Works matching IS 13899600 AND DT 2021 AND VI 20 AND IP 4

Results: 14

Ovarian carcinoma in children with constitutional mutation of SMARCA4: single-family report and literature review.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 355, doi. 10.1007/s10689-021-00258-w

By:

Pastorczak, Agata;
Krajewska, Karolina;
Urbanska, Zuzanna;
Szmyd, Bartosz;
Salacinska-Los, Elzbieta;
Kobos, Józef;
Mlynarski, Wojciech;
Trelinska, Joanna

Publication type:

Article

The paradigm of hematological malignant versus non-malignant manifestations, driven by primary immunodeficiencies: a complex interplay.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 363, doi. 10.1007/s10689-021-00266-w

By:

Kelaidi, C.;
Tzotzola, V.;
Polychronopoulou, S.

Publication type:

Article

Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 337, doi. 10.1007/s10689-021-00264-y

By:

Bakhuizen, Jette J.;
Hanson, Helen;
van der Tuin, Karin;
Lalloo, Fiona;
Tischkowitz, Marc;
Wadt, Karin;
Jongmans, Marjolijn C. J.;
SIOPE Host Genome Working Group;
Dörgeloh, Beate B.;
Farah, Roula A.;
Glentis, Stavros;
Golmard, Lisa;
Hoyer, Juliane;
Jahnukainen, Kirsi;
Jewell, Rosalyn;
Karow, Axel;
Katsibardi, Katharina;
Kuhlen, Michaela;
Meinhardt, Andrea;
Nemes, Karolina

Publication type:

Article

Review of guidelines for the identification and clinical care of patients with genetic predisposition for hematological malignancies.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 295, doi. 10.1007/s10689-021-00263-z

By:

Schlegelberger, Brigitte;
Mecucci, Cristina;
Wlodarski, Marcin

Publication type:

Article

Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 279, doi. 10.1007/s10689-021-00254-0

By:

Byrjalsen, Anna;
Diets, Illja J.;
Bakhuizen, Jette;
Hansen, Thomas van Overeem;
Schmiegelow, Kjeld;
Gerdes, Anne-Marie;
Stoltze, Ulrik;
Kuiper, Roland P.;
Merks, Johannes H. M.;
Wadt, Karin;
Jongmans, Marjolijn

Publication type:

Article

Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG).

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 317, doi. 10.1007/s10689-021-00247-z

By:

Guerrini-Rousseau, L.;
Smith, M. J.;
Kratz, C. P.;
Doergeloh, B.;
Hirsch, S.;
Hopman, S. M. J.;
Jorgensen, M.;
Kuhlen, M.;
Michaeli, O.;
Milde, T.;
Ridola, V.;
Russo, A.;
Salvador, H.;
Waespe, N.;
Claret, B.;
Brugieres, L.;
Evans, D. G.

Publication type:

Article

Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphoma.

Published in:

2021

By:

van Engelen, N.;
van Dijk, F.;
Waanders, E.;
Buijs, A.;
Vermeulen, M. A.;
Loeffen, J. L. C.;
Kuiper, R. P.;
Jongmans, M. C. J.

Publication type:

Case Study

Correction to: Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer.

Published in:

2021

By:

Ripperger, Tim;
Evans, D. Gareth;
Malkin, David;
Kratz, Christian P.

Publication type:

Correction Notice

Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 263, doi. 10.1007/s10689-021-00237-1

By:

Postema, Floor A. M.;
Hopman, Saskia M. J.;
de Borgie, Corianne A. J. M.;
Aalfs, Cora M.;
Anninga, Jakob K.;
Berger, Lieke P. V.;
Bleeker, Fonnet E.;
Dommering, Charlotte J.;
van Eijkelenburg, Natasha K. A.;
Hammond, Peter;
van den Heuvel-Eibrink, Marry M.;
Hol, Janna A.;
Kors, Wijnanda A.;
Letteboer, Tom G. W.;
Loeffen, Jan L. C. M.;
Meijer, Lisethe;
Olderode-Berends, Maran J. W.;
Wagner, Anja;
Hennekam, Raoul C.;
Merks, Johannes H. M.

Publication type:

Article

Proportion of children with cancer that have an indication for genetic counseling and testing based on the cancer type irrespective of other features.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 273, doi. 10.1007/s10689-021-00234-4

By:

Nguyen, Thi Minh Kha;
Behnert, Astrid;
Pietsch, Torsten;
Vokuhl, Christian;
Kratz, Christian Peter

Publication type:

Article

Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 257, doi. 10.1007/s10689-021-00233-5

By:

Schwermer, Miriam;
Behnert, Astrid;
Dörgeloh, Beate;
Ripperger, Tim;
Kratz, Christian P.

Publication type:

Article

Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 305, doi. 10.1007/s10689-021-00229-1

By:

Frühwald, M. C.;
Nemes, K.;
Boztug, H.;
Cornips, M. C. A.;
Evans, D. G.;
Farah, R.;
Glentis, S.;
Jorgensen, M.;
Katsibardi, K.;
Hirsch, S.;
Jahnukainen, K.;
Kventsel, I.;
Kerl, K.;
Kratz, C. P.;
Pajtler, K. W.;
Kordes, U.;
Ridola, V.;
Stutz, E.;
Bourdeaut, F.

Publication type:

Article

Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 289, doi. 10.1007/s10689-021-00228-2

By:

Ripperger, Tim;
Evans, D Gareth;
Malkin, David;
Kratz, Christian P.

Publication type:

Article

Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group.

Published in:

Familial Cancer, 2021, v. 20, n. 4, p. 327, doi. 10.1007/s10689-020-00204-2

By:

Hettmer, Simone;
Dachy, Guillaume;
Seitz, Guido;
Agaimy, Abbas;
Duncan, Catriona;
Jongmans, Marjolijn;
Hirsch, Steffen;
Kventsel, Iris;
Kordes, Uwe;
de Krijger, Ronald R.;
Metzler, Markus;
Michaeli, Orli;
Nemes, Karolina;
Poluha, Anna;
Ripperger, Tim;
Russo, Alexandra;
Smetsers, Stephanie;
Sparber-Sauer, Monika;
Stutz, Eveline;
Bourdeaut, Franck

Publication type:

Article