BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 26274037)

  • 1. Management of Acute Myeloblastic Leukemia in a Child With Biallelic Mismatch Repair Deficiency.
    Elhasid R; Dvir R; Rosenfeld Keidar H; Ben Shachar S; Bitan M; Solar I; Durno C; Aronson M; Malkin D; Hawkins C; Bouffet E; Tabori U;
    J Pediatr Hematol Oncol; 2015 Nov; 37(8):e490-3. PubMed ID: 26274037
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1.
    Wimmer K; Rosenbaum T; Messiaen L
    Clin Genet; 2017 Apr; 91(4):507-519. PubMed ID: 27779754
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium.
    Aronson M; Gallinger S; Cohen Z; Cohen S; Dvir R; Elhasid R; Baris HN; Kariv R; Druker H; Chan H; Ling SC; Kortan P; Holter S; Semotiuk K; Malkin D; Farah R; Sayad A; Heald B; Kalady MF; Penney LS; Rideout AL; Rashid M; Hasadsri L; Pichurin P; Riegert-Johnson D; Campbell B; Bakry D; Al-Rimawi H; Alharbi QK; Alharbi M; Shamvil A; Tabori U; Durno C
    Am J Gastroenterol; 2016 Feb; 111(2):275-84. PubMed ID: 26729549
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome.
    Durno CA; Sherman PM; Aronson M; Malkin D; Hawkins C; Bakry D; Bouffet E; Gallinger S; Pollett A; Campbell B; Tabori U;
    Eur J Cancer; 2015 May; 51(8):977-83. PubMed ID: 25883011
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High frequency of mismatch repair deficiency among pediatric high grade gliomas in Jordan.
    Amayiri N; Tabori U; Campbell B; Bakry D; Aronson M; Durno C; Rakopoulos P; Malkin D; Qaddoumi I; Musharbash A; Swaidan M; Bouffet E; Hawkins C; Al-Hussaini M;
    Int J Cancer; 2016 Jan; 138(2):380-5. PubMed ID: 26293621
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The great mimicker: Phenotypic overlap between constitutional mismatch repair deficiency and Tuberous Sclerosis complex.
    Shapira Rootman M; Goldberg Y; Cohen R; Kropach N; Keidar I; Friedland R; Dotan G; Konen O; Toledano H
    Clin Genet; 2020 Feb; 97(2):296-304. PubMed ID: 31730237
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cancer and constitutional Mismatch Repair Deficiency syndrome due to homozygous MSH 6 mutation in children with Café au Lait Spots and review of literature.
    Özyörük D; Cabı EÜ; Taçyıldız N; Pınarlı F; Erdoğan AO; Hanalioğlu Ş; Erdem AY; Demir AM
    Turk J Pediatr; 2021; 63(5):893-902. PubMed ID: 34738371
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Recommendations on Surveillance and Management of Biallelic Mismatch Repair Deficiency (BMMRD) Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer.
    Durno C; Boland CR; Cohen S; Dominitz JA; Giardiello FM; Johnson DA; Kaltenbach T; Levin TR; Lieberman D; Robertson DJ; Rex DK
    Gastroenterology; 2017 May; 152(6):1605-1614. PubMed ID: 28363489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recommendations on Surveillance and Management of Biallelic Mismatch Repair Deficiency (BMMRD) Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer.
    Durno C; Boland CR; Cohen S; Dominitz JA; Giardiello FM; Johnson DA; Kaltenbach T; Levin TR; Lieberman D; Robertson DJ; Rex DK
    Am J Gastroenterol; 2017 May; 112(5):682-690. PubMed ID: 28349994
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair Deficiency.
    Bouffet E; Larouche V; Campbell BB; Merico D; de Borja R; Aronson M; Durno C; Krueger J; Cabric V; Ramaswamy V; Zhukova N; Mason G; Farah R; Afzal S; Yalon M; Rechavi G; Magimairajan V; Walsh MF; Constantini S; Dvir R; Elhasid R; Reddy A; Osborn M; Sullivan M; Hansford J; Dodgshun A; Klauber-Demore N; Peterson L; Patel S; Lindhorst S; Atkinson J; Cohen Z; Laframboise R; Dirks P; Taylor M; Malkin D; Albrecht S; Dudley RW; Jabado N; Hawkins CE; Shlien A; Tabori U
    J Clin Oncol; 2016 Jul; 34(19):2206-11. PubMed ID: 27001570
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency.
    Wimmer K; Beilken A; Nustede R; Ripperger T; Lamottke B; Ure B; Steinmann D; Reineke-Plaass T; Lehmann U; Zschocke J; Valle L; Fauth C; Kratz CP
    Fam Cancer; 2017 Jan; 16(1):67-71. PubMed ID: 27573199
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Allogeneic stem cell transplant to eliminate germline mutations in the gene for CCAAT-enhancer-binding protein α from hematopoietic cells in a family with AML.
    Stelljes M; Corbacioglu A; Schlenk RF; Döhner K; Frühwald MC; Rossig C; Ehlert K; Silling G; Müller-Tidow C; Juergens H; Döhner H; Berdel WE; Kienast J; Koschmieder S
    Leukemia; 2011 Jul; 25(7):1209-10. PubMed ID: 21455213
    [No Abstract]   [Full Text] [Related]  

  • 13. Synchronous glioblastoma and medulloblastoma in a child with mismatch repair mutation.
    Amayiri N; Al-Hussaini M; Swaidan M; Jaradat I; Qandeel M; Tabori U; Hawkins C; Musharbash A; Alsaad K; Bouffet E
    Childs Nerv Syst; 2016 Mar; 32(3):553-7. PubMed ID: 26293676
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Colorectal Cancer due to Constitutional Mismatch Repair Deficiency Mimicking Neurofibromatosis I.
    Urganci N; Genc DB; Kose G; Onal Z; Vidin OO
    Pediatrics; 2015 Oct; 136(4):e1047-50. PubMed ID: 26391938
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Constitutional mismatch repair-deficiency syndrome (CMMR-D) - a case report of a family with biallelic MSH6 mutation].
    Ilenčíková D
    Klin Onkol; 2012; 25 Suppl():S34-8. PubMed ID: 22920205
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Constitutional mismatch repair deficiency syndrome].
    Jongmans MC; Gidding CE; Loeffen J; Wesseling P; Mensenkamp A; Hoogerbrugge N
    Ned Tijdschr Geneeskd; 2015; 159():A8602. PubMed ID: 26200421
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Constitutional mismatch repair-deficiency and whole-exome sequencing as the means of the rapid detection of the causative MSH6 defect.
    Hoell JI; Gombert M; Ginzel S; Loth S; Landgraf P; Käfer V; Streiter M; Prokop A; Weiss M; Thiele R; Borkhardt A
    Klin Padiatr; 2014 Nov; 226(6-7):357-61. PubMed ID: 25431869
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Constitutional Mismatch Repair Deficiency Syndromes, a Neurofibromatosis 1 Mimicker That Hinders Timely Management.
    Mir A; AlMudhry M; AlOtaibi W; AlHazmi R; AlBaradie R; AlHarbi Q; Bashir S; Chamdine O; Housawi Y
    J Pediatr Hematol Oncol; 2023 Jul; 45(5):e613-e620. PubMed ID: 36897649
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndrome.
    Ripperger T; Schlegelberger B
    Eur J Med Genet; 2016 Mar; 59(3):133-42. PubMed ID: 26743104
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Atypical dermal melanocytosis: a diagnostic clue in constitutional mismatch repair deficiency syndrome.
    Polubothu S; Scott RH; Vabres P; Kinsler VA
    Br J Dermatol; 2017 Nov; 177(5):e185-e186. PubMed ID: 28369758
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.