148 related articles for article (PubMed ID: 27785413)
1. T-lymphoblastic leukemia/lymphoma in macedonian patients with Nijmegen breakage syndrome.
Kocheva SA; Martinova K; Antevska-Trajkova Z; Coneska-Jovanova B; Eftimov A; Dimovski AJ
Balkan J Med Genet; 2016 Jul; 19(1):91-94. PubMed ID: 27785413
[TBL] [Abstract][Full Text] [Related]
2. Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability.
Seemanová E; Sperling K; Neitzel H; Varon R; Hadac J; Butova O; Schröck E; Seeman P; Digweed M
J Med Genet; 2006 Mar; 43(3):218-24. PubMed ID: 16033915
[TBL] [Abstract][Full Text] [Related]
3. 657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls.
Resnick IB; Kondratenko I; Pashanov E; Maschan AA; Karachunsky A; Togoev O; Timakov A; Polyakov A; Tverskaya S; Evgrafov O; Roumiantsev AG
Am J Med Genet A; 2003 Jul; 120A(2):174-9. PubMed ID: 12833396
[TBL] [Abstract][Full Text] [Related]
4. Nijmegen breakage syndrome.
Kondratenko I; Paschenko O; Polyakov A; Bologov A
Adv Exp Med Biol; 2007; 601():61-7. PubMed ID: 17712992
[TBL] [Abstract][Full Text] [Related]
5. [Clinical, cytogenetic and molecular characterization of a new case of Nijmegen breakage syndrome in Chile].
Marcelain K; Aracena M; Be C; Navarrete CL; Moreno R; Santos M; Pincheira J
Rev Med Chil; 2004 Feb; 132(2):211-8. PubMed ID: 15449558
[TBL] [Abstract][Full Text] [Related]
6. Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study Group.
The I
Arch Dis Child; 2000 May; 82(5):400-6. PubMed ID: 10799436
[TBL] [Abstract][Full Text] [Related]
7. Nijmegen breakage syndrome: case report and review of literature.
Hasbaoui BE; Elyajouri A; Abilkassem R; Agadr A
Pan Afr Med J; 2020; 35():85. PubMed ID: 32537088
[TBL] [Abstract][Full Text] [Related]
8. T-cell lymphoblastic leukemia/lymphoma in Nijmegen breakage syndrome.
Pasic S; Vujic D; Fiorini M; Notarangelo LD
Haematologica; 2004 Aug; 89(8):ECR27. PubMed ID: 15339696
[TBL] [Abstract][Full Text] [Related]
9. Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations.
Varon R; Seemanova E; Chrzanowska K; Hnateyko O; Piekutowska-Abramczuk D; Krajewska-Walasek M; Sykut-Cegielska J; Sperling K; Reis A
Eur J Hum Genet; 2000 Nov; 8(11):900-2. PubMed ID: 11093281
[TBL] [Abstract][Full Text] [Related]
10. Determination of the frequency of the common 657Del5 Nijmegen breakage syndrome mutation in the German population: no association with risk of breast cancer.
Carlomagno F; Chang-Claude J; Dunning AM; Ponder BA
Genes Chromosomes Cancer; 1999 Aug; 25(4):393-5. PubMed ID: 10398434
[TBL] [Abstract][Full Text] [Related]
11. Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies.
Chrzanowska KH; Piekutowska-Abramczuk D; Popowska E; Gładkowska-Dura M; Małdyk J; Syczewska M; Krajewska-Walasek M; Goryluk-Kozakiewicz B; Bubała H; Gadomski A; Gaworczyk A; Kazanowska B; Kołtan A; Kuźmicz M; Luszawska-Kutrzeba T; Maciejka-Kapuścińska L; Stolarska M; Stefańska K; Sznurkowska K; Wakulińska A; Wieczorek M; Szczepański T; Kowalczyk J
Int J Cancer; 2006 Mar; 118(5):1269-74. PubMed ID: 16152606
[TBL] [Abstract][Full Text] [Related]
12. NBS1 Heterozygosity and Cancer Risk.
di Masi A; Antoccia A
Curr Genomics; 2008 Jun; 9(4):275-81. PubMed ID: 19452044
[TBL] [Abstract][Full Text] [Related]
13. A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.
Berardinelli F; di Masi A; Salvatore M; Banerjee S; Myung K; De Villartay JP; Revy P; Plebani A; Soresina A; Taruscio D; Tanzarella C; Antoccia A
Eur J Med Genet; 2007; 50(3):176-87. PubMed ID: 17395558
[TBL] [Abstract][Full Text] [Related]
14. Non-Hodgkin's lymphoma in pediatric patients with chromosomal breakage syndromes (AT and NBS): experience from the BFM trials.
Seidemann K; Henze G; Beck JD; Sauerbrey A; Kühl J; Mann G; Reiter A
Ann Oncol; 2000; 11 Suppl 1():141-5. PubMed ID: 10707797
[TBL] [Abstract][Full Text] [Related]
15. Nijmegen breakage syndrome in two half sibs with peripheral T-cell lymphoma and cortical T-cell acute lymphoid leukemia.
Sharapova SO; Golovataya EI; Shepelevich EV; Mareika YE; Guryanova IE; Stegantseva MV; Aleinikova OV
Cent Eur J Immunol; 2020; 45(4):507-510. PubMed ID: 33658897
[TBL] [Abstract][Full Text] [Related]
16. No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence.
Stanulla M; Stümm M; Dieckvoss BO; Seidemann K; Schemmel V; Müller Brechlin A; Schrappe M; Welte K; Reiter A
Br J Haematol; 2000 Apr; 109(1):117-20. PubMed ID: 10848790
[TBL] [Abstract][Full Text] [Related]
17. Unique morphological spectrum of lymphomas in Nijmegen breakage syndrome (NBS) patients with high frequency of consecutive lymphoma formation.
Gładkowska-Dura M; Dzierzanowska-Fangrat K; Dura WT; van Krieken JH; Chrzanowska KH; van Dongen JJ; Langerak AW
J Pathol; 2008 Nov; 216(3):337-44. PubMed ID: 18788073
[TBL] [Abstract][Full Text] [Related]
18. Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL).
Varon R; Reis A; Henze G; von Einsiedel HG; Sperling K; Seeger K
Cancer Res; 2001 May; 61(9):3570-2. PubMed ID: 11325820
[TBL] [Abstract][Full Text] [Related]
19. Chromosomal instability associated with adverse outcome: a case report of patient with Nijmegen breakage syndrome and rapidly developed T-NHL with complex karyotype.
Włodarczyk M; Lejman M
Mol Cytogenet; 2020; 13():35. PubMed ID: 32843899
[TBL] [Abstract][Full Text] [Related]
20. [Clinical and genealogical characteristics in families with Nijmegen breakage syndrome].
Kitsera NI; Polishchuk RS; Akopian HR; Markevych NV; Kostiuchenko LV; Troianovs'ka OO; Skoropad LL
Tsitol Genet; 2005; 39(2):72-8. PubMed ID: 16161417
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]