Thrombotische Mikroangiopathien:
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | German |
| Veröffentlicht: |
Bremen
UNI-MED Verlag AG
[2022]
|
| Schriftenreihe: | UNI-MED Science
|
| Schlagworte: | |
| Online-Zugang: | Inhaltstext Inhaltsverzeichnis Inhaltsverzeichnis |
| Beschreibung: | 47 Seiten Illustrationen, Diagramme 25 cm, 245 g |
| ISBN: | 9783837415933 3837415937 |
Internformat
MARC
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| 264 | 4 | |c © 2022 | |
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Datensatz im Suchindex
| _version_ | 1804184941864419328 |
|---|---|
| adam_text | INHALTSVERZEICHNIS
M|
DEFINITION
UND
KLASSIFIKATION
10
YY
GESCHICHTE
14
YY
DIAGNOSTIK
16
3.1.
DIFFERENTIALDIAGNOSE
.......................................................................................................................
16
YY
THROMBOTISCH-THROMBOZYTOPENISCHE
PURPURA
(TTP)
22
4.1.
BEDEUTUNG
DER
VON-WILLEBRAND-FAKTOR
SPALTENDEN
PROTEASE
ADAMTS1
3
.................................
22
4.2.
IMMUNVERMITTELTE
ERWORBENE
THROMBOTISCH-THROMBOZYTOPENISCHE
PURPURA
(ITTP)
..............
23
4.3.
KONGENITALE
THROMBOTISCH-THROMBOZYTOPENISCHE
PURPURA
(CTTP)
-
UPSHAW-SCHULMAN-SYNDROM
.......................................................................................................
26
4.4.
THERAPIE
EINER
TTP
.........................................................................................................................
26
4.5.
BESONDERE
SITUATIONEN
...................................................................................................................
28
YY
HAEMOLYTISCH-URAEMISCHES
SYNDROM
(HUS)
32
5.1.
DEFINITION
.........................................................................................................................................
32
5.2.
PATHOPHYSIOLOGIE
...........................................................................................................................
32
5.3.
INFEKTIONS-BEDINGTES
TYPISCHES
HUS
-
STEC-HUS,
SP-HUS
...........................................................
33
5.4.
ATYPISCHES
HAEMOLYTISCH-URAEMISCHES
SYNDROM
(AHUS)
-
KOMPLEMENT-BEDINGTE
TMA
(CM-TMA)
........................................................................................................................................
33
5.5.
SEKUNDAERES
HAEMOLYTISCH-URAEMISCHES
SYNDROM
............................................................................
35
5.5.1.
MEDIKAMENTEN-INDUZIERTES
HUS
-
TMA
...........................................................................................
35
5.5.2.
TRANSPLANTATIONS-ASSOZIIERTE
TMA
(TA-TMA)
....................................................................................
35
5.5.3.
SCHWANGERSCHAFT
..............................................................................................................................
35
5.5.4.
MALIGNOM-ASSOZIIERTETMA
..............................................................................................................
36
5.6.
AUTOIMMUNERKRANKUNGEN
MIT
TMA
ODER
TMA
AEHNLICHEN
KRANKHEITSBILDERN
............................
36
5.7.
THERAPIEANSAETZE
.............................................................................................................................
36
5.7.1.
PLASMATHERAPIE
BEI
NICHT-TTP-TMA
.................................................................................................
36
5.7.2.
MEDIKAMENTOESE
THERAPIEANSAETZE
....................................................................................................
36
B
LITERATUR
40
YY
ABKUERZUNGSVERZEICHNIS
46
9
INDEX
47
|
| adam_txt |
INHALTSVERZEICHNIS
M|
DEFINITION
UND
KLASSIFIKATION
10
YY
GESCHICHTE
14
YY
DIAGNOSTIK
16
3.1.
DIFFERENTIALDIAGNOSE
.
16
YY
THROMBOTISCH-THROMBOZYTOPENISCHE
PURPURA
(TTP)
22
4.1.
BEDEUTUNG
DER
VON-WILLEBRAND-FAKTOR
SPALTENDEN
PROTEASE
ADAMTS1
3
.
22
4.2.
IMMUNVERMITTELTE
ERWORBENE
THROMBOTISCH-THROMBOZYTOPENISCHE
PURPURA
(ITTP)
.
23
4.3.
KONGENITALE
THROMBOTISCH-THROMBOZYTOPENISCHE
PURPURA
(CTTP)
-
UPSHAW-SCHULMAN-SYNDROM
.
26
4.4.
THERAPIE
EINER
TTP
.
26
4.5.
BESONDERE
SITUATIONEN
.
28
YY
HAEMOLYTISCH-URAEMISCHES
SYNDROM
(HUS)
32
5.1.
DEFINITION
.
32
5.2.
PATHOPHYSIOLOGIE
.
32
5.3.
INFEKTIONS-BEDINGTES
TYPISCHES
HUS
-
STEC-HUS,
SP-HUS
.
33
5.4.
ATYPISCHES
HAEMOLYTISCH-URAEMISCHES
SYNDROM
(AHUS)
-
KOMPLEMENT-BEDINGTE
TMA
(CM-TMA)
.
33
5.5.
SEKUNDAERES
HAEMOLYTISCH-URAEMISCHES
SYNDROM
.
35
5.5.1.
MEDIKAMENTEN-INDUZIERTES
HUS
-
TMA
.
35
5.5.2.
TRANSPLANTATIONS-ASSOZIIERTE
TMA
(TA-TMA)
.
35
5.5.3.
SCHWANGERSCHAFT
.
35
5.5.4.
MALIGNOM-ASSOZIIERTETMA
.
36
5.6.
AUTOIMMUNERKRANKUNGEN
MIT
TMA
ODER
TMA
AEHNLICHEN
KRANKHEITSBILDERN
.
36
5.7.
THERAPIEANSAETZE
.
36
5.7.1.
PLASMATHERAPIE
BEI
NICHT-TTP-TMA
.
36
5.7.2.
MEDIKAMENTOESE
THERAPIEANSAETZE
.
36
B
LITERATUR
40
YY
ABKUERZUNGSVERZEICHNIS
46
9
INDEX
47 |
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| author_variant | m b mb |
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| bvnumber | BV048836214 |
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| id | DE-604.BV048836214 |
| illustrated | Illustrated |
| index_date | 2024-07-03T21:36:31Z |
| indexdate | 2024-07-10T09:47:21Z |
| institution | BVB |
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| isbn | 9783837415933 3837415937 |
| language | German |
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| owner_facet | DE-19 DE-BY-UBM DE-578 |
| physical | 47 Seiten Illustrationen, Diagramme 25 cm, 245 g |
| publishDate | 2022 |
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| spelling | Bommer, Martin 1967- Verfasser (DE-588)114591120X aut Thrombotische Mikroangiopathien Prof. Dr. Martin Bommer Bremen UNI-MED Verlag AG [2022] © 2022 47 Seiten Illustrationen, Diagramme 25 cm, 245 g txt rdacontent n rdamedia nc rdacarrier UNI-MED Science Thrombotische Mikroangiopathie (DE-588)1268867829 gnd rswk-swf Thrombotische Mikroangiopathie (DE-588)1268867829 s DE-604 UNI-MED Verlag AG (DE-588)1065561733 pbl X:MVB text/html http://deposit.dnb.de/cgi-bin/dokserv?id=b19a044cedfa4169b30f5c7326f071d7&prov=M&dok_var=1&dok_ext=htm Inhaltstext B:DE-101 application/pdf https://d-nb.info/1263587453/04 Inhaltsverzeichnis DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=034101715&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis 1\p vlb 20220726 DE-101 https://d-nb.info/provenance/plan#vlb |
| spellingShingle | Bommer, Martin 1967- Thrombotische Mikroangiopathien Thrombotische Mikroangiopathie (DE-588)1268867829 gnd |
| subject_GND | (DE-588)1268867829 |
| title | Thrombotische Mikroangiopathien |
| title_auth | Thrombotische Mikroangiopathien |
| title_exact_search | Thrombotische Mikroangiopathien |
| title_exact_search_txtP | Thrombotische Mikroangiopathien |
| title_full | Thrombotische Mikroangiopathien Prof. Dr. Martin Bommer |
| title_fullStr | Thrombotische Mikroangiopathien Prof. Dr. Martin Bommer |
| title_full_unstemmed | Thrombotische Mikroangiopathien Prof. Dr. Martin Bommer |
| title_short | Thrombotische Mikroangiopathien |
| title_sort | thrombotische mikroangiopathien |
| topic | Thrombotische Mikroangiopathie (DE-588)1268867829 gnd |
| topic_facet | Thrombotische Mikroangiopathie |
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| work_keys_str_mv | AT bommermartin thrombotischemikroangiopathien AT unimedverlagag thrombotischemikroangiopathien |