Zobrazeno 1 - 10
of 51
pro vyhledávání: '"D M, Layton"'
Autor:
P. Bianchi, R. F. Grace, J.-L. Vives Corrons, B. Glader, A. Glenthøj, H. Kanno, K. H. Kuo, C. Lander, D. M. Layton, D. Pospíŝilová, V. Viprakasit, J. Williams, Y. Yan, B. McGee, E. J. van Beers
Publikováno v:
HemaSphere, Vol 6, Pp 1443-1444 (2022)
Externí odkaz:
https://doaj.org/article/401bfe5c6c394986b676135b33d875b5
Autor:
W. Barcellini, R. F. Grace, H. Al-Samkari, A. Glenthøj, J. A. Rothman, M. Morado Arias, D. M. Layton, O. Andres, M. DiBacco, P. Hawkins, M. P. Judge, F. Tai, J. Morales-Arias, V. Beynon, E. J. van Beers
Publikováno v:
HemaSphere, Vol 6, Pp 1429-1430 (2022)
Externí odkaz:
https://doaj.org/article/5715112410b34e0a910a2c9f3fc2a2df
Autor:
K. H. M. Kuo, D. M. Layton, A. Lal, H. Al-Samkari, J. Bhatia, P. A. Kosinski, B. Tong, M. Lynch, K. Uhlig, E. P. Vichinsky
Publikováno v:
HemaSphere, Vol 6, Pp 1403-1404 (2022)
Externí odkaz:
https://doaj.org/article/b2a98625779f4b66942d8cd26b382e1f
Autor:
R. F. Grace, A. Glenthøj, W. Barcellini, M. Verhovsek, J. A. Rothman, M. Morado Arias, D. M. Layton, O. Andres, F. Galactéros, E. J. van Beers, K. Onodera, V. Viprakasit, S. Chonat, J. B. Porter, M. P. Judge, P. A. Kosinski, P. Hawkins, S. Gheuens, R. Xu, B. McGee, V. Beynon, H. Al-Samkari
Publikováno v:
HemaSphere, Vol 6, Pp 1426-1427 (2022)
Externí odkaz:
https://doaj.org/article/d102fc02d19a4525b0d83f1ccf2a8af3
Autor:
H. Al-Samkari, R. F. Grace, A. Glenthøj, O. Andres, W. Barcellini, F. Galactéros, K. H. M. Kuo, D. M. Layton, M. Morado Arias, V. Viprakasit, Y. Dong, F. Tai, L. Grekas, K. Khoja, S. Gheuens, B. McGee, J. B. Porter, E. J. van Beers
Publikováno v:
HemaSphere, Vol 6, Pp 1425-1426 (2022)
Externí odkaz:
https://doaj.org/article/ee64e4d54d7042caad5c1cd760412896
Autor:
Michel R.A. Lalloz, E.K. Cooper, D. M. Layton, A.D. Stephens, B.N. Green, S. Erten, B.J. Wild
Publikováno v:
Blood Cells, Molecules, and Diseases. 27:691-704
ABSTRACT The precise identification of human hemoglobin variants, over 700 human hemoglobin variants are known, is essential for prediction of their clinical and genetic significance. A systematic approach to their rapid identification is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69d192eefca234d65da8beea8673609e
https://doi.org/10.1006/bcmd.2001.0430
https://doi.org/10.1006/bcmd.2001.0430
Autor:
A. I. Wacey, David Neil Cooper, David Stuart Millar, J. C. Reverter, K. J. Pasi, L. Elliston, D. M. Layton, P. Cachia, Michael Krawczak, Paula H. B. Bolton-Maggs, H. K. Nieuwenhuis, J. Reynaud, P. Deex, P. M. Mannucci
Publikováno v:
Human Genetics. 106:249-257
Factor VII (FVII) deficiency is a rare haemorrhagic condition, normally inherited as an autosomal recessive trait, in which clinical presentation is highly variable and correlates poorly with laboratory phenotype. The FVII (F7) gene was sequenced in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a6837338c088692bd29c5182f461a31
https://doi.org/10.1007/s004390051035
https://doi.org/10.1007/s004390051035
Autor:
Jun Ichi Manabe, Hideki Sumimoto, D. M. Layton, A. J. Bellingham, Yasuyuki Fukumaki, R. Arya, T. Yubisui
Publikováno v:
Scopus-Elsevier
Hereditary methemoglobinemia due to reduced nicotinamide adenine dinucleotide (NADH) cytochrome b5 reductase (b5R) deficiency is classified into two types, an erythrocyte (type I) and a generalized (type II). We investigated the b5R gene of a patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a26f5a38abf5bf715c15270ec7fbbfce
https://doi.org/10.1182/blood.v88.8.3208.bloodjournal8883208
https://doi.org/10.1182/blood.v88.8.3208.bloodjournal8883208
Publikováno v:
Blood Reviews. 9:165-175
The hereditary red cell enzymopathies are an uncommon but important cause of chronic haemolytic anaemia. Their clinical diversity is mirrored by increasingly evident heterogeneity at the molecular level. The structure, function, and expression of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::489a2908e36f2352e4078dd165057d14
https://doi.org/10.1016/0268-960x(95)90022-5
https://doi.org/10.1016/0268-960x(95)90022-5
Autor:
T R, Walton, D M, Layton
Publikováno v:
Journal of oral rehabilitation. 39(9)
The aim of this study was to apply a novel economic tool (cost satisfaction analysis) to assess the utility of fixed prosthodontics, to review its applicability, and to explore the perceived value of treatment. The cost satisfaction analysis employed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::59eee0d920069373e26d9f8f570dcfae
https://pubmed.ncbi.nlm.nih.gov/22642585
https://pubmed.ncbi.nlm.nih.gov/22642585