Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Dan, Bercovich"'
Autor:
Christie M. Ballantyne, Danièle Zoch, Dan Bercovich, Olaf Bodamer, Arthur L. Beaudet, Michael Schlabach
Publikováno v:
Clinical Chemistry. 48:1913-1918
Background: Autosomal dominant familial hypercholesterolemia (FH) attributable to mutations in the LDL receptor (LDLR) gene is one of the most common genetic disorders associated with significant morbidity and mortality. Definitive diagnosis would he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5afc9a4bf8c6ef06739704b1d021db12
https://doi.org/10.1093/clinchem/48.11.1913
https://doi.org/10.1093/clinchem/48.11.1913
Autor:
Ninette Amariglio, Andrea Teigler-Schlegel, Andrea Biondi, Inna Muler, Batia Stark, Oskar A. Haas, Dan Bercovich, Jan Trka, Sabine Strehl, Helena Kempski, Shai Izraeli, Liat Rainis, Gideon Rechavi
Publikováno v:
Blood. 102(3)
Patients with Down syndrome (DS) frequently develop 2 kinds of clonal megakaryocytosis: a common, congenital, spontaneously resolving, transient myeloproliferative disorder (TMD) and, less commonly, childhood acute megakaryoblastic leukemia (AMKL). R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::321cd60e5fa7e69b560627b59669ef97
https://pubmed.ncbi.nlm.nih.gov/12649131
https://pubmed.ncbi.nlm.nih.gov/12649131
Autor:
Olaf A, Bodamer, Dan, Bercovich, Michael, Schlabach, Christie, Ballantyne, Danièle, Zoch, Arthur L, Beaudet
Publikováno v:
Clinical chemistry. 48(11)
Autosomal dominant familial hypercholesterolemia (FH) attributable to mutations in the LDL receptor (LDLR) gene is one of the most common genetic disorders associated with significant morbidity and mortality. Definitive diagnosis would help to initia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d47295c634d0c8b24066e0925d721ad3
https://pubmed.ncbi.nlm.nih.gov/12406975
https://pubmed.ncbi.nlm.nih.gov/12406975
Autor:
Marsha Zeigler, Dan Bercovich, Asaad Khoury, Horachio Plotkin, Avraham Lorber, Gad Bar-Joseph, Deeksha Bali, Priya S. Kishnani, Eli Herskovitz, Dan J. Eldad, Dalia Natan, Hanna Mandel
Publikováno v:
Clinical Therapeutics. 33:S17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9927271e0571a37b222ace7140583d01
https://doi.org/10.1016/j.clinthera.2011.05.058
https://doi.org/10.1016/j.clinthera.2011.05.058
Autor:
Arndt Borkhardt, Martin Schrappe, Dan Bercovich, Linda M. Scott, Giuseppe Basso, Oskar A. Haas, Martin Stanulla, Smadar Avigad, Ithamar Ganmore, Giovanni Cazzaniga, Shai Izraeli, Owen P. Smith, Jean-Pierre Bourquin, Andrea Biondi, Sabine Strehl, Helena Kempski, Batia Stark, Anthony R. Green, Vera Binder, Gunnar Cario, Jan Trka, Bella Bielorei
Publikováno v:
Blood. 110:LB6-LB6
Additional copies of chromosome (chr) 21 are the most common chromosomal aneuploidy in childhood leukemia. Patients with DS have a markedly increased risk for both AML and ALL. Thus trisomy 21 is leukemogenic. DS-AML is uniquely characterized by an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7df9d4de8094037e71a1fb5973bb9a4
https://doi.org/10.1182/blood.v110.11.lb6.lb6
https://doi.org/10.1182/blood.v110.11.lb6.lb6