Zobrazeno 1 - 10 of 33 pro vyhledávání: '"C E, Walsh"'
1
Parvovirus-mediated gene transfer for the haemophilias
Autor: H. Chao, C. E. Walsh
Publikováno v: Haemophilia. 8:60-67
Gene therapy may revolutionize the treatment of haemophilia. Effective gene therapy requires sustained therapeutic levels of factors IX (FIX) and VIII. Adeno-associated virus (AAV) is a member of the parvovirus family, is a nonpathogenic virus with a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3605a34de6f75859a826ff0ae3058395
https://doi.org/10.1046/j.1351-8216.2001.00121.x
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2
Patient- and caregiver-reported bleeding symptoms and reasons for starting and stopping treatment with recombinant factor VIIa: analysis of the Dosing Observational Study in Haemophilia (DOSE)
Autor: L A, Valentino, C E, Walsh, M T, Reding, G A, Young, O, Levendoglu-Tugal, D L, Cooper
Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 18(4)
Acute haemorrhage treatment in patients with congenital haemophilia with inhibitors (CHwI) has transitioned to home. Patient/caregiver perceptions of bleeding symptoms and reasons for starting/stopping treatment were investigated. Frequently bleeding
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dc9690ef2789f0f09272a8d260df7fd3
https://pubmed.ncbi.nlm.nih.gov/22348407
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3
Patient/caregiver-reported recombinant factor VIIa (rFVIIa) dosing: home treatment of acute bleeds in the Dosing Observational Study in Hemophilia (DOSE)
Autor: G, Young, A D, Shapiro, C E, Walsh, R A, Gruppo, R Z, Gut, D L, Cooper
Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 18(3)
Patients with congenital haemophilia with inhibitors experience acute bleeds managed with bypassing agents, such as recombinant FVIIa (rFVIIa). Home-based treatment and dosing patterns in the US remain poorly described. This study aimed to assess the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b8e2b5c3692b218106fe58454968aef4
https://pubmed.ncbi.nlm.nih.gov/22171621
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4
Inflation inertia and optimal disinflation
Autor: C. E. Walsh
Publikováno v: New Zealand Economic Papers. 25:141-150
The Reserve Bank Act of 1989 can be viewed as a means of providing credibility to the Reserve Bank's attempts to lower inflation and as a solution to the inflationary bias inherent in the discretionary conduct of monetary policy. Many of the critics
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bf73229a0308d259fe73c761002ce7f9
https://doi.org/10.1080/00779959109544173
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6
An unanticipated decline in the caesarean section rate
Autor: C E Walsh, G Burke
Publikováno v: Archives of Disease in Childhood - Fetal and Neonatal Edition. 96:Fa89-Fa90
Aim The persistent rise in the rate of caesarean section (CS) is a prominent and contentious feature of modern obstetrics. The aim of this study was to determine which clinical subgroups contributed to an unexpected decline in the CS rate at our inst
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a442ea859db16fbb82e1a6571073839c
https://doi.org/10.1136/archdischild.2011.300162.50
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7
Sustained expression of human factor VIII in mice using a parvovirus-based vector
Autor: H, Chao, L, Mao, A T, Bruce, C E, Walsh
Publikováno v: Blood. 95(5)
Persistent therapeutic levels of human factor VIII (hFVIII) would signify a major advance in the treatment of hemophilia A. Here we report sustained expression of hFVIII in immunocompetent mice using recombinant adeno-associated virus (rAAV) vectors.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bf9b76bff7581b9d2d256a600a6303c0
https://pubmed.ncbi.nlm.nih.gov/10688813
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8
Phenotypic correction of Fanconi anemia group C knockout mice
Autor: K A, Gush, K L, Fu, M, Grompe, C E, Walsh
Publikováno v: Blood. 95(2)
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure, congenital anomalies, and a predisposition to malignancy. FA cells demonstrate hypersensitivity to DNA cross-linking agents, such as mitomycin C (MMC). Mice with a target
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::27663611d9e015d791fe68b78aa98bd6
https://pubmed.ncbi.nlm.nih.gov/10627482
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9
Retroviral gene transfer for the assignment of Fanconi anemia (FA) patients to a FA complementation group
Autor: J M Liu, K L Fu, P C Thuss, Martin Digweed, T Fujino, C E Walsh
Publikováno v: Human genetics. 102(2)
Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, cancer susceptibility, and a variety of developmental defects. The disease is clinically heterogeneous; eight different complementation groups (FA A-H) and,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5fc4c18323104dc32d580541e652aa4
https://pubmed.ncbi.nlm.nih.gov/9521584
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10
Functional correction of Fanconi anemia group A hematopoietic cells by retroviral gene transfer
Autor: K L, Fu, J R, Foe, H, Joenje, K W, Rao, J M, Liu, C E, Walsh
Publikováno v: Blood. 90(9)
Fanconi anemia (FA) is an autosomal recessive genetic disorder characterized by a variety of physical anomalies, bone marrow failure, and an increased risk for malignancy. FA cells exhibit chromosomal instability and are hypersensitive to DNA cross-l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9d5e8b0fe267873be74514f681d28607
https://pubmed.ncbi.nlm.nih.gov/9345011
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