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Academic Journal

46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters.

  • Authors : Yami Channaiah C; Department of Endocrinology, Seth GS Medical College and KEM Hospital, Parel, 400012 Mumbai, India.; Memon SS

Subjects: Infant, Premature* ; Gynecomastia* ; Infertility, Male* Aromatase deficiency

  • Source: Annales d'endocrinologie [Ann Endocrinol (Paris)] 2024 Feb; Vol. 85 (1), pp. 48-55. Date of Electronic Publication: 2023 Jun 20.Publisher: Elsevier Country of Publication: France NLM ID: 0116744 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2213-3941

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Academic Journal

Aromatase deficiency in an Ontario Old Order Mennonite family.

  • Source: Journal of Pediatric Endocrinology & Metabolism; Dec2021, Vol. 34 Issue 12, p1615-1618, 4p

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Academic Journal

Aromatase deficiency caused by mutation of CYP19A1 gene: A case report.

  • Authors : Li H; Department of Endocrinology, First Hospital of Lanzhou University, Lanzhou 730000. .; Fu S

Subjects: 46, XX Disorders of Sex Development*/46, XX Disorders of Sex Development*/46, XX Disorders of Sex Development*/genetics ; Gynecomastia*/Gynecomastia*/Gynecomastia*/genetics; Adult Aromatase deficiency

  • Source: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences [Zhong Nan Da Xue Xue Bao Yi Xue Ban] 2022 Jun 28; Vol. 47 (6), pp. 794-800.Publisher:

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Report

Aromatase deficiency in a tall man: Case report of two novel mutations and review of literature.

  • Authors : Singhania P; Department of Endocrinology and Metabolism, Institute of Post Graduate Medical Education and Research/SSKM Hospital, 244, AJC Bose Road, Kolkata 700020, West Bengal, India.; Dash D

  • Source: Bone reports [Bone Rep] 2022 Nov 23; Vol. 17, pp. 101642. Date of Electronic Publication: 2022 Nov 23 (Print Publication: 2022).Publisher: Elsevier Inc Country of Publication: United States NLM ID: 101646176 Publication Model: eCollection Cited Medium: Print ISSN:

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Report

A Novel Homozygous CYP19A1 Gene Mutation Causing Aromatase Deficiency.

  • Authors : Hathi D; Department of Endocrinology, Nil Ratan Sircar Medical College, Kolkata, IND.; Goswami S

  • Source: Cureus [Cureus] 2022 Feb 09; Vol. 14 (2), pp. e22059. Date of Electronic Publication: 2022 Feb 09 (Print Publication: 2022).Publisher: Cureus, Inc Country of Publication: United States NLM ID: 101596737 Publication Model: eCollection Cited Medium: Print ISSN: 2168-8184

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  • 1-10 of  3,771 results for ""Aromatase deficiency""