Myelodysplastic syndromes / / edited by Ota Fuchs.
This book is a comprehensive overview of myelodysplastic syndromes (MDS). MDS are a heterogeneous group of clonal hematopoietic stem cell disorders characterized by ineffective hematopoiesis, peripheral cytopenias, frequent karyotypic abnormalities, and risk of transformation to acute myeloid leukem...
Saved in:
TeilnehmendeR: | |
---|---|
Place / Publishing House: | Rijeka, Croatia : : IntechOpen,, [2016] ©2016 |
Year of Publication: | 2016 |
Language: | English |
Physical Description: | 1 online resource (210 pages) |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
993545555904498 |
---|---|
ctrlnum |
(CKB)4970000000099139 (NjHacI)994970000000099139 (oapen)https://directory.doabooks.org/handle/20.500.12854/66902 (EXLCZ)994970000000099139 |
collection |
bib_alma |
record_format |
marc |
spelling |
Fuchs, Ota edt Myelodysplastic syndromes / edited by Ota Fuchs. IntechOpen 2016 Rijeka, Croatia : IntechOpen, [2016] ©2016 1 online resource (210 pages) text txt rdacontent computer c rdamedia online resource cr rdacarrier Description based on: online resource; title from PDF information screen (InTech, viewed October 17, 2022). This book is a comprehensive overview of myelodysplastic syndromes (MDS). MDS are a heterogeneous group of clonal hematopoietic stem cell disorders characterized by ineffective hematopoiesis, peripheral cytopenias, frequent karyotypic abnormalities, and risk of transformation to acute myeloid leukemia (AML). Median age of patients with MDS is about 70 years. Various immune abnormalities occur in MDS patients, and the relationship between autoimmune disorders and MDS is described. Accurate prognostication and risk stratification for individual patients with MDS are important for clinical treatment decisions. Patients with MDS are classified into two broad prognostic categories: lower risk and higher risk. The approval of lenalidomide, azacitidine, and decitabine in last 10 years helped to diminish the clinical impact of MDS and delayed its progression to AML. English Myelodysplastic syndromes. Pathology 953-51-2586-9 Fuchs, Ota, editor. |
language |
English |
format |
eBook |
author2 |
Fuchs, Ota, |
author_facet |
Fuchs, Ota, |
author2_variant |
o f of o f of |
author2_role |
TeilnehmendeR |
title |
Myelodysplastic syndromes / |
spellingShingle |
Myelodysplastic syndromes / |
title_full |
Myelodysplastic syndromes / edited by Ota Fuchs. |
title_fullStr |
Myelodysplastic syndromes / edited by Ota Fuchs. |
title_full_unstemmed |
Myelodysplastic syndromes / edited by Ota Fuchs. |
title_auth |
Myelodysplastic syndromes / |
title_new |
Myelodysplastic syndromes / |
title_sort |
myelodysplastic syndromes / |
publisher |
IntechOpen IntechOpen, |
publishDate |
2016 |
physical |
1 online resource (210 pages) |
isbn |
953-51-7296-4 953-51-2587-7 953-51-2586-9 |
callnumber-first |
R - Medicine |
callnumber-subject |
RC - Internal Medicine |
callnumber-label |
RC645 |
callnumber-sort |
RC 3645.73 M945 42016 |
illustrated |
Not Illustrated |
dewey-hundreds |
600 - Technology |
dewey-tens |
610 - Medicine & health |
dewey-ones |
616 - Diseases |
dewey-full |
616.41 |
dewey-sort |
3616.41 |
dewey-raw |
616.41 |
dewey-search |
616.41 |
work_keys_str_mv |
AT fuchsota myelodysplasticsyndromes |
status_str |
n |
ids_txt_mv |
(CKB)4970000000099139 (NjHacI)994970000000099139 (oapen)https://directory.doabooks.org/handle/20.500.12854/66902 (EXLCZ)994970000000099139 |
carrierType_str_mv |
cr |
is_hierarchy_title |
Myelodysplastic syndromes / |
author2_original_writing_str_mv |
noLinkedField |
_version_ |
1787548708996382720 |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>00967nam a2200301 i 4500</leader><controlfield tag="001">993545555904498</controlfield><controlfield tag="005">20221017181556.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr |||||||||||</controlfield><controlfield tag="008">221017s2016 ci o 000 0 eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">953-51-7296-4</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">953-51-2587-7</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(CKB)4970000000099139</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(NjHacI)994970000000099139</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(oapen)https://directory.doabooks.org/handle/20.500.12854/66902</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(EXLCZ)994970000000099139</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">NjHacI</subfield><subfield code="b">eng</subfield><subfield code="e">rda</subfield><subfield code="c">NjHacl</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="050" ind1=" " ind2="4"><subfield code="a">RC645.73</subfield><subfield code="b">.M945 2016</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">616.41</subfield><subfield code="2">23</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Fuchs, Ota</subfield><subfield code="4">edt</subfield></datafield><datafield tag="245" ind1="0" ind2="0"><subfield code="a">Myelodysplastic syndromes /</subfield><subfield code="c">edited by Ota Fuchs.</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="b">IntechOpen</subfield><subfield code="c">2016</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Rijeka, Croatia :</subfield><subfield code="b">IntechOpen,</subfield><subfield code="c">[2016]</subfield></datafield><datafield tag="264" ind1=" " ind2="4"><subfield code="c">©2016</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (210 pages)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="588" ind1=" " ind2=" "><subfield code="a">Description based on: online resource; title from PDF information screen (InTech, viewed October 17, 2022).</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">This book is a comprehensive overview of myelodysplastic syndromes (MDS). MDS are a heterogeneous group of clonal hematopoietic stem cell disorders characterized by ineffective hematopoiesis, peripheral cytopenias, frequent karyotypic abnormalities, and risk of transformation to acute myeloid leukemia (AML). Median age of patients with MDS is about 70 years. Various immune abnormalities occur in MDS patients, and the relationship between autoimmune disorders and MDS is described. Accurate prognostication and risk stratification for individual patients with MDS are important for clinical treatment decisions. Patients with MDS are classified into two broad prognostic categories: lower risk and higher risk. The approval of lenalidomide, azacitidine, and decitabine in last 10 years helped to diminish the clinical impact of MDS and delayed its progression to AML.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Myelodysplastic syndromes.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Pathology</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">953-51-2586-9</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Fuchs, Ota,</subfield><subfield code="e">editor.</subfield></datafield><datafield tag="906" ind1=" " ind2=" "><subfield code="a">BOOK</subfield></datafield><datafield tag="ADM" ind1=" " ind2=" "><subfield code="b">2023-02-22 20:23:35 Europe/Vienna</subfield><subfield code="f">system</subfield><subfield code="c">marc21</subfield><subfield code="a">2019-04-13 22:04:18 Europe/Vienna</subfield><subfield code="g">false</subfield></datafield><datafield tag="AVE" ind1=" " ind2=" "><subfield code="i">DOAB Directory of Open Access Books</subfield><subfield code="P">DOAB Directory of Open Access Books</subfield><subfield code="x">https://eu02.alma.exlibrisgroup.com/view/uresolver/43ACC_OEAW/openurl?u.ignore_date_coverage=true&portfolio_pid=5337979290004498&Force_direct=true</subfield><subfield code="Z">5337979290004498</subfield><subfield code="b">Available</subfield><subfield code="8">5337979290004498</subfield></datafield></record></collection> |