المؤلفون: Demirbilek, Huseyin, Cayir, Atilla, Flanagan, Sarah E., Yıldırım, Ruken, Kor, Yılmaz, Gurbuz, Fatih, Haliloğlu, Belma, Yıldız, Melek, Baran, Rıza Taner, Akbas, Emine Demet, Demiral, Meliha, Ünal, Edip, Arslan, Gulcin, Vuralli, Dogus, Buyukyilmaz, Gonul, Al-Khawaga, Sara, Saeed, Amira, Maadheed, Maryam Al, Khalifa, Amel, Onal, Hasan

المصدر: Journal of Clinical Endocrinology & Metabolism; Dec2020, Vol. 105 Issue 12, p1-9, 9p

مصطلحات موضوعية: PEOPLE with diabetes, PITUITARY dwarfism, FERRITIN, GENE enhancers, FETAL growth retardation, PANCREAS, RESEARCH, GENETICS, CHOLESTASIS, GENETIC mutation, NEONATAL diseases, RESEARCH methodology, DIABETES, EXOCRINE pancreatic insufficiency, MEDICAL cooperation, EVALUATION research, SELF-report inventories, COMPARATIVE studies, SYMPTOMS, RESEARCH funding, TRANSCRIPTION factors, GENETIC techniques, LONGITUDINAL method, DISEASE complications

المؤلفون: Ünal, Edip, Yıldırım, Ruken, Erten, Özlem, Çim, Abdullah, Haspolat, Yusuf Kenan

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Ünal, Edip, Yıldırım, Ruken, Erten, Özlem, Çim, Abdullah, Haspolat, Yusuf Kenan

مصطلحات موضوعية: Noonan sendromu, Short stature, Noonan syndrome, Boy kısalığı

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______3346::606942296579abb61c0a650427043217Test
https://hdl.handle.net/11468/7875Test

المؤلفون: Ünal, Edip, Yıldırım, Ruken, Erten, Özlem, Çim, Abdullah, Haspolat, Yusuf Kenan

مصطلحات موضوعية: Noonan sendromu, Boy kısalığı, Noonan syndrome, Short stature

وصف الملف: application/pdf

العلاقة: Türkiye Klinikleri Journal of Case Reports; Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı; Ünal, E., Yıldırım, R., Erten, Ö., Çim, A. ve Haspolat, Y. K. (2016). Boy kısalığı ile başvuran noonan sendromlu bir olgu. Türkiye Klinikleri Journal of Case Reports, 24(Suppl.), 10-12.; https://hdl.handle.net/11468/7875Test; 24; Supplement; 10; 12

الإتاحة: https://hdl.handle.net/11468/7875Test

المؤلفون: Demirbilek, Huseyin, Cayir, Atilla, Flanagan, Sarah E, Yıldırım, Ruken, Kor, Yılmaz, Gurbuz, Fatih, Haliloğlu, Belma, Yıldız, Melek, Baran, Rıza Taner, Akbas, Emine Demet, Demiral, Meliha, Ünal, Edip, Arslan, Gulcin, Vuralli, Dogus, Buyukyilmaz, Gonul, Al-Khawaga, Sara, Saeed, Amira, Al Maadheed, Maryam, Khalifa, Amel, Onal, Hasan, Yuksel, Bilgin, Ozbek, Mehmet Nuri, Bereket, Abdullah, Hattersley, Andrew T, Hussain, Khalid, De Franco, Elisa

المصدر: The Journal of Clinical Endocrinology & Metabolism; December 2020, Vol. 105 Issue: 12

العنوان البديل: Investigation of adolescents diagnosed with exogenous obesity in terms of Internet, smartphone usage characteristics and psychopathologies.

المؤلفون: Baş, Gülnur¹, Kardaş, Ömer² kardasomer@gmail.com, Kardaş, Burcu², Ünal, Edip³

المصدر: Klinik Psikiyatri Dergisi. 2023, Vol. 26 Issue 3, p209-218. 10p.

المؤلفون: Amine Aktar Karakaya, Aslı Beştaş, Yusuf Kenan Haspolat, Hüseyin Onay, Edip Unal, Feriştah Özkinay, F. Tas, Ruken Yıldırım

المساهمون: Ege Üniversitesi, Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Ünal, Edip, Karakaya, Amine Aktar, Beştaş, Aslı, Haspolat, Yusuf Kenan

المصدر: Journal of Endocrinological Investigation. 44:1301-1307

مصطلحات موضوعية: Persistent müllerian duct syndrome, medicine.medical_specialty, Novel mutation, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, Bioinformatics, Malignancy, medicine.disease_cause, 03 medical and health sciences, Exon, 0302 clinical medicine, Endocrinology, Gene duplication, medicine, Missense mutation, Gene, Persistent Mullerian duct syndrome, Mutation, business.industry, medicine.disease, AMHR2, 030220 oncology & carcinogenesis, Persistent Müllerian duct syndrome, Medical genetics, Undescended testes, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60c6972a7f397577ad2ec2b811c699faTest
https://doi.org/10.1007/s40618-020-01437-9Test

المؤلفون: Yusuf Kenan Haspolat, Edip Unal, Aslı Beştaş, Recep Eröz, Mehmet Tekin, Semih Bolu, Amine Aktar Karakaya

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Beştaş, Aslı, Ünal, Edip, Karakaya, Amine Aktar, Haspolat, Yusuf Kenan, [Belirlenecek]

مصطلحات موضوعية: Male, Delayed puberty, Pediatrics, medicine.medical_specialty, Adolescent, Endocrinology, Diabetes and Metabolism, Mixed Function Oxygenases, Deletion, Endocrinology, Hypergonadotropic hypogonadism, Diabetes mellitus, medicine, Humans, Family, Congenital adrenal hyperplasia, Multiplex ligation-dependent probe amplification, Child, Amenorrhea, Puberty, Delayed, Chinese Patients, Adrenal Hyperplasia, Congenital, business.industry, Gender Identity, Steroid 17-alpha-Hydroxylase, 17,20-Lyase, 17-Hydroxylase/17,20-Lyase Deficiency, medicine.disease, Hypokalemia, Blood pressure, CYP17A1, Cyp17A1 Gene, Mutation, Primary amenorrea, Hypertension, Female, medicine.symptom, business, Mutations

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e70470305c1b015462d97933e714f119Test
https://hdl.handle.net/11468/11092Test

المؤلفون: Funda Feryal Taş, Serdar Ceylaner, Ruken Yıldırım, Suat Tekin, Yusuf Kenan Haspolat, Edip Unal

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Ünal, Edip, Taş, Funda Feryal, Tekin, Suat, Haspolat, Yusuf Kenan

المصدر: Gynecological Endocrinology. 36:739-742

مصطلحات موضوعية: Delayed puberty, medicine.medical_specialty, Cytochrome, biology, Hydroxylase deficiency, Endocrinology, Diabetes and Metabolism, XY karyotype, Obstetrics and Gynecology, CYP17A1 gene, urologic and male genital diseases, medicine.disease, Endocrinology, CYP17A1, Internal medicine, Hypertension, Primary amenorrhea, medicine, biology.protein, Congenital adrenal hyperplasia, medicine.symptom, 17α-hydroxylase, Gene

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0042650033b02bf90e69eedd624801Test
https://doi.org/10.1080/09513590.2019.1707798Test

المؤلفون: Edip Unal, İlyas Yolbaş, Savaş Mert Darakci, Sabahattin Ertuğrul, Sibel Tanriverdi Yilmaz, İbrahim Deger

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Ertuğrul, Sabahattin, Yılmaz, Sibel Tanrıverdi, Ünal, Edip, Yolbaş, İlyas, Değer, İbrahim

مصطلحات موضوعية: Embryology, medicine.medical_specialty, business.industry, Micrognathism, Obstetrics and Gynecology, Hypotonia, medicine.disease, Dermatology, Osteogenesis imperfecta, Congenital clubfoot, Pediatrics, Perinatology and Child Health, medicine, business, Amniotic Band Syndrome, Amniotic band syndrome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32958269c56222ef5fd0d578e3847fbaTest
https://www.degruyter.com/document/doi/10.1515/crpm-2021-0035/htmlTest

المؤلفون: Samim Özen, Gülay Can Yılmaz, Muammer Buyukinan, Deniz Kor, Erdal Eren, Emine Demet Akbaş, Meltem Tayfun, Recep Polat, Edip Unal, Elif Söbü, Ediz Yeşilkaya, Eren Er, Şükran Darcan, Özlem Korkmaz, Ahmet Anık, Gülay Karagüzel, Yilmaz Kor, Damla Gökşen, Saygin Abali, Ayhan Abaci, Olcay Evliyaoğlu, Özlem Nalbantoğlu, Semih Bolu, Merih Berberoğlu, Zeynep Şıklar

المساهمون: Acibadem University Dspace, Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Ünal, Edip

المصدر: JCRPE, Vol 13, Iss 4, Pp 433-438 (2021)
Journal of Clinical Research in Pediatric Endocrinology

مصطلحات موضوعية: Male, Turkey, Endocrinology, Diabetes and Metabolism, Need, Urine, Disease, Pediatrics, Fasting insulin, HNF1A, Endocrinology, Medicine, Age of Onset, Child, biology, High-Throughput Nucleotide Sequencing, early-onset diabetes, HNF1B, Pedigree, Early-onset diabetes, Child, Preschool, Female, Original Article, Mutations, medicine.medical_specialty, Adolescent, Young, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, ABCC8, Monogenic diabetes, Diabetes mellitus, Internal medicine, Mody, Diabetes Mellitus, Genetics, Humans, Monogenic Diabetes, Onset, GCK, business.industry, Infant, RC648-665, medicine.disease, Cross-Sectional Studies, Diabetes Mellitus, Type 2, Pediatrics, Perinatology and Child Health, Next-generation sequencing, biology.protein, next-generation sequencing, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cd9f2d161eae4e859525b5beacd6214Test
https://hdl.handle.net/11454/78746Test