Search Results - "Fatih Gürbüz" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Effects of methylphenidate on appetite and growth in children diagnosed with attention deficit and hyperactivity disorder

Effects of methylphenidate on appetite and growth in children diagnosed with attention deficit and hyperactivity disorder

by Gurbuz, Fatih, Gurbuz, Berrak Bilginer, Celik, Gonca Gul, Yildirim, Veli, Ucakturk, Seyit Ahmet, Seydaoglu, Gulsah, Ucakturk, Eda Mengen, Topaloglu, Ali Kemal, Yuksel, Bilgin
Published in Journal of Pediatric Endocrinology & Metabolism (01.01.2016)

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Loss-of-Function Mutations in SEMA3F and gePLXNA3 Encoding Semaphorin-3F and its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism

Loss-of-Function Mutations in SEMA3F and gePLXNA3 Encoding Semaphorin-3F and its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism

by Kotan, Leman Damla, Ternier, Gaetan, Cakir, Aydilek Dagdeviren, Emeksiz, Hamdi Cihan, Turan, ihsan, Delpouve, Gaspard, Kardelen, Asli Derya, Ozcabi, Bahar, Isik, Emregul, Mengen, Eda, Cakir, Esra Deniz P., Yuksel, Aysegul, Agladioglu, Sabahat Yilmaz, Dilek, Semine Ozdemir, Evliyaoglu, Olcay, Darendeliler, Feyza, Gurbuz, Fatih, Akkus, Gamze, Yuksel, Bilgin, Giacobini, Paolo, Kemal Topaloglu, A.
Published in Genetics in medicine (25.01.2021)

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Ostegenezis İmperfekta Olan Çocuklarda Pamidronat ve Kalsitonin Tedavilerinin Karşılaştırılması

Ostegenezis İmperfekta Olan Çocuklarda Pamidronat ve Kalsitonin Tedavilerinin Karşılaştırılması

by Neslihan Önenli MUNGAN, Fatih GÜRBÜZ, Eda MENGEN, Özden ÖZGÜR, Ali Kemal TOPALOGLU, Bilgin YÜKSEL
Published in Cukurova Medical Journal (01.12.2013)

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Sertoli cell only syndrome with ambiguous genitalia

Sertoli cell only syndrome with ambiguous genitalia

by Gurbuz, Fatih, Ceylaner, Serdar, Erdogan, Seyda, Topaloglu, Ali Kemal, Yuksel, Bilgin
Published in Journal of Pediatric Endocrinology & Metabolism (01.07.2016)

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The effect of lifestyle change and metformin therapy on serum arylesterase and paraoxonase activity in obese children

The effect of lifestyle change and metformin therapy on serum arylesterase and paraoxonase activity in obese children

by Çayır, Atilla, Turan, Mehmet İbrahim, Gurbuz, Fatih, Kurt, Nezahat, Yildirim, Abdulkadir
Published in Journal of Pediatric Endocrinology and Metabolism (01.05.2015)

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An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3)

An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3)

by Dimitri, Paul, De Franco, Elisa, Habeb, Abdelhadi M., Gurbuz, Fatih, Moussa, Khairya, Taha, Doris, Wales, Jerry K. H., Hogue, Jacob, Slavotinek, Anne, Shetty, Ambika, Balasubramanian, Meena
Published in American journal of medical genetics. Part A (01.07.2016)

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Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide

Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide

by Mengen, Eda, Tunc, Selma, Kotan, L Damla, Nalbantoglu, Ozlem, Demir, Korcan, Gurbuz, Fatih, Turan, Ihsan, Seker, Gül, Yuksel, Bilgin, Topaloglu, A Kemal
Published in Hormone research in paediatrics (01.01.2016)

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A Case of Congenital Generalized Lipodystrophy Type 2 with Novel BSCL2 Gene Mutation

A Case of Congenital Generalized Lipodystrophy Type 2 with Novel BSCL2 Gene Mutation

by Gurbuz, Fatih, Turan, Ihsan, Tastan, Mehmet, Topaloglu, Ali Kemal, Yuksel, Bilgin
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)

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Isolated Hypoaldosteronism: A Case Report

Isolated Hypoaldosteronism: A Case Report

by Turan, Ihsan, Gurbuz, Fatih, Tasdan, Mehmet, Kotan, Leman Damla, Topaloglu, Ali Kemal, Yuksel, Bilgin
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)

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Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS 1R gene in three unrelated families

Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS 1R gene in three unrelated families

by Demirbilek, Huseyin, Ozbek, M. Nuri, Demir, Korcan, Kotan, L. Damla, Cesur, Yasar, Dogan, Murat, Temiz, Fatih, Mengen, Eda, Gurbuz, Fatih, Yuksel, Bilgin, Topaloglu, A. Kemal
Published in Clinical endocrinology (Oxford) (01.03.2015)

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The Effect of 7E Learning Model on Academic Achievements and Retention of 6th Grade Science and Technology Course Students in the Unit "Electricity in Our Life"

The Effect of 7E Learning Model on Academic Achievements and Retention of 6th Grade Science and Technology Course Students in the Unit "Electricity in Our Life"

by GÜRBÜZ, Fatih, TURGUT, Ümit, SALAR, Rýza
Published in Journal of Turkish Science Education (01.09.2013)

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Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

by Gürbüz, Fatih, Yüksel, Bilgin, Topaloğlu, Ali Kemal
Published in Journal of clinical research in pediatric endocrinology (01.12.2016)

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Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing

Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing

by Maharaj, Avinaash, Buonocore, Federica, Meimaridou, Eirini, Ruiz-Babot, Gerard, Guasti, Leonardo, Peng, Hwei-Ming, Capper, Cameron P, Burgos-Tirado, Neikelyn, Prasad, Rathi, Hughes, Claire R, Maudhoo, Ashwini, Crowne, Elizabeth, Cheetham, Timothy D, Brain, Caroline E, Suntharalingham, Jenifer P, Striglioni, Niccolò, Yuksel, Bilgin, Gurbuz, Fatih, Gupta, Sangay, Lindsay, Robert, Couch, Robert, Spoudeas, Helen A, Guran, Tulay, Johnson, Stephanie, Fowler, Dallas J, Conwell, Louise S, McInerney-Leo, Aideen M, Drui, Delphine, Cariou, Bertrand, Lopez-Siguero, Juan P, Harris, Mark, Duncan, Emma L, Hindmarsh, Peter C, Auchus, Richard J, Donaldson, Malcolm D, Achermann, John C, Metherell, Louise A
Published in Journal of the Endocrine Society (01.01.2019)

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Effects of Hormone Replacement Therapy on Autoimmune Markers and Clinical Outcomes in Pediatric Patients with Hashimoto's Thyroiditis

Effects of Hormone Replacement Therapy on Autoimmune Markers and Clinical Outcomes in Pediatric Patients with Hashimoto's Thyroiditis

by ALAN TEHÇİ, Başak, GURBUZ, Fatih, BOYRAZ, Mehmet
Published in Turkish Journal of Pediatric Disease (25.12.2023)

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Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study with 241,083 Infants

Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study with 241,083 Infants

by Guran, Tulay, Tezel, Basak, Cakir, Meltem, Akinci, Aysehan, Orbak, Zerrin, Keskin, Mehmet, Selver Eklioglu, Beray, Ozon, Alev, Ozbek, Mehmet Nuri, Karaguzel, Gulay, Hatipoglu, Nihal, Gurbuz, Fatih, Cizmecioglu, Filiz Mine, Kara, Cengiz, Simsek, Enver, Bas, Firdevs, Aydin, Murat, Darendeliler, Feyza
Published in Journal of clinical research in pediatric endocrinology (11.03.2020)

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Etiological Evaluation of Patients Presenting with Isolated Micropenis to an Academic Health Care Center

Etiological Evaluation of Patients Presenting with Isolated Micropenis to an Academic Health Care Center

by Aslan, Tugba Bilmez, Gurbuz, Fatih, Temiz, Fatih, Yuksel, Bilgin, Topaloglu, Ali Kemal
Published in Indian journal of pediatrics (01.08.2014)

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PP-176. Three years follow-up of term and near-term infants with extreme hyperbilirubinemia and predictive value of brain auditory evoke responses

PP-176. Three years follow-up of term and near-term infants with extreme hyperbilirubinemia and predictive value of brain auditory evoke responses

by Unal, Sevim, Gurbuz, Fatih, Guven, Alev, Kose, Gulşen
Published in Early human development (01.11.2010)

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Unusual and early onset IPEX syndrome: a case report

Unusual and early onset IPEX syndrome: a case report

by Doğruel, Dilek, Gürbüz, Fatih, Turan, İhsan, Altıntaş, Derya Ufuk, Yılmaz, Mustafa, Yüksel, Bilgin
Published in The Turkish journal of pediatrics (01.01.2019)

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Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

by Gürbüz, Fatih, Ceylaner, Serdar, Topaloğlu, Ali Kemal, Yüksel, Bilgin
Published in Journal of clinical research in pediatric endocrinology (01.09.2016)

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Evaluation of Neuroimaging and Electroencephalography Findings in Patients with Status Epilepticus [Status Epileptikus Tanisiyla Izlenen Hastalarin Norogoruntuleme ve EEG Bulgularinin Degerlendirilmesi]

Evaluation of Neuroimaging and Electroencephalography Findings in Patients with Status Epilepticus [Status Epileptikus Tanisiyla Izlenen Hastalarin Norogoruntuleme ve EEG Bulgularinin Degerlendirilmesi]

by Gurbuz, Berrak, Gurbuz, Fatih, Cayir, Atilla, Sahin, Irfan, Okdemir, Deniz, Guven, Alev, Degerliyurt, Aydan, Kose, Gulsen
Published in Medicine science (2015)

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