Works matching AU Yüksel, Bilgin

Results: 45

Pulmonary hypertension, heart failure and neutropenia due to diazoxide therapy.

Published in:

Advances in Therapy, 2008, v. 25, n. 5, p. 515, doi. 10.1007/s12325-008-0049-3

By:

Yildizdas, Dincer;
Erdem, Sevcan;
Küçükosmanoǧlu, Osman;
Yilmaz, Mustafa;
Yüksel, Bilgin

Publication type:

Article

CAN BRAIN EDEMA BE PREDICTED WITH OPTIC NERVE SHEATH DIAMETER MEASUREMENT IN CASES WITH DIABETIC KETOACIDOSIS?: A PRELIMINARY STUDY.

Published in:

Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi, 2022, v. 85, n. 2, p. 270, doi. 10.26650/IUITFD.972539

By:

KENDİR, Özlem TOLU;
YILMAZ, Hayri Levent;
ERKEK, Nilgün;
GÖKAY, Sinem SARI;
YILDIZDAŞ, Rıza Dinçer;
YÜKSEL, Bilgin

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:

Turan, Ihsan;
Demir, Korcan;
Mengen, Eda;
Kotan, Leman Damla;
Gürbüz, Fatih;
Yüksel, Bilgin;
Topaloglu, Ali Kemal

Publication type:

Article

The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development.

Published in:

Hormone Research in Paediatrics, 2013, v. 80, n. 3, p. 163, doi. 10.1159/000354086

By:

Yüksel, Bilgin;
Kulle, alexandra E.;
Gürbüz, Fatih;
Welzel, Maik;
Kotan, Damla;
Mengen, Eda;
Holterhus, Paul-Martin;
Topaloğlu, ali Kemal;
Grötzinger, Joachim;
Riepe, Felix G.

Publication type:

Article

A case of ambiguous genitalia with unilateral amelia and unilateral peromelia of the upper limbs.

Published in:

Pediatrics International, 1997, v. 39, n. 5, p. 631, doi. 10.1111/j.1442-200X.1997.tb03656.x

By:

TEMOĈIN, A. KüBRA;
YüKSEL, BILGIN;
TUNCER, RECEP;
ÖZER, GüLER;
ZORLUDEMIR, üNAL

Publication type:

Article

Growth and development of 280 hypothyroids patients at diagnosis.

Published in:

Pediatrics International, 1995, v. 37, n. 2, p. 145, doi. 10.1111/j.1442-200X.1995.tb03286.x

By:

ÖZER, GÜLER;
YÜKSEL, BİLGİN;
KOZANOǦLU, MUSTAFA;
SERBEST, MURAT;
TURGUT, ÇİǦDEM

Publication type:

Article

Clinical features of Bardet-Biedl syndrome.

Published in:

Pediatrics International, 1995, v. 37, n. 2, p. 233, doi. 10.1111/j.1442-200X.1995.tb03306.x

By:

ÖZER, GÜLER;
YÜKSEL, BİLGIN;
SÜLEYMANOVA, DİLARA;
ALHAN, EMRE;
DEMİRCAN, NİHAL;
ÖNENLİ, NESLİHAN

Publication type:

Article

Tuberculous meningitis in children.

Published in:

Pediatrics International, 1994, v. 36, n. 5, p. 480, doi. 10.1111/j.1442-200X.1994.tb03229.x

By:

ALTUNBAŞAK, ŞAKIR;
ALHAN, EMRE;
BAYTOK, VILDAN;
AKSARAY, NECMI;
YÜKSEL, BILGIN;
ÖNENLI, NESLIHAN

Publication type:

Article

Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype.

Published in:

Journal of Bone & Mineral Research, 2003, v. 18, n. 12, p. 2095, doi. 10.1359/jbmr.2003.18.12.2095

By:

Chong, Belinda;
Hegde, Madhuri;
Fawkner, Matthew;
Simonet, Scott;
Cassinelli, Hamilton;
Coker, Mahmut;
Kanis, John;
Seidel, Joerg;
Tau, Cristina;
Tüysüz, Beyhan;
Yüksel, Bilgin;
Love, Donald;
Cundy, Tim

Publication type:

Article

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.

Published in:

Endocrine (1355008X), 2015, v. 49, n. 2, p. 479, doi. 10.1007/s12020-014-0498-1

By:

Baş, Firdevs;
Uyguner, Z.;
Darendeliler, Feyza;
Aycan, Zehra;
Çetinkaya, Ergun;
Berberoğlu, Merih;
Şiklar, Zeynep;
Öcal, Gönül;
Darcan, Şükran;
Gökşen, Damla;
Topaloğlu, Ali;
Yüksel, Bilgin;
Özbek, Mehmet;
Ercan, Oya;
Evliyaoğlu, Olcay;
Çetinkaya, Semra;
Şen, Yaşar;
Atabek, Emre;
Toksoy, Güven;
Aydin, Banu

Publication type:

Article

P160 - MUTATIONS ANALYSIS OF 21 HYDROXYLASE ENZYME DEFICIENCIES IN PATIENTS WITH CONGENITAL ADRENAL HYPERPLAZIA IN ÇUKUROVA REGION OF TURKEY.

Published in:

2012

By:

YENİLMEZ, Ebru DÜNDAR;
BOĞA, Duygu DÜZGÜNCE;
TULİ, Abdullah;
YÜKSEL, Bilgin

Publication type:

Abstract

P160 - ÇUKUROVA BÖLGESİNDEKİ KONJENİTAL ADRENAL HİPERPLAZİLİ HASTALARDA 21 HİDROKSİLAZ ENZİM EKSİKLİKLERİNE YOL AÇAN MUTASYONLARIN ANALİZİ.

Published in:

Turkish Journal of Biochemistry / Turk Biyokimya Dergisi, 2012, v. 37, n. S1, p. 301

By:

YENİLMEZ, Ebru DÜNDAR;
BOĞA, Duygu DÜZGÜNCE;
TULİ, Abdullah;
YÜKSEL, Bilgin

Publication type:

Article

Congenital Lipoid Adrenal Hyperplasia: Functional Characterization of Three Novel Mutations in the STAR Gene.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 3, p. 1301, doi. 10.1210/jc.2009-1176

By:

Bens, Susanne;
Mohn, Angelika;
Yüksel, Bilgin;
Kulle, Alexandra E.;
Michalek, Matthias;
Chiarelli, Franco;
Özbek, Mehmet Nuri;
Leuschner, Ivo;
Grötzinger, Joachim;
Holterhus, Paul-Martin;
Riepe, Felix G.

Publication type:

Article

Serebral palsili hastaların klinik bulguları ve kemik mineral metabolizmalarının değerlendirilmesi.

Published in:

Cocuk Sagligi ve Hastaliklari Dergisi, 2015, v. 58, n. 4, p. 140

By:

Yeşilmen, Mehmet Can;
Hergüner, Mihriban Özlem;
Yüksel, Bilgin;
Altunbaşak, Şakir;
İncecik, Faruk;
Mert, Gülen Gül;
Aynacı, Eser;
Besen, Şeyda;
Haytoğlu, Zeliha

Publication type:

Article

Unusual and early onset IPEX syndrome: a case report.

Published in:

Turkish Journal of Pediatrics, 2019, v. 61, n. 4, p. 580, doi. 10.24953/turkjped.2019.04.015

By:

Doğruel, Dilek;
Gürbüz, Fatih;
Turan, İhsan;
Altıntaş, Derya Ufuk;
Yılmaz, Mustafa;
Yüksel, Bilgin

Publication type:

Article

Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations.

Published in:

Turkish Journal of Pediatrics, 2017, v. 59, n. 4, p. 434, doi. 10.24953/turkjped.2017.04.010

By:

Şeker-Yılmaz, Berna;
Kör, Deniz;
Derya Bulut, Fatma;
Yüksel, Bilgin;
Karabay-Bayazıt, Aysun;
Kemal Topaloğlu, Ali;
Ceylaner, Gülay;
Önenli-Mungan, Neslihan

Publication type:

Article

Relationship between metabolic control and neurocognitive functions in children diagnosed with type I diabetes mellitus before and after 5 years of age.

Published in:

Turkish Journal of Pediatrics, 2012, v. 54, n. 4, p. 352

By:

Tolu-Kendir, Özlem;
Kiriş, Nurcihan;
Temiz, Fatih;
Gürbüz, Fatih;
Önenli-Mungan, Neslihan;
Topaloğlu, Ali Kemal;
Yüksel, Bilgin

Publication type:

Article

EV TİPİ MEKANİK VENTİLATÖR İLE İZLENEN ÇOCUK HASTALARDA DÜŞÜK KEMİK MİNERAL DANSİTE SIKLIĞI VE RİSK FAKTÖRLERİ.

Published in:

Journal of Pediatric Emergency & Intensive Care Medicine / Çocuk Acil ve Voğun Bakım Dergisi, 2018, v. 5, p. 195

By:

Tolunay, İlknur;
Yıldızdaş, Dinçer;
Horoz, Özden Özgür;
Yüksel, Bilgin;
Turan, İhsan;
Melek, Engin;
Atmış, Bahriye

Publication type:

Article

Ev Tipi Vantilatör ile İzlenen Trakeostomili Hastalarda Ürolitiazis Sıklığı ve Risk Faktörleri.

Published in:

Journal of Pediatric Emergency & Intensive Care Medicine / Çocuk Acil ve Voğun Bakım Dergisi, 2017, v. 4, n. 3, p. 92, doi. 10.4274/cayd.96158

By:

Tolunay, İlknur;
Yıldızdaş, R. Dinçer;
Horoz, Özden Özgür;
Melek, Engin;
Atmış, Bahriye;
Yüksel, Bilgin;
Turan, İhsan

Publication type:

Article

Long-term Impact of Continuous Glucose Monitoring Assistance on Glycemic Control in Children and Adolescents with Type 1 Diabetes Following the 2023 Kahramanmaras Earthquake.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2025, v. 17, n. 2, p. 161, doi. 10.4274/jcrpe.galenos.2024.2024-9-9

By:

Tarçın, Gürkan;
Ataş, Nurgül;
Yaşar, Mevra;
Şahin, Kadriye Cansu;
Trabzon, Gül;
Dündar, İsmail;
Çiçek, Dilek;
Balkı, Hanife Gül;
Manyas, Hayrullah;
Bitkay, Abdurrahman;
Celiloğlu, Can;
Dilek, Semine Özdemir;
Kılıç, Sümeyra;
Kilimci, Duygu Düzcan;
Ata, Aysun;
Çamtosun, Emine;
Mengen, Eda;
Karaoğlan, Murat;
Yüksel, Bilgin;
Uçaktürk, Seyit Ahmet

Publication type:

Article

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 2, p. 180, doi. 10.4274/jcrpe.galenos.2020.2020.0216

By:

Savaş-Erdeve, Şenay;
Aycan, Zehra;
Çetinkaya, Semra;
Öztürk, Ayşe Pınar;
Baş, Firdevs;
Poyrazoğlu, Şükran;
Darendeliler, Feyza;
Özsu, Elif;
Şıklar, Zeynep;
Demiral, Meliha;
Unal, Edip;
Özbek, Mehmet Nuri;
Gürbüz, Fatih;
Yüksel, Bilgin;
Evliyaoğlu, Olcay;
Akyürek, Nesibe;
Berberoğlu, Merih

Publication type:

Article

Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years' Experience and Challenges.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 4, p. 347, doi. 10.4274/jcrpe.galenos.2020.2020.0009

By:

Gürbüz, Fatih;
Alkan, Murat;
Çelik, Gonca;
Bişgin, Atıl;
Çekin, Necmi;
Ünal, İlker;
Topaloğlu, Ali Kemal;
Zorludemir, Ünal;
Avcı, Ayşe;
Yüksel, Bilgin

Publication type:

Article

Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 3, p. 261, doi. 10.4274/jcrpe.galenos.2020.2019.0191

By:

Bulut, Fatma Derya;
Dilek, Semine Özdemir;
Kotan, Damla;
Mengen, Eda;
Gürbüz, Fatih;
Yüksel, Bilgin

Publication type:

Article

Efficiency of Single Dose of Tolvaptan Treatment During the Triphasic Episode After Surgery for Craniopharyngioma.

Published in:

2019

By:

Gürbüz, Fatih;
Taştan, Mehmet;
Turan, İhsan;
Yüksel, Bilgin

Publication type:

Case Study

Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2019, v. 11, n. 1, p. 94, doi. 10.4274/jcrpe.galenos.2018.2018.0134

By:

Kışla Ekinci, Rabia Miray;
Gürbüz, Fatih;
Balcı, Sibel;
Bişgin, Atıl;
Taştan, Mehmet;
Yüksel, Bilgin;
Yılmaz, Mustafa

Publication type:

Article

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 2, p. 95, doi. 10.4274/jcrpe.3908

By:

Akkuş, Gamze;
Kotan, Leman Damla;
Durmaz, Erdem;
Mengen, Eda;
Turan, İhsan;
Ulubay, Ayça;
Gürbüz, Fatih;
Yüksel, Bilgin;
Tetiker, Tamer;
Topaloğlu, A. Kemal

Publication type:

Article

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2016, p. 496, doi. 10.4274/jcrpe.3065

By:

Gürbüz, Fatih;
Yüksel, Bilgin;
Topaloğlu, Ali Kemal

Publication type:

Article

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis.

Published in:

2016

By:

Gürbüz, Fatih;
Ceylaner, Serdar;
Topaloğlu, Ali Kemal;
Yüksel, Bilgin

Publication type:

Letter to the Editor

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, n. 2, p. 125, doi. 10.4274/jcrpe.3248

By:

Kotan, Leman Damla;
Cooper, Charlton;
Darcan, Şükran;
Carr, Ian M.;
Özen, Samim;
Yi Yan;
Hamedani, Mohammad K.;
Gürbüz, Fatih;
Mengen, Eda;
Turan, İhsan;
Ulubay, Ayça;
Akkuş, Gamze;
Yüksel, Bilgin;
Kemal Topaloğlu, A.;
Leygue, Etienne

Publication type:

Article

Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, p. 17

By:

Ulubay, Ayça;
Kotan, L. Damla;
Cooper, Charlton;
Darcan, Şükran;
Carr, Ian M.;
Özen, Samim;
Yi Yan;
Hamedani, Mohammad K.;
Gürbüz, Fatih;
Mengen, Eda;
Turan, İhsan;
Akkuş, Gamze;
Yüksel, Bilgin;
Leygue, Etienne;
Topaloğlu, A. Kemal

Publication type:

Article

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis.

Published in:

2016

By:

Gürbüz, Fatih;
Yüreğir, Özge Özalp;
Ceylaner, Serdar;
Topaloğlu, Ali Kemal;
Yüksel, Bilgin

Publication type:

Letter to the Editor

Wolcott-Rallison Syndrome.

Published in:

2015

By:

Gürbüz, Fatih;
Yüksel, Bilgin;
Topaloğlu, Ali Kemal

Publication type:

Abstract

Crouzon Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis.

Published in:

2015

By:

Gürbüz, Fatih;
Ceylaner, Serdar;
Topaloğlu, Ali Kemal;
Yüksel, Bilgin

Publication type:

Abstract

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis.

Published in:

2015

By:

Gürbüz, Fatih;
Yüreğir, Özge Özalp;
Ceylaner, Serdar;
Topaloğlu, Ali Kemal;
Yüksel, Bilgin

Publication type:

Abstract

Wolcott-Rallison Syndrome.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 84

By:

Gürbüz, Fatih;
Yüksel, Bilgin;
Topaloğlu, Ali Kemal

Publication type:

Article

Crouzon Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 83

By:

Gürbüz, Fatih;
Ceylaner, Serdar;
Topaloğlu, Ali Kemal;
Yüksel, Bilgin

Publication type:

Article

A Novel GH1 Functional Mutation in a Family with Isolated Growth Hormone Deficiency.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 13

By:

Gürbüz, Fatih;
Yüksel, Bilgin;
Bişgin, Atıl;
Mengen, Eda;
Topalo287;lu, Ali Kemal

Publication type:

Article

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2012, v. 4, n. 3, p. 121, doi. 10.4274/Jcrpe.725

By:

Gurbuz, Fatih;
Damla Kotan, L.;
Mengen, Eda;
Şıklar, Zeynep;
Berberoğlu, Merih;
Dokmetaş, Sebila;
Kılıclı, Mehmet Fatih;
Güven, Ayla;
Kirel, Birgül;
Saka, Nurçin;
Poyrazoğlu, Şükran;
Cesur, Yaşar;
Doğan, Murat;
Özen, Samim;
Nuri Özbek, Mehmet;
Demirbilek, Hüseyin;
Burcu Kekil, M.;
Temiz, Fatih;
Mungan, NeslihanÖnenli;
Yüksel, Bilgin

Publication type:

Article

Vitamin D Deficiency in Obsessive--Compulsive Disorder Patients with Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infections: A Case Control Study.

Published in:

Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2016, v. 53, n. 1, p. 33, doi. 10.5152/npa.2015.8763

By:

ÇELİK, Gonca;
TAŞ, Didem;
TAHİROĞLU, Ayşegül;
AVCI, Ayşe;
YÜKSEL, Bilgin;
ÇAM, Perihan

Publication type:

Article

Mosaic Isodicentric Y Chromosome in a Patient with Mixed Gonadal Dysgenesis.

Published in:

Erciyes Medical Journal / Erciyes Tip Dergisi, 2014, v. 36, n. 4, p. 177, doi. 10.5152/etd.2014.5663

By:

Yılmaz, Zerrin;
Yüksel, Bilgin;
Özer, Özge;
Şahin, Feride İffet

Publication type:

Article

Optimal timing of repeat thyroid fine-needle aspiration biopsy.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2025, v. 38, n. 5, p. 494, doi. 10.1515/jpem-2024-0594

By:

Cay, Mevra;
Turan, Ihsan;
Mengen, Eda;
Çimen, Ayse Merve;
Celebi, Şükriye Tuğçe;
Yüksel, Bilgin

Publication type:

Article

Changes in the presentation of newly diagnosed type 1 diabetes in children during the COVID-19 pandemic in a tertiary center in Southern Turkey.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 10, p. 1303, doi. 10.1515/jpem-2021-0287

By:

Dilek, Semine Özdemir;
Gürbüz, Fatih;
Turan, İhsan;
Celiloğlu, Can;
Yüksel, Bilgin

Publication type:

Article

The first report of cabergoline-induced immune hemolytic anemia in an adolescent with prolactinoma.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 1/2, p. 159, doi. 10.1515/jpem-2013-0151

By:

Gürbüz, Fatih;
Yağcı-Küpeli, Begül;
Kör, Yılmaz;
Yüksel, Bilgin;
Zorludemir, Suzan;
Gürbüz, Berrak Bilginer;
Küpeli, Serhan

Publication type:

Article

Novel Growth Hormone Receptor Gene Mutation in a Patient with Laron Syndrome.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2010, v. 23, n. 4, p. 407, doi. 10.1515/jpem.2010.064

By:

Arman, Ahmet;
Yüksel, Bilgin;
Coker, Ajda;
Sarioz, Ozlem;
Temiz, Fatih;
Topaloglu, Ali Kemal

Publication type:

Article

Thyroid Hormone Levels and their Relationship to Survival in Children with Bacterial Sepsis and Septic Shock.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2004, v. 17, n. 10, p. 1435, doi. 10.1515/jpem.2004.17.10.1435

By:

Yildizdaş, Dinçer;
Önenli-Mungan, Neslihan;
Yapicioglu, Hacer;
Topaloğlu, Ali Kemal;
Sertdemir, Yaşar;
Yüksel, Bilgin

Publication type:

Article