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: 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

المؤلفون: Alper Akın, Mehmet Türe, Ruken Yıldırım, Edip Unal, Hasan Balık, Yusuf Kenan Haspolat

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Akın, Alper, Ünal, Edip, Yıldırım, Ruken, Türe, Mehmet, Balık, Hasan, Haspolat, Yusuf Kenan

المصدر: Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)

مصطلحات موضوعية: Male, Performance, Ventricular Dysfunction, Right, Doppler-echocardiograhy, lcsh:Medicine, Cardiac-function, 030204 cardiovascular system & hematology, Adolescents, Doppler imaging, Ventricular Dysfunction, Left, 0302 clinical medicine, Disease, Myocardial Performance Index, Patient group, lcsh:Science, Child, L-Thyroxine therapy, Subclinical infection, Multidisciplinary, Ventricular function, Echocardiography, Doppler, Child, Preschool, Cardiology, cardiovascular system, Female, Thyroid-hormone, Risk, Cardiac function curve, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Diastole, 030209 endocrinology & metabolism, Article, 03 medical and health sciences, Diastolic-function, Hypothyroidism, Internal medicine, medicine, Humans, cardiovascular diseases, Normal range, business.industry, lcsh:R, Cardiovascular biology, Thyroid diseases, Thyroxine, Dysfunction, Case-Control Studies, lcsh:Q, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc98e2dd35f6d28b5b5264f1c693ca69Test
http://europepmc.org/articles/PMC7661521Test

المؤلفون: Edip Unal, Yusuf Kenan Haspolat

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

المصدر: Journal of Surgery and Medicine, Vol 4, Iss 11, Pp 1003-1007 (2020)
Volume: 4, Issue: 11 1003-1007
Journal of Surgery and Medicine

مصطلحات موضوعية: obezite, medicine.medical_specialty, obesity, Medicine (General), RD1-811, plazma aterojenik indeks,monosit HDL oranı,obezite,metabolik sendrom,çocuklar, Pediatrics, metabolic syndrome, monosit hdl oranı, chemistry.chemical_compound, High-density lipoprotein, R5-920, children, Internal medicine, monocyte to hdl cholesterol ratio, medicine, Obesity, Children, Cholesterol, business.industry, Monocyte, atherogenic index of plasma,monocyte to HDL cholesterol ratio,obesity,metabolic syndrome,children, Atherogenic index of plasma, nutritional and metabolic diseases, Non alcoholic, metabolik sendrom, atherogenic index of plasma, medicine.disease, plazma aterojenik indeks, Metabolic syndrome, medicine.anatomical_structure, Endocrinology, çocuklar, Pediatri, chemistry, Monocyte to HDL cholesterol ratio, Medicine, lipids (amino acids, peptides, and proteins), Surgery, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0dc39a23842685a0101d39840b1f0f8Test
https://hdl.handle.net/11468/8371Test

المؤلفون: Saygin Abali, Ihsan Esen, Ahmet Uçaktürk, Semra Cetinkaya, Ayhan Abacı, Azad Akberzade, Korcan Demir, Gönül Çatlı, Tulay Guran, Serap Turan, Damla Gökşen, Birgül Kirel, Yilmaz Kor, Ömer Tarım, Nihal Hatipoglu, Mehmet Nuri Ozbek, Zeynep Şıklar, Aslı Derya Kardelen, Ahmet Anık, Nesibe Akyürek, Atilla Cayir, Elvan Bayramoğlu, Murat Aydin, Ece Böber, Sukran Poyrazoglu, Erdal Eren, Onur Akın, Merih Berberoğlu, Edip Unal, Cengiz Kara, Ruken Yıldırım, Beray Selver Eklioğlu, Abdullah Bereket, Firdevs Bas, Emine Dilek, Muammer Buyukinan

المساهمون: Bursa Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Endokrinoloji Anabilim Dalı., Tarım, Ömer, CCU-8073-2022, Siklar, Zeynep, Turan, Serap, Bereket, Abdullah, Bas, Firdevs, Guran, Tulay, Akberzade, Azad, Abaci, Ayhan, Demir, Korcan, Bober, Ece, Ozbek, Mehmet Nuri, Kara, Cengiz, Poyrazoglu, Sukran, Aydin, Murat, Kardelen, Asli, Tarim, Omer, Eren, Erdal, Hatipoglu, Nihal, Buyukinan, Muammer, Akyurek, Nesibe, Cetinkaya, Semra, Bayramoglu, Elvan, Eklioglu, Beray Selver, Ucakturk, Ahmet, Abali, Saygin, Goksen, Damla, Kor, Yilmaz, Unal, Edip, Esen, Ihsan, Yildirim, Ruken, Akin, Onur, Cayir, Atilla, Dilek, Emine, Kirel, Birgul, Anik, Ahmet, Catli, Gonul, Berberoglu, Merih, Ege Üniversitesi, OMÜ, Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Ünal, Edip

المصدر: Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 12, Iss 2, Pp 150-159 (2020)

مصطلحات موضوعية: Fibroblast growth factor 23, Male, Turkey, Endocrinology, Diabetes and Metabolism, Parathyroid hormone, Gene sequence, Treatment response, Gastroenterology, Pediatrics, Gene, 0302 clinical medicine, Endocrinology, Medicine, Child, Endocrinology & metabolism, Linear growth, Dentin matrix protein 1, Depression, Parathyroid hyperplasia, Phosphorus, Hip dysplasia, Management, Osteotomy, Hypophosphatemic rickets, Tooth abscess, Blood, Cohort studies, Cohort analysis, Cohort study, Human, medicine.medical_specialty, Entesopathy, Phosphate, Major clinical study, Article, 0-Belirlenecek, 03 medical and health sciences, Sodium phosphate cotransporter 2c, Alkaline phosphatase, Genetic screening, Wrist disease, Genetics, Humans, Short children, Cross-sectional study, Growth-hormone treatment, Questionnaire, PHEX, Puberty, Infant, Frontal bossing, lcsh:Pediatrics, Follow up, medicine.disease, 030104 developmental biology, Albright syndrome, Calcium-regulating hormones and agents, 0301 basic medicine, Cystinosis, Rickets, hypophosphatemic, lcsh:Diseases of the endocrine glands. Clinical endocrinology, Bone pain, Turkey (bird), PHEX protein, Hyperparathyroidism, Phosphaturia, Genetic analysis, Kidney tubule absorption, lcsh:RJ1-570, Tyrosinemia, Combination drug therapy, Hypertension, Lordosis, Original Article, Female, Nephrocalcinosis, medicine.drug, Phosphate regulating neutral endopeptidase, Kidney tubule disorder, Ligament disease, Calcitriol, Adolescent, Child, preschool, CLCN5 gene, Oncogenic Osteomalacia, Familial Hypophosphatemic Rickets, Cancer, Drug therapy, combination, 030209 endocrinology & metabolism, Administration and dosage, Follow-up studies, Widening of wrist, Phosphates, PHEX phosphate regulating neutral endopeptidase, Internal medicine, Valgus knee, Gene mutation, Growth hormone, Craniofacial synostosis, Outcome assessment, health care, Kidney calcification, Prepuberty, lcsh:RC648-665, business.industry, Treatment, Hypophosphatemic Rickets, 25 hydroxyvitamin D, Clinical feature, Preschool child, Pediatrics, Perinatology and Child Health, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0e1f85da3399c9bfa3c4fa363aaad19Test
http://hdl.handle.net/11452/30611Test

المؤلفون: Funda Feryal Taş, Yusuf Kenan Haspolat, Süleyman Yıldız, Edip Unal, Ruken Yıldırım, Vasfiye Demir

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

المصدر: Journal of Surgery and Medicine, Vol 3, Iss 4, Pp 335-337 (2019)
Volume: 3, Issue: 4 335-337
Journal of Surgery and Medicine

مصطلحات موضوعية: medicine.medical_specialty, General and Internal Medicine, Medicine (General), neonatal diabet, endocrine system diseases, RD1-811, ATP-sensitive potassium channel,Neonatal diabetes,ABCC8 gene, R5-920, Neonatal diabet, medicine, Genel ve Dahili Tıp, ATP duyarlı K kanalı, ABCC8 gene, Gynecology, business.industry, abcc8 gene, Neonatal diabetes, nutritional and metabolic diseases, atp duyarlı k kanalı, abcc8 geni, medicine.disease, Neonatal diabet,ATP duyarlı K kanalı,ABCC8 geni, ABCC8 geni, Transient neonatal diabetes mellitus, ATP-sensitive potassium channel, Medicine, Surgery, atp-sensitive potassium channel, neonatal diabetes, business, Novel mutation

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842527bc5e8cb1a6ff2174f4c31029a3Test
https://dergipark.org.tr/en/pub/josam/issue/44120/515839Test

المؤلفون: Yusuf Kenan Haspolat, Edip Unal, Ruken Yıldırım, Alper Akın, Hasan Balık, Mehmet Türe

المساهمون: Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Akın, Alper, Ünal, Edip, Yıldırım, Ruken, Türe, Mehmet, Balık, Hasan, Haspolat, Yusuf Kenan

مصطلحات موضوعية: medicine.medical_specialty, medicine.diagnostic_test, business.industry, Corrected qt, Case-control study, 030209 endocrinology & metabolism, Mean age, General Medicine, 030204 cardiovascular system & hematology, QT interval, 03 medical and health sciences, Ventricular repolarization, 0302 clinical medicine, QT dispersion, Subclinical hypothyroidism, Qt dispersion, Internal medicine, medicine, Cardiology, Cardiology and Cardiovascular Medicine, business, Electrocardiography, Children, Qtc dispersion, Subclinical infection

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2d9cc50fe665a5c0d56dc03b73600ceTest
https://hdl.handle.net/11468/8342Test

المؤلفون: Unal, Edip, Yıldırım, Ruken, Taş, Funda Feryal, Demir, Vasfiye, Onay, Hüseyin, Haspolat, Yusuf Kenan

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

المصدر: Journal of Clinical Research in Pediatric Endocrinology

مصطلحات موضوعية: medicine.medical_specialty, endocrine system, ambiguous genitalia, 46, XX Disorders of Sex Development, medicine.drug_class, Endocrinology, Diabetes and Metabolism, Disorders of Sex Development, Endokrinoloji ve Metabolizma, Case Report, 030209 endocrinology & metabolism, maternal virilization, Maternal virilization, 03 medical and health sciences, Aromatase, 0302 clinical medicine, Endocrinology, Internal medicine, Ambiguous genitalia, medicine, Humans, Genetic Predisposition to Disease, Congenital adrenal hyperplasia, Infertility, Male, Testosterone, hirsutism, Pregnancy, biology, business.industry, CYP19A1 gene, Virilization, Homozygote, Aromatase deficiency, Infant, medicine.disease, Pediatri, Estrogen, Mutation, Pediatrics, Perinatology and Child Health, biology.protein, Gynecomastia, Female, medicine.symptom, business, Metabolism, Inborn Errors, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c68f4d7fd51cdd510694c6bf393bf2bTest
https://hdl.handle.net/11454/29703Test