131 related articles for article (PubMed ID: 16760553)
1. Frasier syndrome: a rare cause of delayed puberty.
Chan WK; To KF; But WM; Lee KW
Hong Kong Med J; 2006 Jun; 12(3):225-7. PubMed ID: 16760553
[TBL] [Abstract][Full Text] [Related]
2. Laparoscopically Removed Streak Gonad Revealed Gonadoblastoma in Frasier Syndrome.
Hashimoto K; Horibe YU; Ezaki J; Kanno T; Takahashi N; Akizawa Y; Matsui H; Yamamoto T; Shibata N
Anticancer Res; 2017 Jul; 37(7):3975-3979. PubMed ID: 28668903
[TBL] [Abstract][Full Text] [Related]
3. Lack of puberty despite elevated estradiol in a 46,XY phenotypic female with Frasier syndrome.
Miyoshi Y; Santo Y; Tachikawa K; Namba N; Hirai H; Mushiake S; Nakajima S; Michigami T; Ozono K
Endocr J; 2006 Jun; 53(3):371-6. PubMed ID: 16717397
[TBL] [Abstract][Full Text] [Related]
4. WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes.
Aucella F; Bisceglia L; De Bonis P; Gigante M; Caridi G; Barbano G; Mattioli G; Perfumo F; Gesualdo L; Ghiggeri GM
Pediatr Nephrol; 2006 Oct; 21(10):1393-8. PubMed ID: 16909243
[TBL] [Abstract][Full Text] [Related]
5. Frasier syndrome: early gonadoblastoma and cyclosporine responsiveness.
Sinha A; Sharma S; Gulati A; Sharma A; Agarwala S; Hari P; Bagga A
Pediatr Nephrol; 2010 Oct; 25(10):2171-4. PubMed ID: 20419325
[TBL] [Abstract][Full Text] [Related]
6. Bilateral Gonadoblastoma in a 6-Year-old Girl With Frasier Syndrome: Need for Early Preventive Gonadectomy.
Kollios K; Karipiadou A; Papagianni M; Traeger-Synodinos J; Kosta K; Savvidou P; Stabouli S; Roilides E
J Pediatr Hematol Oncol; 2022 Nov; 44(8):471-473. PubMed ID: 35700406
[TBL] [Abstract][Full Text] [Related]
7. A female infant with Frasier syndrome showing splice site mutation in Wilms' tumor gene (WT1) intron 9.
Fujita S; Sugimoto K; Miyazawa T; Yanagida H; Tabata N; Okada M; Takemura T
Clin Nephrol; 2010 Jun; 73(6):487-91. PubMed ID: 20497763
[TBL] [Abstract][Full Text] [Related]
8. Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutation.
Kitsiou-Tzeli S; Deligiorgi M; Malaktari-Skarantavou S; Vlachopoulos C; Megremis S; Fylaktou I; Traeger-Synodinos J; Kanaka-Gantenbein C; Stefanadis C; Kanavakis E
Hormones (Athens); 2012; 11(3):361-7. PubMed ID: 22908070
[TBL] [Abstract][Full Text] [Related]
9. [Frasier syndrome: a rare syndrome with WT1 gene mutation in pediatric urology].
Zugor V; Zenker M; Schrott KM; Schott GE
Aktuelle Urol; 2006 Jan; 37(1):64-6. PubMed ID: 16440249
[TBL] [Abstract][Full Text] [Related]
10. Frasier syndrome: four new cases with unusual presentations.
Guaragna MS; Lutaif AC; Bittencourt VB; Piveta CS; Soardi FC; Castro LC; Belangero VM; Maciel-Guerra AT; Guerra-Junior G; Mello MP
Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):525-32. PubMed ID: 23295293
[TBL] [Abstract][Full Text] [Related]
11. A Unique Presentation of XY Gonadal Dysgenesis in Frasier Syndrome due to WT1 Mutation and a Literature Review.
Lavi E; Zighan M; Abu Libdeh A; Klopstock T; Weinberg-Shukron A; Renbaum P; Levy-Lahad E; Zangen D
Pediatr Endocrinol Rev; 2020 Aug; 17(4):302-307. PubMed ID: 32780953
[TBL] [Abstract][Full Text] [Related]
12. [WT1 mutation as a cause of progressive nephropathy in Frasier syndrome--case report].
Wasilewska A; Zoch-Zwierz W; Tenderenda E; Rybi-Szumińska A; Kołodziejczyk Z
Pol Merkur Lekarski; 2009 Jun; 26(156):642-4. PubMed ID: 19711733
[TBL] [Abstract][Full Text] [Related]
13. Frasier Syndrome: A 15-Year-Old Phenotypically Female Adolescent Presenting with Delayed Puberty and Nephropathy.
Shao Q; Xie X; Geng J; Yang X; Li W; Zhang Y
Children (Basel); 2023 Mar; 10(3):. PubMed ID: 36980135
[TBL] [Abstract][Full Text] [Related]
14. A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male.
Yang Y; Feng D; Huang J; Nie X; Yu Z
Eur J Pediatr; 2013 Jan; 172(1):127-9. PubMed ID: 22763603
[TBL] [Abstract][Full Text] [Related]
15. Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46,XX female.
Demmer L; Primack W; Loik V; Brown R; Therville N; McElreavey K
J Am Soc Nephrol; 1999 Oct; 10(10):2215-8. PubMed ID: 10505699
[TBL] [Abstract][Full Text] [Related]
16. Recurrence of a dysgerminoma in Frasier syndrome.
Mestrallet G; Bertholet-Thomas A; Ranchin B; Bouvier R; Frappaz D; Cochat P
Pediatr Transplant; 2011 May; 15(3):e53-5. PubMed ID: 20408995
[TBL] [Abstract][Full Text] [Related]
17. Gonadal tumor in Frasier syndrome: a review and classification.
Ezaki J; Hashimoto K; Asano T; Kanda S; Akioka Y; Hattori M; Yamamoto T; Shibata N
Cancer Prev Res (Phila); 2015 Apr; 8(4):271-6. PubMed ID: 25623218
[TBL] [Abstract][Full Text] [Related]
18. Prophylactic bilateral salpingo-oopherectomy in a 17-year-old with Frasier syndrome reveals gonadoblastoma and seminoma: a case report.
Love JD; DeMartini SD; Coppola CP
J Pediatr Surg; 2006 Nov; 41(11):e1-4. PubMed ID: 17101338
[TBL] [Abstract][Full Text] [Related]
19. Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.
Chernin G; Vega-Warner V; Schoeb DS; Heeringa SF; Ovunc B; Saisawat P; Cleper R; Ozaltin F; Hildebrandt F;
Clin J Am Soc Nephrol; 2010 Sep; 5(9):1655-62. PubMed ID: 20595692
[TBL] [Abstract][Full Text] [Related]
20. Expanding the clinical spectrum of Frasier syndrome.
Gwin K; Cajaiba MM; Caminoa-Lizarralde A; Picazo ML; Nistal M; Reyes-Múgica M
Pediatr Dev Pathol; 2008; 11(2):122-7. PubMed ID: 17378674
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]