Found: 120
Select item for more details and to access through your institution.
Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2024, v. 16, n. 3, p. 288, doi. 10.4274/jcrpe.galenos.2024.2024-1-3
- By:
- Publication type:
- Article
Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics.
- Published in:
- Diabetologia, 2022, v. 65, n. 2, p. 336, doi. 10.1007/s00125-021-05597-y
- By:
- Publication type:
- Article
MANF supports the inner hair cell synapse and the outer hair cell stereocilia bundle in the cochlea.
- Published in:
- Life Science Alliance, 2022, v. 5, n. 2, p. 1, doi. 10.26508/lsa.202101068
- By:
- Publication type:
- Article
Nadir Görülen Bir Turner Sendromu Karyotipi: 45,X/47,XXX.
- Published in:
- Journal of Current Pediatrics / Guncel Pediatri, 2014, v. 12, n. 1, p. 43, doi. 10.4274/jcp.02996
- By:
- Publication type:
- Article
The frequency and associated factors of diabetic ketoacidosis at diagnosis in children with type 1 diabetes.
- Published in:
- 2010
- By:
- Publication type:
- Journal Article
Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3.
- Published in:
- PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0193388
- By:
- Publication type:
- Article
PHOTO QUIZ.
- Published in:
- Marmara Medical Journal, 2010, v. 23, n. 1, p. 67
- By:
- Publication type:
- Article
Aromatase Inhibitors May Increase the Risk of Cardiometabolic Complications in Adolescent Boys.
- Published in:
- Pediatric Cardiology, 2024, v. 45, n. 2, p. 228, doi. 10.1007/s00246-023-03260-4
- By:
- Publication type:
- Article
A case of Takayasu disease with findings of incomplete Alagille syndrome.
- Published in:
- Rheumatology International, 2005, v. 25, n. 7, p. 555, doi. 10.1007/s00296-004-0557-7
- By:
- Publication type:
- Article
A Novel De Novo Missense Mutation in HNF4A Resulting in Sulfonylurea-Responsive Maturity-onset Diabetes of the Young.
- Published in:
- Journal of Pediatric Research, 2018, v. 5, n. 3, p. 1, doi. 10.4274/jpr.60252
- By:
- Publication type:
- Article
Early-Onset Isolated Bilateral Pheochromocytoma As a Major Clinical Manifestation of von-Hippel Lindau Syndrome Type 2C.
- Published in:
- Journal of Pediatric Research, 2018, v. 5, n. 1, p. 48, doi. 10.4274/jpr.58661
- By:
- Publication type:
- Article
Tip I Diabetes Mellitus Olgularının Tanı Anındaki Diyabetik Ketoasidoz Sıklığının Değişimi: On Beş Yıllık Tek Merkez Deneyimi.
- Published in:
- Journal of Pediatric Research, 2017, v. 4, n. 3, p. 143, doi. 10.4274/jpr.16768
- By:
- Publication type:
- Article
Bedside sonographic measurements of optic nerve sheath diameter in children with diabetic ketoacidosis.
- Published in:
- Pediatric Diabetes, 2021, v. 22, n. 4, p. 618, doi. 10.1111/pedi.13188
- By:
- Publication type:
- Article
Comparison of the Efficacy of Daily and Weekly ID Oral Alendronate Treatment in Patients with Secondary Osteoporosis.
- Published in:
- Journal of Dr. Behcet Uz Children's Hospital, 2019, v. 9, n. 3, p. 191, doi. 10.5222/buchd.2019.25349
- By:
- Publication type:
- Article
46, XY cinsiyet gelişim bozukluğunun nadir bir nedeni: Persistan müller kanalı sendromu.
- Published in:
- Journal of Dr. Behcet Uz Children's Hospital, 2017, v. 7, n. 3, p. 242, doi. 10.5222/buchd.2017.242
- By:
- Publication type:
- Article
Infantile Graves Disease.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Erken başlangıçlı Graves olgusu.
- Published in:
- Türk Pediatri Arşivi, 2013, v. 48, n. 4, p. 332, doi. 10.4274/tpa.833
- By:
- Publication type:
- Article
Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum Stress.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Predictive value of clinical and laboratory variables for vesicoureteral reflux in children.
- Published in:
- Pediatric Nephrology, 2007, v. 22, n. 6, p. 844, doi. 10.1007/s00467-006-0418-6
- By:
- Publication type:
- Article
DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism.
- Published in:
- Hormone Research in Paediatrics, 2021, v. 94, n. 9/10, p. 364, doi. 10.1159/000520409
- By:
- Publication type:
- Article
Serum Level of Biotin Rather than the Daily Dosage Is the Main Determinant of Interference on Thyroid Function Assays.
- Published in:
- Hormone Research in Paediatrics, 2019, v. 92, n. 2, p. 92, doi. 10.1159/000502740
- By:
- Publication type:
- Article
Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide.
- Published in:
- Hormone Research in Paediatrics, 2016, v. 85, n. 2, p. 107, doi. 10.1159/000441977
- By:
- Publication type:
- Article
GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in Adolescents.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 83, n. 3, p. 177, doi. 10.1159/000369013
- By:
- Publication type:
- Article
Psychomotor Retardation Caused by a Defective Thyroid Hormone Transporter: Report of Two Families with Different MCT8 Mutations.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 82, n. 4, p. 261, doi. 10.1159/000365191
- By:
- 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
- By:
- Publication type:
- Article
Efficacy of aromatase inhibitor therapy in a case with large cell calcifying Sertoli cell tumour-associated prepubertal gynaecomastia.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 12, p. 1565, doi. 10.1515/jpem-2022-0368
- By:
- Publication type:
- Article
Hemoglobin A<sub>1C</sub> can differentiate subjects with GCK mutations among patients suspected to have MODY.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 12, p. 1528, doi. 10.1515/jpem-2022-0381
- By:
- Publication type:
- Article
Biochemical indicators of euthyroid sick syndrome in critically ill children.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 10, p. 1285, doi. 10.1515/jpem-2022-0232
- By:
- Publication type:
- Article
Initial neutrophil/lymphocyte and lymphocyte/monocyte ratios can predict future insulin need in newly diagnosed type 1 diabetes mellitus.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 5, p. 593, doi. 10.1515/jpem-2021-0564
- By:
- Publication type:
- Article
A nonsense variant in FGFR1: a rare cause of combined pituitary hormone deficiency.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 12, p. 1613, doi. 10.1515/jpem-2020-0029
- By:
- Publication type:
- Article
Graves' disease following allogenic hematopoietic stem cell transplantation for severe aplastic anemia: case report and literature review.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 5, p. 589, doi. 10.1515/jpem-2017-0358
- By:
- Publication type:
- Article
Changes of thyroid hormonal status in patients receiving ketogenic diet due to intractable epilepsy.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 4, p. 411, doi. 10.1515/jpem-2016-0281
- By:
- Publication type:
- Article
A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1111, doi. 10.1515/jpem-2015-0482
- By:
- Publication type:
- Article
Relationship between oxidative stress and blood glucose fluctuations evaluated with daily glucose monitoring in children with type 1 diabetes mellitus.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 4, p. 435, doi. 10.1515/jpem-2015-0212
- By:
- Publication type:
- Article
Levothyroxine replacement in primary congenital hypothyroidism: the higher the initial dose the higher the rate of overtreatment.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 2, p. 133, doi. 10.1515/jpem-2015-0047
- By:
- Publication type:
- Article
Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 11/12, p. 1265, doi. 10.1515/jpem-2014-0430
- By:
- Publication type:
- Article
A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 11/12, p. 1379, doi. 10.1515/jpem-2014-0501
- By:
- Publication type:
- Article
Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiency.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 7/8, p. 961, doi. 10.1515/jpem-2014-0365
- By:
- Publication type:
- Article
Management of central diabetes insipidus with oral desmopressin lyophilisate in infants.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 923, doi. 10.1515/jpem-2013-0368
- By:
- Publication type:
- Article
A novel mutation in a mother and a son with Aarskog-Scott syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 3/4, p. 385, doi. 10.1515/jpem-2012-0233
- By:
- Publication type:
- Article
Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 147, doi. 10.1515/jpem-2012-0239
- By:
- Publication type:
- Article
Hyperprolactinemia in children: clinical features and long-term results.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 11/12, p. 1123, doi. 10.1515/jpem-2012-0130
- By:
- Publication type:
- Article
Evaluation of neutrophil gelatinase-associated lipocalin in normoalbuminuric normotensive type 1 diabetic adolescents.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 5/6, p. 517, doi. 10.1515/jpem-2011-0487
- By:
- Publication type:
- Article
Clinical profile and etiologies of children with central diabetes insipidus: a single-center experience from Turkey.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 5/6, p. 499, doi. 10.1515/jpem-2012-0006
- By:
- Publication type:
- Article
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 5/6, p. 419, doi. 10.1515/jpem-2012-0053
- By:
- Publication type:
- Article
A Comparison of Multiple Daily Insulin Therapy with Continuous Subcutaneous Insulin Infusion Therapy in Adolescents with Type 1 Diabetes Mellitus: A Single-Center Experience From Turkey.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2009, v. 22, n. 6, p. 539, doi. 10.1515/JPEM.2009.22.6.539
- By:
- Publication type:
- Article
Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 3, p. e1204, doi. 10.1210/clinem/dgad606
- By:
- Publication type:
- Article
A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 9, p. 2371, doi. 10.1210/clinem/dgad099
- By:
- Publication type:
- Article
Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal Insufficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 5, p. e1924, doi. 10.1210/clinem/dgac016
- By:
- Publication type:
- Article
Clinical course of primary empty sella in children: a single-center experience.
- Published in:
- Turkish Journal of Pediatrics, 2022, v. 64, n. 5, p. 900, doi. 10.24953/turkjped.2021.4953
- By:
- Publication type:
- Article