Çukurova Üniversitesi
Akademik Veri Yönetim Sistemi
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Akkuş G., Kotan D., Durmaz E., Mengen E., Turan İ., Ulubay A., et al.,"Idiopathic Hypogonadothropic Hypogonadism Due To Novel FGFR1 Mutations.", JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.-, 2016
Topaloğlu A.K., "Normosmic Idiopathic Hypogonadotropic Hypogonadism Due To A Novel Homozygous Nonsense C.C969a (P.Y323x) Mutation In The Kiss1r Gene In Three Unrelated Families.", Clin Endocrinol (Oxf), vol.82, pp.429-438, 2015
Topaloğlu A.K., "Etiological Evaluation Of Patients Presenting With Isolated Micropenis To An Academic Health Care Center", INDIAN JOURNAL OF PEDIATRICS, vol.81, pp.775-779, 2014
Topaloğlu A.K., "Mutations In Fezf1 Cause Kallmann Syndrome", AMERICAN JOURNAL OF HUMAN GENETICS, vol.95, pp.326-331, 2014
Topaloğlu A.K., "A Rare Variant In Human Fibroblast Activation Protein Associated With Er Stress, Loss Of Enzymatic Function And Loss Of Cell Surface Localisation", BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, vol.1844, pp.1248-1259, 2014
Koç A.F., Topaloğlu A.K., Kretzschmar D., Dissen G.A., Kotan L.D., Mcardle C.A., Hamel B.C., Guclu M., Papatya E.D., Eren E., Mengen E., Gurbuz F., Cook M., Castellano J.M., Kekil M.B., Mungan N.O., Yüksel B., Ojeda S.R., Koc A.F., "Loss-Of-Function Mutations In Pnpla6 Encoding Neuropathy Target Esterase Underlie Pubertal Failure And Neurological Deficits In Gordon Holmes Syndrome", JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.99, pp.0-0, 2014
Topaloğlu A.K., "Mcm9 Mutations Are Associated With Ovarian Failure, Short Stature, And Chromosomal Instability.", Am J Hum Genet. , pp.754-762, 2014
Topaloğlu A.K., "The Novel Mutation P.Trp147arg Of The Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia With Adrenal Insufficiency And 46,Xy Disorder Of Sex Development", HORMONE RESEARCH IN PAEDIATRICS, vol.80, pp.163-169, 2013
Topaloğlu A.K., "Quantitation Of Fibroblast Activation Protein (Fap)-Specific Protease Activity In Mouse, Baboon And Human Fluids And Organs.", FEBS Open Bio., vol.4, pp.43-54, 2013
Topaloğlu A.K., "Chromium Levels In Healthy And Newly Diagnosed Type 1 Diabetic Children", PEDIATRICS INTERNATIONAL, vol.54, pp.780-785, 2012
Topaloğlu A.K., "Inactivating Kiss1 Mutation And Hypogonadotropic Hypogonadism", NEW ENGLAND JOURNAL OF MEDICINE, vol.366, pp.629-635, 2012
Topaloğlu A.K., "Relationship Between Metabolic Control And Neurocognitive Functions In Children Diagnosed With Type I Diabetes Mellitus Before And After 5 Years Of Age", TURKISH JOURNAL OF PEDIATRICS, vol.54, pp.352-361, 2012
Topaloğlu A.K., "A Homozygous Recurring Mutation In Wisp3 Causing Progressive Pseudorheumatoid Arthropathy", JOURNAL OF PEDIATRIC ENDOCRINOLOGY, vol.24, pp.105-108, 2011
Topaloğlu A.K., "Neurokinin B Signalling In The Human Reproductive Axis", MOLECULAR AND CELLULAR ENDOCRINOLOGY, vol.346, pp.57-64, 2011
Topaloğlu A.K., "The Effects Of Neurokinin B Upon Gonadotrophin Release In Male Rodents", JOURNAL OF NEUROENDOCRINOLOGY, vol.22, pp.181-187, 2010
Topaloğlu A.K., "Wolcott-Rallison Syndrome Due To The Same Mutation (W522x) In Eif2ak3 In Two Unrelated Families And Review Of The Literature*", PEDIATRIC DIABETES, vol.11, pp.279-285, 2010
Topaloğlu A.K., "Neurokinin B Signalling In Human Puberty", JOURNAL OF NEUROENDOCRINOLOGY, vol.22, pp.765-770, 2010
Topaloğlu A.K., "Molecular Causes Of Hypogonadotropic Hypogonadism", CURRENT OPINION IN OBSTETRICS, vol.22, pp.264-270, 2010
Topaloğlu A.K., "The Recent Genetics Of Hypogonadotrophic Hypogonadism - Novel Insights And New Questions", CLINICAL ENDOCRINOLOGY, vol.72, pp.427-435, 2010
Li Y., Laue K., Temtamy S., Aglan M., Kotan L.D., Yigit G., et al., "Temtamy Preaxial Brachydactyly Syndrome Is Caused By Loss-Of-Function Mutations In Chondroitin Synthase 1, A Potential Target Of Bmp Signaling", AMERICAN JOURNAL OF HUMAN GENETICS, vol.87, pp.757-767, 2010
Topaloğlu A.K., "Neurokinin B Signaling In Puberty: Human And Animal Studies", MOLECULAR AND CELLULAR ENDOCRINOLOGY, vol.324, pp.64-69, 2010
Topaloğlu A.K., "Novel Growth Hormone Receptor Gene Mutation In A Patient With Laron Syndrome", JOURNAL OF PEDIATRIC ENDOCRINOLOGY, vol.23, pp.407-414, 2010
Topaloğlu A.K., "Thyroid Peroxidase Gene Mutations Causing Congenital Hypothyroidism In Three Turkish Families", JOURNAL OF PEDIATRIC ENDOCRINOLOGY, vol.22, pp.1033-1039, 2009
Topaloğlu A.K., "Ambulatory Blood Pressure Monitoring And Serum Nitric Oxide Concentration In Type 1 Diabetic Children", ENDOCRINE JOURNAL, vol.56, pp.477-485, 2009
Topaloğlu A.K., "Hypogonadotropic Hypogonadism Due To A Novel Missense Mutation In The First Extracellular Loop Of The Neurokinin B Receptor", JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM, vol.94, pp.3633-3639, 2009
Topaloğlu A.K., "Tac3 And Tacr3 Mutations In Familial Hypogonadotropic Hypogonadism Reveal A Key Role For Neurokinin B In The Central Control Of Reproduction", NATURE GENETICS, vol.41, pp.354-358, 2009
Topaloğlu A.K., "Metabolic Acidosis In A Patient With Type 1 Diabetes Mellitus Complicated By Methanol And Amitriptyline Intoxication", EUROPEAN JOURNAL OF EMERGENCY MEDICINE, vol.16, pp.45-48, 2009
Topaloğlu A.K., "P450c17 Deficiency: Clinical And Molecular Characterization Of Six Patients", JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM, vol.92, pp.1000-1007, 2007
Topaloğlu A.K., "Molecular Genetic Analysis Of Normosmic Hypogonadotropic Hypogonadism In A Turkish Population: Identification And Detailed Functional Characterization Of A Novel Mutation In The Gonadotropin-Releasing Hormone Receptor Gene", NEUROENDOCRINOLOGY, vol.84, pp.301-308, 2006
Topaloğlu A.K., "Bone Calcium Changes During Diabetic Ketoacidosis: A Comparison With Lactic Acidosis Due To Volume Depletion", BONE, vol.37, pp.122-127, 2005
Topaloğlu A.K., "Wolcott-Rallison Syndrome - Clinical, Genetic, And Functional Study Of Eif2ak3 Mutations And Suggestion Of Genetic Heterogeneity", DIABETES, vol.53, pp.1876-1883, 2004
Topaloğlu A.K., "Thyroid Hormone Levels And Their Relationship To Survival In Children With Bacterial Sepsis And Septic Shock", JOURNAL OF PEDIATRIC ENDOCRINOLOGY, vol.17, pp.1435-1442, 2004
Topaloğlu A.K., "Three Children With Triple A Syndrome Due To A Mutation (R478x) In The Aaas Gene", HORMONE RESEARCH, vol.61, pp.3-6, 2004
Topaloğlu A.K., "Familial Thyroxin-Binding Globulin Excess With Ichthyosis: A Case Report", TURKISH JOURNAL OF PEDIATRICS, vol.46, pp.174-176, 2004
Topaloğlu A.K., "Fucosidosis With Hypothyroidism: A Case Report", TURKISH JOURNAL OF PEDIATRICS, vol.46, pp.170-173, 2004
Topaloğlu A.K., "Type Ii Hyperprolinemia: A Case Report", TURKISH JOURNAL OF PEDIATRICS, vol.46, pp.167-169, 2004
Topaloğlu A.K., "Four New Cases Of Congenital Secondary Hypothyroidism Due To A Splice Site Mutation In The Thyrotropin-Beta Gene: Phenotypic Variability And Founder Effect", JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM, vol.89, pp.4136-4141, 2004
Topaloğlu A.K., "Growth Hormone And Insulin-Like Growth Factor 1 Levels And Their Relation To Survival In Children With Bacterial Sepsis And Septic Shock", JOURNAL OF PAEDIATRICS AND CHILD HEALTH, vol.40, pp.221-226, 2004
Topaloğlu A.K., "A Newborn Infant With Generalized Glutathione Synthetase Deficiency", TURKISH JOURNAL OF PEDIATRICS, vol.46, pp.72-75, 2004
Topaloğlu A.K., "Bone Mineral Changes In Acute Metabolic Acidosis Due To Acute Gastroenteritis", CALCIFIED TISSUE INTERNATIONAL, vol.75, pp.380-383, 2004
Topaloğlu A.K., "Extremely Immature Infant Who Developed Clitoromegaly During The Second Month Of Her Postnatal Life Probably Due To Frequent Whole Blood Transfusion From An Adult Male", PEDIATRICS INTERNATIONAL, vol.45, pp.347-348, 2003
Topaloğlu A.K., "Serum Il-1, Il-2, Tnf Alpha And Inf Gamma Levels Of Patients With Type 1 Diabetes Mellitus And Their Siblings", JOURNAL OF PEDIATRIC ENDOCRINOLOGY, vol.16, pp.203-210, 2003
Topaloğlu A.K., "Coexistence Of Common Variable Immunodeficiency And Autoimmune Polyglandular Syndrome Type 2", JOURNAL OF PEDIATRIC ENDOCRINOLOGY, vol.14, pp.565-566, 2001
Topaloğlu A.K., "Influence Of Metabolic Control On Growth In Homocystinuria Due To Cystathionine B-Synthase Deficiency", PEDIATRIC RESEARCH, vol.49, pp.796-798, 2001
Topaloğlu A.K., "Lack Of Association Between Plasma Leptin Levels And Appetite In Children With Iron Deficiency", NUTRITION, vol.17, pp.657-659, 2001
Topaloğlu A.K., "Chronic Mercury Intoxication Simulating Pheochromocytoma: Effect Of Captopril On Urinary Mercury Excretion", PEDIATRICS INTERNATIONAL, vol.43, pp.429-430, 2001
Topaloğlu A.K., "A Practical Gnrh Analogue (Triptorelin) Stimulation Test To Distinguish Constitutional Delay Of Puberty From Hypogonadotropic Hypogonadism In Prepubertal Boys", TURKISH JOURNAL OF PEDIATRICS, vol.43, pp.114-117, 2001
Topaloğlu A.K., "Effect Of Gestational Age On Plasma Fibronectin Concentrations In The Neonate", PEDIATRICS INTERNATIONAL, vol.43, pp.26-28, 2001
Topaloğlu A.K., "Primary Hyperparathyroidism In An Infant With Three Parathyroid Glands And Pulmonary Calcinosis", JOURNAL OF PEDIATRIC ENDOCRINOLOGY, vol.14, pp.1173-1175, 2001
Topaloğlu A.K., "Evaluation Of Cerebral Maturation By Visual And Quantitative Analysis Of Resting Electroencephalography In Children With Primary Nocturnal Enuresis", JOURNAL OF CHILD NEUROLOGY, vol.16, pp.714-718, 2001
Topaloğlu A.K., "Twenty Novel Mutations In The Alpha-Galactosidase A Gene Causing Fabry Disease", MOLECULAR MEDICINE, vol.5, pp.806-811, 1999
Topaloğlu A.K., "Prenatal Molecular Diagnosis Of Severe Ornithine Carbamoyltransferase Deficiency Due To A Novel Mutation, E181g", JOURNAL OF INHERITED METABOLIC DISEASE, vol.22, pp.82-83, 1999
Topaloğlu A.K., "Congenital Adrenal Hyperplasia And Bilateral Ovarian Cysts In A Neonate", CLINICAL PEDIATRICS, vol.36, pp.719-720, 1997
Yildizdaş R.D., Topaloğlu A.K., Yüksel B., Yapicioğlu Yildizdaş H., Mungan N., Sertdemir Y., Ulutan S., "Bakteriyel Sepsis Ve Septik Şoktaki Çocuklarda Tiroid Hormon Düzeyleri Ve Sağ Kalım Oranları Arasındaki Ilişki", II. Ulusal Çocuk Acil ve Yoğun Bakım Kongresi, NEVŞEHİR, TÜRKIYE, 8-12 Haziran 2005, ss.0-0
Yildizdaş R.D., Topaloğlu A.K., Tanyeli A., Erbey F., Bayram İ., Özcan K., Büyükçelik M., Kendirli S., "Ağır Laktik Asidoz Ile Seyreden Bir Histiositoz Olgusu", 39. Türk Pediatri Kongresi, NEVŞEHİR, TÜRKIYE, 17-22 Haziran 2003, cilt.0, ss.0-0
Topaloğlu A.K., Yildizdaş R.D., Yüksel B., Özer G., Mungan N., Özden Ö., "Sepsis Ve Septik Şokda Büyüme Hormonu Ve Igf-I Düzeyleri", VII. Ulusal Pediatrik Endokrinoloji Kongresi, TRABZON, TÜRKIYE, 9-11 Ekim 2002, cilt.C1-7, ss.0-0
Topaloğlu A.K., Yildizdaş R.D., Yüksel B., Özer G., Mungan N., Özden Ö., "Sepsis Ve Septik Şokda Büyüme Hormonu Ve Igf-I Düzeyleri", VII. Ulusal Pediatrik Endokrinoloji Kongresi, TRABZON, TÜRKIYE, 9-11 Ekim 2002, cilt.C1-7, ss.0-0
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