Hasil Pencarian - Hüseyin DEMİRBİLEK

Perbaiki Hasil
  1. 1
    The ımportance of art therapy ın the qualıty of lıfe ın hemodıalysıs patıents

    The ımportance of art therapy ın the qualıty of lıfe ın hemodıalysıs patıents oleh Ergün Parmaksız, Hüseyin Demirbilek

    Diterbitkan 2020-10-01
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  2. 2
    Cystoscopy-Guided Laparoscopic Excision of Prostatic Utricle: Report of a Case

    Cystoscopy-Guided Laparoscopic Excision of Prostatic Utricle: Report of a Case oleh Ozlem Boybeyi-Turer, Huseyin Demirbilek, Tutku Soyer

    Diterbitkan 2020-01-01
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  3. 3
    The role of the resistive index in Hashimoto's thyroiditis: a Sonographic pilot study in children

    The role of the resistive index in Hashimoto's thyroiditis: a Sonographic pilot study in children oleh Basar Sarikaya, Huseyin Demirbilek, Deniz Akata, Nurgun Kandemir

    Diterbitkan 2012-11-01
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  4. 4
    The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism

    The Genetic and Molecular Mechanisms of Congenital Hyperinsulinism oleh Sonya Galcheva, Hüseyin Demirbilek, Sara Al-Khawaga, Khalid Hussain

    Diterbitkan 2019-02-01
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  5. 5
    Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p. Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother

    Type A insulin resistance syndrome due to a novel heterozygous c.3486_3503del (p. Arg1163_Ala1168del) INSR gene mutation in an adolescent girl and her mother oleh Serkan Bilge Koca, Melike Ataseven Kulali, Başak Güğüş, Hüseyin Demirbilek

    Diterbitkan 2024-02-01
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  6. 6
    Severe hyponatremia and repeated intestinal resections for intestinal dysmotility mimicking congenital aganglionic megacolon due to delay in the diagnosis of congenital hypothyroidism

    Severe hyponatremia and repeated intestinal resections for intestinal dysmotility mimicking congenital aganglionic megacolon due to delay in the diagnosis of congenital hypothyroid... oleh Gonul Buyukyilmaz, Demet Baltu, Tutku Soyer, Murat Tanyıldız, Huseyin Demirbilek

    Diterbitkan 2016-12-01
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  7. 7
    Ion Transporters, Channelopathies, and Glucose Disorders

    Ion Transporters, Channelopathies, and Glucose Disorders oleh Huseyin Demirbilek, Sonya Galcheva, Dogus Vuralli, Sara Al-Khawaga, Khalid Hussain

    Diterbitkan 2019-05-01
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  8. 8
    Çocukluk çağında nadir görülen idiyopatik hipoparatiroidizm ve bazal gangliyon kalsifikasyonu birlikteliği: Fahr hastalığı

    Çocukluk çağında nadir görülen idiyopatik hipoparatiroidizm ve bazal gangliyon kalsifikasyonu birlikteliği: Fahr hastalığı oleh Rıza Taner BARAN, Hüseyin DEMİRBİLEK, Serpil BARAN, Mesut PARLAK, Eda PARLAK

    Diterbitkan 2018-03-01
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  9. 9
    Neurofibromatosis type 1 and autoimmune hyperthyroidism in a 10,5 years-old girl

    Neurofibromatosis type 1 and autoimmune hyperthyroidism in a 10,5 years-old girl oleh Huseyin Demirbilek, Serhan Kupeli, Mehmet Nuri Ozbek, Semra Saygi, Aysen Turedi Yildirim

    Diterbitkan 2013-08-01
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  10. 10
    Onbuçuk yaşındaki bir kız çocuğunda Nörofibromatoziz tip 1 ve otoimmün hipertiroidizm birlikteliği

    Onbuçuk yaşındaki bir kız çocuğunda Nörofibromatoziz tip 1 ve otoimmün hipertiroidizm birlikteliği oleh Hüseyin DEMİRBİLEK, Serhan KÜPELİ, Mehmet Nuri ÖZBEK, Semra SAYGI, Aysen Türedi YILDIRIM

    Diterbitkan 2013-12-01
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  11. 11
    Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism

    Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism oleh Muhammet Asena, Meliha Demiral, Edip Unal, Murat Öcal, Hüseyin Demirbilek, Mehmet Nuri Özbek

    Diterbitkan 2020-09-01
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  12. 12
    Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the <italic>GLI2</italic> Gene

    Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the <italic... oleh Meliha Demiral, Hüseyin Demirbilek, Edip Unal, Ceren Damla Durmaz, Serdar Ceylaner, Mehmet Nuri Özbek

    Diterbitkan 2020-09-01
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  13. 13
    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

    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 oleh Meliha Demiral, Edip Unal, Birsen Baysal, Rıza Taner Baran, Hüseyin Demirbilek, Mehmet Nuri Özbek

    Diterbitkan 2020-09-01
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  14. 14
    Continuous Hepatogonodal and Splenogonogal Fusion: A Rare Cause of Bilateral Intra-Abdominal Testis in an 18-Month-Old Boy

    Continuous Hepatogonodal and Splenogonogal Fusion: A Rare Cause of Bilateral Intra-Abdominal Testis in an 18-Month-Old Boy oleh Gül Durmuş, Ozlem Boybeyi-Turer, Hatice Nursun Özcan, Onur Gözmen, Hüseyin Demirbilek, Tutku Soyer

    Diterbitkan 2022-01-01
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  15. 15
    Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation

    Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation oleh Emregül Işık, Hüseyin Demirbilek, Jayne A. Houghton, Sian Ellard, Sarah E. Flanagan, Khalid Hussain

    Diterbitkan 2019-03-01
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  16. 16
    Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes

    Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes oleh Edip Unal, Meliha Demiral, Birsen Baysal, Mehmet Ağın, Elif Gökçe Devecioğlu, Hüseyin Demirbilek, Mehmet Nuri Özbek

    Diterbitkan 2021-03-01
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  17. 17
    Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year

    Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year oleh Şervan Özalkak, Meliha Demiral, Edip Ünal, Funda Feryal Taş, Hüseyin Onay, Hüseyin Demirbilek, Mehmet Nuri Ozbek

    Diterbitkan 2023-09-01
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  18. 18
    Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report

    Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report oleh Şervan Özalkak, Ruken Yıldırım, Selma Tunç, Edip Ünal, Funda Feryal Taş, Hüseyin Demirbilek, Mehmet Nuri Özbek

    Diterbitkan 2022-06-01
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  19. 19
    Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism.

    Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism. oleh Ved Bhushan Arya, Senthil Senniappan, Huseyin Demirbilek, Syeda Alam, Sarah E Flanagan, Sian Ellard, Khalid Hussain

    Diterbitkan 2014-01-01
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  20. 20
    The effects of the covid-19 pandemic on puberty: a cross-sectional, multicenter study from Turkey

    The effects of the covid-19 pandemic on puberty: a cross-sectional, multicenter study from Turkey oleh Gul Yesiltepe Mutlu, Elif Eviz, Belma Haliloglu, Heves Kirmizibekmez, Fatma Dursun, Servan Ozalkak, Atilla Cayir, Beste Yuksel Sacli, Mehmet Nuri Ozbek, Huseyin Demirbilek, Sukru Hatun

    Diterbitkan 2022-08-01
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