Etiology of primary ovarian insufficiency in a series young girls presenting at a pediatric endocrinology center

Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome

(2013) Sarah B. Pierce et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Resumption of Ovarian Function and Pregnancies in 358 Patients with Premature Ovarian Failure

(2011) Maud Bidet et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Premature Ovarian Failure in Patients with Autoimmune Addison's Disease: Clinical, Genetic, and Immunological Evaluation

(2011) G. Reato et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Five mutations of mitochondrial DNA polymerase-gamma (POLG) are not a prevalent etiology for spontaneous 46,XX primary ovarian insufficiency

(2010) Zhi-Bin Tong et al.   FERTILITY AND STERILITY

Phenotyping and genetic studies of 357 consecutive patients presenting with premature ovarian failure

(2009) Anne Bachelot et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Mutations inNR5A1Associated with Ovarian Insufficiency

(2009) Diana Lourenço et al.   NEW ENGLAND JOURNAL OF MEDICINE

Primary Ovarian Insufficiency

(2009) Lawrence M. Nelson   NEW ENGLAND JOURNAL OF MEDICINE

Primary ovarian insufficiency: a more accurate term for premature ovarian failure

(2007) Corrine K. Welt   CLINICAL ENDOCRINOLOGY