148 related articles for article (PubMed ID: 33351351)
1. [A clinical case of aromatase excess syndrome associated with 15Q21.2 duplication].
Kasyanova YV; Chernyak IY; Voronina IK; Kalinchenko NY
Probl Endokrinol (Mosk); 2020 Aug; 66(2):79-84. PubMed ID: 33351351
[TBL] [Abstract][Full Text] [Related]
2. Aromatase excess syndrome in a Chinese boy due to a novel duplication at 15q21.2.
Tan X; Wu X; Chen J; Wu Y; Li S; Chen X; Zhang X
J Pediatr Endocrinol Metab; 2019 Jan; 32(1):85-88. PubMed ID: 30530883
[TBL] [Abstract][Full Text] [Related]
3. Aromatase excess syndrome: a rare autosomal dominant disorder leading to pre- or peri-pubertal onset gynecomastia.
Fukami M; Miyado M; Nagasaki K; Shozu M; Ogata T
Pediatr Endocrinol Rev; 2014 Mar; 11(3):298-305. PubMed ID: 24716396
[TBL] [Abstract][Full Text] [Related]
4. Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency.
Verma N; Jain V; Birla S; Jain R; Sharma A
J Pediatr Endocrinol Metab; 2012; 25(11-12):1185-90. PubMed ID: 23329769
[TBL] [Abstract][Full Text] [Related]
5. Genomic basis of aromatase excess syndrome: recombination- and replication-mediated rearrangements leading to CYP19A1 overexpression.
Fukami M; Tsuchiya T; Vollbach H; Brown KA; Abe S; Ohtsu S; Wabitsch M; Burger H; Simpson ER; Umezawa A; Shihara D; Nakabayashi K; Bulun SE; Shozu M; Ogata T
J Clin Endocrinol Metab; 2013 Dec; 98(12):E2013-21. PubMed ID: 24064691
[TBL] [Abstract][Full Text] [Related]
6. Aromatase deficiency, a rare syndrome: case report.
Baykan EK; Erdoğan M; Özen S; Darcan Ş; Saygılı LF
J Clin Res Pediatr Endocrinol; 2013; 5(2):129-32. PubMed ID: 23748068
[TBL] [Abstract][Full Text] [Related]
7. Aromatase and estrogen receptor α deficiency.
Bulun SE
Fertil Steril; 2014 Feb; 101(2):323-9. PubMed ID: 24485503
[TBL] [Abstract][Full Text] [Related]
8. Aromatase Deficiency due to a Novel Mutation in
Unal E; Yıldırım R; Taş FF; Demir V; Onay H; Haspolat YK
J Clin Res Pediatr Endocrinol; 2018 Nov; 10(4):377-381. PubMed ID: 29553041
[TBL] [Abstract][Full Text] [Related]
9. Aromatase deficiency caused by mutation of
Li H; Fu S; Dai R; Sheng Z; Liu W
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2022 Jun; 47(6):794-800. PubMed ID: 35837780
[TBL] [Abstract][Full Text] [Related]
10. Aromatase Deficiency due to a Homozygous CYP19A1 Mutation in a 46,XX Egyptian Patient with Ambiguous Genitalia.
Mazen I; McElreavey K; Elaidy A; Kamel AK; Abdel-Hamid MS
Sex Dev; 2017; 11(5-6):275-279. PubMed ID: 29324451
[TBL] [Abstract][Full Text] [Related]
11. Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolism.
Chen Z; Wang O; Nie M; Elison K; Zhou D; Li M; Jiang Y; Xia W; Meng X; Chen S; Xing X
Mol Cell Endocrinol; 2015 Jan; 399():32-42. PubMed ID: 25301327
[TBL] [Abstract][Full Text] [Related]
12. Congenital disorders of estrogen biosynthesis and action.
Fukami M; Ogata T
Best Pract Res Clin Endocrinol Metab; 2022 Jan; 36(1):101580. PubMed ID: 34538723
[TBL] [Abstract][Full Text] [Related]
13. Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the
Özen S; Atik T; Korkmaz Ö; Onay H; Gökşen D; Özkınay F; Çoğulu Ö; Darcan Ş
J Clin Res Pediatr Endocrinol; 2020 Mar; 12(1):109-112. PubMed ID: 30968679
[TBL] [Abstract][Full Text] [Related]
14. Aromatase deficiency: rare cause of virilization.
Ludwikowski B; Heger S; Datz N; Richter-Unruh A; González R
Eur J Pediatr Surg; 2013 Oct; 23(5):418-22. PubMed ID: 23093430
[No Abstract] [Full Text] [Related]
15. Long-term Effect of Aromatase Inhibition in Aromatase Excess Syndrome.
Binder G; Nakamura A; Schweizer R; Ogata T; Fukami M; Nagasaki K
J Clin Endocrinol Metab; 2021 Apr; 106(5):1491-1500. PubMed ID: 33513243
[TBL] [Abstract][Full Text] [Related]
16. A potential rearrangement between CYP19 and TRPM7 genes on chromosome 15q21.2 as a cause of aromatase excess syndrome.
Tiulpakov A; Kalintchenko N; Semitcheva T; Polyakov A; Dedov I; Sverdlova P; Kolesnikova G; Peterkova V; Rubtsov P
J Clin Endocrinol Metab; 2005 Jul; 90(7):4184-90. PubMed ID: 15811932
[TBL] [Abstract][Full Text] [Related]
17. Aromatase deficiency in an Ontario Old Order Mennonite family.
Kim SY; Colaiacovo S; Dave S; Coughlin K; Langdon K; Stein R; Saleh M
J Pediatr Endocrinol Metab; 2021 Dec; 34(12):1615-1618. PubMed ID: 34348419
[TBL] [Abstract][Full Text] [Related]
18. A Novel Homozygous
Dursun F; Ceylaner S
J Clin Res Pediatr Endocrinol; 2019 May; 11(2):196-201. PubMed ID: 30074481
[TBL] [Abstract][Full Text] [Related]
19. Aromatase deficiency: a novel compound heterozygous mutation identified in a Chinese girl with severe phenotype and obvious maternal virilization.
Zhu WJ; Cheng T; Zhu H; Han B; Fan MX; Gu T; Zhao SX; Liu Y; Cheng KX; Song HD; Qiao J
Mol Cell Endocrinol; 2016 Sep; 433():66-74. PubMed ID: 27256151
[TBL] [Abstract][Full Text] [Related]
20. Aromatase deficiency: A case series of 46, XX Chinese children and a systematic review of the literature.
Fan L; Zhang B; Li L; Gong C
Clin Endocrinol (Oxf); 2020 Dec; 93(6):687-695. PubMed ID: 32623730
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]