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Items: 1 to 20 of 147

1.

Mother-to-son transmission of a luteinizing hormone receptor activating mutation in a prepubertal child with testotoxicosis.

Eunice M, Philibert P, Kulshreshtha B, Audran F, Paris F, Sultan C, Ammini AC.

J Pediatr Endocrinol Metab. 2009 Mar;22(3):275-9.

PMID:
19492585
2.

The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes.

Latronico AC, Lins TS, Brito VN, Arnhold IJ, Mendonca BB.

Clin Endocrinol (Oxf). 2000 Nov;53(5):609-13.

PMID:
11106922
3.
4.

Preclinical diagnosis of testotoxicosis in a boy with an activating mutation of the luteinizing hormone receptor.

Teles M, Brito VN, Arnhold IJ, Mendonca BB, Latronico AC.

J Pediatr Endocrinol Metab. 2006 Apr;19(4):541-4.

PMID:
16759041
5.
6.

[A report of familial male-limited precocious puberty caused by a germ-line heterozygous mutation (M398T) in luteinizing hormone receptor gene].

Mao JF, Wu XY, Nie M, Lu SY, Gong FY, Dai YF.

Zhonghua Nei Ke Za Zhi. 2010 Dec;49(12):1024-7. Chinese.

PMID:
21211360
7.

Japanese familial patients with male-limited precocious puberty.

Shinagawa T, Katsumata N, Sato N, Horikawa R, Tanae A, Tanaka T.

Endocr J. 2000 Dec;47(6):777-82.

8.

Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious puberty.

Kosugi S, Van Dop C, Geffner ME, Rabl W, Carel JC, Chaussain JL, Mori T, Merendino JJ Jr, Shenker A.

Hum Mol Genet. 1995 Feb;4(2):183-8.

PMID:
7757065
9.
10.

A case of male-limited precocious puberty caused by a point mutation in the second transmembrane domain of the luteinizing hormone choriogonadotropin receptor gene.

Yano K, Kohn LD, Saji M, Kataoka N, Okuno A, Cutler GB Jr.

Biochem Biophys Res Commun. 1996 Mar 27;220(3):1036-42.

PMID:
8607787
11.

[Analysis of a family affected with familial male-limited precocious puberty due to a Ala568Val mutation in LHCGR gene].

Chen RM, Zhang Y, Yang XH, Lin XQ.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):631-4. doi: 10.3760/cma.j.issn.1003-9406.2012.06.002. Chinese.

PMID:
23225038
13.

Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: a novel constitutively activating mutation in the first transmembrane helix.

Latronico AC, Shinozaki H, Guerra G Jr, Pereira MA, Lemos Marini SH, Baptista MT, Arnhold IJ, Fanelli F, Mendonca BB, Segaloff DL.

J Clin Endocrinol Metab. 2000 Dec;85(12):4799-805.

PMID:
11134146
14.

A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty.

Latronico AC, Abell AN, Arnhold IJ, Liu X, Lins TS, Brito VN, Billerbeck AE, Segaloff DL, Mendonca BB.

J Clin Endocrinol Metab. 1998 Jul;83(7):2435-40.

PMID:
9661624
15.

Sexual pseudo-precocity caused by a somatic activating mutation of the LH receptor preceding true sexual precocity.

Kiepe D, Richter-Unruh A, Autschbach F, Kessler M, Schenk JP, Bettendorf M.

Horm Res. 2008;70(4):249-53. doi: 10.1159/000151598. Epub 2008 Sep 5.

PMID:
18772599
16.
17.

Peripheral precocious puberty in a male caused by Leydig cell adenoma harboring a somatic mutation of the LHR gene: report of a case.

Sangkhathat S, Kanngurn S, Jaruratanasirikul S, Tubtawee T, Chaiyapan W, Patrapinyokul S, Chiengkriwate P.

J Med Assoc Thai. 2010 Sep;93(9):1093-7.

PMID:
20873084
18.

A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty.

Shenker A, Laue L, Kosugi S, Merendino JJ Jr, Minegishi T, Cutler GB Jr.

Nature. 1993 Oct 14;365(6447):652-4.

PMID:
7692306
20.

A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty.

Latronico AC, Anasti J, Arnhold IJ, Mendonça BB, Domenice S, Albano MC, Zachman K, Wajchenberg BL, Tsigos C.

J Clin Endocrinol Metab. 1995 Aug;80(8):2490-4.

PMID:
7629248
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