Publications by authors named "Huseyin Demirbilek"

54Publications

Identification of Three Novel and One Known Mutation in the Gene in Four Unrelated Turkish Families; the Role of Homozygosity Mapping in the Early Diagnosis.

J Clin Res Pediatr Endocrinol 2020 Sep 17. Epub 2020 Sep 17.

Developmental Endocrinology Research Group, Clinical and Molecular Genetics Unit, Institute of Child Health, University College London, WC1N 1EH, London, United Kingdom.

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http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0152DOI Listing
September 2020

Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes.

J Clin Res Pediatr Endocrinol 2020 Aug 21. Epub 2020 Aug 21.

Gazi Yaşargil Training and Research Hospital, Department of Pediatric Endocrinology, Diyarbakır, Turkey.

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http://dx.doi.org/10.4274/jcrpe.galenos.2020.2020.0108DOI Listing
August 2020

Neonatal diabetes due to homozygous INS gene promoter mutations: Highly variable phenotype, remission and early relapse during the first 3 years of life.

Pediatr Diabetes 2020 Jul 13. Epub 2020 Jul 13.

Gazi Yaşargil Research and Training Hospital, Pediatric Endocrinology, Diyarbakır, Turkey.

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http://dx.doi.org/10.1111/pedi.13079DOI Listing
July 2020

Cystoscopy-Guided Laparoscopic Excision of Prostatic Utricle: Report of a Case.

European J Pediatr Surg Rep 2020 Jan 28;8(1):e35-e38. Epub 2020 Apr 28.

Department of Pediatric Surgery, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1055/s-0040-1705155DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188514PMC
January 2020

A novel diagnostic tool for the evaluation of hypothalamic-pituitary region and diagnosis of growth hormone deficiency: pons ratio.

J Pediatr Endocrinol Metab 2020 May 21;33(6):735-742. Epub 2020 May 21.

Gazi Yasargil Training and Research Hospital Clinics of Paediatric Endocrinology, Diyarbakır, Turkey.

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http://dx.doi.org/10.1515/jpem-2019-0321DOI Listing
May 2020

Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-Eastern Region of Turkey

J Clin Res Pediatr Endocrinol 2020 09 11;12(3):295-302. Epub 2020 Mar 11.

Gazi Yaşargil Training and Research Hospital, Clinic of Paediatric Endocrinology, Diyarbakır, Turkey

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http://dx.doi.org/10.4274/jcrpe.galenos.2020.2019.0218DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499137PMC
September 2020

Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism

J Clin Res Pediatr Endocrinol 2020 09 28;12(3):275-280. Epub 2020 Jan 28.

Diyarbakır University of Health Sciences Turkey, Gazi Yaşargil Training and Research Hospital, Clinic of Paediatric Endocrinology, Diyarbakır, Turkey

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http://dx.doi.org/10.4274/jcrpe.galenos.2020.2019.0170DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499143PMC
September 2020

A Distinct Clinical Phenotype in Two Siblings with X-linked Adrenoleukodystrophy.

Neuro Endocrinol Lett 2019 Mar;40(1):36-40

Hacettepe University Faculty of Medicine, Department of Pediatrics Endocrinology, Ankara, Turkey.

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March 2019

Ion Transporters, Channelopathies, and Glucose Disorders.

Int J Mol Sci 2019 May 27;20(10). Epub 2019 May 27.

Department of Paediatric Medicine, Division of Endocrinology, Sidra Medicine, Doha, Qatar.

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http://dx.doi.org/10.3390/ijms20102590DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566632PMC
May 2019

Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in SCNN1Aand SCNN1BGenes.

Horm Res Paediatr 2019 24;91(3):175-185. Epub 2019 Apr 24.

Department of Paediatric Endocrinology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1159/000498860DOI Listing
December 2019

The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism.

Front Endocrinol (Lausanne) 2019 26;10:111. Epub 2019 Feb 26.

Division of Endocrinology, Department of Paediatric Medicine, Sidra Medicine, Doha, Qatar.

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http://dx.doi.org/10.3389/fendo.2019.00111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401612PMC
February 2019

Permanent neonatal diabetes mellitus and neurological abnormalities due to a novel homozygous missense mutation in NEUROD1.

Pediatr Diabetes 2018 08 27;19(5):898-904. Epub 2018 Mar 27.

Department of Paediatric Endocrinology, Erciyes University Medical Faculty, Kayseri, Turkey.

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http://dx.doi.org/10.1111/pedi.12669DOI Listing
August 2018

Congenital Hyperinsulinism: Diagnosis and Treatment Update.

J Clin Res Pediatr Endocrinol 2017 Dec 27;9(Suppl 2):69-87. Epub 2017 Dec 27.

Sidra Medical and Research Center, Clinic of Paediatric Medicine, Doha, Qatar.

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http://cms.galenos.com.tr/Uploads/Article_16630/JCRPE-9-2-En
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http://dx.doi.org/10.4274/jcrpe.2017.S007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790328PMC
December 2017

Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology.

Int J Pediatr Endocrinol 2017 29;2017. Epub 2017 Aug 29.

Department of Paediatric Medicine Sidra Medical & Research Center, OPC, C6-337, PO Box 26999, Doha, Qatar.

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http://dx.doi.org/10.1186/s13633-017-0048-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575922PMC
August 2017

Clinical and biochemical characteristics and bone mineral density of homozygous, compound heterozygous and heterozygous carriers of three novel mutations.

Eur J Endocrinol 2017 Jun 1;176(6):657-667. Epub 2017 Mar 1.

Departments of PediatricsLeiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.1530/EJE-16-0999DOI Listing
June 2017

Severe hyponatremia and repeated intestinal resections for intestinal dysmotility mimicking congenital aganglionic megacolon due to delay in the diagnosis of congenital hypothyroidism.

Ann Pediatr Endocrinol Metab 2016 Dec 31;21(4):230-234. Epub 2016 Dec 31.

Department of Paediatric Endocrinology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.6065/apem.2016.21.4.230DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290179PMC
December 2016

Hyperinsulinaemic hypoglycaemia in children and adults.

Lancet Diabetes Endocrinol 2017 09 1;5(9):729-742. Epub 2016 Dec 1.

Department of Pediatric Medicine, Sidra Medical & Research Center, Outpatient Clinic, Doha, Qatar. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S22138587163032
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http://dx.doi.org/10.1016/S2213-8587(16)30323-0DOI Listing
September 2017

Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism.

J Clin Res Pediatr Endocrinol 2016 Jun 18;8(2):163-9. Epub 2016 Apr 18.

Diyarbakır Children State Hospital, Clinic of Pediatric Endocrinology, Diyarbakır, Turkey; Present position: Hacettepe University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey, Phone: +90 543 370 54 91 E-mail:

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http://dx.doi.org/10.4274/jcrpe.2228DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096471PMC
June 2016

Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type I.

Horm Res Paediatr 2016 17;85(5):309-17. Epub 2016 Mar 17.

Genetics and Epigenetics in Health and Disease, Genetics and Genomic Medicine Programme, UCL Institute of Child Health, Great Ormond Street Hospital for Children, London, UK.

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http://dx.doi.org/10.1159/000444483DOI Listing
April 2017

Severe Hypercalcemia in a Child With Acute Lymphoblastic Leukemia Relapse: Successful Management With Combination of Calcitonin and Bisphosphonate.

J Pediatr Hematol Oncol 2016 Apr;38(3):232-4

*Pediatric Hematology Unit †Pediatric Endocrinology Unit, Hacettepe University Faculty of Medicine, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.

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http://dx.doi.org/10.1097/MPH.0000000000000525DOI Listing
April 2016

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group.

J Clin Res Pediatr Endocrinol 2015 Sep;7(3):183-91

Gülhane Military Medicine Academy, Department of Pediatric Endocrinology, Ankara, Turkey Phone: +90 312 304 18 98 E-mail:

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http://dx.doi.org/10.4274/jcrpe.2023DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677552PMC
September 2015

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort.

J Clin Endocrinol Metab 2016 Jan 2;101(1):284-92. Epub 2015 Nov 2.

Department of Pediatric Endocrinology and Diabetes (T.G., Z.A., A.B., S.T.), Marmara University, Istanbul 34899, Turkey; Institute of Metabolism and Systems Research (T.G.), University of Birmingham, Birmingham B15 2TT, United Kingdom; Department of Genetics and Genomic Medicine (F.B., J.S., J.C.A.), University College London Institute of Child Health, University College London, London WC1N 1EH, United Kingdom; Department of Pediatric Endocrinology and Diabetes (N.S., F.B., B.K.A., Z.Y.A.), Istanbul Faculty of Medicine, Istanbul University, 34452 Istanbul, Turkey; Clinics of Pediatric Endocrinology (M.N.O., H.D.), Diyarbakir Children's Hospital, 21100 Diyarbakir, Turkey; Clinics of Pediatric Endocrinology (Z.A., S.Y.A.), Dr Sami Ulus Obstetrics and Gynecology, Children's Health and Disease Training and Research Hospital, 06100 Ankara, Turkey; Department of Pediatric Endocrinology and Diabetes (S.D., S.O.), Ege University, 35040 Izmir, Turkey; Department of Pediatric Endocrinology and Diabetes (A.B., E.D.), Gazi University, 06550 Ankara, Turkey; Pediatric Endocrinology Clinic (A.G., M.Y.), Goztepe Educational and Research Hospital, 34810 Istanbul, Turkey; Department of Pediatrics (A.G.), Amasya University Medical Faculty, 05189 Amasya, Turkey; Pediatric Endocrinology Clinic (K.D.), Dr Behçet Uz Children's Hospital, Izmir, Turkey; Department of Pediatric Endocrinology and Diabetes (A.A.), Inonu University, Malatya, Turkey; Clinics of Pediatric Endocrinology (M.B.), Konya Training and Research Hospital, 42100 Konya, Turkey; Department of Pediatric Endocrinology and Diabetes (O.T.), Uludag University, 16059 Bursa, Turkey; Department of Pediatric Endocrinology and Diabetes (G.C.), Eylul University, 35210 Izmir, Turkey; Department of Pediatric Endocrinology and Diabetes (B.Y.), Cukurova University, 01330 Adana, Turkey; Clinics of Pediatric Endocrinology (T.A.), Kanuni Sultan Suleyman Education and Research Hospital, 34303 Istanbul, Turkey; Pediatric Endocrinology Clinic

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https://academic.oup.com/jcem/article-pdf/101/1/284/8920007/
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https://academic.oup.com/jcem/article-lookup/doi/10.1210/jc.
Publisher Site
http://dx.doi.org/10.1210/jc.2015-3250DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701852PMC
January 2016

Capillary bedside blood glucose measurement in neonates: missing a diagnosis of galactosemia.

J Clin Res Pediatr Endocrinol 2015 Mar;7(1):83-5

acettepe University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey. E-mail:

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http://dx.doi.org/10.4274/jcrpe.1805DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439900PMC
March 2015

Turner syndrome and associated problems in Turkish children: a multicenter study.

J Clin Res Pediatr Endocrinol 2015 Mar;7(1):27-36

Gülhane Military Medicine Academy, Department of Pediatric Endocrinology, Ankara, Turkey. E-mail:

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http://dx.doi.org/10.4274/jcrpe.1771DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439889PMC
March 2015

Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.

Eur J Endocrinol 2015 Jun 9;172(6):697-705. Epub 2015 Mar 9.

Departments of Paediatric EndocrinologyGreat Ormond Street Hospital for Children NHS Trust, London WC1N 3JH, UKThe Institute of Child HealthUniversity College London, London WC1N 1EH, UKDepartments of Paediatric EndocrinologyChildren State Hospital, 21100 Diyarbakir, TurkeyInstitute of Biomedical and Clinical ScienceUniversity of Exeter Medical School, Exeter EX2 5DW, UKDepartments of NeonatologyChildren State Hospital, 21100 Diyarbakir, TurkeyDepartment of Medical Biology and GeneticsDicle University, 21100 Diyarbakir, TurkeyFaculty of MedicineUniversity of Southampton, Southampton SO16 6YD, UK Departments of Paediatric EndocrinologyGreat Ormond Street Hospital for Children NHS Trust, London WC1N 3JH, UKThe Institute of Child HealthUniversity College London, London WC1N 1EH, UKDepartments of Paediatric EndocrinologyChildren State Hospital, 21100 Diyarbakir, TurkeyInstitute of Biomedical and Clinical ScienceUniversity of Exeter Medical School, Exeter EX2 5DW, UKDepartments of NeonatologyChildren State Hospital, 21100 Diyarbakir, TurkeyDepartment of Medical Biology and GeneticsDicle University, 21100 Diyarbakir, TurkeyFaculty of MedicineUniversity of Southampton, Southampton SO16 6YD, UK

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http://dx.doi.org/10.1530/EJE-14-0852DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411707PMC
June 2015

Prepubertal unilateral gynecomastia: report of 2 cases.

J Clin Res Pediatr Endocrinol 2014 Dec;6(4):250-3

Diyarbakır Children State Hospital, Clinic of Pediatric Endocrinology, Diyarbakır, Turkey. E-mail:

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http://dx.doi.org/10.4274/Jcrpe.1477DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4293661PMC
December 2014

Familial isolated growth hormone deficiency due to a novel homozygous missense mutation in the growth hormone releasing hormone receptor gene: clinical presentation with hypoglycemia.

J Clin Endocrinol Metab 2014 Dec;99(12):E2730-4

Developmental Endocrinology Research Group (H.D., S.T., M.S., P.S., V.B.A., K.H.), Clinical and Molecular Genetics Unit, Institute of Child Health, University College London, WC1N 1EH London, United Kingdom; Department of Paediatric Endocrinology (H.D., P.S., V.B.A., K.H.), Great Ormond Street Hospital for Children, NHS Foundation Trust, WC1N 3JH London, United Kingdom; Department of Paediatric Endocrinology (H.D., R.T.B., M.N.O.) and Department of Radiology (N.H., A.B.), Diyarbakir Children's State Hospital, 21100 Diyarbakir, Turkey.

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http://dx.doi.org/10.1210/jc.2014-2696DOI Listing
December 2014

Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability.

Hum Mol Genet 2014 Dec 11;23(24):6432-40. Epub 2014 Jul 11.

Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter EX2 5DW, UK, Molecular Genetics Laboratory, Royal Devon and Exeter NHS Foundation Trust, Exeter EX2 5DW, UK.

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http://dx.doi.org/10.1093/hmg/ddu360DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240195PMC
December 2014

Long-term follow-up of children with congenital hyperinsulinism on octreotide therapy.

J Clin Endocrinol Metab 2014 Oct 17;99(10):3660-7. Epub 2014 Jun 17.

Developmental Endocrinology Research Group (H.D., P.S., V.B.A., L.H., K.H.), Clinical and Molecular Genetics Unit, Institute of Child Health, University College London, London WC1N 1EH, United Kingdom; Department of Paediatric Endocrinology (H.D., P.S., V.B.A., L.H., K.H.), Great Ormond Street Hospital for Children, London WC1N 3JH, United Kingdom; and Institute of Biomedical and Clinical Science (S.E.F., S.E.), University of Exeter Medical School, Exeter EX2 5DW, United Kingdom.

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https://academic.oup.com/jcem/article-lookup/doi/10.1210/jc.
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http://dx.doi.org/10.1210/jc.2014-1866DOI Listing
October 2014

Persistent hyperinsulinaemic hypoglycaemia in infancy.

Semin Pediatr Surg 2014 Apr 15;23(2):76-82. Epub 2014 Mar 15.

Department of Developmental Endocrinology Research Group, Clinical and Molecular Genetics Unit, Institute of Child Health, University College London; Department of Paediatric Endocrinology, Great Ormond Street Hospital for Children, London. Electronic address:

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http://dx.doi.org/10.1053/j.sempedsurg.2014.03.005DOI Listing
April 2014

Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism.

PLoS One 2014 19;9(5):e98054. Epub 2014 May 19.

Department of Paediatric Endocrinology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom; Institute of Child Health, University College London, London, United Kingdom.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0098054PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026387PMC
January 2015

Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations.

Eur J Endocrinol 2014 Jun 31;170(6):885-92. Epub 2014 Mar 31.

Departments of NeonatologyPaediatric EndocrinologyGreat Ormond Street Hospital for Children NHS Trust, London WC1N 3JH, UKDevelopmental Endocrinology Research GroupMolecular Genetics Unit, The Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UKDepartments of Paediatric EndocrinologyAnkara Children's Hematology and Oncology Training Hospital, Ankara, TurkeyDepartments of Paediatric EndocrinologyChildren State Hospital, Diyarbakır, TurkeyDepartments of Paediatric EndocrinologyInönü University, Malatya, TurkeyDepartments of Paediatric EndocrinologyYüzüncü Yıl University, Van, TurkeyInstitute of Biomedical and Clinical ScienceUniversity of Exeter Medical School, Exeter EX2 5DW, UKDepartment of Medical Biology and GeneticsDicle University, Diyarbakır, TurkeyDepartments of NeonatologyPaediatric EndocrinologyGreat Ormond Street Hospital for Children NHS Trust, London WC1N 3JH, UKDevelopmental Endocrinology Research GroupMolecular Genetics Unit, The Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UKDepartments of Paediatric EndocrinologyAnkara Children's Hematology and Oncology Training Hospital, Ankara, TurkeyDepartments of Paediatric EndocrinologyChildren State Hospital, Diyarbakır, TurkeyDepartments of Paediatric EndocrinologyInönü University, Malatya, TurkeyDepartments of Paediatric EndocrinologyYüzüncü Yıl University, Van, TurkeyInstitute of Biomedical and Clinical ScienceUniversity of Exeter Medical School, Exeter EX2 5DW, UKDepartment of Medical Biology and GeneticsDicle University, Diyarbakır, Turkey

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http://dx.doi.org/10.1530/EJE-14-0045DOI Listing
June 2014

Oncologic manifestations in children with neurofibromatosis type 1 in Turkey.

Turk J Pediatr 2013 May-Jun;55(3):266-70

Divisions of 1Pediatric Neurology, Department of Pediatrics, Faculty of Medicine, Çukurova University, Adana, Turkey.

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July 2014

Multiple pituitary hormone deficiency due to gunshot injury in a 6-year-old girl.

J Clin Res Pediatr Endocrinol 2013 Sep;5(3):209-11

Diyarbakır Children's State Hospital, Pediatric Endocrinology, Diyarbakır, Turkey. E-mail:

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http://dx.doi.org/10.4274/jcrpe.1027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814539PMC
September 2013

Incidence of type 1 diabetes mellitus in Turkish children from the southeastern region of the country: a regional report.

J Clin Res Pediatr Endocrinol 2013 ;5(2):98-103

Diyarbakır Children State Hospital, Division of Pediatric Endocrinology, Diyarbakır, Turkey.

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http://dx.doi.org/10.4274/Jcrpe.954DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701930PMC
January 2014

The role of the resistive index in Hashimoto's thyroiditis: a sonographic pilot study in children.

Clinics (Sao Paulo) 2012 Nov;67(11):1253-7

Department of Radiology, Medical Faculty, Hacettepe University, Ankara, Turkey.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488981PMC
http://dx.doi.org/10.6061/clinics/2012(11)05DOI Listing
November 2012

17beta-hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17betaHSD3 gene.

J Pediatr Endocrinol Metab 2012 ;25(5-6):561-3

Hacettepe University Faculty of Medicine, Division of Pediatric Endocrinology, Ankara, 06100 Turkey.

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http://dx.doi.org/10.1515/jpem-2012-0009DOI Listing
September 2012

Evaluation of serum kisspeptin levels in girls in the diagnosis of central precocious puberty and in the assessment of pubertal suppression.

J Pediatr Endocrinol Metab 2012 ;25(3-4):313-6

Division of Pediatric Endocrinology, Hacettepe University Medical School, Sihhiye, Ankara, Turkey.

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http://dx.doi.org/10.1515/jpem-2011-0445DOI Listing
July 2012

Vitamin D-deficient rickets mimicking ankylosing spondylitis in an adolescent girl.

Turk J Pediatr 2012 Mar-Apr;54(2):177-9

Division of Paediatric Endocrinology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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August 2012

Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient.

J Pediatr Endocrinol Metab 2011 ;24(1-2):109-12

Department of Pediatric Endocrinology, Hacettepe University, Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.1515/jpem.2011.118DOI Listing
May 2011

GnRH stimulation test in precocious puberty: single sample is adequate for diagnosis and dose adjustment.

J Clin Res Pediatr Endocrinol 2011 23;3(1):12-7. Epub 2011 Feb 23.

Pediatric Endocrinology Unit, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

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http://dx.doi.org/10.4274/jcrpe.v3i1.03DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065310PMC
December 2011