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 *

145 related articles for article (PubMed ID: 37907964)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 6. Gorlin syndrome presenting with a unilateral ovarian fibroma in a 22-year-old woman: a case report.
    Finch T; Pushpanathan C; Brown K; El-Gohary Y
    J Med Case Rep; 2012 Jun; 6():148. PubMed ID: 22691621
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ovarian preservation in a young patient with Gorlin syndrome and multiple bilateral ovarian masses.
    Morse CB; McLaren JF; Roy D; Siegelman ES; Livolsi VA; Gracia CR
    Fertil Steril; 2011 Jul; 96(1):e47-50. PubMed ID: 21565340
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Mutiple keratocystic odontogenic tumors (KCOT) in a patient with Gorlin syndrome: a case report with late presentation and absence of skin manifestations.
    Hashmi AA; Edhi MM; Faridi N; Hosein M; Khan M
    BMC Res Notes; 2016 Jul; 9():357. PubMed ID: 27448602
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. Bilateral ovarian fibroma associated with Gorlin syndrome.
    Aram S; Moghaddam NA
    J Res Med Sci; 2009 Jan; 14(1):57-61. PubMed ID: 21772861
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel PTCH1 mutations in patients with keratocystic odontogenic tumors screened for nevoid basal cell carcinoma (NBCC) syndrome.
    Pastorino L; Pollio A; Pellacani G; Guarneri C; Ghiorzo P; Longo C; Bruno W; Giusti F; Bassoli S; Bianchi-ScarrĂ  G; Ruini C; Seidenari S; Tomasi A; Ponti G
    PLoS One; 2012; 7(8):e43827. PubMed ID: 22952776
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Radiological features in 82 patients with nevoid basal cell carcinoma (NBCC or Gorlin) syndrome.
    Kimonis VE; Mehta SG; Digiovanna JJ; Bale SJ; Pastakia B
    Genet Med; 2004; 6(6):495-502. PubMed ID: 15545745
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gorlin syndrome with an ovarian leiomyoma associated with a PTCH1 second hit.
    Akizawa Y; Miyashita T; Sasaki R; Nagata R; Aoki R; Ishitani K; Nagashima Y; Matsui H; Saito K
    Am J Med Genet A; 2016 Apr; 170A(4):1029-34. PubMed ID: 26782978
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nevoid basal cell carcinoma syndrome (Gorlin syndrome).
    Lo Muzio L
    Orphanet J Rare Dis; 2008 Nov; 3():32. PubMed ID: 19032739
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Skeletal and dermatological manifestations of the nevoid Basal cell carcinoma syndrome (Gorlin-Goltz syndrome). Results of 8 patients in 12 years].
    Rupprecht M; Mensing CH; Barvencik F; Ittrich H; Heiland M; Rueger JM; Amling M; Pogoda P
    Rofo; 2007 Jun; 179(6):618-26. PubMed ID: 17492539
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gorlin-Goltz syndrome with familial manifestation.
    Pazdera J; Santava A; Kolar Z
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2022 Mar; 166(1):112-116. PubMed ID: 33542540
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple nevoid basal cell carcinoma syndrome associated with congenital orbital teratoma, caused by a PTCH1 frameshift mutation.
    Rodrigues AL; Carvalho A; Cabral R; Carneiro V; Gilardi P; Duarte CP; Puente-Prieto J; Santos P; Mota-Vieira L
    Genet Mol Res; 2014 Jul; 13(3):5654-63. PubMed ID: 25117323
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiac fibroma as an inherited manifestation of nevoid basal-cell carcinoma syndrome.
    Bossert T; Walther T; Vondrys D; Gummert JF; Kostelka M; Mohr FW
    Tex Heart Inst J; 2006; 33(1):88-90. PubMed ID: 16572881
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.