147 related articles for article (PubMed ID: 35133534)
21.
Zeng W; Li J; Wang X; Jiang F; Men M
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2022 Jul; 47(7):847-857. PubMed ID: 36039580
[TBL] [Abstract][Full Text] [Related]
22. GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in
Neocleous V; Fanis P; Toumba M; Tanteles GA; Schiza M; Cinarli F; Nicolaides NC; Oulas A; Spyrou GM; Mantzoros CS; Vlachakis D; Skordis N; Phylactou LA
Front Endocrinol (Lausanne); 2020; 11():626. PubMed ID: 32982993
[No Abstract] [Full Text] [Related]
23. Additional mutation in
Ichioka K; Yoshikawa T; Kimura H; Saito R
BMJ Case Rep; 2024 Jan; 17(1):. PubMed ID: 38272512
[TBL] [Abstract][Full Text] [Related]
24. [Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadism].
Tusset C; Trarbach EB; Silveira LF; Beneduzzi D; Montenegro L; Latronico AC
Arq Bras Endocrinol Metabol; 2011 Nov; 55(8):501-11. PubMed ID: 22218430
[TBL] [Abstract][Full Text] [Related]
25. Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes.
Valdes-Socin H; Rubio Almanza M; Tomé Fernández-Ladreda M; Debray FG; Bours V; Beckers A
Front Endocrinol (Lausanne); 2014; 5():109. PubMed ID: 25071724
[TBL] [Abstract][Full Text] [Related]
26. Congenital hypogonadotropic hypogonadism in females: clinical spectrum, evaluation and genetics.
Bry-Gauillard H; Trabado S; Bouligand J; Sarfati J; Francou B; Salenave S; Chanson P; Brailly-Tabard S; Guiochon-Mantel A; Young J
Ann Endocrinol (Paris); 2010 May; 71(3):158-62. PubMed ID: 20363464
[TBL] [Abstract][Full Text] [Related]
27. Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience.
Shin SJ; Sul Y; Kim JH; Cho JH; Kim GH; Kim JH; Choi JH; Yoo HW
Ann Pediatr Endocrinol Metab; 2015 Mar; 20(1):27-33. PubMed ID: 25883924
[TBL] [Abstract][Full Text] [Related]
28. Prevalence of pathogenic variants and digenic disease in patients diagnosed with normosmic hypogonadotropic hypogonadism/Kallmann Syndrome.
Poch A; Dougherty MP; Roman RA; Chorich L; Hawkins Z; Kim SH; Kim HG; Layman LC
Mol Cell Endocrinol; 2024 Aug; 589():112224. PubMed ID: 38593951
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Two families with normosmic congenital hypogonadotropic hypogonadism and biallelic mutations in KISS1R (KISS1 receptor): clinical evaluation and molecular characterization of a novel mutation.
Brioude F; Bouligand J; Francou B; Fagart J; Roussel R; Viengchareun S; Combettes L; Brailly-Tabard S; Lombès M; Young J; Guiochon-Mantel A
PLoS One; 2013; 8(1):e53896. PubMed ID: 23349759
[TBL] [Abstract][Full Text] [Related]
31. Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism.
Kim JH; Seo GH; Kim GH; Huh J; Hwang IT; Jang JH; Yoo HW; Choi JH
Exp Clin Endocrinol Diabetes; 2019 Sep; 127(8):538-544. PubMed ID: 30216942
[TBL] [Abstract][Full Text] [Related]
32. The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
Quaynor SD; Kim HG; Cappello EM; Williams T; Chorich LP; Bick DP; Sherins RJ; Layman LC
Fertil Steril; 2011 Dec; 96(6):1424-1430.e6. PubMed ID: 22035731
[TBL] [Abstract][Full Text] [Related]
33. Identification of gene variants in a cohort of hypogonadotropic hypogonadism: Diagnostic utility of custom NGS panel and WES in unravelling genetic complexity of the disease.
Gach A; Pinkier I; Sałacińska K; Szarras-Czapnik M; Salachna D; Kucińska A; Rybak-Krzyszkowska M; Sakowicz A
Mol Cell Endocrinol; 2020 Nov; 517():110968. PubMed ID: 32763379
[TBL] [Abstract][Full Text] [Related]
34. Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism.
Zhou C; Niu Y; Xu H; Li Z; Wang T; Yang W; Wang S; Wang DW; Liu J
Fertil Steril; 2018 Aug; 110(3):486-495.e5. PubMed ID: 30098700
[TBL] [Abstract][Full Text] [Related]
35. Clinical and genetic features of 64 young male paediatric patients with congenital hypogonadotropic hypogonadism.
Wang Y; Gong C; Qin M; Liu Y; Tian Y
Clin Endocrinol (Oxf); 2017 Dec; 87(6):757-766. PubMed ID: 28833369
[TBL] [Abstract][Full Text] [Related]
36. Genetic Analysis of Patients with Congenital Hypogonadotropic Hypogonadism: A Case Series.
Cannarella R; Gusmano C; Condorelli RA; Bernini A; Kaftalli J; Maltese PE; Paolacci S; Dautaj A; Marceddu G; Bertelli M; La Vignera S; Calogero AE
Int J Mol Sci; 2023 Apr; 24(8):. PubMed ID: 37108593
[TBL] [Abstract][Full Text] [Related]
37. Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism.
Beranova M; Oliveira LM; Bédécarrats GY; Schipani E; Vallejo M; Ammini AC; Quintos JB; Hall JE; Martin KA; Hayes FJ; Pitteloud N; Kaiser UB; Crowley WF; Seminara SB
J Clin Endocrinol Metab; 2001 Apr; 86(4):1580-8. PubMed ID: 11297587
[TBL] [Abstract][Full Text] [Related]
38. Homozygous p.R31H GNRH1 mutation and normosmic congenital hypogonadotropic hypogonadism in a patient and self-limited delayed puberty in his relatives.
Brachet C; Gernay C; Boros E; Soblet J; Vilain C; Heinrichs C
J Pediatr Endocrinol Metab; 2020 Sep; 33(9):1237-1240. PubMed ID: 32813678
[TBL] [Abstract][Full Text] [Related]
39. Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease.
Cangiano B; Swee DS; Quinton R; Bonomi M
Hum Genet; 2021 Jan; 140(1):77-111. PubMed ID: 32200437
[TBL] [Abstract][Full Text] [Related]
40. Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships.
Brioude F; Bouligand J; Trabado S; Francou B; Salenave S; Kamenicky P; Brailly-Tabard S; Chanson P; Guiochon-Mantel A; Young J
Eur J Endocrinol; 2010 May; 162(5):835-51. PubMed ID: 20207726
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
