Hepatitis B Virus Reactivation with Discontinuation of Nucleoside Analogue in Patients Who Received Allogeneic Hematopoietic Stem Cell Transplantation
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Hepatitis B Virus Reactivation with Discontinuation of Nucleoside Analogue in Patients Who Received Allogeneic Hematopoietic Stem Cell Transplantation ; volume:15 ; number:1 ; year:2021 ; pages:178-187 ; extent:10
Case reports in gastroenterology ; 15, Heft 1 (2021), 178-187 (gesamt 10)
- Creator
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Tsuruoka, Mio
Inoue, Jun
Onishi, Yasushi
Ninomiya, Masashi
Kakazu, Eiji
Iwata, Tomoaki
Sano, Akitoshi
Sato, Kosuke
Harigae, Hideo
Masamune, Atsushi
- DOI
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10.1159/000512397
- URN
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urn:nbn:de:101:1-2021051301090558866418
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:01 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Tsuruoka, Mio
- Inoue, Jun
- Onishi, Yasushi
- Ninomiya, Masashi
- Kakazu, Eiji
- Iwata, Tomoaki
- Sano, Akitoshi
- Sato, Kosuke
- Harigae, Hideo
- Masamune, Atsushi
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Differences between intrinsic and acquired nucleoside analogue resistance in acute myeloid leukaemia cells
Differences between intrinsic and acquired nucleoside analogue resistance in acute myeloid leukaemia cells
Nucleoside analogue 2’-C-methylcytidine inhibits hepatitis E virus replication but antagonizes ribavirin
Tenofovir rescue therapy in chronic hepatitis B patients who failed previous nucleoside analogue treatment
Uridine supplementation with Mitocnol antagonizes antiretroviral nucleoside analogue-induced mitochondrial peripheral and cerebral neuropathy in vivo
An enantioselective and modular platform for C4ʹ-modified nucleoside analogue synthesis enabled by intramolecular trans-acetalizations
Synthese carbocyclischer Nucleoside
Books received
Interferon-Free Strategies with a Nucleoside/Nucleotide Analogue
Interferon-Free Strategies without a Nucleoside/Nucleotide Analogue
Disease Reactivation after Fingolimod Discontinuation in Pregnant Multiple Sclerosis Patients
Nucleoside analogue activators of cyclic AMP-independent protein kinase A of Trypanosoma
Differences between intrinsic and acquired nucleoside analogue resistance in acute myeloid leukaemia cells
Differences between intrinsic and acquired nucleoside analogue resistance in acute myeloid leukaemia cells
Nucleoside analogue 2’-C-methylcytidine inhibits hepatitis E virus replication but antagonizes ribavirin
Tenofovir rescue therapy in chronic hepatitis B patients who failed previous nucleoside analogue treatment
Uridine supplementation with Mitocnol antagonizes antiretroviral nucleoside analogue-induced mitochondrial peripheral and cerebral neuropathy in vivo
An enantioselective and modular platform for C4ʹ-modified nucleoside analogue synthesis enabled by intramolecular trans-acetalizations
Synthese carbocyclischer Nucleoside
Books received
Interferon-Free Strategies with a Nucleoside/Nucleotide Analogue
Interferon-Free Strategies without a Nucleoside/Nucleotide Analogue
Disease Reactivation after Fingolimod Discontinuation in Pregnant Multiple Sclerosis Patients
Nucleoside analogue activators of cyclic AMP-independent protein kinase A of Trypanosoma
Differences between intrinsic and acquired nucleoside analogue resistance in acute myeloid leukaemia cells
Differences between intrinsic and acquired nucleoside analogue resistance in acute myeloid leukaemia cells
Nucleoside analogue 2’-C-methylcytidine inhibits hepatitis E virus replication but antagonizes ribavirin
Tenofovir rescue therapy in chronic hepatitis B patients who failed previous nucleoside analogue treatment
Uridine supplementation with Mitocnol antagonizes antiretroviral nucleoside analogue-induced mitochondrial peripheral and cerebral neuropathy in vivo
An enantioselective and modular platform for C4ʹ-modified nucleoside analogue synthesis enabled by intramolecular trans-acetalizations
Synthese carbocyclischer Nucleoside