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 *

347 related articles for article (PubMed ID: 29544218)

  • 21.
    Ponti G; Manfredini M; Pastorino L; Maccaferri M; Tomasi A; Pellacani G
    Anticancer Res; 2018 Jan; 38(1):471-476. PubMed ID: 29277811
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance.
    Casano K; Meddaugh H; Zambrano RM; Marble M; Torres JI; Lacassie Y
    Eur J Med Genet; 2020 Apr; 63(4):103842. PubMed ID: 31945512
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel patched 1 mutations in patients with nevoid basal cell carcinoma syndrome--case report.
    Škodrić-Trifunović V; Stjepanović M; Savić Ž; Ilić M; Kavečan I; Jovanović Privrodski J; Spasovski V; Stojiljković M; Pavlović S
    Croat Med J; 2015 Feb; 56(1):63-7. PubMed ID: 25727044
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Basal Cell Nevus (Gorlin) Syndrome with a Novel Heterozygous Deletion Frameshift Mutation (C.959delc, P.val322 Phe Fsx2) in the Ptch1 Gene Associated with Epiretinal Membrane, Odontogenic Keratocysts and without Skin Lesions and Falx Cerebri Calcification.
    Akaltun A; Eroz R; Dogan M; Bolu S; Onder HI; Onbas O; Kocabay K
    Genet Couns; 2016; 27(2):259-62. PubMed ID: 29485834
    [No Abstract]   [Full Text] [Related]  

  • 25. [From gene to disease: basal cell naevus syndrome].
    de Meij TG; Baars MJ; Gille JJ; Hack WW; Haasnoot K; van Hagen JM
    Ned Tijdschr Geneeskd; 2005 Jan; 149(2):78-81. PubMed ID: 15688838
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Nevoid Basal Cell Carcinoma Syndrome:
    Martinez MF; Romano MV; Martinez AP; González A; Muchnik C; Stengel FM; Mazzuoccolo LD; Azurmendi PJ
    Cells; 2019 Feb; 8(2):. PubMed ID: 30754660
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles.
    Savino M; d'Apolito M; Formica V; Baorda F; Mari F; Renieri A; Carabba E; Tarantino E; Andreucci E; Belli S; Lo Muzio L; Dallapiccola B; Zelante L; Savoia A
    Hum Mutat; 2004 Nov; 24(5):441. PubMed ID: 15459969
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Somatic mosaicism containing double mutations in
    Ikemoto Y; Takayama Y; Fujii K; Masuda M; Kato C; Hatsuse H; Fujitani K; Nagao K; Kameyama K; Ikehara H; Toyoda M; Umezawa A; Miyashita T
    J Med Genet; 2017 Aug; 54(8):579-584. PubMed ID: 28363938
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome.
    Hasan Ali O; Yurchenko AA; Pavlova O; Sartori A; Bomze D; Higgins R; Ring SS; Hartmann F; Bühler D; Fritzsche FR; Jochum W; Navarini AA; Kim A; French LE; Dermitzakis E; Christiano AM; Hohl D; Bickers DR; Nikolaev SI; Flatz L
    J Eur Acad Dermatol Venereol; 2021 Feb; 35(2):396-402. PubMed ID: 32564428
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Novel PTCH1 Mutation in a Young Child With Gorlin Syndrome and Medulloblastoma.
    Gloude NJ; Yoon JM; Crawford JR
    Pediatr Blood Cancer; 2016 Jun; 63(6):1128-9. PubMed ID: 26840755
    [No Abstract]   [Full Text] [Related]  

  • 34. Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literature.
    Lacombe D; Chateil JF; Fontan D; Battin J
    Genet Couns; 1990; 1(3-4):273-7. PubMed ID: 2098052
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Skeletal stigmata as keys to access to the composite and ancient Gorlin-Goltz syndrome history: The Egypt, Pompeii and Herculaneum lessons.
    Ponti G; Pellacani G; Tomasi A; Sammaria G; Manfredini M
    Gene; 2016 Sep; 589(2):104-11. PubMed ID: 26794802
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Manifestations of Gorlin-Goltz syndrome.
    Larsen AK; Mikkelsen DB; Hertz JM; Bygum A
    Dan Med J; 2014 May; 61(5):A4829. PubMed ID: 24814739
    [TBL] [Abstract][Full Text] [Related]  

  • 37. PTCH1 and SMO gene alterations in keratocystic odontogenic tumors.
    Sun LS; Li XF; Li TJ
    J Dent Res; 2008 Jun; 87(6):575-9. PubMed ID: 18502968
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome.
    Kimonis VE; Goldstein AM; Pastakia B; Yang ML; Kase R; DiGiovanna JJ; Bale AE; Bale SJ
    Am J Med Genet; 1997 Mar; 69(3):299-308. PubMed ID: 9096761
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Heterozygous tandem duplication within the PTCH1 gene results in nevoid basal cell carcinoma syndrome.
    Kosaki R; Nagao K; Kameyama K; Suzuki M; Fujii K; Miyashita T
    Am J Med Genet A; 2012 Jul; 158A(7):1724-8. PubMed ID: 22711650
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Multifocal desmoplastic medulloblastoma in an african-american child with nevoid basal cell carcinoma (gorlin) syndrome. Case report.
    Smucker PS; Smith JL
    J Neurosurg; 2006 Oct; 105(4 Suppl):315-20. PubMed ID: 17328283
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.