Ali K Topaloglu

Summary

Affiliation: Cukurova University
Country: Turkey

Publications

  1. doi request reprint Inactivating KISS1 mutation and hypogonadotropic hypogonadism
    A Kemal Topaloglu
    Faculty of Medicine, Department of Pediatric Endocrinology, Cukurova University, Adana, Turkey
    N Engl J Med 366:629-35. 2012
  2. doi request reprint Neurokinin B signalling in the human reproductive axis
    A Kemal Topaloglu
    Cukurova University, Department of Pediatric Endocrinology, Balcali, Adana, Turkey
    Mol Cell Endocrinol 346:57-64. 2011
  3. doi request reprint Molecular causes of hypogonadotropic hypogonadism
    Ali kemal Topaloglu
    Department of Pediatric Endocrinology, Faculty of Medicine, Cukurova University, Balcali, Adana 01330, Turkey
    Curr Opin Obstet Gynecol 22:264-70. 2010
  4. doi request reprint Neurokinin B signalling in human puberty
    A K Topaloglu
    Faculty of Medicine, Department of Pediatric Endocrinology and Metabolism, Cukurova University, Balcali, Adana, Turkey
    J Neuroendocrinol 22:765-70. 2010
  5. doi request reprint Neurokinin B signaling in puberty: human and animal studies
    A Kemal Topaloglu
    Cukurova University, Faculty of Medicine, Department of Pediatric Endocrinology and Metabolism, Balcali, Adana 01330, Turkey
    Mol Cell Endocrinol 324:64-9. 2010
  6. doi request reprint TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction
    A Kemal Topaloglu
    Cukurova University, Faculty of Medicine, Department of Pediatric Endocrinology and Metabolism, Balcali, Adana 01330, Turkey
    Nat Genet 41:354-8. 2009
  7. ncbi request reprint Athyreosis, dysgenesis, and dyshormonogenesis in congenital hypothyroidism
    Ali K Topaloglu
    Division of Pediatric Endocrinology and Metabolism, Ukurova University, Faculty of Medicine, Adana, Turkey
    Pediatr Endocrinol Rev 3:498-502. 2006
  8. ncbi request reprint 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
    A Kemal Topaloglu
    Division of Paediatric Endocrinology and Metabolism, Cukurova University, Faculty of Medicine, Adana, Turkey
    Neuroendocrinology 84:301-8. 2006
  9. ncbi request reprint Bone calcium changes during diabetic ketoacidosis: a comparison with lactic acidosis due to volume depletion
    A Kemal Topaloglu
    Division of Pediatric Endocrinology and Metabolism, Cukurova University, Faculty of Medicine, Balcali, Adana 10330, Turkey
    Bone 37:122-7. 2005
  10. ncbi request reprint Ambulatory blood pressure monitoring and serum nitric oxide concentration in type 1 diabetic children
    Ozden O Horoz
    Cukurova University, School of Medicine, Department of Pediatrics, Division of Pediatric Intensive Care Unit, Adana, Turkey
    Endocr J 56:477-85. 2009

Collaborators

Detail Information

Publications15

  1. doi request reprint Inactivating KISS1 mutation and hypogonadotropic hypogonadism
    A Kemal Topaloglu
    Faculty of Medicine, Department of Pediatric Endocrinology, Cukurova University, Adana, Turkey
    N Engl J Med 366:629-35. 2012
    ..Funded by the Scientific and Technological Research Council of Turkey [TÜBİTAK] and others.)...
  2. doi request reprint Neurokinin B signalling in the human reproductive axis
    A Kemal Topaloglu
    Cukurova University, Department of Pediatric Endocrinology, Balcali, Adana, Turkey
    Mol Cell Endocrinol 346:57-64. 2011
    ....
  3. doi request reprint Molecular causes of hypogonadotropic hypogonadism
    Ali kemal Topaloglu
    Department of Pediatric Endocrinology, Faculty of Medicine, Cukurova University, Balcali, Adana 01330, Turkey
    Curr Opin Obstet Gynecol 22:264-70. 2010
    ..Lately important developments have occurred in this field...
  4. doi request reprint Neurokinin B signalling in human puberty
    A K Topaloglu
    Faculty of Medicine, Department of Pediatric Endocrinology and Metabolism, Cukurova University, Balcali, Adana, Turkey
    J Neuroendocrinol 22:765-70. 2010
    ....
  5. doi request reprint Neurokinin B signaling in puberty: human and animal studies
    A Kemal Topaloglu
    Cukurova University, Faculty of Medicine, Department of Pediatric Endocrinology and Metabolism, Balcali, Adana 01330, Turkey
    Mol Cell Endocrinol 324:64-9. 2010
    ..In this communication, NKB involvement in puberty is reviewed from the perspective of the fundamental question of "what controls puberty?"..
  6. doi request reprint TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction
    A Kemal Topaloglu
    Cukurova University, Faculty of Medicine, Department of Pediatric Endocrinology and Metabolism, Balcali, Adana 01330, Turkey
    Nat Genet 41:354-8. 2009
    ..These findings implicate Neurokinin B as a critical central regulator of human gonadal function and suggest new approaches to the pharmacological control of human reproduction and sex hormone-related diseases...
  7. ncbi request reprint Athyreosis, dysgenesis, and dyshormonogenesis in congenital hypothyroidism
    Ali K Topaloglu
    Division of Pediatric Endocrinology and Metabolism, Ukurova University, Faculty of Medicine, Adana, Turkey
    Pediatr Endocrinol Rev 3:498-502. 2006
    ..Thus there is new insight into the pathophysiology of congenital hypothyroidism...
  8. ncbi request reprint 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
    A Kemal Topaloglu
    Division of Paediatric Endocrinology and Metabolism, Cukurova University, Faculty of Medicine, Adana, Turkey
    Neuroendocrinology 84:301-8. 2006
    ..Currently known mutations account for less than 15% of cases with normosmic hypogonadotropic hypogonadism (nIHH). The objective of the study was to identify novel hereditary associations in the pathogenesis of nIHH...
  9. ncbi request reprint Bone calcium changes during diabetic ketoacidosis: a comparison with lactic acidosis due to volume depletion
    A Kemal Topaloglu
    Division of Pediatric Endocrinology and Metabolism, Cukurova University, Faculty of Medicine, Balcali, Adana 10330, Turkey
    Bone 37:122-7. 2005
    ..Observed changes appear to be independent of calcitrophic hormones...
  10. ncbi request reprint Ambulatory blood pressure monitoring and serum nitric oxide concentration in type 1 diabetic children
    Ozden O Horoz
    Cukurova University, School of Medicine, Department of Pediatrics, Division of Pediatric Intensive Care Unit, Adana, Turkey
    Endocr J 56:477-85. 2009
    ..A prospective follow-up study on diabetic patients with normo- and micro- albuminuria is needed to confirm the predictive values of increased NO concentrations and ABPM parameters on the development of albuminuria...
  11. ncbi request reprint P450c17 deficiency: clinical and molecular characterization of six patients
    S Rosa
    University Children s Hospital, Division of Endocrinology and Diabetology, Steinwiesstrasse 75, 8032 Zurich, Switzerland
    J Clin Endocrinol Metab 92:1000-7. 2007
    ..The characteristics of P450c17 deficiency include 46,XY disorder of sex development, hypertension, hypokalemia, and lack of pubertal development...
  12. ncbi request reprint Bone mineral changes in acute metabolic acidosis due to acute gastroenteritis
    Dincer Yildizdas
    Pediatric Intensive Care Unit, Faculty of Medicine, Cukurova University, Adana, Turkey
    Calcif Tissue Int 75:380-3. 2004
    ..This study provides data regarding acute metabolic acidosis-induced changes in noninvasive parameters of bone modeling, assessed for the first time in humans...
  13. ncbi request reprint Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity
    Valérie Senée
    Génétique des Maladies Infectieuses et Autoimmunes, INSERM E102, Institut Pasteur, Paris, France
    Diabetes 53:1876-83. 2004
    ....
  14. ncbi request reprint Three children with triple A syndrome due to a mutation (R478X) in the AAAS gene
    Bilgin Yuksel
    Division of Pediatric Endocrinology and Metabolism, Cukurova University, Faculty of Medicine, Adana, Turkey
    Horm Res 61:3-6. 2004
    ..To investigate the phenotype and genotype of 3 unrelated children with triple A syndrome from southern Turkey...
  15. ncbi request reprint Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect
    Guntram Borck
    Children s Hospital of the Johannes Gutenberg University, Mainz, Germany
    J Clin Endocrinol Metab 89:4136-41. 2004
    ....