-
1
-
-
79851507687
-
Clinical spectrum, pathophysiology and treatment of the Wiskott-Aldrich syndrome
-
Albert, M.H., Notarangelo, L.D., Ochs, H.D., Clinical spectrum, pathophysiology and treatment of the Wiskott-Aldrich syndrome. Curr. Opin. Hematol. 18:1 (2011), 42–48.
-
(2011)
Curr. Opin. Hematol.
, vol.18
, Issue.1
, pp. 42-48
-
-
Albert, M.H.1
Notarangelo, L.D.2
Ochs, H.D.3
-
2
-
-
40549106508
-
Diagnosis, genetics, and management of inherited bone marrow failure syndromes
-
Alter, B.P., Diagnosis, genetics, and management of inherited bone marrow failure syndromes. Hematology/the Education Program of the American Society of Hematology American Society of Hematology Education Program, 2007, 29–39.
-
(2007)
Hematology/the Education Program of the American Society of Hematology American Society of Hematology Education Program
, pp. 29-39
-
-
Alter, B.P.1
-
3
-
-
84899934875
-
Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c. 547G > A
-
Auer, F., Ruschendorf, F., Gombert, M., et al. Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c. 547G > A. Leukemia 28:5 (2014), 1136–1138.
-
(2014)
Leukemia
, vol.28
, Issue.5
, pp. 1136-1138
-
-
Auer, F.1
Ruschendorf, F.2
Gombert, M.3
-
4
-
-
84999959126
-
Reduced penetrance of inherited susceptibility to pre B-all caused by germline transmission of Pax5 C.547g > A
-
11-
-
Auer, F., Ruschendorf, F., Gombert, M., et al. Reduced penetrance of inherited susceptibility to pre B-all caused by germline transmission of Pax5 C.547g > A. Haematologica, 99, 2014 11-.
-
(2014)
Haematologica
, vol.99
-
-
Auer, F.1
Ruschendorf, F.2
Gombert, M.3
-
5
-
-
32544457420
-
Population-based study of cancer among carriers of a constitutional structural chromosomal rearrangement
-
Bache, I., Hasle, H., Tommerup, N., Olsen, J.H., Population-based study of cancer among carriers of a constitutional structural chromosomal rearrangement. Gene Chromosome Cancer 45:3 (2006), 231–246.
-
(2006)
Gene Chromosome Cancer
, vol.45
, Issue.3
, pp. 231-246
-
-
Bache, I.1
Hasle, H.2
Tommerup, N.3
Olsen, J.H.4
-
6
-
-
84896717941
-
Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium
-
Bakry, D., Aronson, M., Durno, C., et al. Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium. Eur. J. Cancer 50:5 (2014), 987–996.
-
(2014)
Eur. J. Cancer
, vol.50
, Issue.5
, pp. 987-996
-
-
Bakry, D.1
Aronson, M.2
Durno, C.3
-
7
-
-
84999976270
-
Novel genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the CMMRD consortium
-
Bakry, D., Campbell, B., Durno, C., et al. Novel genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the CMMRD consortium. Cancer Res., 74(23), 2014.
-
(2014)
Cancer Res.
, vol.74
, Issue.23
-
-
Bakry, D.1
Campbell, B.2
Durno, C.3
-
8
-
-
80054972817
-
Promising therapy results for lymphoid malignancies in children with chromosomal breakage syndromes (Ataxia teleangiectasia or Nijmegen-breakage syndrome): a retrospective survey
-
Bienemann, K., Burkhardt, B., Modlich, S., et al. Promising therapy results for lymphoid malignancies in children with chromosomal breakage syndromes (Ataxia teleangiectasia or Nijmegen-breakage syndrome): a retrospective survey. Br. J. Haematol. 155:4 (2011), 468–476.
-
(2011)
Br. J. Haematol.
, vol.155
, Issue.4
, pp. 468-476
-
-
Bienemann, K.1
Burkhardt, B.2
Modlich, S.3
-
9
-
-
84942342366
-
Diagnosis of constitutional mismatch repair-deficiency syndrome based on microsatellite instability and lymphocyte tolerance to methylating agents
-
Bodo, S., Colas, C., Buhard, O., et al. Diagnosis of constitutional mismatch repair-deficiency syndrome based on microsatellite instability and lymphocyte tolerance to methylating agents. Gastroenterology 149 (2015), 1017–1029.
-
(2015)
Gastroenterology
, vol.149
, pp. 1017-1029
-
-
Bodo, S.1
Colas, C.2
Buhard, O.3
-
10
-
-
84876159587
-
Physicians compliance during maintenance therapy in children with down syndrome and acute lymphoblastic leukemia
-
Bohnstedt, C., Levinsen, M., Rosthoj, S., et al. Physicians compliance during maintenance therapy in children with down syndrome and acute lymphoblastic leukemia. Leukemia 27:4 (2013), 866–870.
-
(2013)
Leukemia
, vol.27
, Issue.4
, pp. 866-870
-
-
Bohnstedt, C.1
Levinsen, M.2
Rosthoj, S.3
-
11
-
-
84938215333
-
Revisiting Li-Fraumeni syndrome from TP53 mutation carriers
-
Bougeard, G., Renaux-Petel, M., Flaman, J.M., et al. Revisiting Li-Fraumeni syndrome from TP53 mutation carriers. J. Clin. Oncol. Official J. Am. Soc. Clin. Oncol. 33:21 (2015), 2345–2352.
-
(2015)
J. Clin. Oncol. Official J. Am. Soc. Clin. Oncol.
, vol.33
, Issue.21
, pp. 2345-2352
-
-
Bougeard, G.1
Renaux-Petel, M.2
Flaman, J.M.3
-
12
-
-
77954519312
-
Methotrexate-induced side effects are not due to differences in pharmacokinetics in children with down syndrome and acute lymphoblastic leukemia
-
Buitenkamp, T.D., Mathot, R.A., de Haas, V., Pieters, R., Zwaan, C.M., Methotrexate-induced side effects are not due to differences in pharmacokinetics in children with down syndrome and acute lymphoblastic leukemia. Haematologica 95:7 (2010), 1106–1113.
-
(2010)
Haematologica
, vol.95
, Issue.7
, pp. 1106-1113
-
-
Buitenkamp, T.D.1
Mathot, R.A.2
de Haas, V.3
Pieters, R.4
Zwaan, C.M.5
-
13
-
-
84891823402
-
Acute lymphoblastic leukemia in children with down syndrome: a retrospective analysis from the Ponte di Legno study group
-
Buitenkamp, T.D., Izraeli, S., Zimmermann, M., et al. Acute lymphoblastic leukemia in children with down syndrome: a retrospective analysis from the Ponte di Legno study group. Blood 123:1 (2014), 70–77.
-
(2014)
Blood
, vol.123
, Issue.1
, pp. 70-77
-
-
Buitenkamp, T.D.1
Izraeli, S.2
Zimmermann, M.3
-
14
-
-
0027303705
-
Acute lymphoidic leukemia in a patient with thrombocytopenia/absent radii (Tar) syndrome
-
Camitta, B.M., Rock, A., Acute lymphoidic leukemia in a patient with thrombocytopenia/absent radii (Tar) syndrome. Am. J. Pediatr. Hematol. Oncol. 15:3 (1993), 335–337.
-
(1993)
Am. J. Pediatr. Hematol. Oncol.
, vol.15
, Issue.3
, pp. 335-337
-
-
Camitta, B.M.1
Rock, A.2
-
15
-
-
17344370416
-
Profound abnormality of the B/T lymphocyte ratio during chemotherapy for pediatric acute lymphoblastic leukemia
-
Caver, T.E., Slobod, K.S., Flynn, P.M., et al. Profound abnormality of the B/T lymphocyte ratio during chemotherapy for pediatric acute lymphoblastic leukemia. Leukemia 12:4 (1998), 619–622.
-
(1998)
Leukemia
, vol.12
, Issue.4
, pp. 619-622
-
-
Caver, T.E.1
Slobod, K.S.2
Flynn, P.M.3
-
16
-
-
78651103619
-
Analysis of peripheral blood T-cell subsets, natural killer cells and serum levels of cytokines in children with Down syndrome
-
Cetiner, S., Demirhan, O., Inal, T.C., Tastemir, D., Sertdemir, Y., Analysis of peripheral blood T-cell subsets, natural killer cells and serum levels of cytokines in children with Down syndrome. Int. J. Immunogenet. 37:4 (2010), 233–237.
-
(2010)
Int. J. Immunogenet.
, vol.37
, Issue.4
, pp. 233-237
-
-
Cetiner, S.1
Demirhan, O.2
Inal, T.C.3
Tastemir, D.4
Sertdemir, Y.5
-
17
-
-
84887538621
-
The inherited bone marrow failure syndromes
-
Chirnomas, S.D., Kupfer, G.M., The inherited bone marrow failure syndromes. Pediatr. Clin. N. Am. 60:6 (2013), 1291–1310.
-
(2013)
Pediatr. Clin. N. Am.
, vol.60
, Issue.6
, pp. 1291-1310
-
-
Chirnomas, S.D.1
Kupfer, G.M.2
-
18
-
-
18844428558
-
The risk of developing second cancers among survivors of childhood soft tissue sarcoma
-
Cohen, R.J., Curtis, R.E., Inskip, P.D., Fraumeni, J.F. Jr., The risk of developing second cancers among survivors of childhood soft tissue sarcoma. Cancer 103:11 (2005), 2391–2396.
-
(2005)
Cancer
, vol.103
, Issue.11
, pp. 2391-2396
-
-
Cohen, R.J.1
Curtis, R.E.2
Inskip, P.D.3
Fraumeni, J.F.4
-
19
-
-
84928963165
-
Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome
-
Durno, C.A., Sherman, P.M., Aronson, M., et al. Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome. Eur. J. Cancer 51:8 (2015), 977–983.
-
(2015)
Eur. J. Cancer
, vol.51
, Issue.8
, pp. 977-983
-
-
Durno, C.A.1
Sherman, P.M.2
Aronson, M.3
-
20
-
-
9344265760
-
The p53 gene in pediatric therapy-related leukemia and myelodysplasia
-
Felix, C.A., Hosler, M.R., Provisor, D., et al. The p53 gene in pediatric therapy-related leukemia and myelodysplasia. Blood 87:10 (1996), 4376–4381.
-
(1996)
Blood
, vol.87
, Issue.10
, pp. 4376-4381
-
-
Felix, C.A.1
Hosler, M.R.2
Provisor, D.3
-
21
-
-
84891835299
-
Complying with the European clinical trials directive while surviving the administrative pressure – an alternative approach to toxicity registration in a cancer trial
-
Frandsen, T.L., Heyman, M., Abrahamsson, J., et al. Complying with the European clinical trials directive while surviving the administrative pressure – an alternative approach to toxicity registration in a cancer trial. Eur. J. Cancer 50:2 (2014), 251–259.
-
(2014)
Eur. J. Cancer
, vol.50
, Issue.2
, pp. 251-259
-
-
Frandsen, T.L.1
Heyman, M.2
Abrahamsson, J.3
-
22
-
-
0023200576
-
Pharmacokinetics and toxicity of methotrexate in children with down-syndrome and acute lymphocytic-leukemia
-
Garre, M.L., Relling, M.V., Kalwinsky, D., et al. Pharmacokinetics and toxicity of methotrexate in children with down-syndrome and acute lymphocytic-leukemia. J. Pediatr US 111:4 (1987), 606–612.
-
(1987)
J. Pediatr US
, vol.111
, Issue.4
, pp. 606-612
-
-
Garre, M.L.1
Relling, M.V.2
Kalwinsky, D.3
-
23
-
-
84856909174
-
Congenital pancytopenia and absence of B lymphocytes in a neonate with a mutation in the ikaros gene
-
Goldman, F.D., Gurel, Z., Al-Zubeidi, D., et al. Congenital pancytopenia and absence of B lymphocytes in a neonate with a mutation in the ikaros gene. Pediatr. Blood Cancer 58:4 (2012), 591–597.
-
(2012)
Pediatr. Blood Cancer
, vol.58
, Issue.4
, pp. 591-597
-
-
Goldman, F.D.1
Gurel, Z.2
Al-Zubeidi, D.3
-
24
-
-
0033509951
-
Lymphoblastic lymphoma and excessive toxicity from chemotherapy: an unusual presentation for Fanconi anemia
-
Goldsby, R.E., Perkins, S.L., Virshup, D.M., Brothman, A.R., Bruggers, C.S., Lymphoblastic lymphoma and excessive toxicity from chemotherapy: an unusual presentation for Fanconi anemia. J. Pediatr. Hematol. Oncol. 21:3 (1999), 240–243.
-
(1999)
J. Pediatr. Hematol. Oncol.
, vol.21
, Issue.3
, pp. 240-243
-
-
Goldsby, R.E.1
Perkins, S.L.2
Virshup, D.M.3
Brothman, A.R.4
Bruggers, C.S.5
-
25
-
-
0029892336
-
Occurrence of cancer in women with Turner syndrome
-
Hasle, H., Olsen, J.H., Nielsen, J., Hansen, J., Friedrich, U., Tommerup, N., Occurrence of cancer in women with Turner syndrome. Br. J. Cancer 73:9 (1996), 1156–1159.
-
(1996)
Br. J. Cancer
, vol.73
, Issue.9
, pp. 1156-1159
-
-
Hasle, H.1
Olsen, J.H.2
Nielsen, J.3
Hansen, J.4
Friedrich, U.5
Tommerup, N.6
-
26
-
-
0342905433
-
Risks of leukaemia and solid tumours in individuals with down's syndrome
-
Hasle, H., Clemmensen, I.H., Mikkelsen, M., Risks of leukaemia and solid tumours in individuals with down's syndrome. Lancet 355:9199 (2000), 165–169.
-
(2000)
Lancet
, vol.355
, Issue.9199
, pp. 165-169
-
-
Hasle, H.1
Clemmensen, I.H.2
Mikkelsen, M.3
-
27
-
-
77954664195
-
DNA incorporation of 6-thioguanine nucleotides during maintenance therapy of childhood acute lymphoblastic leukaemia and non-Hodgkin lymphoma
-
Hedeland, R.L., Hvidt, K., Nersting, J., et al. DNA incorporation of 6-thioguanine nucleotides during maintenance therapy of childhood acute lymphoblastic leukaemia and non-Hodgkin lymphoma. Cancer Chemother. Pharmacol. 66:3 (2010), 485–491.
-
(2010)
Cancer Chemother. Pharmacol.
, vol.66
, Issue.3
, pp. 485-491
-
-
Hedeland, R.L.1
Hvidt, K.2
Nersting, J.3
-
28
-
-
13044264463
-
Hypodiploidy with less than 45 chromosomes confers adverse risk in childhood acute lymphoblastic leukemia: a report from the children's cancer group
-
Heerema, N.A., Nachman, J.B., Sather, H.N., et al. Hypodiploidy with less than 45 chromosomes confers adverse risk in childhood acute lymphoblastic leukemia: a report from the children's cancer group. Blood 94:12 (1999), 4036–4045.
-
(1999)
Blood
, vol.94
, Issue.12
, pp. 4036-4045
-
-
Heerema, N.A.1
Nachman, J.B.2
Sather, H.N.3
-
29
-
-
3843096077
-
Familial association of leukemia with colorectal cancer
-
Hemminki, K., Chen, B., Familial association of leukemia with colorectal cancer. Leukemia Res. 28:10 (2004), 1113–1115.
-
(2004)
Leukemia Res.
, vol.28
, Issue.10
, pp. 1113-1115
-
-
Hemminki, K.1
Chen, B.2
-
30
-
-
84924267622
-
T-cell all in ataxia telangiectasia cured with only 7 Weeks of Anti-leukemic therapy
-
Hersby, D.S., Sehested, A., Kristensen, K., Schmiegelow, K., T-cell all in ataxia telangiectasia cured with only 7 Weeks of Anti-leukemic therapy. J. Pediat Hematol. Oncol. 37:2 (2015), 154–155.
-
(2015)
J. Pediat Hematol. Oncol.
, vol.37
, Issue.2
, pp. 154-155
-
-
Hersby, D.S.1
Sehested, A.2
Kristensen, K.3
Schmiegelow, K.4
-
31
-
-
84874647204
-
The genomic landscape of hypodiploid acute lymphoblastic leukemia
-
Holmfeldt, L., Wei, L., Diaz-Flores, E., et al. The genomic landscape of hypodiploid acute lymphoblastic leukemia. Nat. Genet. 45:3 (2013), 242–252.
-
(2013)
Nat. Genet.
, vol.45
, Issue.3
, pp. 242-252
-
-
Holmfeldt, L.1
Wei, L.2
Diaz-Flores, E.3
-
32
-
-
79551513215
-
Pharmacogenetic and germline prognostic markers of lung cancer
-
Horgan, A.M., Yang, B., Azad, A.K., et al. Pharmacogenetic and germline prognostic markers of lung cancer. J. Thorac. Oncol. Official Publ. Int. Assoc. Study Lung Cancer 6:2 (2011), 296–304.
-
(2011)
J. Thorac. Oncol. Official Publ. Int. Assoc. Study Lung Cancer
, vol.6
, Issue.2
, pp. 296-304
-
-
Horgan, A.M.1
Yang, B.2
Azad, A.K.3
-
33
-
-
84925512075
-
X-linked agammaglobulinemia associated with B-precursor acute lymphoblastic leukemia
-
Hoshino, A., Okuno, Y., Migita, M., et al. X-linked agammaglobulinemia associated with B-precursor acute lymphoblastic leukemia. J. Clin. Immunol. 35:2 (2015), 108–111.
-
(2015)
J. Clin. Immunol.
, vol.35
, Issue.2
, pp. 108-111
-
-
Hoshino, A.1
Okuno, Y.2
Migita, M.3
-
34
-
-
84871145966
-
The thirteenth international childhood acute lymphoblastic leukemia workshop report: La Jolla, CA, USA, December 7-9, 2011
-
Hunger, S.P., Baruchel, A., Biondi, A., et al. The thirteenth international childhood acute lymphoblastic leukemia workshop report: La Jolla, CA, USA, December 7-9, 2011. Pediatr. Blood Cancer 60:2 (2013), 344–348.
-
(2013)
Pediatr. Blood Cancer
, vol.60
, Issue.2
, pp. 344-348
-
-
Hunger, S.P.1
Baruchel, A.2
Biondi, A.3
-
35
-
-
84924540717
-
A functional variant in miR-605 modifies the age of onset in Li-Fraumeni syndrome
-
Id Said, B., Malkin, D., A functional variant in miR-605 modifies the age of onset in Li-Fraumeni syndrome. Cancer Genet. 208:1–2 (2015), 47–51.
-
(2015)
Cancer Genet.
, vol.208
, Issue.1-2
, pp. 47-51
-
-
Id Said, B.1
Malkin, D.2
-
36
-
-
84891816797
-
How I treat ALL in down's syndrome: pathobiology and management
-
Izraeli, S., Vora, A., Zwaan, C.M., Whitlock, J., How I treat ALL in down's syndrome: pathobiology and management. Blood 123:1 (2014), 35–40.
-
(2014)
Blood
, vol.123
, Issue.1
, pp. 35-40
-
-
Izraeli, S.1
Vora, A.2
Zwaan, C.M.3
Whitlock, J.4
-
37
-
-
84939265615
-
Dyskeratosis congenita with acute pre B cell lymphoblastic leukemia in a 10-year-old Girl
-
Kalasekhar, V., Ranjith, S., Venkatesh, C., Bhat, B.V., Biswajith, D., Kayal, S., Dyskeratosis congenita with acute pre B cell lymphoblastic leukemia in a 10-year-old Girl. Indian J. Pediatr. 82:9 (2015), 867–868.
-
(2015)
Indian J. Pediatr.
, vol.82
, Issue.9
, pp. 867-868
-
-
Kalasekhar, V.1
Ranjith, S.2
Venkatesh, C.3
Bhat, B.V.4
Biswajith, D.5
Kayal, S.6
-
38
-
-
84930272290
-
TP53 germline mutation may affect response to anticancer treatments: analysis of an intensively treated Li-Fraumeni family
-
Kappel, S., Janschek, E., Wolf, B., et al. TP53 germline mutation may affect response to anticancer treatments: analysis of an intensively treated Li-Fraumeni family. Breast Cancer Res. Treat. 151:3 (2015), 671–678.
-
(2015)
Breast Cancer Res. Treat.
, vol.151
, Issue.3
, pp. 671-678
-
-
Kappel, S.1
Janschek, E.2
Wolf, B.3
-
39
-
-
84862777927
-
Regulation of Rev1 by the Fanconi anemia core complex
-
Kim, H., Yang, K., Dejsuphong, D., D'Andrea, A.D., Regulation of Rev1 by the Fanconi anemia core complex. Nat. Struct. Mol. Biol. 19:2 (2012), 164–170.
-
(2012)
Nat. Struct. Mol. Biol.
, vol.19
, Issue.2
, pp. 164-170
-
-
Kim, H.1
Yang, K.2
Dejsuphong, D.3
D'Andrea, A.D.4
-
40
-
-
79955043471
-
Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes
-
Kratz, C.P., Rapisuwon, S., Reed, H., Hasle, H., Rosenberg, P.S., Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes. Am. J. Med. Genet. C 157C:2 (2011), 83–89.
-
(2011)
Am. J. Med. Genet. C
, vol.157C
, Issue.2
, pp. 83-89
-
-
Kratz, C.P.1
Rapisuwon, S.2
Reed, H.3
Hasle, H.4
Rosenberg, P.S.5
-
41
-
-
84928205738
-
Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes
-
Kratz, C.P., Franke, L., Peters, H., et al. Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes. Br. J. Cancer 112:8 (2015), 1392–1397.
-
(2015)
Br. J. Cancer
, vol.112
, Issue.8
, pp. 1392-1397
-
-
Kratz, C.P.1
Franke, L.2
Peters, H.3
-
42
-
-
84932628341
-
PD-1 Blockade in tumors with mismatch-repair deficiency
-
Le, D.T., Uram, J.N., Wang, H., et al. PD-1 Blockade in tumors with mismatch-repair deficiency. New Engl. J. Med. 372:26 (2015), 2509–2520.
-
(2015)
New Engl. J. Med.
, vol.372
, Issue.26
, pp. 2509-2520
-
-
Le, D.T.1
Uram, J.N.2
Wang, H.3
-
43
-
-
84898945538
-
Domains of genome-wide gene expression dysregulation in down's syndrome
-
Letourneau, A., Santoni, F.A., Bonilla, X., et al. Domains of genome-wide gene expression dysregulation in down's syndrome. Nature 508:7496 (2014), 345–350.
-
(2014)
Nature
, vol.508
, Issue.7496
, pp. 345-350
-
-
Letourneau, A.1
Santoni, F.A.2
Bonilla, X.3
-
44
-
-
80053646494
-
Familial myelodysplastic syndromes: a review of the literature
-
Liew, E., Owen, C., Familial myelodysplastic syndromes: a review of the literature. Haematol Hematol J. 96:10 (2011), 1536–1542.
-
(2011)
Haematol Hematol J.
, vol.96
, Issue.10
, pp. 1536-1542
-
-
Liew, E.1
Owen, C.2
-
45
-
-
84923301480
-
How i treat juvenile myelomonocytic leukemia
-
Locatelli, F., Niemeyer, C.M., How i treat juvenile myelomonocytic leukemia. Blood 125:7 (2015), 1083–1090.
-
(2015)
Blood
, vol.125
, Issue.7
, pp. 1083-1090
-
-
Locatelli, F.1
Niemeyer, C.M.2
-
46
-
-
1942487219
-
Immunologic monitoring of maintenance therapy for acute lymphoblastic leukaemia in children-preliminary report
-
Luczynski, W., Stasiak-Barmuta, A., Krawczuk-Rybak, M., Immunologic monitoring of maintenance therapy for acute lymphoblastic leukaemia in children-preliminary report. Pediatr. Blood Cancer 42:5 (2004), 416–420.
-
(2004)
Pediatr. Blood Cancer
, vol.42
, Issue.5
, pp. 416-420
-
-
Luczynski, W.1
Stasiak-Barmuta, A.2
Krawczuk-Rybak, M.3
-
47
-
-
79551623766
-
Risk factors for treatment related mortality in childhood acute lymphoblastic leukaemia
-
Lund, B., Asberg, A., Heyman, M., et al. Risk factors for treatment related mortality in childhood acute lymphoblastic leukaemia. Pediatr. Blood Cancer 56:4 (2011), 551–559.
-
(2011)
Pediatr. Blood Cancer
, vol.56
, Issue.4
, pp. 551-559
-
-
Lund, B.1
Asberg, A.2
Heyman, M.3
-
48
-
-
84964698756
-
Predisposition to pediatric and hematologic cancers: a moving target
-
Malkin, D., Nichols, K.E., Zelley, K., Schiffman, J.D., Predisposition to pediatric and hematologic cancers: a moving target. American Society of Clinical Oncology Educational Book/ASCO American Society of Clinical Oncology Meeting, 2014, e44–e55.
-
(2014)
American Society of Clinical Oncology Educational Book/ASCO American Society of Clinical Oncology Meeting
, pp. e44-e55
-
-
Malkin, D.1
Nichols, K.E.2
Zelley, K.3
Schiffman, J.D.4
-
49
-
-
34248198839
-
Chemotherapy for myeloid malignancy in children with Fanconi anemia
-
Mehta, P.A., Ileri, T., Harris, R.E., et al. Chemotherapy for myeloid malignancy in children with Fanconi anemia. Pediatr. Blood Cancer 48:7 (2007), 668–672.
-
(2007)
Pediatr. Blood Cancer
, vol.48
, Issue.7
, pp. 668-672
-
-
Mehta, P.A.1
Ileri, T.2
Harris, R.E.3
-
50
-
-
70350152582
-
Genetic risk factors for melanoma
-
Meyle, K.D., Guldberg, P., Genetic risk factors for melanoma. Hum. Genet. 126:4 (2009), 499–510.
-
(2009)
Hum. Genet.
, vol.126
, Issue.4
, pp. 499-510
-
-
Meyle, K.D.1
Guldberg, P.2
-
51
-
-
84999968324
-
Germline aberrations of PAX5 cause susceptibility to pre-B cell acute lymphoblastic leukemia
-
52-
-
Miething, C., Shah, S., Schrader, K., et al. Germline aberrations of PAX5 cause susceptibility to pre-B cell acute lymphoblastic leukemia. Onkologie, 36, 2013 52-.
-
(2013)
Onkologie
, vol.36
-
-
Miething, C.1
Shah, S.2
Schrader, K.3
-
52
-
-
84933518382
-
Inherited genetic variation in childhood acute lymphoblastic leukemia
-
Moriyama, T., Relling, M.V., Yang, J.J., Inherited genetic variation in childhood acute lymphoblastic leukemia. Blood 125:26 (2015), 3988–3995.
-
(2015)
Blood
, vol.125
, Issue.26
, pp. 3988-3995
-
-
Moriyama, T.1
Relling, M.V.2
Yang, J.J.3
-
53
-
-
34548027243
-
Outcome of treatment in children with hypodiploid acute lymphoblastic leukemia
-
Nachman, J.B., Heerema, N.A., Sather, H., et al. Outcome of treatment in children with hypodiploid acute lymphoblastic leukemia. Blood 110:4 (2007), 1112–1115.
-
(2007)
Blood
, vol.110
, Issue.4
, pp. 1112-1115
-
-
Nachman, J.B.1
Heerema, N.A.2
Sather, H.3
-
54
-
-
84929130522
-
Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia
-
Noetzli, L., Lo, R.W., Lee-Sherick, A.B., et al. Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia. Nat. Genet. 47:5 (2015), 535–538.
-
(2015)
Nat. Genet.
, vol.47
, Issue.5
, pp. 535-538
-
-
Noetzli, L.1
Lo, R.W.2
Lee-Sherick, A.B.3
-
55
-
-
84888311432
-
Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse
-
Perez-Andreu, V., Roberts, K.G., Harvey, R.C., et al. Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse. Nat. Genet. 45:12 (2013), 1494–1498.
-
(2013)
Nat. Genet.
, vol.45
, Issue.12
, pp. 1494-1498
-
-
Perez-Andreu, V.1
Roberts, K.G.2
Harvey, R.C.3
-
56
-
-
84921750869
-
A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults
-
Perez-Andreu, V., Roberts, K.G., Xu, H., et al. A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults. Blood 125:4 (2015), 680–686.
-
(2015)
Blood
, vol.125
, Issue.4
, pp. 680-686
-
-
Perez-Andreu, V.1
Roberts, K.G.2
Xu, H.3
-
57
-
-
67651125091
-
Clinical radiation sensitivity with DNA repair disorders: an overview
-
Pollard, J.M., Gatti, R.A., Clinical radiation sensitivity with DNA repair disorders: an overview. Int. J. Radiat. Oncol. 74:5 (2009), 1323–1331.
-
(2009)
Int. J. Radiat. Oncol.
, vol.74
, Issue.5
, pp. 1323-1331
-
-
Pollard, J.M.1
Gatti, R.A.2
-
58
-
-
67650866716
-
Induction death and treatment-related mortality in first remission of children with acute lymphoblastic leukemia: a population-based analysis of the Austrian Berlin-Frankfurt-Munster study group
-
Prucker, C., Attarbaschi, A., Peters, C., et al. Induction death and treatment-related mortality in first remission of children with acute lymphoblastic leukemia: a population-based analysis of the Austrian Berlin-Frankfurt-Munster study group. Leukemia 23:7 (2009), 1264–1269.
-
(2009)
Leukemia
, vol.23
, Issue.7
, pp. 1264-1269
-
-
Prucker, C.1
Attarbaschi, A.2
Peters, C.3
-
59
-
-
84865168175
-
Pediatric acute lymphoblastic leukemia: where are we going and how do we get there?
-
Pui, C.H., Mullighan, C.G., Evans, W.E., Relling, M.V., Pediatric acute lymphoblastic leukemia: where are we going and how do we get there?. Blood 120:6 (2012), 1165–1174.
-
(2012)
Blood
, vol.120
, Issue.6
, pp. 1165-1174
-
-
Pui, C.H.1
Mullighan, C.G.2
Evans, W.E.3
Relling, M.V.4
-
60
-
-
79952495602
-
Infections and immunodeficiency in down syndrome
-
Ram, G., Chinen, J., Infections and immunodeficiency in down syndrome. Clin. Exp. Immunol. 164:1 (2011), 9–16.
-
(2011)
Clin. Exp. Immunol.
, vol.164
, Issue.1
, pp. 9-16
-
-
Ram, G.1
Chinen, J.2
-
61
-
-
84865165714
-
Childhood Acute Lymphoblastic Leukemia Collaborative G. Systematic review and meta-analysis of randomized trials of central nervous system directed therapy for childhood acute lymphoblastic leukemia
-
Richards, S., Pui, C.H., Gayon, P., Childhood Acute Lymphoblastic Leukemia Collaborative G. Systematic review and meta-analysis of randomized trials of central nervous system directed therapy for childhood acute lymphoblastic leukemia. Pediatr. Blood Cancer 60:2 (2013), 185–195.
-
(2013)
Pediatr. Blood Cancer
, vol.60
, Issue.2
, pp. 185-195
-
-
Richards, S.1
Pui, C.H.2
Gayon, P.3
-
62
-
-
0031729512
-
Treatment of lymphoid malignancies in patients with ataxia-telangiectasia
-
Sandoval, C., Swift, M., Treatment of lymphoid malignancies in patients with ataxia-telangiectasia. Med. Pediatr. Oncol. 31:6 (1998), 491–497.
-
(1998)
Med. Pediatr. Oncol.
, vol.31
, Issue.6
, pp. 491-497
-
-
Sandoval, C.1
Swift, M.2
-
63
-
-
57849157777
-
Etiology of common childhood acute lymphoblastic leukemia: the adrenal hypothesis
-
Schmiegelow, K., Vestergaard, T., Nielsen, S.M., Hjalgrim, H., Etiology of common childhood acute lymphoblastic leukemia: the adrenal hypothesis. Leukemia 22:12 (2008), 2137–2141.
-
(2008)
Leukemia
, vol.22
, Issue.12
, pp. 2137-2141
-
-
Schmiegelow, K.1
Vestergaard, T.2
Nielsen, S.M.3
Hjalgrim, H.4
-
64
-
-
84859651186
-
High concordance of subtypes of childhood acute lymphoblastic leukemia within families: lessons from sibships with multiple cases of leukemia
-
Schmiegelow, K., Lausten Thomsen, U., Baruchel, A., et al. High concordance of subtypes of childhood acute lymphoblastic leukemia within families: lessons from sibships with multiple cases of leukemia. Leukemia 26:4 (2012), 675–681.
-
(2012)
Leukemia
, vol.26
, Issue.4
, pp. 675-681
-
-
Schmiegelow, K.1
Lausten Thomsen, U.2
Baruchel, A.3
-
65
-
-
84883119415
-
Second malignant neoplasms after treatment of childhood acute lymphoblastic leukemia
-
Schmiegelow, K., Levinsen, M.F., Attarbaschi, A., et al. Second malignant neoplasms after treatment of childhood acute lymphoblastic leukemia. J. Clin. Oncol. Official J. Am. Soc. Clin. Oncol. 31:19 (2013), 2469–2476.
-
(2013)
J. Clin. Oncol. Official J. Am. Soc. Clin. Oncol.
, vol.31
, Issue.19
, pp. 2469-2476
-
-
Schmiegelow, K.1
Levinsen, M.F.2
Attarbaschi, A.3
-
66
-
-
84864318773
-
Germline mutations in the DNA damage response genes BRCA1, BRCA2, BARD1 and TP53 in patients with therapy related myeloid neoplasms
-
Schulz, E., Valentin, A., Ulz, P., et al. Germline mutations in the DNA damage response genes BRCA1, BRCA2, BARD1 and TP53 in patients with therapy related myeloid neoplasms. J. Med. Genet. 49:7 (2012), 422–428.
-
(2012)
J. Med. Genet.
, vol.49
, Issue.7
, pp. 422-428
-
-
Schulz, E.1
Valentin, A.2
Ulz, P.3
-
67
-
-
84884999671
-
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
-
1226–U179
-
Shah, S., Schrader, K.A., Waanders, E., et al. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia. Nat. Genet., 45(10), 2013 1226–U179.
-
(2013)
Nat. Genet.
, vol.45
, Issue.10
-
-
Shah, S.1
Schrader, K.A.2
Waanders, E.3
-
68
-
-
84879010315
-
Acute lymphoblastic leukemia with treatment–naive Fanconi anemia
-
Shah, A., John, B.M., Sondhi, V., Acute lymphoblastic leukemia with treatment–naive Fanconi anemia. Indian Pediatr. 50:5 (2013), 508–510.
-
(2013)
Indian Pediatr.
, vol.50
, Issue.5
, pp. 508-510
-
-
Shah, A.1
John, B.M.2
Sondhi, V.3
-
69
-
-
84873459266
-
Tumor protein p53 (TP53) testing and Li-Fraumeni syndrome: current status of clinical applications and future directions
-
Sorrell, A.D., Espenschied, C.R., Culver, J.O., Weitzel, J.N., Tumor protein p53 (TP53) testing and Li-Fraumeni syndrome: current status of clinical applications and future directions. Mol. Diagn. Ther. 17:1 (2013), 31–47.
-
(2013)
Mol. Diagn. Ther.
, vol.17
, Issue.1
, pp. 31-47
-
-
Sorrell, A.D.1
Espenschied, C.R.2
Culver, J.O.3
Weitzel, J.N.4
-
70
-
-
84937693478
-
Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes
-
Spinella, J.F., Healy, J., Saillour, V., et al. Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes. BMC Cancer, 15, 2015, 539.
-
(2015)
BMC Cancer
, vol.15
, pp. 539
-
-
Spinella, J.F.1
Healy, J.2
Saillour, V.3
-
71
-
-
0029822592
-
Role of postreplicative DNA mismatch repair in the cytotoxic action of thioguanine
-
Swann, P.F., Waters, T.R., Moulton, D.C., et al. Role of postreplicative DNA mismatch repair in the cytotoxic action of thioguanine. Science 273:5278 (1996), 1109–1111.
-
(1996)
Science
, vol.273
, Issue.5278
, pp. 1109-1111
-
-
Swann, P.F.1
Waters, T.R.2
Moulton, D.C.3
-
72
-
-
77954332797
-
Myelodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome
-
Talwalkar, S.S., Yin, C.C., Naeem, R.C., Hicks, M.J., Strong, L.C., Abruzzo, L.V., Myelodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome. Arch. Pathol. Lab. Med. 134:7 (2010), 1010–1015.
-
(2010)
Arch. Pathol. Lab. Med.
, vol.134
, Issue.7
, pp. 1010-1015
-
-
Talwalkar, S.S.1
Yin, C.C.2
Naeem, R.C.3
Hicks, M.J.4
Strong, L.C.5
Abruzzo, L.V.6
-
73
-
-
84937779216
-
Germline ETV6 mutations confer susceptibility to acute lymphoblastic leukemia and thrombocytopenia
-
Topka, S., Vijai, J., Walsh, M.F., et al. Germline ETV6 mutations confer susceptibility to acute lymphoblastic leukemia and thrombocytopenia. PLoS Genet., 11(6), 2015.
-
(2015)
PLoS Genet.
, vol.11
, Issue.6
-
-
Topka, S.1
Vijai, J.2
Walsh, M.F.3
-
74
-
-
69349091330
-
Germline genomic variants associated with childhood acute lymphoblastic leukemia
-
Trevino, L.R., Yang, W., French, D., et al. Germline genomic variants associated with childhood acute lymphoblastic leukemia. Nat. Genet. 41:9 (2009), 1001–1005.
-
(2009)
Nat. Genet.
, vol.41
, Issue.9
, pp. 1001-1005
-
-
Trevino, L.R.1
Yang, W.2
French, D.3
-
75
-
-
84938690611
-
Mercaptopurine metabolite levels are predictors of bone marrow toxicity following high-dose methotrexate therapy of childhood acute lymphoblastic leukaemia
-
Vang, S.I., Schmiegelow, K., Frandsen, T., Rosthoj, S., Nersting, J., Mercaptopurine metabolite levels are predictors of bone marrow toxicity following high-dose methotrexate therapy of childhood acute lymphoblastic leukaemia. Cancer Chemother. Pharmacol. 75:5 (2015), 1089–1093.
-
(2015)
Cancer Chemother. Pharmacol.
, vol.75
, Issue.5
, pp. 1089-1093
-
-
Vang, S.I.1
Schmiegelow, K.2
Frandsen, T.3
Rosthoj, S.4
Nersting, J.5
-
76
-
-
79957474904
-
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study
-
Villani, A., Tabori, U., Schiffman, J., et al. Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study. Lancet Oncol. 12:6 (2011), 559–567.
-
(2011)
Lancet Oncol.
, vol.12
, Issue.6
, pp. 559-567
-
-
Villani, A.1
Tabori, U.2
Schiffman, J.3
-
77
-
-
84860338982
-
Incidence of neoplasia in diamond blackfan anemia: a report from the diamond blackfan anemia registry
-
Vlachos, A., Rosenberg, P.S., Atsidaftos, E., Alter, B.P., Lipton, J.M., Incidence of neoplasia in diamond blackfan anemia: a report from the diamond blackfan anemia registry. Blood 119:16 (2012), 3815–3819.
-
(2012)
Blood
, vol.119
, Issue.16
, pp. 3815-3819
-
-
Vlachos, A.1
Rosenberg, P.S.2
Atsidaftos, E.3
Alter, B.P.4
Lipton, J.M.5
-
78
-
-
0031037835
-
Cytotoxic mechanism of 6-thioguanine: hMutS alpha, the human mismatch binding heterodimer, binds to DNA containing S-6-methylthioguanine
-
Waters, T.R., Swann, P.F., Cytotoxic mechanism of 6-thioguanine: hMutS alpha, the human mismatch binding heterodimer, binds to DNA containing S-6-methylthioguanine. Biochem. Us 36:9 (1997), 2501–2506.
-
(1997)
Biochem. Us
, vol.36
, Issue.9
, pp. 2501-2506
-
-
Waters, T.R.1
Swann, P.F.2
-
79
-
-
0033969694
-
Diamond-Blackfan anemia
-
Willig, T.N., Gazda, H., Sieff, C.A., Diamond-Blackfan anemia. Curr. Opin. Hematol. 7:2 (2000), 85–94.
-
(2000)
Curr. Opin. Hematol.
, vol.7
, Issue.2
, pp. 85-94
-
-
Willig, T.N.1
Gazda, H.2
Sieff, C.A.3
-
80
-
-
77952317756
-
Constitutional mismatch repair-deficiency syndrome
-
Wimmer, K., Kratz, C.P., Constitutional mismatch repair-deficiency syndrome. Haematol Hematol J. 95:5 (2010), 699–701.
-
(2010)
Haematol Hematol J.
, vol.95
, Issue.5
, pp. 699-701
-
-
Wimmer, K.1
Kratz, C.P.2
-
81
-
-
84901470161
-
Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD)
-
Wimmer, K., Kratz, C.P., Vasen, H.F., et al. Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD). J. Med. Genet. 51:6 (2014), 355–365.
-
(2014)
J. Med. Genet.
, vol.51
, Issue.6
, pp. 355-365
-
-
Wimmer, K.1
Kratz, C.P.2
Vasen, H.F.3
-
82
-
-
84903514900
-
How safe is a standard-risk child with ALL?
-
Winther, J.F., Schmiegelow, K., How safe is a standard-risk child with ALL?. Lancet Oncol. 15:8 (2014), 782–783.
-
(2014)
Lancet Oncol.
, vol.15
, Issue.8
, pp. 782-783
-
-
Winther, J.F.1
Schmiegelow, K.2
-
83
-
-
0035448564
-
Cancer in siblings of children with cancer in the Nordic countries: a population-based cohort study
-
Winther, J.F., Sankila, R., Boice, J.D., et al. Cancer in siblings of children with cancer in the Nordic countries: a population-based cohort study. Lancet 358:9283 (2001), 711–717.
-
(2001)
Lancet
, vol.358
, Issue.9283
, pp. 711-717
-
-
Winther, J.F.1
Sankila, R.2
Boice, J.D.3
-
84
-
-
84898797335
-
Lack of toxicity in a patient with germline TP53 mutation treated with radiotherapy
-
Wong, P., Han, K., Lack of toxicity in a patient with germline TP53 mutation treated with radiotherapy. Curr. Oncol. 21:2 (2014), e349–e353.
-
(2014)
Curr. Oncol.
, vol.21
, Issue.2
, pp. e349-e353
-
-
Wong, P.1
Han, K.2
-
85
-
-
84933060281
-
Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children
-
Xu, H., Zhang, H., Yang, W., et al. Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children. Nat. Commun., 6, 2015, 7553.
-
(2015)
Nat. Commun.
, vol.6
, pp. 7553
-
-
Xu, H.1
Zhang, H.2
Yang, W.3
-
86
-
-
84926216729
-
Germ line ETV6 mutations in familial thrombocytopenia and hematologic malignancy
-
Zhang, M.Y., Churpek, J.E., Kee, S.B., et al. Germ line ETV6 mutations in familial thrombocytopenia and hematologic malignancy. Nat. Genet. 47:2 (2015), 180–185.
-
(2015)
Nat. Genet.
, vol.47
, Issue.2
, pp. 180-185
-
-
Zhang, M.Y.1
Churpek, J.E.2
Kee, S.B.3
-
87
-
-
84949449519
-
Germline mutations in predisposition genes in pediatric Cancer
-
Zhang, J., Walsh, M.F., Wu, G., et al. Germline mutations in predisposition genes in pediatric Cancer. N. Engl. J. Med., 2015.
-
(2015)
N. Engl. J. Med.
-
-
Zhang, J.1
Walsh, M.F.2
Wu, G.3
|