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A Novel Variant in SYNE4 Confirms its Causative Role in Sensorineural Hearing Loss

Masterson, John ; Yıldırım, Busegül ; Gökkaya, Ece ; Tokgöz Yılmaz, Suna ; Tekin, Mustafa

Balkan Medical Journal, 2018, Vol.35(2), p.196-198 [Peer Reviewed Journal]

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Peripheral Neuropathy as a Complication of Diabetic Ketoacidosis in a Child with Newly Diagnosed Diabetes Type 1: A Case Report

Baszyńska-Wilk, Marta ; Wysocka-Mincewicz, Marta ; Świercz, Anna ; Świderska, Jolanta ; Marszał, Magdalena ; Szalecki, Mieczysław

Journal of Clinical Research in Pediatric Endocrinology, 2018, Vol.10(3), p.289-293 [Peer Reviewed Journal]

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Inflammatory Myofibroblastic Tumor Presenting with Diabetes Insipidus in an Eight-Year-Old Boy: A Case Report

Sarı, Erkan ; Ataş, Erman ; Bulut, Engin Burak ; Sarı, Sebahattin ; Akın, Onur ; Saldır, Mehmet ; Karslıoğlu, Yıldırım ; Yeşilkaya, Ediz

Journal of Clinical Research in Pediatric Endocrinology, 2015, Vol.7(4), p.340-343 [Peer Reviewed Journal]

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Novel Founder Mutation in FANCA Gene (c.3446_3449dupCCCT) Among Romani Patients from the Balkan Region

Dimishkovska, Marija ; Kotori, Vjosa Mulliqi ; Gucev, Zoran ; Kocheva, Svetlana ; Polenakovic, Momir ; Plaseska-Karanfilska, Dijana

Balkan Medical Journal, 2018, Vol.35(1), p.108-111 [Peer Reviewed Journal]

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Hyperthyroidism After Allogeneic Hematopoietic Stem Cell Transplantation: A Report of Four Cases

Sağ, Erdal ; Gönç, Nazlı ; Alikaşifoğlu, Ayfer ; Kuşkonmaz, Barış ; Uçkan, Duygu ; Özön, Alev ; Kandemir, Nurgün

Journal of Clinical Research in Pediatric Endocrinology, 2015, Vol.7(4), p.349-354 [Peer Reviewed Journal]

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Tolvaptan Treatment in Children with Chronic Hyponatremia due to Inappropriate Antidiuretic Hormone Secretion: A Report of Three Cases

Tuli, Gerdi ; Tessaris, Daniele ; Einaudi, Silvia ; De Sanctis, Luisa ; Matarazzo, Patrizia

Journal of Clinical Research in Pediatric Endocrinology, 2017, Vol.9(3), p.288-292 [Peer Reviewed Journal]

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Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis

Karahan, Feryal ; Çıtak, Elvan Çağlar ; Yaman, Emel ; Alakaya, Mehmet ; Sağcan, Fatih ; Yılmaz, Eda Bengi ; Kuş, Funda ; Gürses, İclal ; Balcı, Yüksel

Journal of Clinical Research in Pediatric Endocrinology, 2018, Vol.10(1), p.87-90 [Peer Reviewed Journal]

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Premature Coronary Artery Disease due to Homozygous Familial Hypercholesterolemia in a 12-Year-Old Girl

Ekici, Filiz ; Özçobanoğlu, Salih ; Kardelen, Fırat

Balkan Medical Journal, 2018, Vol.35(2), p.208-211 [Peer Reviewed Journal]

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Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

Yekedüz, Merve Koç ; Şıklar, Zeynep ; Burgu, Berk ; Kuloğlu, Zarife ; Kocaay, Pınar ; Çamtosun, Emine ; İsakoca, Mehmet ; Kansu, Aydan ; Soygür, Tarkan ; Berberoğlu, Merih

Journal of Clinical Research in Pediatric Endocrinology, 2017, Vol.9(2), p.168-171 [Peer Reviewed Journal]

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Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome

Hulle, Severine Van ; Craen, Margarita ; Callewaert, Bert ; Joustra, Sjoerd ; Oostdijk, Wilma ; Losekoot, Monique ; Wit, Jan Maarten ; Turgeon, Marc Olivier ; Bernard, Daniel J ; Schepper, Jean De

Journal of Clinical Research in Pediatric Endocrinology, 2016, Vol.8(1), p.86-91 [Peer Reviewed Journal]

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  1. Sarı, Erkan
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