Prof. Dr. Tülay Güran
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Which diseases does this doctor work on?
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Adrenal Hyperplasia, Congenital 30 publicationsSource: OpenAlex / PubMed MeSHView publications
- Adrenal Insufficiency 18 publications
- Puberty, Precocious 16 publications
- Addison Disease 7 publications
- Diabetes Mellitus, Type 1 7 publications
- Disorders of Sex Development 7 publications
- Hypertension 6 publications
- Obesity 6 publications
- Nephrocalcinosis 5 publications
- Hypoglycemia 4 publications
- Adrenal Cortex Neoplasms 4 publications
- Hypercalcemia 4 publications
- Osteochondrodysplasias 4 publications
- Gonadal Dysgenesis, 46,XY 4 publications
- Androgen-Insensitivity Syndrome 4 publications
- Hypogonadism 4 publications
- Diabetes Mellitus, Type 2 4 publications
- Adenoma 3 publications
- Nephrotic Syndrome 3 publications
- Hypokalemia 3 publications
- Adrenocortical Carcinoma 3 publications
- Rickets 3 publications
- Renal Tubular Transport, Inborn Errors 3 publications
- Pseudohypoaldosteronism 3 publications
- Ovarian Cysts 3 publications
- Bronchiectasis 3 publications
- Cystic Fibrosis 2 publications
- Turner Syndrome 2 publications
- Pituitary Neoplasms 2 publications
- Hypophosphatemia, Familial 2 publications
- Puberty, Delayed 2 publications
- Adrenal Rest Tumor 2 publications
- Testicular Neoplasms 2 publications
- Hyperandrogenism 2 publications
- Pseudohypoparathyroidism 2 publications
- ACTH Syndrome, Ectopic 2 publications
- Atrophy 2 publications
- Cushing Syndrome 2 publications
- Hypospadias 2 publications
- Hypopituitarism 2 publications
- Hypocalcemia 2 publications
- Hypophosphatasia 2 publications
- Abnormalities, Multiple 2 publications
- Weight Gain 2 publications
- Developmental Disabilities 2 publications
- Primary Ovarian Insufficiency 2 publications
- Alkalosis 2 publications
- Bartter Syndrome 2 publications
- Birth Weight 2 publications
- Hypothalamic Neoplasms 2 publications
- Tooth Abnormalities 2 publications
- Exostoses, Multiple Hereditary 2 publications
- Congenital Hypothyroidism 2 publications
- Insulin Resistance 2 publications
- Thyroid Hormone Resistance Syndrome 2 publications
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Where does this information come from?
The source is stated next to each piece of information. If you see something wrong, you can suggest a correction.
- SpecialtyPaediatric Endocrinologysaglik.gov.trFrom source
- InstitutionMarmara Üniversitesi Pendik Eğitim ve Araştırma Hastanesisaglik.gov.trFrom source
- Area of workAdrenal Hyperplasia, CongenitalExtracted from 30 publications · Model version —From source
- Publications389 publicationsOpenAlex, ORCID, Europe PMCFrom source
- ORCID0000-0003-2658-6866ORCIDFrom source
- Last synchronised5 November 2026 10:37https://marmaraeah.saglik.gov.tr/TR-1393155/doktorlarimiz.html#tulay-guransaglik.gov.tr
Scientific work
Publications on Adrenal Hyperplasia, Congenital
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Long-term clinical outcomes of primary adrenal insufficiency caused by homozygous CYP11A1 p.R451W variant
European Journal of Endocrinology, 2026
DOI 10.1093/ejendo/lvag110 PMID 42340003 Open-access full textSource: OpenAlex
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Isolated Hyperchlorhidrosis Caused by Novel Biallelic CA12 Variants Mimicking Pseudohypoaldosteronism
2026
DOI 10.1159/hrp/adaag054 Source: ORCID
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Determinants of pubertal progression and final height in premature pubarche
Journal of Endocrinological Investigation, 2026
DOI 10.1007/s40618-026-02957-6 PMID 42340620 Open-access full textSource: ORCID
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Response to Letter to the Editor from Ting and Chen: “Impact of Growth-Promoting Therapies on Puberty, Growth, and Final Height in Classical 21-Hydroxylase Deficiency”
The Journal of Clinical Endocrinology & Metabolism, 2026
DOI 10.1210/clinem/dgag029 PMID 41711662 Source: ORCID
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Positive neonatal screening test for congenital adrenal hyperplasia in a case with 3β-hydroxysteroid dehydrogenase type 2 deficiency
Journal of Pediatric Endocrinology and Metabolism, 2026
DOI 10.1515/jpem-2025-0403 PMID 41111433 Source: ORCID
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Utility of a 40-minute LH level after depot leuprolide for diagnosis and treatment monitoring in girls with CPP
Journal of endocrinological investigation, 2026
DOI 10.1007/s40618-026-02925-0 PMID 42189483 Open-access full textSource: Europe PMC
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BMI-SDS Changes During GnRHa Therapy in 150 Girls with Idiopathic Central Precocious Puberty: Follow-up Through Final Height
Journal of clinical research in pediatric endocrinology, 2026
DOI 10.4274/jcrpe.galenos.2026.2026-3-6 PMID 42028850 1 citation (Europe PMC) Open-access full textSource: Europe PMC
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Isolated Hypoglycemia in Children with Cystic Fibrosis: Role of Pancreatic Insufficiency and Glucagon Response
Journal of clinical research in pediatric endocrinology, 2026
DOI 10.4274/jcrpe.galenos.2025.2025-2-6 PMID 41090401 Open-access full textSource: Europe PMC
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Machine learning algorithms to accelerate etiological diagnosis of congenital disorders of adrenal steroidogenesis
The Journal of Clinical Endocrinology & Metabolism, 2026
DOI 10.1210/clinem/dgag237 PMID 42359583 2 citations (Europe PMC) Open-access full textSource: ORCID
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The 40<sup>th</sup> Minute Cortisol Measurement is the Key Time-Point in the Low-Dose Synacthen Stimulation Test: A Large, Assay-Specific Pediatric Validation Study
Journal of clinical research in pediatric endocrinology, 2026
DOI 10.4274/jcrpe.galenos.2026.2026-1-17 PMID 42043277 Open-access full textSource: Europe PMC