Found: 122
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Comparison of capillary blood ketone measurement by electrochemical method and urinary ketone in treatment of diabetic ketosis and ketoacidosis in children.
- Published in:
- Acta Diabetologica, 2008, v. 45, n. 2, p. 83, doi. 10.1007/s00592-008-0026-y
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- Publication type:
- Article
Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers.
- Published in:
- 2020
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- Publication type:
- Question & Answer
Rare cause of severe hypertension in an adolescent boy presenting with short stature: Questions.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
A rare cause of hypertension in childhood: Answers.
- Published in:
- 2020
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- Publication type:
- Case Study
A rare cause of hypertension in childhood: Questions.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
Development of external genitalia during mini-puberty: is it related to somatic growth or reproductive hormones?
- Published in:
- European Journal of Pediatrics, 2024, v. 183, n. 3, p. 1325, doi. 10.1007/s00431-023-05393-3
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- Publication type:
- Article
Evaluation of Glucose Intolerance in Adolescents Relative to Adults with Type 2 Diabetes Mellitus.
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- Journal of Pediatric Endocrinology & Metabolism, 2006, v. 19, n. 11, p. 1319
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- Publication type:
- Article
Effect of Zinc Supplementation on Growth Hormone Secretion, IGF-I, IGFBP-3, Somatomedin Generation, Alkaline Phosphatase, Osteocalcin and Growth in Prepubertal Children with Idiopathic Short Stature.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2005, v. 18, n. 1, p. 69, doi. 10.1515/jpem.2005.18.1.69
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- Publication type:
- Article
Analysis of the PAX8 Gene in Congenital Hypothyroidism Caused by Different Forms of Thyroid Dysgenesis in a Father and Daughter.
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- Journal of Pediatric Endocrinology & Metabolism, 2004, v. 17, n. 7, p. 1021, doi. 10.1515/jpem.2004.17.7.1021
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- Publication type:
- Article
Two Patients with Kabuki Syndrome Presenting with Endocrine Problems.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2001, v. 14, n. 2, p. 215, doi. 10.1515/jpem.2001.14.2.215
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- Publication type:
- Article
Excessive Growth in a Girl with Weaver Syndrome.
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- Journal of Pediatric Endocrinology & Metabolism, 2000, v. 13, n. 8, p. 1147, doi. 10.1515/jpem.2000.13.8.1147
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- Publication type:
- Article
Effect of Hyperthyroidism on Insulin-like Growth Factor-I (IGF-I) and IGF-Binding Proteins in Adolescent Children.
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- Journal of Pediatric Endocrinology & Metabolism, 2000, v. 13, n. 8, p. 1073
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- Publication type:
- Article
Triple A Syndrome Mimicking Cystic Fibrosis.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2000, v. 13, n. 3, p. 329, doi. 10.1515/jpem.2000.13.3.329
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- Publication type:
- Article
Effect of Alendronate Treatment on the Clinical Picture and Bone Turnover Markers in Chronic Idiopathic Hyperphosphatasia.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2000, v. 13, n. 2, p. 217, doi. 10.1515/jpem.2000.13.2.217
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- Publication type:
- Article
Normal Growth in a Patient with Septo-Optic Dysplasia despite both Growth Hormone and IGF-I Deficiency.
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- Journal of Pediatric Endocrinology & Metabolism, 1998, v. 11, n. 1, p. 69, doi. 10.1515/jpem.1998.11.1.69
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- Publication type:
- Article
Growth Hormone Treatment in Growth Retarded Children with End Stage Renal Failure: Effect on Free/Dissociable IGF-I Levels.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 1997, v. 10, n. 2, p. 197, doi. 10.1515/jpem.1997.10.2.197
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- Publication type:
- Article
Acquired modification of sphingosine-1-phosphate lyase activity is not related to adrenal insufficiency.
- Published in:
- BMC Neurology, 2018, v. 18, n. 1, p. N.PAG, doi. 10.1186/s12883-018-1049-9
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- Publication type:
- Article
Effects of leukemia inhibitory receptor gene mutations on human hypothalamo-pituitary-adrenal function.
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- Pituitary, 2015, v. 18, n. 4, p. 456, doi. 10.1007/s11102-014-0594-5
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- Publication type:
- Article
Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features.
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- 2022
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- Publication type:
- Case Study
Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature.
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- Calcified Tissue International, 2021, v. 108, n. 5, p. 576, doi. 10.1007/s00223-020-00784-2
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- Publication type:
- Article
A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age.
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- 2020
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- Publication type:
- journal article
Clinical Significance of Hypophosphatasemia in Children.
- Published in:
- 2020
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- Publication type:
- journal article
Bone Mineral Density in Children with Non-Cystic Fibrosis Bronchiectasis.
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- Respiration, 2008, v. 75, n. 4, p. 432, doi. 10.1159/000105386
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- Publication type:
- Article
Misalignment among adolescents living with obesity, caregivers, and healthcare professionals: ACTION Teens global survey study.
- Published in:
- Pediatric Obesity, 2022, v. 17, n. 11, p. 1, doi. 10.1111/ijpo.12957
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- Publication type:
- Article
Personalized approach to childhood obesity: Lessons from gut microbiota and omics studies. Narrative review and insights from the 29th European childhood obesity congress.
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- Pediatric Obesity, 2021, v. 16, n. 10, p. 1, doi. 10.1111/ijpo.12835
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- Publication type:
- Article
Cardiac decompensation due to massive pericardial effusion.
- Published in:
- Clinical Pediatrics, 1994, v. 33, n. 12, p. 749, doi. 10.1177/000992289403301209
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- Publication type:
- Article
Persistent Müllerian Duct Syndrome: A Rare But Important Etiology of Inguinal Hernia and Cryptorchidism.
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- Sexual Development, 2019, v. 13, n. 5/6, p. 264, doi. 10.1159/000510466
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- Publication type:
- Article
Homozygosity for a novel INHA mutation in two male siblings with hypospadias, primary hypogonadism, and high-normal testicular volume.
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- European Journal of Endocrinology, 2022, v. 186, n. 5, p. K25, doi. 10.1530/EJE-21-1230
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- Publication type:
- Article
Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C.
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- European Journal of Endocrinology, 2022, v. 186, n. 1, p. 65, doi. 10.1530/EJE-21-0910
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- Publication type:
- Article
PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans.
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- European Journal of Endocrinology, 2019, v. 180, n. 5, p. 291, doi. 10.1530/EJE-19-0067
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- Publication type:
- Article
Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy.
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- European Journal of Endocrinology, 2012, v. 166, n. 1, p. 43, doi. 10.1530/EJE-11-0140
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- Publication type:
- Article
Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes.
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- Nephrology Dialysis Transplantation, 2012, v. 27, n. 2, p. 667, doi. 10.1093/ndt/gfr300
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- Publication type:
- Article
Membranous nephropathy in Schimke immuno-osseous dysplasia.
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- Pediatric Nephrology, 2006, v. 21, n. 6, p. 870, doi. 10.1007/s00467-006-0082-x
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- Publication type:
- Article
Peritoneal loss of insulin-like growth factor-I and binding proteins in end-stage renal disease.
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- Pediatric Nephrology, 1998, v. 12, n. 7, p. 581, doi. 10.1007/s004670050510
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- Publication type:
- Article
Venous Thrombosis in a Pseudohypoparathyroidism Patient with a Novel GNAS Frameshift Mutation and Complete Resolution of Vascular Calcifications with Acetazolamide Treatment.
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- Hormone Research in Paediatrics, 2024, v. 97, n. 4, p. 404, doi. 10.1159/000534456
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- Publication type:
- Article
Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature.
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- Hormone Research in Paediatrics, 2023, v. 96, n. 5, p. 527, doi. 10.1159/000529070
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- Publication type:
- Article
Postoperative and Long-Term Endocrinologic Complications of Craniopharyngioma.
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- Hormone Research in Paediatrics, 2020, v. 93, n. 9-10, p. 497, doi. 10.1159/000515347
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- Publication type:
- Article
Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency.
- Published in:
- Hormone Research in Paediatrics, 2020, v. 93, n. 9-10, p. 558, doi. 10.1159/000515079
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- Publication type:
- Article
Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation.
- Published in:
- Hormone Research in Paediatrics, 2020, v. 93, n. 5, p. 313, doi. 10.1159/000510623
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- Publication type:
- Article
Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty.
- Published in:
- Hormone Research in Paediatrics, 2020, v. 93, n. 1, p. 66, doi. 10.1159/000505329
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- Publication type:
- Article
Fibroblast Growth Factor-23 and Matrix Extracellular Phosphoglycoprotein Levels in Healthy Children and, Pregnant and Puerperal Women.
- Published in:
- Hormone Research in Paediatrics, 2019, v. 92, n. 5, p. 302, doi. 10.1159/000506477
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- Publication type:
- Article
Low DHEAS Concentration in a Girl Presenting with Short Stature and Premature Pubarche: A Novel PAPSS2 Gene Mutation.
- Published in:
- Hormone Research in Paediatrics, 2019, v. 92, n. 4, p. 262, doi. 10.1159/000502114
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- Publication type:
- Article
Restoration of Height after 11 Years of Letrozole Treatment in 11β-Hydroxylase Deficiency.
- Published in:
- Hormone Research in Paediatrics, 2019, v. 92, n. 3, p. 203, doi. 10.1159/000501456
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- Publication type:
- Article
Premature Pubarche, Hyperinsulinemia and Hypothyroxinemia: Novel Manifestations of Congenital Portosystemic Shunts (Abernethy Malformation) in Children.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 83, n. 4, p. 282, doi. 10.1159/000369395
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- Publication type:
- Article
The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study.
- Published in:
- Hormone Research in Paediatrics, 2012, v. 77, n. 2, p. 85, doi. 10.1159/000335172
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- Publication type:
- Article
T4 plus T3 Treatment in Children with Hypothyroidism and Inappropriately Elevated Thyroid-Stimulating Hormone despite Euthyroidism on T4 Treatment.
- Published in:
- Hormone Research in Paediatrics, 2010, v. 73, n. 2, p. 108, doi. 10.1159/000277627
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- Publication type:
- Article
Development of Insulin Detemir/Insulin Aspart Cross-Reacting Antibodies Following Treatment with Insulin Detemir: 104-week Study in Children and Adolescents with Type 1 Diabetes Aged 2-16 Years.
- Published in:
- Diabetes Therapy, 2016, v. 7, n. 4, p. 713, doi. 10.1007/s13300-016-0196-5
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- Publication type:
- Article
The Frequency and the Effects of 21-Hydroxylase Gene Defects in Congenital Adrenal Hyperplasia Patients.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 6, p. 399, doi. 10.1111/ahg.12083
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- Publication type:
- Article
Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2023, v. 36, n. 4, p. 401, doi. 10.1515/jpem-2022-0645
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- Publication type:
- Article
Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 4, p. 557, doi. 10.1515/jpem-2019-0466
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- Publication type:
- Article