167 related articles for article (PubMed ID: 36313636)
1. Congenital medulloblastoma in two brothers with SUFU-mutated Gorlin-Goltz syndrome: Case reports and literature review.
Chen Y; Zhang H; Zhao Y; Ma J
Front Oncol; 2022; 12():988798. PubMed ID: 36313636
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations.
Smith MJ; Beetz C; Williams SG; Bhaskar SS; O'Sullivan J; Anderson B; Daly SB; Urquhart JE; Bholah Z; Oudit D; Cheesman E; Kelsey A; McCabe MG; Newman WG; Evans DG
J Clin Oncol; 2014 Dec; 32(36):4155-61. PubMed ID: 25403219
[TBL] [Abstract][Full Text] [Related]
4. [Identification of a Family with SUFU Germline Deletion Based on a Case of Desmoplastic Medulloblastoma in an Infant].
Šoukalová J; Vejmělková K; Cermanová T; Kašíková K; Mikulášová A; Janyšková H; Melichárková K; Pavelka Z; Ježová M; Pospíšilová Š; Kuglík P; Valášková I; Gaillyová R; Štěrba J; Zitterbart K
Klin Onkol; 2016; 29 Suppl 1():S83-8. PubMed ID: 26691947
[TBL] [Abstract][Full Text] [Related]
5. High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age.
Brugières L; Remenieras A; Pierron G; Varlet P; Forget S; Byrde V; Bombled J; Puget S; Caron O; Dufour C; Delattre O; Bressac-de Paillerets B; Grill J
J Clin Oncol; 2012 Jun; 30(17):2087-93. PubMed ID: 22508808
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Defining the Spectrum, Treatment and Outcome of Patients With Genetically Confirmed Gorlin Syndrome From the HIT-MED Cohort.
Kloth K; Obrecht D; Sturm D; Pietsch T; Warmuth-Metz M; Bison B; Mynarek M; Rutkowski S
Front Oncol; 2021; 11():756025. PubMed ID: 34888241
[TBL] [Abstract][Full Text] [Related]
8. Retrospective investigation of hereditary syndromes in patients with medulloblastoma in a single institution.
Wang Y; Wu J; Li W; Li J; Liu R; Yang B; Li C; Jiang T
Childs Nerv Syst; 2021 Feb; 37(2):411-417. PubMed ID: 32930885
[TBL] [Abstract][Full Text] [Related]
9. Medulloblastoma in a toddler with Gorlin syndrome.
Al-Rahawan MG; Trevino S; Jacob R; Murray JC; Al-Rahawan MM
Proc (Bayl Univ Med Cent); 2018 Apr; 31(2):216-218. PubMed ID: 29706825
[TBL] [Abstract][Full Text] [Related]
10. Gorlin-Goltz Syndrome: A Case Report and Literature Review with
Kim HS; Heo S; Kim KS; Choi J; Yang JY
Arch Plast Surg; 2023 Jul; 50(4):384-388. PubMed ID: 37564720
[TBL] [Abstract][Full Text] [Related]
11. Clinical, pathological, and molecular data on desmoplastic/nodular medulloblastoma: case studies and a review of the literature.
Siegfried A; Bertozzi AI; Bourdeaut F; Sevely A; Loukh N; Grison C; Miquel C; Lafon D; Sevenet N; Pietsch T; Dufour C; Delisle MB
Clin Neuropathol; 2016; 35(3):106-13. PubMed ID: 26857864
[TBL] [Abstract][Full Text] [Related]
12. Differences in RNA and microRNA Expression Between PTCH1- and SUFU-mutated Medulloblastoma.
Gershanov S; Toledano H; Pernicone N; Fichman S; Michowiz S; Pinhasov A; Goldenberg-Cohen N; Listovsky T; Salmon-Divon M
Cancer Genomics Proteomics; 2021; 18(3):335-347. PubMed ID: 33893086
[TBL] [Abstract][Full Text] [Related]
13. Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations.
Brugières L; Pierron G; Chompret A; Paillerets BB; Di Rocco F; Varlet P; Pierre-Kahn A; Caron O; Grill J; Delattre O
J Med Genet; 2010 Feb; 47(2):142-4. PubMed ID: 19833601
[TBL] [Abstract][Full Text] [Related]
14. Spontaneous recovery from a medulloblastoma by a female with Gorlin-Goltz syndrome.
Su CW; Lin KL; Hou JW; Jung SM; Zen EC
Pediatr Neurol; 2003 Mar; 28(3):231-4. PubMed ID: 12770681
[TBL] [Abstract][Full Text] [Related]
15. Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same.
Huq AJ; Walsh M; Rajagopalan B; Finlay M; Trainer AH; Bonnet F; Sevenet N; Winship IM
Fam Cancer; 2018 Oct; 17(4):601-606. PubMed ID: 29356994
[TBL] [Abstract][Full Text] [Related]
16. Gorlin-Goltz syndrome.
Şereflican B; Tuman B; Şereflican M; Halıcıoğlu S; Özyalvaçlı G; Bayrak S
Turk Pediatri Ars; 2017 Sep; 52(3):173-177. PubMed ID: 29062253
[TBL] [Abstract][Full Text] [Related]
17. Gorlin-Goltz Syndrome: A Case Report and Literature Review.
Al-Jarboua MN; Al-Husayni AH; Al-Mgran M; Al-Omar AF
Cureus; 2019 Jan; 11(1):e3849. PubMed ID: 30891389
[TBL] [Abstract][Full Text] [Related]
18. SHH desmoplastic/nodular medulloblastoma and Gorlin syndrome in the setting of Down syndrome: case report, molecular profiling, and review of the literature.
Mangum R; Varga E; Boué DR; Capper D; Benesch M; Leonard J; Osorio DS; Pierson CR; Zumberge N; Sahm F; Schrimpf D; Pfister SM; Finlay JL
Childs Nerv Syst; 2016 Dec; 32(12):2439-2446. PubMed ID: 27444290
[TBL] [Abstract][Full Text] [Related]
19. Basal cell carcinoma of the eyelid associated with Gorlin-Goltz syndrome.
Honavar SG; Shields JA; Shields CL; Eagle RC; Demirci H; Mahmood EZ
Ophthalmology; 2001 Jun; 108(6):1115-23. PubMed ID: 11382639
[TBL] [Abstract][Full Text] [Related]
20. Gorlin-Goltz Syndrome with Intracranial Meningioma: Case Report and Review of Literature.
Narang A; Maheshwari C; Aggarwal V; Bansal P; Singh P
World Neurosurg; 2020 Jan; 133():324-330. PubMed ID: 31605858
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]