183 related articles for article (PubMed ID: 35775118)
1. Case report of bilateral ovarian fibromas associated with de novo germline variants in PTCH1 and SMARCA4.
Higashimoto T; Smith CH; Hopkins MR; Gross J; Xing D; Lee JW; Morris T; Bodurtha J
Mol Genet Genomic Med; 2022 Sep; 10(9):e2005. PubMed ID: 35775118
[TBL] [Abstract][Full Text] [Related]
2. Bilateral ovarian fibromas as the sole manifestation of Gorlin syndrome in a 22-year-old woman: a case report and literature review.
Zhu M; Li J; Duan J; Yang J; Gu W; Jiang W
Diagn Pathol; 2023 Oct; 18(1):118. PubMed ID: 37907964
[TBL] [Abstract][Full Text] [Related]
3. Nevoid basal cell carcinoma syndrome with a unilateral giant ovarian fibroma in a Japanese 6-year-old girl.
Jimbo T; Masumoto K; Urita Y; Takayasu H; Shinkai T; Uesugi T; Gotoh C; Sakamoto N; Sasaki T; Oto T; Fukushima T; Noguchi E; Nakano Y
Eur J Pediatr; 2014 May; 173(5):667-70. PubMed ID: 24257914
[TBL] [Abstract][Full Text] [Related]
4. Imaging features of uterine and ovarian fibromatosis in Nevoid Basal Cell Carcinoma Syndrome.
Scalia AC; Farulla A; Fiocchi F; Alboni C; Torricelli P
J Radiol Case Rep; 2018 Sep; 12(9):21-30. PubMed ID: 30651920
[TBL] [Abstract][Full Text] [Related]
5. Complex karyotypic abnormality in ovarian fibroma associated with Gorlin syndrome.
Smith LM; Hu P; Meyer LJ; Coffin CM
Am J Med Genet; 2002 Sep; 112(1):61-4. PubMed ID: 12239722
[TBL] [Abstract][Full Text] [Related]
6. Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome.
Foulkes WD; Kamihara J; Evans DGR; Brugières L; Bourdeaut F; Molenaar JJ; Walsh MF; Brodeur GM; Diller L
Clin Cancer Res; 2017 Jun; 23(12):e62-e67. PubMed ID: 28620006
[TBL] [Abstract][Full Text] [Related]
7. Nevoid basal cell carcinoma syndrome: bilateral ovarian fibromas in a 3 1/2-year-old girl.
Johnson AD; Hebert AA; Esterly NB
J Am Acad Dermatol; 1986 Feb; 14(2 Pt 2):371-4. PubMed ID: 3950141
[TBL] [Abstract][Full Text] [Related]
8. Gorlin syndrome: two unusual cases of recurrent, bilateral, multinodular, calcified ovarian fibromas with conservative surgical treatment.
Fedele L; Motta F; Frontino G; Pallotti F
J Minim Invasive Gynecol; 2012; 19(2):248-51. PubMed ID: 22381971
[TBL] [Abstract][Full Text] [Related]
9. Medulloblastoma and other neoplasms in patients with heterozygous germline SUFU variants: A scoping review.
Lee SG; Evans G; Stephen M; Goren R; Bondy M; Goodman S
Am J Med Genet A; 2024 Jun; 194(6):e63496. PubMed ID: 38282294
[TBL] [Abstract][Full Text] [Related]
10. [Recurrent ovarian fibromas in condition of Gorlin syndrome].
Omrani H; Hui Bon Hoa I; Bennis H; Lehmann M; Zerr V
J Gynecol Obstet Biol Reprod (Paris); 2010 Nov; 39(7):584-7. PubMed ID: 20599329
[TBL] [Abstract][Full Text] [Related]
11. Meigs Syndrome Superimposed on Gorlin Syndrome in a 14-Year-Old Girl.
Iwasaki K; Matsushita H; Murakami H; Watanabe K; Wakatsuki A
J Pediatr Adolesc Gynecol; 2016 Oct; 29(5):e75-e77. PubMed ID: 27079916
[TBL] [Abstract][Full Text] [Related]
12. Is loss of heterozygosity at 9q22.3 (PTCH gene) and 19p13.3 (STK11 gene) involved in the pathogenesis of ovarian stromal tumors?
Tsuji T; Catasus L; Prat J
Hum Pathol; 2005 Jul; 36(7):792-6. PubMed ID: 16084949
[TBL] [Abstract][Full Text] [Related]
13. Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.
Garavelli L; Piemontese MR; Cavazza A; Rosato S; Wischmeijer A; Gelmini C; Albertini E; Albertini G; Forzano F; Franchi F; Carella M; Zelante L; Superti-Furga A
Am J Med Genet A; 2013 Nov; 161A(11):2894-901. PubMed ID: 24124115
[TBL] [Abstract][Full Text] [Related]
14. Heterozygous PTCH1 Mutations Impact the Bone Metabolism in Patients With Nevoid Basal Cell Carcinoma Syndrome Likely by Regulating SPARC Expression.
Hong Y; Zhang J; Zhang H; Li X; Qu J; Zhai J; Zhang L; Chen F; Li T
J Bone Miner Res; 2016 Jul; 31(7):1413-28. PubMed ID: 26890308
[TBL] [Abstract][Full Text] [Related]
15. Concurrent medulloblastoma and cardiac fibroma: a rare presentation of Gorlin-Goltz syndrome.
Alanazi R; Alkhaibary A; Alfaqawwy W; AlSufiani F; Ahmad N; Aljared T
Childs Nerv Syst; 2023 Sep; 39(9):2499-2504. PubMed ID: 37160435
[TBL] [Abstract][Full Text] [Related]
16. Case 128: Bilateral ovarian fibromas in nevoid basal cell carcinoma syndrome.
Fonseca RB; Grzeszczak EF
Radiology; 2008 Jan; 246(1):318-21. PubMed ID: 18096544
[No Abstract] [Full Text] [Related]
17. A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndrome.
Zhou J; Zhang G; Shi M; Liu Z; Xiao M; Fu S; Gong X; Shi X
Med Mol Morphol; 2019 Dec; 52(4):235-237. PubMed ID: 30997576
[TBL] [Abstract][Full Text] [Related]
18. Conservative treatment of recurrent ovarian fibromas in a young patient affected by Gorlin syndrome.
Seracchioli R; Bagnoli A; Colombo FM; Missiroli S; Venturoli S
Hum Reprod; 2001 Jun; 16(6):1261-3. PubMed ID: 11387302
[TBL] [Abstract][Full Text] [Related]
19. Bilateral ovarian fibromas in children.
Howell CG; Rogers DA; Gable DS; Falls GD
J Pediatr Surg; 1990 Jun; 25(6):690-1. PubMed ID: 2359009
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]