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1
المؤلفون: Özalkak, Şervan, Yıldırım, Ruken, Tunç, Selma, Ünal, Edip, Taş, Funda Feryal, Demirbilek, Hüseyin, Özbek, Mehmet Nuri
المساهمون: 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. 14:172-178
مصطلحات موضوعية: Male, Adolescent, Turkey, Annual incidence, Incidence, Endocrinology, Diabetes and Metabolism, Type 1 diabetes mellitus, Diabetic Ketoacidosis, Southeastern Anatolian, Diabetes Mellitus, Type 1, Endocrinology, Pediatrics, Perinatology and Child Health, Humans, Female, Child, Aged
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d36cda77b2b02cebd4ff1318dfaf390Test
https://doi.org/10.4274/jcrpe.galenos.2021.2021-10-7Test -
2
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 -
3
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 Endocrinologyمصطلحات 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 -
4
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 -
5
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