v. 93, n. 5, p. 322, doi. 10.1159/000510764
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- Publication type:
- Article
Height Gain and Safety Outcomes in Growth Hormone-Treated Children with Idiopathic Short Stature: Experience from a Prospective Observational Study.
- Published in:
- Hormone Research in Paediatrics, 2019, v. 91, n. 4, p. 241, doi. 10.1159/000500087
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- Publication type:
- Article
Expanding Genetic and Functional Diagnoses of IGF1R Haploinsufficiencies.
- Published in:
- Hormone Research in Paediatrics, 2017, v. 87, n. 6, p. 412, doi. 10.1159/000464143
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- Publication type:
- Article
Pharmacokinetic and Pharmacodynamic Modeling of MOD-4023, a Long-Acting Human Growth Hormone, in Growth Hormone Deficiency Children.
- Published in:
- Hormone Research in Paediatrics, 2017, v. 87, n. 5, p. 324, doi. 10.1159/000470842
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- Publication type:
- Article
How Aggressively Should We Treat Short Stature?
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- Hormone Research in Paediatrics, 2015, v. 83, n. 4, p. 280, doi. 10.1159/000374114
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- Publication type:
- Article
A Novel ERCC6 Splicing Variant Associated with a Mild Cockayne Syndrome Phenotype.
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- Hormone Research in Paediatrics, 2014, v. 82, n. 5, p. 344, doi. 10.1159/000368192
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- Publication type:
- Article
A Novel GHR Intronic Variant, c.266+83G>T, Activates a Cryptic 5′ Splice Site Causing Severe GHR Deficiency and Classical GH Insensitivity Syndrome.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 80, n. 6, p. 397, doi. 10.1159/000355404
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- Publication type:
- Article
A Database and Website for Molecular Defects of the GH-IGF Axis: www.growthgenetics.com.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 80, n. 6, p. 443, doi. 10.1159/000355543
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- Publication type:
- Article
A Novel Exonic GHR Splicing Mutation (c.784G>C) in a Patient with Classical Growth Hormone Insensitivity Syndrome.
- Published in:
- 2013
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- Publication type:
- Case Study
Identification of a Novel Heterozygous IGF1 Splicing Mutation in a Large Kindred with Familial Short Stature.
- Published in:
- Hormone Research in Paediatrics, 2012, v. 78, n. 1, p. 59, doi. 10.1159/000337249
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- Publication type:
- Article
Triple A Syndrome in a Patient with Genetic Growth Hormone Insensitivity: Phenotypic Effects of Two Genetic Disorders.
- Published in:
- 2012
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- Publication type:
- Case Study
A Novel Y332C Missense Mutation in the Intracellular Domain of The Human Growth Hormone Receptor Does Not Alter STAT5b Signaling: Redundancy of GHR Intracellular Tyrosines Involved in STAT5b Signaling.
- Published in:
- Hormone Research in Paediatrics, 2011, v. 75, n. 3, p. 187, doi. 10.1159/000320461
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- Publication type:
- Article
Atypical GH Insensitivity Syndrome and Severe Insulin-Like Growth Factor-I Deficiency Resulting from Compound Heterozygous Mutations of the GH Receptor, Including a Novel Frameshift Mutation Affecting the Intracellular Domain.
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- Hormone Research in Paediatrics, 2010, v. 74, n. 6, p. 406, doi. 10.1159/000314968
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- Publication type:
- Article
Growth and growth hormone in Turner syndrome: Looking back, looking ahead.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2019, v. 181, n. 1, p. 86, doi. 10.1002/ajmg.c.31680
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- Publication type:
- Article
Short Stature in Partially Corrected X-linked Severe Combined Immunodeficiency - Suboptimal Response to Growth Hormone.
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- Journal of Pediatric Endocrinology & Metabolism, 2008, v. 21, n. 11, p. 1057, doi. 10.1515/JPEM.2008.21.11.1057
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- Publication type:
- Article
What Is the Role for Pediatric Endocrinologists in the Management of Skeletal Dysplasias?
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 5, p. e1410, doi. 10.1210/clinem/dgad726
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- Publication type:
- Article
Bone Mineral, Histomorphometry, and Body Composition in Adults with Growth Hormone Receptor Deficiency.
- Published in:
- Journal of Bone & Mineral Research, 1998, v. 13, n. 3, p. 415, doi. 10.1359/jbmr.1998.13.3.415
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- Publication type:
- Article
Variable Degree of Growth Hormone (GH) and Insulin-Like Growth Factor (IGF) Sensitivity in Children with Idiopathic Short Stature Compared with GH-Deficient Patients: Evidence from an IGF-Based Dosing Study of Short Children.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 5, p. 2089, doi. 10.1210/jc.2009-2139
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- Publication type:
- Article
Familial Short Stature Caused by Haploinsufficiency of the Insulin-Like Growth Factor I Receptor due to Nonsense-Mediated Messenger Ribonucleic Acid Decay.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 5, p. 1740, doi. 10.1210/jc.2008-1903
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- Publication type:
- Article
Growth Hormone (GH) Insensitivity and Insulin-Like Growth Factor-I Deficiency in Inuit Subjects and an Ecuadorian Cohort: Functional Studies of Two Codon 180 GH Receptor Gene Mutations.
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- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 3, p. 1030, doi. 10.1210/jc.2007-2022
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- Publication type:
- Article
Height Velocity Targets from the National Cooperative Growth Study for First-Year Growth Hormone Responses in Short Children.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 2, p. 352, doi. 10.1210/jc.2007-1581
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- Publication type:
- Article
Insulin Growth Factor-Based Dosing of Growth Hormone Therapy in Children: A Randomized, Controlled Study.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 7, p. 2480, doi. 10.1210/jc.2007-0204
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- Publication type:
- Article
Primary Growth Hormone (GH) Insensitivity and Insulin-Like Growth Factor Deficiency Caused by Novel Compound Heterozygous Mutations of the GH Receptor Gene: Genetic and Functional Studies of Simple and Compound Heterozygous States.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 6, p. 2223, doi. 10.1210/jc.2006-2624
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- Publication type:
- Article
Total Absence of Functional Acid Labile Subunit, Resulting in Severe Insulin-Like Growth Factor Deficiency and Moderate Growth Failure.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 5, p. 1826, doi. 10.1210/jc.2005-2842
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- Publication type:
- Article
Editorial: The Pharmacogenomics of Human Growth.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 3, p. 795, doi. 10.1210/jc.2006-0026
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- Publication type:
- Article
Circulating Ghrelin Levels Are Suppressed by Meals and Octreotide Therapy in Children with Prader-Willi Syndrome.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 8, p. 3573, doi. 10.1210/jc.2003-030205
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- Publication type:
- Article