Zobrazeno 1 - 9
of 9
pro vyhledávání: '"C P, Kratz"'
Publikováno v:
Der Pathologe. 40:592-599
Das Li-Fraumeni-Syndrom (LFS; „Online Mendelian Inheritance in Man“, OMIM #151623) gilt als eines der aggressivsten derzeit bekannten Krebspradispositionssyndrome. Das heterogene Tumorspektrum wird dominiert von Knochen- und Weichteilsarkomen, ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa25a7219f2e4e69a606041ce6761353
https://doi.org/10.1007/s00292-019-00657-y
https://doi.org/10.1007/s00292-019-00657-y
Publikováno v:
Der Pathologe. 40(6)
The Li-Fraumeni syndrome (LFS, online Mendelian inheritance in man, OMIM #151623) is considered to be one of the currently known most aggressive cancer predisposition syndromes. The heterogeneous spectrum of tumors is dominated by bone and soft tissu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2091afdbeb80a002f8bf8786dd6c41bc
https://pubmed.ncbi.nlm.nih.gov/31511974
https://pubmed.ncbi.nlm.nih.gov/31511974
Publikováno v:
WHO/IARC Classification of Tumours; 2021, Vol. 6, p429-433, 5p
Autor:
D. A., Solomon, C. P., Kratz
Publikováno v:
WHO/IARC Classification of Tumours; 2021, Vol. 6, p478-480, 3p
Publikováno v:
WHO/IARC Classification of Tumours; 2021, Vol. 6, p446-448, 3p
Publikováno v:
International journal of andrology. 34(4 Pt 2)
Three genome-wide association studies of testicular cancer have uncovered predisposition alleles in or near KITLG, BAK1, SPRY4, TERT, ATF7IP and DMRT1. We investigated whether testicular cancer-risk alleles can be utilized in the clinical setting. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3de4abfe78d05d75ac10e4a55987550c
https://pubmed.ncbi.nlm.nih.gov/21564132
https://pubmed.ncbi.nlm.nih.gov/21564132
Autor:
Dominik Schneider, Peter Vorwerk, C. P. Kratz, Norbert Graf, R. E. Schultze-Florey, E. Koscielniak
Publikováno v:
Klinische Pädiatrie. 225:177-178
Recently, germline mutations of DICER1 have been identified in patients with rare neoplasms suggesting the existence of a newly discovered cancer prone syndrome. Initially, DICER1 mutations were identified in patients with familial pleuropulmonary bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cc6a472b00122610c1f6789536202b
https://doi.org/10.1055/s-0033-1337976
https://doi.org/10.1055/s-0033-1337976
Publikováno v:
Klinische Padiatrie. 216(6)
Essential Thrombocythemia (ET) is an acquired myeloproliferative disorder (MPD) characterized by excessive production of platelets. The disorder is usually affecting adults and is rarely diagnosed in children.In this retrospective study we describe 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3509b09257967f8b3f73f93927c503cb
https://pubmed.ncbi.nlm.nih.gov/15565550
https://pubmed.ncbi.nlm.nih.gov/15565550
Publikováno v:
Medicine & Science in Sports & Exercise; May 1993, Vol. 25 Issue: Supplement 5 pS107-S107, 1p