PubMed for id: 82883

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Year	Number of Results
1967	1
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1982	10
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2013	80
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2024	16

2,041 results

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Fertility outcomes in male adults with congenital hypogonadotropic hypogonadism treated during puberty with human chorionic gonadotropin and recombinant follicle stimulating hormone.

Grob F, Keshwani R, Angley E, Zacharin M. Grob F, et al. J Paediatr Child Health. 2024 Apr 4. doi: 10.1111/jpc.16540. Online ahead of print. J Paediatr Child Health. 2024. PMID: 38572627

Case report: Novel SIN3A loss-of-function variant as causative for hypogonadotropic hypogonadism in Witteveen-Kolk syndrome.

Correa Brito L, Keselman A, Villegas F, Scaglia P, Esnaola Azcoiti M, Castro S, Sanguineti N, Izquierdo A, Maier M, Bergadá I, Arberas C, Rey RA, Ropelato MG. Correa Brito L, et al. Front Genet. 2024 Mar 11;15:1354715. doi: 10.3389/fgene.2024.1354715. eCollection 2024. Front Genet. 2024. PMID: 38528912 Free PMC article.

Contributions of common genetic variants to constitutional delay of puberty and idiopathic hypogonadotropic hypogonadism.

Lippincott MF, Schafer EC, Hindman AA, He W, Brauner R, Delaney A, Grinspon R, Hall JE, Hirschhorn JN, McElreavey K, Palmert MR, Rey R, Seminara SB, Salem RM, Chan YM; Delayed Puberty Genetics Consortium. Lippincott MF, et al. J Clin Endocrinol Metab. 2024 Mar 13:dgae166. doi: 10.1210/clinem/dgae166. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38477512

Classes and predictors of reversal in male patients with congenital hypogonadotropic hypogonadism: a cross-sectional study of six international referral centres.

Dwyer AA, McDonald IR, Cangiano B, Giovanelli L, Maione L, Silveira LFG, Raivio T, Latronico AC, Young J, Quinton R, Bonomi M, Persani L, Seminara SB, Lee CS. Dwyer AA, et al. Lancet Diabetes Endocrinol. 2024 Apr;12(4):257-266. doi: 10.1016/S2213-8587(24)00028-7. Epub 2024 Mar 1. Lancet Diabetes Endocrinol. 2024. PMID: 38437850

Heavy Metal Levels in Males With Idiopathic Hypogonadotropic Hypogonadism.

Ciftel S, Ozkaya AL. Ciftel S, et al. Cureus. 2024 Jan 28;16(1):e53128. doi: 10.7759/cureus.53128. eCollection 2024 Jan. Cureus. 2024. PMID: 38420092 Free PMC article.

Additional mutation in PROKR2 and phenotypic differences in a Kallmann syndrome/normosmic congenital hypogonadotropic hypogonadism family carrying FGFR1 missense mutation.

Ichioka K, Yoshikawa T, Kimura H, Saito R. Ichioka K, et al. BMJ Case Rep. 2024 Jan 25;17(1):e258042. doi: 10.1136/bcr-2023-258042. BMJ Case Rep. 2024. PMID: 38272512 Free PMC article.

Clinical manifestations and spermatogenesis outcomes in Chinese patients with congenital hypogonadotropic hypogonadism caused by inherited or de novo FGFR1 mutations.

Yang YF, Ma HL, Wang X, Nie M, Mao JF, Wu XY. Yang YF, et al. Asian J Androl. 2024 Jan 9. doi: 10.4103/aja202366. Online ahead of print. Asian J Androl. 2024. PMID: 38227553 Free article.

Digenic CHD7 and SMCHD1 inheritance Unveils phenotypic variability in a family mainly presenting with hypogonadotropic hypogonadism.

Wang T, Ren W, Fu F, Wang H, Li Y, Duan J. Wang T, et al. Heliyon. 2023 Dec 6;10(1):e23272. doi: 10.1016/j.heliyon.2023.e23272. eCollection 2024 Jan 15. Heliyon. 2023. PMID: 38148819 Free PMC article.

Gonadotropins for pubertal induction in males with hypogonadotropic hypogonadism: systematic review and meta-analysis.

Alexander EC, Faruqi D, Farquhar R, Unadkat A, Ng Yin K, Hoskyns R, Varughese R, Howard SR. Alexander EC, et al. Eur J Endocrinol. 2024 Jan 3;190(1):S1-S11. doi: 10.1093/ejendo/lvad166. Eur J Endocrinol. 2024. PMID: 38128110 Free PMC article.

Epiphysiolysis in a 22-year-old Patient with Congenital Hypogonadotropic Hypogonadism: Case Report.

Nicolini AP, Kuga CT. Nicolini AP, et al. Rev Bras Ortop (Sao Paulo). 2021 Apr 19;58(6):e960-e963. doi: 10.1055/s-0041-1726071. eCollection 2023 Dec. Rev Bras Ortop (Sao Paulo). 2021. PMID: 38077755 Free PMC article.

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