Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ladislav Chrobak"'
Autor:
Thorsten Marquardt, Hermann Heimpel, Antje Griesshammer, Gritta Janka-Schaub, Kerstin Gallmeier, Jonas Denecke, Ladislav Chrobak, Volker Anselstetter, Martina Kron, Elisabeth Kohne, Beate Einsiedler
Publikováno v:
Blood. 102:4576-4581
Congenital dyserythropoietic anemia type II (CDA II) is the most frequent type of congenital dyserythropoietic anemia. More than 200 cases have been described, but with the exception of a report by the International CDA II Registry, these reports inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3741204cab40ecf61c8aac96f2608ab
https://doi.org/10.1182/blood-2003-02-0613
https://doi.org/10.1182/blood-2003-02-0613
Autor:
Josef T. Prchal, Ladislav Chrobak, H. L. Rubin, Jiri Palek, Vaclav Brabec, J. L. Murray, LM Snyder, WD Melrose, WM Taylor, Petr Jarolim, S.K. Ballas
Publikováno v:
Blood. 88:4366-4374
Hereditary spherocytosis (HS) is a common hemolytic anemia of variable clinical expression. Pathogenesis of HS has been associated with defects of several red cell membrane proteins including erythroid band 3. We have studied erythrocyte membrane pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::515392f790c6722ed395723d58320652
https://doi.org/10.1182/blood.v88.11.4366.4366
https://doi.org/10.1182/blood.v88.11.4366.4366
Autor:
Petr Jarolim, H. L. Rubin, Carlo Brugnara, Seth L. Alper, Hynek Wichterle, Ladislav Chrobak, Vaclav Brabec, Alexander S. Zolotarev, Jiri Palek
Publikováno v:
Blood. 85:634-640
To elucidate the molecular basis of band 3 deficiency in a recently defined subset of patients with autosomal dominant hereditary spherocytosis (HS), we screened band 3 cDNA for single-strand conformation polymorphism (SSCP). In 5 of 17 (29%) unrelat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9cb1ad4fac203b7fc67e962af46f089
https://doi.org/10.1182/blood.v85.3.634.bloodjournal853634
https://doi.org/10.1182/blood.v85.3.634.bloodjournal853634
Autor:
Titus H.J. Huisman, Yuan chao Gu, You jun Fei, Jaroslav Cermak, Jarmila Indrakova, Ferdane Kutlar, Vaclav Brabec, Adriana Sakalova, E. Baysal, Ladislav Chrobak, Marie Jarošová, Karel Indrák
Publikováno v:
Human Genetics. 88:399-404
We have identified different beta-thalassemia mutations in 93 members of 34 families of Czech or Slovakian descent using gene amplification, hybridization with specific 32P-labeled oligonucleotide probes, sequencing of amplified DNA, and gene mapping
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422f1de01f9f48d906e272a631a5abdf
https://doi.org/10.1007/bf00215673
https://doi.org/10.1007/bf00215673
Autor:
Ladislav Chrobák, Jaroslava Voglová
Publikováno v:
Acta Medica, Vol 46, Iss 3, Pp 85-89 (2003)
The publication provides an up-to-date review of the significance of cytogenetic abnormalities in chronic myelogenous leukemia (CML) and the development of a promising agent with specific molecular target against tyrosine kinase, product of the BCR-A
Externí odkaz:
https://doaj.org/article/3277de885eaf4aeab26932a0315baae9
Autor:
Ladislav Chrobák
Publikováno v:
Acta Medica, Vol 43, Iss 1, Pp 3-8 (2000)
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disorder in which intravascular hemolysis results from the somatic mutation of the totipotent stem cells causing an intrinsic defect in red cell membrane. PNH cells lack glycosylphosphat
Externí odkaz:
https://doaj.org/article/5d6fa259969f4d1db737a9379097653e
Publikováno v:
Acta Medica, Vol 42, Iss 3, Pp 85-88 (1999)
As minimal residual disease (MRD) is considered the detection of hairy cells (HCs) in a patient with hairy cell leukemia (HCL) in complete remission with the absence of detectable HCs by routine morphology of peripheral blood, aspirates and bone marr
Externí odkaz:
https://doaj.org/article/1249320ee78b4bf2b1edd1cbe53368dc
Autor:
Petr Dulíček, Ladislav Chrobák, Ivo Kalousek, Lenka Pešavová, Miroslav Pecka, Pravoslav Stránský
Publikováno v:
Acta Medica, Vol 42, Iss 3, Pp 93-96 (1999)
A successful pregnancy is dependent on the development of adequate placental circulation. The abnormalities of placental vasculature may result in a number of gestational pathologies, including fetal loss. The aim of our study was to determine whethe
Externí odkaz:
https://doaj.org/article/b17c683a3cd24f479197abc453bc23ef
Publikováno v:
Acta Medica, Vol 41, Iss 1, Pp 23-26 (1998)
Red cell distribution width (RDW) was examined in 18 patients with hairy cell leukemia (HCL) treated with 2- chlorodeoxyadenosine (2-CdA), in 5 patients treated with Interferon alpha (IFN-alpha) and in 9 patients subjected to splenectomy. Out of 18 p
Externí odkaz:
https://doaj.org/article/36441046924c47c7892af425fec8dc4a
Autor:
Ladislav Chrobák, Milan Bláha
Publikováno v:
Acta Medica, Vol 41, Iss 3, Pp 145-153 (1998)
Article without abstract.
Externí odkaz:
https://doaj.org/article/dc09ba7554e3489e8378e4515e803b82