Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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Letter to the Editor regarding "Testotoxicosis: Report of Two Cases, One with a Novel Mutation in Luteinizing Hormone/Choriogonadotropin Receptor Gene".A Case of Familial Male-Limited Precocious Puberty in a Child With Klinefelter Syndrome

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Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

@en

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

@en

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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Bahar Özcabı

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Beyhan Tüysüz

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Cenk Büyükünal

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Feride Tahmiscioğlu Bucak

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Olcay Evliyaoğlu

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Oya Ercan

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Rahşan Özcan

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Serdar Ceylaner

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

Bicalutamide and third-generation aromatase inhibitors in testotoxicosis

Bicalutamide plus anastrozole for the treatment of gonadotropin-independent precocious puberty in boys with testotoxicosis: a phase II, open-label pilot study (BATT).

Aromatase inhibitors in pediatrics.

Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty.

Gonadotropin-independent familial sexual precocity with premature Leydig and germinal cell maturation (familial testotoxicosis): effects of a potent luteinizing hormone-releasing factor agonist and medroxyprogesterone acetate therapy in four cases.

A mutation in the first transmembrane domain of the lutropin receptor causes male precocious puberty.

Testicular leydig cell hyperplasia as a cause of familial sexual precocity.

Novel C617Y mutation in the 7th transmembrane segment of luteinizing hormone/choriogonadotropin receptor in a Japanese boy with peripheral precocious puberty.

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

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242-248

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scholarly article

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10.4274/JCRPE.2067

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P478

http://www.w3.org/2001/XMLSchema#string

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2015-09-01T00:00:00Z

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282422736

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26831561

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4677562

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Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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P2860

P2860

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932