174 related articles for article (PubMed ID: 23650337)
1. Clinical genetic testing for Kallmann syndrome.
Layman LC
J Clin Endocrinol Metab; 2013 May; 98(5):1860-2. PubMed ID: 23650337
[No Abstract] [Full Text] [Related]
2. Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes.
Costa-Barbosa FA; Balasubramanian R; Keefe KW; Shaw ND; Al-Tassan N; Plummer L; Dwyer AA; Buck CL; Choi JH; Seminara SB; Quinton R; Monies D; Meyer B; Hall JE; Pitteloud N; Crowley WF
J Clin Endocrinol Metab; 2013 May; 98(5):E943-53. PubMed ID: 23533228
[TBL] [Abstract][Full Text] [Related]
3. Kallmann syndrome in women: from genes to diagnosis and treatment.
Meczekalski B; Podfigurna-Stopa A; Smolarczyk R; Katulski K; Genazzani AR
Gynecol Endocrinol; 2013 Apr; 29(4):296-300. PubMed ID: 23368665
[TBL] [Abstract][Full Text] [Related]
4. Complex genetics in idiopathic hypogonadotropic hypogonadism.
Pitteloud N; Durrani S; Raivio T; Sykiotis GP
Front Horm Res; 2010; 39():142-153. PubMed ID: 20389092
[TBL] [Abstract][Full Text] [Related]
5. [Kallmann syndrome].
Fujieda K; Mukai T
Nihon Rinsho; 2006 Apr; 64 Suppl 4():47-53. PubMed ID: 16689283
[No Abstract] [Full Text] [Related]
6. [Advances in the studies of Kallmann syndrome].
Hao LJ; Cui YX
Zhonghua Nan Ke Xue; 2006 Jul; 12(7):647-9. PubMed ID: 16894948
[TBL] [Abstract][Full Text] [Related]
7. Next-generation sequencing of patients with congenital anosmia.
Alkelai A; Olender T; Dode C; Shushan S; Tatarskyy P; Furman-Haran E; Boyko V; Gross-Isseroff R; Halvorsen M; Greenbaum L; Milgrom R; Yamada K; Haneishi A; Blau I; Lancet D
Eur J Hum Genet; 2017 Dec; 25(12):1377-1387. PubMed ID: 29255181
[TBL] [Abstract][Full Text] [Related]
8. [Kallmann syndrome].
Sato N; Ogata T
Nihon Rinsho; 2006 Jun; Suppl 2():220-4. PubMed ID: 16817388
[No Abstract] [Full Text] [Related]
9. Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.
Sarfati J; Bouvattier C; Bry-Gauillard H; Cartes A; Bouligand J; Young J
Orphanet J Rare Dis; 2015 Jun; 10():71. PubMed ID: 26051373
[TBL] [Abstract][Full Text] [Related]
10. [Hypogonadotropic hypogonadism: new aspects in the regulation of hypothalamic-pituitary-gonadal axis].
Brioude F; Bouvattier CE; Lombès M
Ann Endocrinol (Paris); 2010 Sep; 71 Suppl 1():S33-41. PubMed ID: 21237329
[TBL] [Abstract][Full Text] [Related]
11. Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism.
Aoyama K; Mizuno H; Tanaka T; Togawa T; Negishi Y; Ohashi K; Hori I; Izawa M; Hamajima T; Saitoh S
J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1111-1118. PubMed ID: 28915117
[TBL] [Abstract][Full Text] [Related]
12. Clinical genetics of Kallmann syndrome.
Dodé C; Hardelin JP
Ann Endocrinol (Paris); 2010 May; 71(3):149-57. PubMed ID: 20362962
[TBL] [Abstract][Full Text] [Related]
13. [Isolated hypogonadotropic hypogonadism].
Shozu M
Nihon Rinsho; 2006 Apr; 64 Suppl 4():202-6. PubMed ID: 16689309
[No Abstract] [Full Text] [Related]
14. Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.
Sarfati J; Fouveaut C; Leroy C; Jeanpierre M; Hardelin JP; Dodé C
Eur J Endocrinol; 2013 Dec; 169(6):805-9. PubMed ID: 24031091
[TBL] [Abstract][Full Text] [Related]
15. The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.
Hardelin JP; Dodé C
Sex Dev; 2008; 2(4-5):181-93. PubMed ID: 18987492
[TBL] [Abstract][Full Text] [Related]
16. Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients.
Gu WJ; Zhang Q; Wang YQ; Yang GQ; Hong TP; Zhu DL; Yang JK; Ning G; Jin N; Chen K; Zang L; Wang AP; Du J; Wang XL; Yang LJ; Ba JM; Lv ZH; Dou JT; Mu YM
Exp Biol Med (Maywood); 2015 Nov; 240(11):1480-9. PubMed ID: 26031747
[TBL] [Abstract][Full Text] [Related]
17. [Molecular genetics of Kallmann syndrome: an update].
Fu C; Feng Z; Liu RZ
Zhonghua Nan Ke Xue; 2011 Apr; 17(4):361-5. PubMed ID: 21548217
[TBL] [Abstract][Full Text] [Related]
18. Mechanisms of disease: Insights into X-linked and autosomal-dominant Kallmann syndrome.
Tsai PS; Gill JC
Nat Clin Pract Endocrinol Metab; 2006 Mar; 2(3):160-71. PubMed ID: 16932275
[TBL] [Abstract][Full Text] [Related]
19. Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.
Raivio T; Avbelj M; McCabe MJ; Romero CJ; Dwyer AA; Tommiska J; Sykiotis GP; Gregory LC; Diaczok D; Tziaferi V; Elting MW; Padidela R; Plummer L; Martin C; Feng B; Zhang C; Zhou QY; Chen H; Mohammadi M; Quinton R; Sidis Y; Radovick S; Dattani MT; Pitteloud N
J Clin Endocrinol Metab; 2012 Apr; 97(4):E694-9. PubMed ID: 22319038
[TBL] [Abstract][Full Text] [Related]
20. Genetics of congenital hypogonadotropic hypogonadism in Denmark.
Tommiska J; Känsäkoski J; Christiansen P; Jørgensen N; Lawaetz JG; Juul A; Raivio T
Eur J Med Genet; 2014 Jul; 57(7):345-8. PubMed ID: 24732674
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]