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 *

136 related articles for article (PubMed ID: 25415177)

  • 21. Ovarian and uterine development and hormonal feedback mechanism in a 46 XX patient with CYP19A1 deficiency under low dose estrogen replacement.
    Burckhardt MA; Obmann V; Wolf R; Janner M; Flück CE; Mullis PE
    Gynecol Endocrinol; 2015 May; 31(5):349-54. PubMed ID: 25585547
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters.
    Yami Channaiah C; Memon SS; Sarathi V; Lila AR; Barnabas R; Raghav D; Bhandare VV; Arya S; Thakkar H; Patil VA; Karlekar M; Kunwar A; Bandgar T
    Ann Endocrinol (Paris); 2024 Feb; 85(1):48-55. PubMed ID: 37348676
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype.
    Parween S; Fernández-Cancio M; Benito-Sanz S; Camats N; Rojas Velazquez MN; López-Siguero JP; Udhane SS; Kagawa N; Flück CE; Audí L; Pandey AV
    J Clin Endocrinol Metab; 2020 Apr; 105(4):. PubMed ID: 32060549
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Aromatase deficiency in an adolescent girl misdiagnosed as congenital adrenal hyperplasia in infancy and childhood.
    Eklioglu BS; Atabek ME; Akyurek N; Piskin MM; Kılınc M
    J Pediatr Endocrinol Metab; 2014 Jul; 27(7-8):593-4. PubMed ID: 24825080
    [No Abstract]   [Full Text] [Related]  

  • 26. 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]  

  • 27. Impact of estrogen replacement throughout childhood on growth, pituitary-gonadal axis and bone in a 46,XX patient with CYP19A1 deficiency.
    Janner M; Flück CE; Mullis PE
    Horm Res Paediatr; 2012; 78(4):261-8. PubMed ID: 22964562
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel compound heterozygous mutation of the aromatase gene in an adult man: reinforced evidence on the relationship between congenital oestrogen deficiency, adiposity and the metabolic syndrome.
    Maffei L; Rochira V; Zirilli L; Antunez P; Aranda C; Fabre B; Simone ML; Pignatti E; Simpson ER; Houssami S; Clyne CD; Carani C
    Clin Endocrinol (Oxf); 2007 Aug; 67(2):218-24. PubMed ID: 17547681
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: evaluation of gonadal function after puberty.
    Alos N; Moisan AM; Ward L; Desrochers M; Legault L; Leboeuf G; Van Vliet G; Simard J
    J Clin Endocrinol Metab; 2000 May; 85(5):1968-74. PubMed ID: 10843183
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Estrogen deficiency reversibly induces telomere shortening in mouse granulosa cells and ovarian aging in vivo.
    Bayne S; Li H; Jones ME; Pinto AR; van Sinderen M; Drummond A; Simpson ER; Liu JP
    Protein Cell; 2011 Apr; 2(4):333-46. PubMed ID: 21574023
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Aromatase deficiency: an unusual cause for primary amenorrhea with virilization.
    Sudeep K; Abraham J; Seshadri L; Seshadri MS
    J Assoc Physicians India; 2013 May; 61(5):340-3. PubMed ID: 24482950
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Child with '46, XX' disorder of sex development: clues to diagnose aromatase deficiency.
    Agrawal SS; Chakraborty PP; Sinha A; Maiti A
    BMJ Case Rep; 2019 Dec; 12(12):. PubMed ID: 31801784
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Aromatase excess syndrome: identification of cryptic duplications and deletions leading to gain of function of CYP19A1 and assessment of phenotypic determinants.
    Fukami M; Shozu M; Soneda S; Kato F; Inagaki A; Takagi H; Hanaki K; Kanzaki S; Ohyama K; Sano T; Nishigaki T; Yokoya S; Binder G; Horikawa R; Ogata T
    J Clin Endocrinol Metab; 2011 Jun; 96(6):E1035-43. PubMed ID: 21470988
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hypothesis: Persistently elevated hCG causes gestational ovarian overstimulation associated with prolonged postpartum hyperandrogenism in mothers of aromatase-deficient babies.
    Riedl S; Springer A; Häusler G; Price G; Richter-Unruh A; Stener-Victorin E; Wudy SA
    J Clin Endocrinol Metab; 2013 Aug; 98(8):3115-20. PubMed ID: 23824416
    [TBL] [Abstract][Full Text] [Related]  

  • 36. An Intron 9 CYP19 Gene Variant (IVS9+5G>A), Present in an Aromatase-Deficient Girl, Affects Normal Splicing and Is Also Present in Normal Human Steroidogenic Tissues.
    Saraco N; Nesi-Franca S; Sainz R; Marino R; Marques-Pereira R; La Pastina J; Perez Garrido N; Sandrini R; Rivarola MA; de Lacerda L; Belgorosky A
    Horm Res Paediatr; 2015; 84(4):275-82. PubMed ID: 26279340
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Impact of estrogen replacement therapy in a male with congenital aromatase deficiency caused by a novel mutation in the CYP19 gene.
    Herrmann BL; Saller B; Janssen OE; Gocke P; Bockisch A; Sperling H; Mann K; Broecker M
    J Clin Endocrinol Metab; 2002 Dec; 87(12):5476-84. PubMed ID: 12466340
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Recognizing rare disorders: aromatase deficiency.
    Jones ME; Boon WC; McInnes K; Maffei L; Carani C; Simpson ER
    Nat Clin Pract Endocrinol Metab; 2007 May; 3(5):414-21. PubMed ID: 17452968
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic and clinical spectrum of aromatase deficiency in infancy, childhood and adolescence.
    Belgorosky A; Guercio G; Pepe C; Saraco N; Rivarola MA
    Horm Res; 2009; 72(6):321-30. PubMed ID: 19844120
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 17β-Estradiol is critical for the preovulatory induction of prostaglandin E(2) synthesis in mice.
    Toda K; Ono M; Yuhki K; Ushikubi F; Saibara T
    Mol Cell Endocrinol; 2012 Oct; 362(1-2):176-82. PubMed ID: 22713853
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.