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Article

Familial Gestational Hyperthyroidism Caused by a Mutant Thyrotropin Receptor Hypersensitive to Human Chorionic Gonadotropin

17 Dec 1998

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9854118
DOI: 10.1056/nejm199812173392505

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Familial Gestational Hyperthyroidism Caused by a Mutant Thyrotropin Receptor Hypersensitive to Human Chorionic GonadotropinPMID 9854118Read ↗

Prolonged and Severe Gestational Thyrotoxicosis Due to Enhanced hCG Sensitivity of a Mutant Thyrotropin Receptor.Semantic proximity Read ↗

TSH receptor gene mutations and familial gestational hyperthyroidism.Semantic proximity Read ↗

Mutations of the Human Thyrotropin Receptor Gene Causing Thyroid Hypoplasia and Persistent Congenital HypothyroidismSemantic proximity Read ↗

A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementation.Semantic proximity Read ↗

Sporadic Congenital Hyperthyroidism due to a Spontaneous Germline Mutation in the Thyrotropin Receptor Gene*Semantic proximity Read ↗

Abnormal stimulation of the thyrotrophin receptor during gestation.Semantic proximity Read ↗

Sporadic Congenital Hyperthyroidism due to a Germline Mutation in the Thyrotropin Receptor Gene (Leu 512 Gln) in a Japanese PatientSemantic proximity Read ↗

Three cases report of resistance to thyroid hormone and the genetic mutation of these patients and their family membersSemantic proximity Read ↗

Germline mutations in the thyrotropin receptor gene cause non–autoimmune autosomal dominant hyperthyroidismSemantic proximity Read ↗

Congenital Hyperthyroidism Caused by a Mutation in the Thyrotropin-Receptor GeneSemantic proximity Read ↗

A Chorionic Gonadotropin–Sensitive Mutation in the Follicle-Stimulating Hormone Receptor as a Cause of Familial Gestational Spontaneous Ovarian Hyperstimulation SyndromeSemantic proximity Read ↗

Congenital Neonatal Hyperthyroidism Caused by Germline Mutations in the TSH Receptor GeneSemantic proximity Read ↗

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