These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 27256151)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene.
    Hauri-Hohl A; Meyer-Böni M; Lang-Muritano M; Hauri-Hohl M; Schoenle EJ; Biason-Lauber A
    Clin Endocrinol (Oxf); 2011 Jul; 75(1):39-43. PubMed ID: 21521281
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of a novel CYP19A1 (aromatase) R192H mutation causing virilization of a 46,XX newborn, undervirilization of the 46,XY brother, but no virilization of the mother during pregnancies.
    Bouchoucha N; Samara-Boustani D; Pandey AV; Bony-Trifunovic H; Hofer G; Aigrain Y; Polak M; Flück CE
    Mol Cell Endocrinol; 2014 Jun; 390(1-2):8-17. PubMed ID: 24705274
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Five new cases of 46,XX aromatase deficiency: clinical follow-up from birth to puberty, a novel mutation, and a founder effect.
    Marino R; Perez Garrido N; Costanzo M; Guercio G; Juanes M; Rocco C; Ramirez P; Warman DM; Ciaccio M; Pena G; Feyling JG; Miras M; Rivarola MA; Belgorosky A; Saraco N
    J Clin Endocrinol Metab; 2015 Feb; 100(2):E301-7. PubMed ID: 25415177
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Aromatase and estrogen receptor α deficiency.
    Bulun SE
    Fertil Steril; 2014 Feb; 101(2):323-9. PubMed ID: 24485503
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissue.
    Acar S; Erbaş İM; Paketçi A; Onay H; Çankaya T; Gürsoy S; Özhan B; Abacı A; Özer E; Olguner M; Böber E; Demir K
    Turk J Pediatr; 2020; 62(5):826-830. PubMed ID: 33108086
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. A Novel Homozygous CYP19A1 Gene Mutation Causing Aromatase Deficiency.
    Hathi D; Goswami S; Sengupta N; Baidya A
    Cureus; 2022 Feb; 14(2):e22059. PubMed ID: 35340461
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.