Your search returned 31 results.

Results
	1.	Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism. [electronic resource] by Topaloğlu, A Kemal Producer: 20180806 In: Journal of clinical research in pediatric endocrinology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Neurokinin B signaling in puberty: human and animal studies. [electronic resource] by Topaloglu, A Kemal Producer: 20101005 In: Molecular and cellular endocrinology vol. 324 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Neurokinin B signalling in the human reproductive axis. [electronic resource] by Topaloglu, A Kemal Semple, Robert K Producer: 20120409 In: Molecular and cellular endocrinology vol. 346 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Neurokinin B and its receptor in hypogonadotropic hypogonadism. [electronic resource] by Semple, Robert K Topaloglu, A Kemal Producer: 20101206 In: Frontiers of hormone research vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions. [electronic resource] by Semple, Robert K Topaloglu, A Kemal Producer: 20100728 In: Clinical endocrinology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Genetics of Hypogonadotropic Hypogonadism. [electronic resource] by Topaloglu, A Kemal Kotan, L Damla Producer: 20160715 In: Endocrine development vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A newborn infant with generalized glutathione synthetase deficiency. [electronic resource] by Yapicioğlu, Hacer Satar, Mehmet Tutak, Ercan Narli, Nejat Topaloğlu, A Kemal Producer: 20040608 In: The Turkish journal of pediatrics vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	8.	Bone mineral changes in acute metabolic acidosis due to acute gastroenteritis. [electronic resource] by Yildizdas, Dincer Topaloglu, A Kemal Mungan, Neslihan O Yuksel, Bilgin Ozer, Guler Producer: 20050421 In: Calcified tissue international vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Three children with triple A syndrome due to a mutation (R478X) in the AAAS gene. [electronic resource] by Yuksel, Bilgin Braun, Regina Topaloglu, A Kemal Mungan, Neslihan O Ozer, Guler Huebner, Angela Producer: 20041202 In: Hormone research vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Bone calcium changes during diabetic ketoacidosis: a comparison with lactic acidosis due to volume depletion. [electronic resource] by Topaloglu, A Kemal Yildizdas, Dincer Yilmaz, H Levent Mungan, Neslihan O Yuksel, Bilgin Ozer, Guler Producer: 20051123 In: Bone vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	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. [electronic resource] by Topaloglu, A Kemal Lu, Zhi-Liang Farooqi, I Sadaf Mungan, Neslihan O Yuksel, Bilgin O'Rahilly, Stephen Millar, Robert P Producer: 20070521 In: Neuroendocrinology vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. [electronic resource] by Kotan, Leman D Isik, Emregul Turan, Ihsan Mengen, Eda Akkus, Gamze Tastan, Mehmet Gurbuz, Fatih Yuksel, Bilgin Topaloglu, A Kemal Producer: 20200330 In: Clinical genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature. [electronic resource] by Ozbek, M Nuri Senée, Valérie Aydemir, Sehnaz Kotan, L Damla Mungan, Neslihan O Yuksel, Bilgin Julier, Cécile Topaloglu, A Kemal Producer: 20120112 In: Pediatric diabetes vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide. [electronic resource] by Mengen, Eda Tunc, Selma Kotan, L Damla Nalbantoglu, Ozlem Demir, Korcan Gurbuz, Fatih Turan, Ihsan Seker, Gül Yuksel, Bilgin Topaloglu, A Kemal Producer: 20161102 In: Hormone research in paediatrics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations. [electronic resource] by Akkuş, Gamze Kotan, Leman Damla Durmaz, Erdem Mengen, Eda Turan, İhsan Ulubay, Ayça Gürbüz, Fatih Yüksel, Bilgin Tetiker, Tamer Topaloğlu, A Kemal Producer: 20180319 In: Journal of clinical research in pediatric endocrinology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism. [electronic resource] by Turan, Ihsan Hutchins, B Ian Hacihamdioglu, Bulent Kotan, L Damla Gurbuz, Fatih Ulubay, Ayca Mengen, Eda Yuksel, Bilgin Wray, Susan Topaloglu, A Kemal Producer: 20170911 In: The Journal of clinical endocrinology and metabolism vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families. [electronic resource] 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 Producer: 20151221 In: Clinical endocrinology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Inactivating KISS1 mutation and hypogonadotropic hypogonadism. [electronic resource] by Topaloglu, A Kemal Tello, Javier A Kotan, L Damla Ozbek, Mehmet N Yilmaz, M Bertan Erdogan, Seref Gurbuz, Fatih Temiz, Fatih Millar, Robert P Yuksel, Bilgin Producer: 20120224 In: The New England journal of medicine vol. 366 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration. [electronic resource] by Hutchins, B Ian Kotan, L Damla Taylor-Burds, Carol Ozkan, Yusuf Cheng, Paul J Gurbuz, Fatih Tiong, Jean D R Mengen, Eda Yuksel, Bilgin Topaloglu, A Kemal Wray, Susan Producer: 20170605 In: Endocrinology vol. 157 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	P450c17 deficiency: clinical and molecular characterization of six patients. [electronic resource] by Rosa, S Duff, C Meyer, M Lang-Muritano, M Balercia, G Boscaro, M Topaloglu, A Kemal Mioni, R Fallo, F Zuliani, L Mantero, F Schoenle, E J Biason-Lauber, A Producer: 20070510 In: The Journal of clinical endocrinology and metabolism vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 31 results.