Disorders of hemoglobin: genetics, pathophysiology, and clinical management
This book is a completely revised new edition of the definitive reference on disorders of hemoglobin. Authored by world-renowned experts, the book focuses on basic science aspects and clinical features of hemoglobinopathies, covering diagnosis, treatment, and future applications of current research....
Gespeichert in:
Weitere Verfasser: | |
---|---|
Format: | Elektronisch E-Book |
Sprache: | English |
Veröffentlicht: |
Cambridge
Cambridge University Press
2009
|
Ausgabe: | Second edition |
Schlagworte: | |
Online-Zugang: | BSB01 FHN01 URL des Erstveröffentlichers |
Zusammenfassung: | This book is a completely revised new edition of the definitive reference on disorders of hemoglobin. Authored by world-renowned experts, the book focuses on basic science aspects and clinical features of hemoglobinopathies, covering diagnosis, treatment, and future applications of current research. While the second edition continues to address the important molecular, cellular, and genetic components, coverage of clinical issues has been significantly expanded, and there is more practical emphasis on diagnosis and management throughout. The book opens with a review of the scientific underpinnings. Pathophysiology of common hemoglobin disorders is discussed next in an entirely new section devoted to vascular biology, the erythrocyte membrane, nitric oxide biology, and hemolysis. Four sections deal with α and β thalassemia, sickle cell disease, and related conditions, followed by special topics. The second edition concludes with current and developing approaches to treatment, incorporating new agents for iron chelation, methods to induce fetal hemoglobin production, novel treatment approaches, stem cell transplantation, and progress in gene therapy |
Beschreibung: | Title from publisher's bibliographic system (viewed on 05 Oct 2015) |
Beschreibung: | 1 online resource (xx, 826 pages) |
ISBN: | 9780511596582 |
DOI: | 10.1017/CBO9780511596582 |
Internformat
MARC
LEADER | 00000nmm a2200000zc 4500 | ||
---|---|---|---|
001 | BV043944349 | ||
003 | DE-604 | ||
005 | 00000000000000.0 | ||
007 | cr|uuu---uuuuu | ||
008 | 161206s2009 |||| o||u| ||||||eng d | ||
020 | |a 9780511596582 |c Online |9 978-0-511-59658-2 | ||
024 | 7 | |a 10.1017/CBO9780511596582 |2 doi | |
035 | |a (ZDB-20-CBO)CR9780511596582 | ||
035 | |a (OCoLC)967779211 | ||
035 | |a (DE-599)BVBBV043944349 | ||
040 | |a DE-604 |b ger |e rda | ||
041 | 0 | |a eng | |
049 | |a DE-12 |a DE-92 | ||
082 | 0 | |a 616.1/51 |2 22 | |
084 | |a XG 6600 |0 (DE-625)152819:13129 |2 rvk | ||
084 | |a YC 2400 |0 (DE-625)153201:12905 |2 rvk | ||
245 | 1 | 0 | |a Disorders of hemoglobin |b genetics, pathophysiology, and clinical management |c edited by Martin H. Steinberg [and others] |
250 | |a Second edition | ||
264 | 1 | |a Cambridge |b Cambridge University Press |c 2009 | |
300 | |a 1 online resource (xx, 826 pages) | ||
336 | |b txt |2 rdacontent | ||
337 | |b c |2 rdamedia | ||
338 | |b cr |2 rdacarrier | ||
500 | |a Title from publisher's bibliographic system (viewed on 05 Oct 2015) | ||
520 | |a This book is a completely revised new edition of the definitive reference on disorders of hemoglobin. Authored by world-renowned experts, the book focuses on basic science aspects and clinical features of hemoglobinopathies, covering diagnosis, treatment, and future applications of current research. While the second edition continues to address the important molecular, cellular, and genetic components, coverage of clinical issues has been significantly expanded, and there is more practical emphasis on diagnosis and management throughout. The book opens with a review of the scientific underpinnings. Pathophysiology of common hemoglobin disorders is discussed next in an entirely new section devoted to vascular biology, the erythrocyte membrane, nitric oxide biology, and hemolysis. Four sections deal with α and β thalassemia, sickle cell disease, and related conditions, followed by special topics. The second edition concludes with current and developing approaches to treatment, incorporating new agents for iron chelation, methods to induce fetal hemoglobin production, novel treatment approaches, stem cell transplantation, and progress in gene therapy | ||
650 | 4 | |a Hemoglobinopathy | |
650 | 0 | 7 | |a Hämoglobinopathie |0 (DE-588)4022815-0 |2 gnd |9 rswk-swf |
689 | 0 | 0 | |a Hämoglobinopathie |0 (DE-588)4022815-0 |D s |
689 | 0 | |8 1\p |5 DE-604 | |
700 | 1 | |a Steinberg, Martin H. |4 edt | |
776 | 0 | 8 | |i Erscheint auch als |n Druckausgabe |z 978-0-521-87519-6 |
856 | 4 | 0 | |u https://doi.org/10.1017/CBO9780511596582 |x Verlag |z URL des Erstveröffentlichers |3 Volltext |
912 | |a ZDB-20-CBO | ||
999 | |a oai:aleph.bib-bvb.de:BVB01-029353319 | ||
883 | 1 | |8 1\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk | |
966 | e | |u https://doi.org/10.1017/CBO9780511596582 |l BSB01 |p ZDB-20-CBO |q BSB_PDA_CBO |x Verlag |3 Volltext | |
966 | e | |u https://doi.org/10.1017/CBO9780511596582 |l FHN01 |p ZDB-20-CBO |q FHN_PDA_CBO |x Verlag |3 Volltext |
Datensatz im Suchindex
_version_ | 1804176889123700736 |
---|---|
any_adam_object | |
author2 | Steinberg, Martin H. |
author2_role | edt |
author2_variant | m h s mh mhs |
author_facet | Steinberg, Martin H. |
building | Verbundindex |
bvnumber | BV043944349 |
classification_rvk | XG 6600 YC 2400 |
collection | ZDB-20-CBO |
ctrlnum | (ZDB-20-CBO)CR9780511596582 (OCoLC)967779211 (DE-599)BVBBV043944349 |
dewey-full | 616.1/51 |
dewey-hundreds | 600 - Technology (Applied sciences) |
dewey-ones | 616 - Diseases |
dewey-raw | 616.1/51 |
dewey-search | 616.1/51 |
dewey-sort | 3616.1 251 |
dewey-tens | 610 - Medicine and health |
discipline | Medizin |
doi_str_mv | 10.1017/CBO9780511596582 |
edition | Second edition |
format | Electronic eBook |
fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>03029nmm a2200469zc 4500</leader><controlfield tag="001">BV043944349</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">161206s2009 |||| o||u| ||||||eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780511596582</subfield><subfield code="c">Online</subfield><subfield code="9">978-0-511-59658-2</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1017/CBO9780511596582</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ZDB-20-CBO)CR9780511596582</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)967779211</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV043944349</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-12</subfield><subfield code="a">DE-92</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">616.1/51</subfield><subfield code="2">22</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">XG 6600</subfield><subfield code="0">(DE-625)152819:13129</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">YC 2400</subfield><subfield code="0">(DE-625)153201:12905</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Disorders of hemoglobin</subfield><subfield code="b">genetics, pathophysiology, and clinical management</subfield><subfield code="c">edited by Martin H. Steinberg [and others]</subfield></datafield><datafield tag="250" ind1=" " ind2=" "><subfield code="a">Second edition</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Cambridge</subfield><subfield code="b">Cambridge University Press</subfield><subfield code="c">2009</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (xx, 826 pages)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Title from publisher's bibliographic system (viewed on 05 Oct 2015)</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">This book is a completely revised new edition of the definitive reference on disorders of hemoglobin. Authored by world-renowned experts, the book focuses on basic science aspects and clinical features of hemoglobinopathies, covering diagnosis, treatment, and future applications of current research. While the second edition continues to address the important molecular, cellular, and genetic components, coverage of clinical issues has been significantly expanded, and there is more practical emphasis on diagnosis and management throughout. The book opens with a review of the scientific underpinnings. Pathophysiology of common hemoglobin disorders is discussed next in an entirely new section devoted to vascular biology, the erythrocyte membrane, nitric oxide biology, and hemolysis. Four sections deal with α and β thalassemia, sickle cell disease, and related conditions, followed by special topics. The second edition concludes with current and developing approaches to treatment, incorporating new agents for iron chelation, methods to induce fetal hemoglobin production, novel treatment approaches, stem cell transplantation, and progress in gene therapy</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Hemoglobinopathy</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Hämoglobinopathie</subfield><subfield code="0">(DE-588)4022815-0</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Hämoglobinopathie</subfield><subfield code="0">(DE-588)4022815-0</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="8">1\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Steinberg, Martin H.</subfield><subfield code="4">edt</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Druckausgabe</subfield><subfield code="z">978-0-521-87519-6</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1017/CBO9780511596582</subfield><subfield code="x">Verlag</subfield><subfield code="z">URL des Erstveröffentlichers</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-20-CBO</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-029353319</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">1\p</subfield><subfield code="a">cgwrk</subfield><subfield code="d">20201028</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#cgwrk</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1017/CBO9780511596582</subfield><subfield code="l">BSB01</subfield><subfield code="p">ZDB-20-CBO</subfield><subfield code="q">BSB_PDA_CBO</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1017/CBO9780511596582</subfield><subfield code="l">FHN01</subfield><subfield code="p">ZDB-20-CBO</subfield><subfield code="q">FHN_PDA_CBO</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield></record></collection> |
id | DE-604.BV043944349 |
illustrated | Not Illustrated |
indexdate | 2024-07-10T07:39:21Z |
institution | BVB |
isbn | 9780511596582 |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-029353319 |
oclc_num | 967779211 |
open_access_boolean | |
owner | DE-12 DE-92 |
owner_facet | DE-12 DE-92 |
physical | 1 online resource (xx, 826 pages) |
psigel | ZDB-20-CBO ZDB-20-CBO BSB_PDA_CBO ZDB-20-CBO FHN_PDA_CBO |
publishDate | 2009 |
publishDateSearch | 2009 |
publishDateSort | 2009 |
publisher | Cambridge University Press |
record_format | marc |
spelling | Disorders of hemoglobin genetics, pathophysiology, and clinical management edited by Martin H. Steinberg [and others] Second edition Cambridge Cambridge University Press 2009 1 online resource (xx, 826 pages) txt rdacontent c rdamedia cr rdacarrier Title from publisher's bibliographic system (viewed on 05 Oct 2015) This book is a completely revised new edition of the definitive reference on disorders of hemoglobin. Authored by world-renowned experts, the book focuses on basic science aspects and clinical features of hemoglobinopathies, covering diagnosis, treatment, and future applications of current research. While the second edition continues to address the important molecular, cellular, and genetic components, coverage of clinical issues has been significantly expanded, and there is more practical emphasis on diagnosis and management throughout. The book opens with a review of the scientific underpinnings. Pathophysiology of common hemoglobin disorders is discussed next in an entirely new section devoted to vascular biology, the erythrocyte membrane, nitric oxide biology, and hemolysis. Four sections deal with α and β thalassemia, sickle cell disease, and related conditions, followed by special topics. The second edition concludes with current and developing approaches to treatment, incorporating new agents for iron chelation, methods to induce fetal hemoglobin production, novel treatment approaches, stem cell transplantation, and progress in gene therapy Hemoglobinopathy Hämoglobinopathie (DE-588)4022815-0 gnd rswk-swf Hämoglobinopathie (DE-588)4022815-0 s 1\p DE-604 Steinberg, Martin H. edt Erscheint auch als Druckausgabe 978-0-521-87519-6 https://doi.org/10.1017/CBO9780511596582 Verlag URL des Erstveröffentlichers Volltext 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
spellingShingle | Disorders of hemoglobin genetics, pathophysiology, and clinical management Hemoglobinopathy Hämoglobinopathie (DE-588)4022815-0 gnd |
subject_GND | (DE-588)4022815-0 |
title | Disorders of hemoglobin genetics, pathophysiology, and clinical management |
title_auth | Disorders of hemoglobin genetics, pathophysiology, and clinical management |
title_exact_search | Disorders of hemoglobin genetics, pathophysiology, and clinical management |
title_full | Disorders of hemoglobin genetics, pathophysiology, and clinical management edited by Martin H. Steinberg [and others] |
title_fullStr | Disorders of hemoglobin genetics, pathophysiology, and clinical management edited by Martin H. Steinberg [and others] |
title_full_unstemmed | Disorders of hemoglobin genetics, pathophysiology, and clinical management edited by Martin H. Steinberg [and others] |
title_short | Disorders of hemoglobin |
title_sort | disorders of hemoglobin genetics pathophysiology and clinical management |
title_sub | genetics, pathophysiology, and clinical management |
topic | Hemoglobinopathy Hämoglobinopathie (DE-588)4022815-0 gnd |
topic_facet | Hemoglobinopathy Hämoglobinopathie |
url | https://doi.org/10.1017/CBO9780511596582 |
work_keys_str_mv | AT steinbergmartinh disordersofhemoglobingeneticspathophysiologyandclinicalmanagement |