These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
157 related articles for article (PubMed ID: 9238276)
1. Luteinizing hormone resistance syndromes. Tsigos C; Latronico C; Chrousos GP Ann N Y Acad Sci; 1997 Jun; 816():263-73. PubMed ID: 9238276 [TBL] [Abstract][Full Text] [Related]
2. An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46,XX female. Toledo SP; Brunner HG; Kraaij R; Post M; Dahia PL; Hayashida CY; Kremer H Themmen AP J Clin Endocrinol Metab; 1996 Nov; 81(11):3850-4. PubMed ID: 8923827 [TBL] [Abstract][Full Text] [Related]
3. A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptor. Latronico AC; Chai Y; Arnhold IJ; Liu X; Mendonca BB; Segaloff DL Mol Endocrinol; 1998 Mar; 12(3):442-50. PubMed ID: 9514160 [TBL] [Abstract][Full Text] [Related]
4. Ovarian resistance to luteinizing hormone: a novel cause of amenorrhea and infertility. Arnhold IJ; Latronico AC; Batista MC; Carvalho FM; Chrousos GP; Mendonça BB Fertil Steril; 1997 Feb; 67(2):394-7. PubMed ID: 9022621 [TBL] [Abstract][Full Text] [Related]
5. Brief report: testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene. Latronico AC; Anasti J; Arnhold IJ; Rapaport R; Mendonca BB; Bloise W; Castro M; Tsigos C; Chrousos GP N Engl J Med; 1996 Feb; 334(8):507-12. PubMed ID: 8559204 [No Abstract] [Full Text] [Related]
6. A novel mutation of the human luteinizing hormone receptor in 46XY and 46XX sisters. Stavrou SS; Zhu YS; Cai LQ; Katz MD; Herrera C; Defillo-Ricart M; Imperato-McGinley J J Clin Endocrinol Metab; 1998 Jun; 83(6):2091-8. PubMed ID: 9626144 [TBL] [Abstract][Full Text] [Related]
7. Male hypogonadism caused by homozygous deletion of exon 10 of the luteinizing hormone (LH) receptor: differential action of human chorionic gonadotropin and LH. Gromoll J; Eiholzer U; Nieschlag E; Simoni M J Clin Endocrinol Metab; 2000 Jun; 85(6):2281-6. PubMed ID: 10852464 [TBL] [Abstract][Full Text] [Related]
9. Inactivating mutations of luteinizing hormone beta-subunit or luteinizing hormone receptor cause oligo-amenorrhea and infertility in women. Arnhold IJ; Lofrano-Porto A; Latronico AC Horm Res; 2009; 71(2):75-82. PubMed ID: 19129711 [TBL] [Abstract][Full Text] [Related]
10. Inactivating mutations of the human luteinizing hormone receptor in both sexes. Latronico AC; Arnhold IJ Semin Reprod Med; 2012 Oct; 30(5):382-6. PubMed ID: 23044874 [TBL] [Abstract][Full Text] [Related]
11. Naturally occurring mutations of the luteinizing hormone receptor gene affecting reproduction. Latronico AC Semin Reprod Med; 2000; 18(1):17-20. PubMed ID: 11299516 [TBL] [Abstract][Full Text] [Related]
12. Evidence for genetic heterogeneity in male pseudohermaphroditism due to Leydig cell hypoplasia. Zenteno JC; Canto P; Kofman-Alfaro S; Mendez JP J Clin Endocrinol Metab; 1999 Oct; 84(10):3803-6. PubMed ID: 10523033 [TBL] [Abstract][Full Text] [Related]
13. Homozygous mutation within the conserved Ala-Phe-Asn-Glu-Thr motif of exon 7 of the LH receptor causes male pseudohermaphroditism. Gromoll J; Schulz A; Borta H; Gudermann T; Teerds KJ; Greschniok A; Nieschlag E; Seif FJ Eur J Endocrinol; 2002 Nov; 147(5):597-608. PubMed ID: 12444891 [TBL] [Abstract][Full Text] [Related]
14. A novel variant in Aktar Karakaya A; Unal E; Beştaş A; Taş F; Onay H; Haspolat YK Gynecol Endocrinol; 2020 Dec; 36(12):1136-1139. PubMed ID: 32654531 [TBL] [Abstract][Full Text] [Related]
15. Clinical features of women with resistance to luteinizing hormone. Arnhold IJ; Latronico AC; Batista MC; Izzo CR; Mendonca BB Clin Endocrinol (Oxf); 1999 Dec; 51(6):701-7. PubMed ID: 10619974 [TBL] [Abstract][Full Text] [Related]
16. Menstrual disorders and infertility caused by inactivating mutations of the luteinizing hormone receptor gene. Arnhold IJ; Latronico AC; Batista MC; Mendonca BB Fertil Steril; 1999 Apr; 71(4):597-601. PubMed ID: 10202864 [TBL] [Abstract][Full Text] [Related]
17. A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases. Yano K; Hidaka A; Saji M; Polymeropoulos MH; Okuno A; Kohn LD; Cutler GB J Clin Endocrinol Metab; 1994 Dec; 79(6):1818-23. PubMed ID: 7527413 [TBL] [Abstract][Full Text] [Related]
18. Mutations in a novel, cryptic exon of the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism. Kossack N; Simoni M; Richter-Unruh A; Themmen AP; Gromoll J PLoS Med; 2008 Apr; 5(4):e88. PubMed ID: 18433292 [TBL] [Abstract][Full Text] [Related]
19. Mutant luteinizing hormone receptors in a compound heterozygous patient with complete Leydig cell hypoplasia: abnormal processing causes signaling deficiency. Martens JW; Lumbroso S; Verhoef-Post M; Georget V; Richter-Unruh A; Szarras-Czapnik M; Romer TE; Brunner HG; Themmen AP; Sultan Ch J Clin Endocrinol Metab; 2002 Jun; 87(6):2506-13. PubMed ID: 12050206 [TBL] [Abstract][Full Text] [Related]
20. A novel inactivating mutation of the LH/chorionic gonadotrophin receptor with impaired membrane trafficking leading to Leydig cell hypoplasia type 1. Rivero-Müller A; Potorac I; Pintiaux A; Daly AF; Thiry A; Rydlewski C; Nisolle M; Parent AS; Huhtaniemi I; Beckers A Eur J Endocrinol; 2015 Jun; 172(6):K27-36. PubMed ID: 25795638 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]