Scientific work

Prof. Dr. Teoman Akçay

103 publications. The source of the information is stated next to each publication.

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  1. Molecular findings of three different male under virilization cases with 47,XXY karyotype

    Endocrine Abstracts, 2014

    DOI 10.1530/endoabs.35.p821 1 citation (OpenAlex) Source: OpenAlex

  2. Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation

    American Journal of Human Genetics, 2013

    DOI 10.1016/j.ajhg.2012.11.017 PMID 23273570 67 citations (Europe PMC) Open-access full textSource: ORCID

  3. Suprasellar mass mimicking a hypothalamic glioma in a patient with a complete PROP1 deletion

    European Journal of Medical Genetics, 2013

    DOI 10.1016/j.ejmg.2013.06.006 PMID 23831233 9 citations (Europe PMC) Source: ORCID

  4. Transient neonatal diabetes mellitus in a Turkish patient with three novel homozygous variants in the ZFP57 gene

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2013

    DOI 10.4274/jcrpe.928 PMID 23748067 4 citations (Europe PMC) Open-access full textSource: ORCID

  5. MSX1 intronic CA repeat polymorphism is associated with non-syndromic cleft lip with/without palate in a Turkish family.

    Disease and Molecular Medicine, 2013

    DOI 10.5455/dmm.20131024011602 1 citation (OpenAlex) Open-access full textSource: OpenAlex

  6. Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: Novel mutations in TRPM6 and CLDN16 genes

    Nephrology Dialysis Transplantation, 2012

    DOI 10.1093/ndt/gfr300 PMID 21669885 25 citations (Europe PMC) Open-access full textSource: ORCID

  7. Congenital hyperinsulinism and cardiomyopathy

    Fetal and Pediatric Pathology, 2012

    DOI 10.3109/15513815.2012.656831 PMID 22413945 1 citation (Europe PMC) Open-access full textSource: ORCID

  8. Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase

    Orphanet Journal of Rare Diseases, 2012

    DOI 10.1186/1750-1172-7-25 PMID 22583614 30 citations (Europe PMC) Open-access full textSource: ORCID

  9. Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy

    European Journal of Endocrinology, 2012

    DOI 10.1530/eje-11-0140 PMID 22004907 27 citations (Europe PMC) Open-access full textSource: ORCID

  10. Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individuals

    Journal of Clinical Endocrinology and Metabolism, 2012

    DOI 10.1210/jc.2011-3169 PMID 22549935 98 citations (Europe PMC) Open-access full textSource: ORCID

  11. Regional dispersion of non-syndromic cleft lip withwithout palate Turkish children patients and possible geographical effects

    Clinical and Experimental Health Sciences, 2012

    DOI 10.5455/musbed.20121231011251 4 citations (OpenAlex) Open-access full textSource: OpenAlex

  12. İzole dudak-damak yarıklı Türk çocuk hastaların bölgesel dağılımı ve olası bölgesel etkiler

    DergiPark (Istanbul University), 2012

    Source: OpenAlex

  13. Cognitive and psychosocial development in children with familial hypomagnesaemia

    Magnesium Research, 2011

    DOI 10.1684/mrh.2011.0278 PMID 21489917 3 citations (Europe PMC) Open-access full textSource: ORCID

  14. Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees

    Journal of Clinical Endocrinology and Metabolism, 2011

    DOI 10.1210/jc.2010-1906 PMID 21252247 44 citations (Europe PMC) Open-access full textSource: ORCID

  15. Investigation of the MMP1 and MMP3 promoter polymorphisms in temporomandibular joint disorder,Temporomandibular baǧlantı bozukluklarnda MMP1 ve MMP3 promotor polimorfizmlerinin incelenmesi

    Journal of Cell and Molecular Biology, 2011

    Source: ORCID

  16. Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet-Biedl syndrome

    Clinical Dysmorphology, 2011

    DOI 10.1097/mcd.0b013e32833fd528 PMID 20966747 16 citations (Europe PMC) Open-access full textSource: ORCID

  17. Serum alkaline phosphatase levels in healthy children and evaluation of alkaline phosphatase z-scores in different types of rickets

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2011

    DOI 10.4274/jcrpe.v3i1.02 PMID 21448327 98 citations (Europe PMC) Open-access full textSource: ORCID

  18. Circulating insulin-like growth factor binding protein-4 (IGFBP-4) is not regulated by parathyroid hormone and vitamin D in vivo: Evidence from children with rickets

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2010

    DOI 10.4274/jcrpe.v2i1.17 PMID 21274331 22 citations (Europe PMC) Open-access full textSource: ORCID

  19. Content analysis of food advertising in Turkish television

    Journal of Paediatrics and Child Health, 2010

    DOI 10.1111/j.1440-1754.2010.01753.x PMID 20546099 18 citations (Europe PMC) Open-access full textSource: ORCID

  20. Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations

    European Journal of Endocrinology, 2010

    DOI 10.1530/eje-09-0861 PMID 20164212 114 citations (Europe PMC) Open-access full textSource: ORCID

  21. Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia

    Bone, 2010

    DOI 10.1016/j.bone.2009.09.016 PMID 19796717 43 citations (Europe PMC) Open-access full textSource: ORCID

  22. Molecular approach to tooth decays,Diş çürüklerinin oluşumuna moleküler yaklaşım

    Journal of Cell and Molecular Biology, 2010

    Source: ORCID

  23. Recessive versus imprinted disorder: Consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib

    European Journal of Endocrinology, 2010

    DOI 10.1530/eje-10-0348 PMID 20538864 4 citations (Europe PMC) Open-access full textSource: ORCID

  24. T4 plus T3 treatment in children with hypothyroidism and inappropriately elevated thyroid-stimulating hormone despite euthyroidism on T4 treatment

    Hormone Research in Paediatrics, 2010

    DOI 10.1159/000277627 PMID 20190547 10 citations (Europe PMC) Open-access full textSource: ORCID

  25. Irradiation-Induced Growth Hormone Neurosecretory Disfunction In ALL Patients

    Blood, 2010

    DOI 10.1182/blood.v116.21.4329.4329 Source: OpenAlex

  26. EVALUATION OF GROWTH PARAMETERS AND PUBERTAL CONDITIONS IN PATIENTS WITH BETA-THALASSEMIA MAJOR

    Bursa Uludag University - AVESIS, 2010

    Source: OpenAlex

  27. Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor

    Journal of Clinical Endocrinology and Metabolism, 2009

    DOI 10.1210/jc.2009-0551 PMID 19755480 100 citations (Europe PMC) Open-access full textSource: ORCID

  28. Puberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hair

    European Journal of Endocrinology, 2009

    DOI 10.1530/eje-08-0632 PMID 18996963 11 citations (Europe PMC) Open-access full textSource: ORCID

  29. The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children

    European Journal of Pediatrics, 2009

    DOI 10.1007/s00431-008-0876-x PMID 19043735 29 citations (Europe PMC) Open-access full textSource: ORCID

  30. Constitutional Growth Delay Pattern of Growth in Velo-Cardio-Facial Syndrome: Longitudinal follow up and final height of two cases

    Journal of Clinical Research in Pediatric Endocrinology, 2008

    DOI 10.4008/jcrpe.v1i1.13 PMID 21318064 4 citations (Europe PMC) Open-access full textSource: OpenAlex

  31. Alendronate treatment in children with osteogenesis imperfecta.

    Indian pediatrics, 2008

    PMID 18310788 12 citations (Europe PMC) Source: ORCID

  32. Erratum: Evaluation of diagnosis and treatment results in children with grave's disease with emphasis on the pubertal status of patients (Journal of Pediatric Endocrinology and Metabolism (2008) vol. 21 (8) (745-751))

    Journal of Pediatric Endocrinology and Metabolism, 2008

    Source: ORCID

  33. Evaluation of diagnosis and treatment results in children with graves' disease with emphasis on the pubertal status of patients

    Journal of Pediatric Endocrinology and Metabolism, 2008

    DOI 10.1515/jpem.2008.21.8.745 PMID 18825874 13 citations (Europe PMC) Source: ORCID

  34. Significance of acanthosis nigricans in childhood obesity

    Journal of Paediatrics and Child Health, 2008

    DOI 10.1111/j.1440-1754.2007.01272.x PMID 18476925 35 citations (Europe PMC) Open-access full textSource: ORCID

  35. Alopecia areata: A new association with resistance to thyroid hormones in a family with novel TRb mutation

    Dspace Repository (Marmara Üniversitesi), 2008

    Open-access full textSource: OpenAlex

  36. Prognostic significances of oxidative DNA damage evaluated by 8-hydroxy-deoxyguanosine and antioxidant enzymes in patients undergoing resection of gastric and colon carcinoma.

    Neoplasma, 2007

    PMID 17319786 15 citations (Europe PMC) Source: ORCID

  37. Hypophysis hyperplasia and growth hormon deficiency that immitate hypophysis macro adenoma secondary to hypothyroidism,Hipotiroidiye ikincil hipofiz makroadenomunu taklit eden hipofiz hiperplazisi ve büyüme hormonu eksikliǧi

    Goztepe Tip Dergisi, 2006

    Source: ORCID

  38. Severe diabetic ketoacidosis: Hyperventilation or relative hypoventilation [1]

    Pediatric Critical Care Medicine, 2006

    DOI 10.1097/01.pcc.0000216417.23633.be PMID 16682898 Open-access full textSource: ORCID

  39. Factors associated with obesity in children with hypothalamo-pituitary tumors

    Dspace Repository (Marmara Üniversitesi), 2006

    Open-access full textSource: OpenAlex

  40. Evaluation of patients with Graves' disease

    Bursa Uludag University - AVESIS, 2006

    Source: OpenAlex

  41. Fahr disease,Fahr hastaliǧi

    Goztepe Tip Dergisi, 2006

    Source: ORCID

  42. The relationship between antioxidant enzymes and bladder cancer.

    PubMed, 2005

    PMID 16059648 10 citations (Europe PMC) Source: OpenAlex

  43. DNA damage, DNA susceptibility to oxidation and glutathione level in women with polycystic ovary syndrome.

    Scandinavian journal of clinical and laboratory investigation, 2005

    DOI 10.1080/00365510500375263 PMID 16509054 49 citations (Europe PMC) Source: ORCID

  44. Oxidative protein damage parameters in plasma in chronic experimental diabetes in rats.

    European journal of medical research, 2003

    PMID 12911868 12 citations (Europe PMC) Source: ORCID

  45. Levels of plasma vitamin E, vitamin C, TBARS, and cholesterol in male patients with colorectal tumors.

    Biochemistry. Biokhimiia, 2003

    DOI 10.1023/a:1023010418230 PMID 12733974 18 citations (Europe PMC) Source: ORCID

  46. Asemptomatik Türk çocuklarında idrarla kalsiyum atılımı ve idiyopatik hiperkalsiüri sıklığı

    2002

    Source: OpenAlex

  47. Zinc deficiency,Çinko eksikligi

    SENDROM, 2001

    Source: ORCID

  48. Effect of alpha-lipoic acid supplementation on oxidative protein damage in the streptozotocin-diabetic rat.

    Research in experimental medicine. Zeitschrift fur die gesamte experimentelle Medizin einschliesslich experimenteller Chirurgie, 2000

    DOI 10.1007/s004330050007 PMID 10743682 26 citations (Europe PMC) Source: ORCID

  49. Changes in bone turnover and deoxypyridinoline levels in epileptic patients.

    Clinical chemistry and laboratory medicine, 2000

    DOI 10.1515/cclm.2000.008 PMID 10774961 18 citations (Europe PMC) Source: ORCID

  50. Oxidative protein damage in plasma of type 2 diabetic patients.

    Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 2000

    DOI 10.1055/s-2007-978584 PMID 10727013 78 citations (Europe PMC) Source: ORCID