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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 -
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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 -
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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 -
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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 -
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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 -
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المؤلفون: Suat Tekin, Yusuf Kenan Haspolat, Edip Unal, Ruken Yıldırım, Funda Feryal Taş, Askin Sen
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: Hormones (Athens, Greece). 17(2)
مصطلحات موضوعية: 0301 basic medicine, Male, Pediatrics, medicine.medical_specialty, Isolated ACTH deficiency, TBX19 gene, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, Adrenocorticotropic hormone, Hypoglycemia, Gene mutation, Endocrine System Diseases, Infant, Newborn, Diseases, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Adrenocorticotropic Hormone, medicine, Adrenal insufficiency, Humans, Sibling, Hydrocortisone, Homeodomain Proteins, business.industry, Neonatal hypoglycemia, Siblings, Genetic Diseases, Inborn, Infant, Newborn, Infant, General Medicine, medicine.disease, 030104 developmental biology, Female, business, T-Box Domain Proteins, medicine.drug, Adrenal Insufficiency
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8e3d0fed2a18a4fda2768f9b0b4f04fTest
https://pubmed.ncbi.nlm.nih.gov/29858850Test