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Quoted phrase not found in phrase index: "Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma"
Page 1
Germline SUFU mutation carriers and medulloblastoma: clinical characteristics, cancer risk, and prognosis.
Guerrini-Rousseau L, Dufour C, Varlet P, Masliah-Planchon J, Bourdeaut F, Guillaud-Bataille M, Abbas R, Bertozzi AI, Fouyssac F, Huybrechts S, Puget S, Bressac-De Paillerets B, Caron O, Sevenet N, Dimaria M, Villebasse S, Delattre O, Valteau-Couanet D, Grill J, Brugières L. Guerrini-Rousseau L, et al. Neuro Oncol. 2018 Jul 5;20(8):1122-1132. doi: 10.1093/neuonc/nox228. Neuro Oncol. 2018. PMID: 29186568 Free PMC article.
BACKGROUND: Germline mutations of suppressor of fused homolog (SUFU) predispose to sonic hedgehog (SHH) medulloblastoma. Germline SUFU mutations have been reported in nevoid basal cell carcinoma syndrome (NBCCS), but little is known about …
BACKGROUND: Germline mutations of suppressor of fused homolog (SUFU) predispose to sonic hedgehog (SHH) medulloblastoma. Germline SUF …
Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation.
Kijima C, Miyashita T, Suzuki M, Oka H, Fujii K. Kijima C, et al. Fam Cancer. 2012 Dec;11(4):565-70. doi: 10.1007/s10689-012-9548-0. Fam Cancer. 2012. PMID: 22829011
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by developmental defects and tumorigenesis. ...Together with the previous report describing three cases of non-NBCCS medulloblastoma carrying a g …
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by developme …
Nevoid basal cell carcinoma syndrome: relation with desmoplastic medulloblastoma in infancy. A population-based study and review of the literature.
Amlashi SF, Riffaud L, Brassier G, Morandi X. Amlashi SF, et al. Cancer. 2003 Aug 1;98(3):618-24. doi: 10.1002/cncr.11537. Cancer. 2003. PMID: 12879481 Free article. Review.
BACKGROUND: Patients with nevoid basal cell carcinoma syndrome (NBCCS) are believed to be predisposed to develop early-onset neoplasms including medulloblastomas (MB). ...Although patients with NBCCS are predisposed to develop multiple basal …
BACKGROUND: Patients with nevoid basal cell carcinoma syndrome (NBCCS) are believed to be predisposed to …
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective.
Garrè ML, Cama A, Bagnasco F, Morana G, Giangaspero F, Brisigotti M, Gambini C, Forni M, Rossi A, Haupt R, Nozza P, Barra S, Piatelli G, Viglizzo G, Capra V, Bruno W, Pastorino L, Massimino M, Tumolo M, Fidani P, Dallorso S, Schumacher RF, Milanaccio C, Pietsch T. Garrè ML, et al. Clin Cancer Res. 2009 Apr 1;15(7):2463-71. doi: 10.1158/1078-0432.CCR-08-2023. Epub 2009 Mar 10. Clin Cancer Res. 2009. PMID: 19276247
PURPOSE: We aimed to test the hypothesis that medulloblastoma (MB) variants show a different age distribution and clinical behavior reflecting their specific biology, and that MB occurring at very young age is associated with cancer predisposition syndromes such as …
PURPOSE: We aimed to test the hypothesis that medulloblastoma (MB) variants show a different age distribution and clinical behavior r …
Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literature.
Lacombe D, Chateil JF, Fontan D, Battin J. Lacombe D, et al. Genet Couns. 1990;1(3-4):273-7. Genet Couns. 1990. PMID: 2098052 Review.
The nevoid basal-cell carcinoma syndrome (NBCCS) is a rare autosomal-dominant inherited disorder. Its clinical manifestations are multiple basal-cell nevi and cysts of the jaw along with skeletal anomalies and various combinations …
The nevoid basal-cell carcinoma syndrome (NBCCS) is a rare autosomal-dominant inherited disorder. Its cli …
Complications of the naevoid basal cell carcinoma syndrome: results of a population based study.
Evans DG, Ladusans EJ, Rimmer S, Burnell LD, Thakker N, Farndon PA. Evans DG, et al. J Med Genet. 1993 Jun;30(6):460-4. doi: 10.1136/jmg.30.6.460. J Med Genet. 1993. PMID: 8326488 Free PMC article.
There are many potential complications which have been reported in association with the naevoid basal cell carcinoma syndrome. We have been able to show the relative frequencies of these problems in a population based study of 84 cases in …
There are many potential complications which have been reported in association with the naevoid basal cell ca …
Ovarian fibromas in pediatric patients with basal cell nevus (Gorlin) syndrome.
Ball A, Wenning J, Van Eyk N. Ball A, et al. J Pediatr Adolesc Gynecol. 2011 Feb;24(1):e5-7. doi: 10.1016/j.jpag.2010.07.005. J Pediatr Adolesc Gynecol. 2011. PMID: 20817576
BACKGROUND: Gorlin syndrome is a rare genetic condition consisting of multiple basal cell nevi associated with other entities such as medulloblastoma, skeletal abnormalities, and ovarian fibromas. ...At laparoscopy, 10 ovarian fibromas, ranging …
BACKGROUND: Gorlin syndrome is a rare genetic condition consisting of multiple basal cell nevi associated with o …
Primary malignant skin tumors in children: etiology, treatment and prognosis.
Varan A, Gököz A, Akyüz C, Kutluk T, Yalçin B, Köksal Y, Büyükpamukçu M. Varan A, et al. Pediatr Int. 2005 Dec;47(6):653-7. doi: 10.1111/j.1442-200x.2005.02145.x. Pediatr Int. 2005. PMID: 16354219
We had nine (42.9%) patients with malignant melanoma, five (23.8%) with primary skin non-Hodgkin lymphoma, three (14.3%) with Kaposi sarcoma (KS), two (9.5%) with basal cell carcinoma (BCC), and two (9.5%) with squamous cell carcinoma (SCC). RES …
We had nine (42.9%) patients with malignant melanoma, five (23.8%) with primary skin non-Hodgkin lymphoma, three (14.3%) with Kaposi sarcoma …
Identification of PATCHED mutations in medulloblastomas by direct sequencing.
Dong J, Gailani MR, Pomeroy SL, Reardon D, Bale AE. Dong J, et al. Hum Mutat. 2000 Jul;16(1):89-90. doi: 10.1002/1098-1004(200007)16:1<89::AID-HUMU18>3.0.CO;2-7. Hum Mutat. 2000. PMID: 10874314
Medulloblastoma is the most common malignant embryonic tumors of the central nervous system. The nevoid basal cell carcinoma syndrome (NBCCS), which is caused by mutations of PTCH gene on chromosome 9q22, accounts for about 2% of all medu …
Medulloblastoma is the most common malignant embryonic tumors of the central nervous system. The nevoid basal cell …
Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: support for a gatekeeper mechanism in skin tumorigenesis.
Vorechovský I, Undén AB, Sandstedt B, Toftgård R, Ståhle-Bäckdahl M. Vorechovský I, et al. Cancer Res. 1997 Nov 1;57(21):4677-81. Cancer Res. 1997. PMID: 9354420
The nevoid basal cell carcinoma (Gorlin) syndrome (NBCCS) is an autosomal dominant disorder characterized by multiple developmental defects and cancer susceptibility. ...Because basal cell carcinomas have been observed to develop i …
The nevoid basal cell carcinoma (Gorlin) syndrome (NBCCS) is an autosomal dominant disorder characterized …