Works matching Vulliamy, C. E., 1886-1971

Results: 21

Multiple organ dysfunction after trauma.

Published in:

British Journal of Surgery, 2020, v. 107, n. 4, p. 402, doi. 10.1002/bjs.11361

By:

Cole, E.;
Gillespie, S.;
Vulliamy, P.;
Brohi, K.;
Akkad, H.;
Apostolidou, K.;
Ardley, R.;
Aylwin, C.;
Bassford, C.;
Bonner, S.;
Brooks, A.;
Cairns, T.;
Cecconi, M.;
Clark, F.;
Dempsey, G.;
Denison Davies, E.;
Docking, R.;
Eddlestone, J.;
Ellis, D.;
Evans, J.

Publication type:

Article

A ribosome-related signature in peripheral blood CLL B cells is linked to reduced survival following treatment.

Published in:

Cell Death & Disease, 2016, v. 7, n. 6, p. e2249, doi. 10.1038/cddis.2016.148

By:

Sbarrato, T;
Horvilleur, E;
Pöyry, T;
Hill, K;
Chaplin, L C;
Spriggs, R V;
Stoneley, M;
Wilson, L;
Jayne, S;
Vulliamy, T;
Beck, D;
Dokal, I;
Dyer, M J S;
Yeomans, A M;
Packham, G;
Bushell, M;
Wagner, S D;
Willis, A E

Publication type:

Article

Postoperative Elevation of the Neutrophil: Lymphocyte Ratio Predicts Complications Following Esophageal Resection.

Published in:

World Journal of Surgery, 2016, v. 40, n. 6, p. 1397, doi. 10.1007/s00268-016-3427-z

By:

Vulliamy, Paul;
McCluney, Simon;
Mukherjee, Samrat;
Ashby, Luke;
Amalesh, Thangadorai

Publication type:

Article

Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data.

Published in:

Bioinformatics, 2017, v. 33, n. 15, p. 2421, doi. 10.1093/bioinformatics/btx147

By:

Pontikos, Nikolas;
Jing Yu;
Moghul, Ismail;
Withington, Lucy;
Blanco-Kelly, Fiona;
Vulliamy, Tom;
Wong, Tsz Lun Ernest;
Murphy, Cian;
Cipriani, Valentina;
Fiorentino, Alessia;
Arno, Gavin;
Greene, Daniel;
Jacobsen, Julius O. B.;
Clark, Tristan;
Gregory, David S.;
Nemeth, Andrea M.;
Halford, Stephanie;
Inglehearn, Chris F.;
Downes, Susan;
Black, Graeme C.

Publication type:

Article

Characterisation and Validation of Insertions and Deletions in 173 Patient Exomes.

Published in:

PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051292

By:

Lescai, Francesco;
Bonfiglio, Silvia;
Bacchelli, Chiara;
Chanudet, Estelle;
Waters, Aoife;
Sisodiya, Sanjay M.;
Kasperavičiū tė, Dalia;
Williams, Julie;
Harold, Denise;
Hardy, John;
Kleta, Robert;
Cirak, Sebahattin;
Williams, Richard;
Achermann, John C.;
Anderson, John;
Kelsell, David;
Vulliamy, Tom;
Houlden, Henry;
Wood, Nicholas;
Sheerin, Una

Publication type:

Article

Viscoelastic haemostatic assay augmented protocols for major trauma haemorrhage (ITACTIC): a randomized, controlled trial.

Published in:

Intensive Care Medicine, 2021, v. 47, n. 1, p. 49, doi. 10.1007/s00134-020-06266-1

By:

Baksaas-Aasen, K.;
Gall, L. S.;
Stensballe, J.;
Juffermans, N. P.;
Curry, N.;
Maegele, M.;
Brooks, A.;
Rourke, C.;
Gillespie, S.;
Murphy, J.;
Maroni, R.;
Vulliamy, P.;
Henriksen, H. H.;
Pedersen, K. Holst;
Kolstadbraaten, K. M.;
Wirtz, M. R.;
Kleinveld, D. J. B.;
Schäfer, N.;
Chinna, S.;
Davenport, R. A.

Publication type:

Article

Exogenous TERC alone can enhance proliferative potential, telomerase activity and telomere length in lymphocytes from dyskeratosis congenita patients.

Published in:

British Journal of Haematology, 2009, v. 144, n. 5, p. 771, doi. 10.1111/j.1365-2141.2008.07516.x

By:

Kirwan, Michael;
Beswick, Richard;
Vulliamy, Tom;
Nathwani, Amit C.;
Walne, Amanda J.;
Casimir, Colin;
Dokal, Inderjeet

Publication type:

Article

Alterations in platelet behavior after major trauma: adaptive or maladaptive?

Published in:

Platelets, 2021, v. 32, n. 3, p. 295, doi. 10.1080/09537104.2020.1718633

By:

Vulliamy, Paul;
Kornblith, Lucy Z.;
Kutcher, Matthew E.;
Cohen, Mitchell J.;
Brohi, Karim;
Neal, Matthew D.

Publication type:

Article

A large ventricular septal defect complicating resuscitation after blunt trauma.

Published in:

2012

By:

De'Ath, Henry D. I.;
Vulliamy, Paul E. D.;
Davies, Ceri;
Uppal, Rakesh

Publication type:

Case Study

Molecular Characterization of Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency in Al-Ain District, United Arab Emirates.

Published in:

Human Heredity, 1996, v. 46, n. 3, p. 136, doi. 10.1159/000154342

By:

Bayoumi, R.A.;
Nur-E-Kamal, M.S.A.;
Tadayyon, M.;
Mohamed, K.K.A.;
Mahboob, B.H.;
Qureshi, M.M.;
Lakhani, M.S.;
Awaad, M.O.;
Kaeda, J.;
Vulliamy, T.J.;
Luzzatto, L.

Publication type:

Article

Coarctation repair mimicking acute aortic dissection.

Published in:

2012

By:

Vulliamy, Paul E.;
McCormack, David J.;
Szczeklik, Michal;
Lall, Kulvinder S.

Publication type:

Case Study

Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome).

Published in:

2003

By:

Sznajer, Yves;
Baumann, Clarisse;
David, Albert;
Journel, Hubert;
Lacombe, Didier;
Perel, Yves;
Blouin, Pascale;
Segura, Jean-François;
Cezard, Jean-Pierre;
Peuchmaur, Michel;
Vulliamy, Tomy;
Dokal, Inderjeet;
Verloes, Alain;
Segura, Jean-François

Publication type:

journal article

Characterization of G6PD deficiency in southern Croatia: description of a new variant, G6PD Split.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 11, p. 547, doi. 10.1007/s10038-005-0292-2

By:

Barišić, Marin;
Korać, Jelena;
Pavlinac, Ivana;
Krželj, Vjekoslav;
Marušić, Eugenija;
Vulliamy, Tom;
Terzić, Janoš

Publication type:

Article

A novel DKC1 mutation, severe combined immunodeficiency (T+ B– NK– SCID) and bone marrow transplantation in an infant with Hoyeraal–Hreidarsson syndrome.

Published in:

British Journal of Haematology, 2002, v. 119, n. 3, p. 765, doi. 10.1046/j.1365-2141.2002.03822.x

By:

Cossu, Fausto;
Vulliamy, Tom J.;
Marrone, Anna;
Badiali, Manuela;
Cao, Antonio;
Dokal, Inderjeet

Publication type:

Article

Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1.

Published in:

British Journal of Haematology, 1999, v. 107, n. 2, p. 335, doi. 10.1046/j.1365-2141.1999.01690.x

By:

Knight;
Heiss;
Vulliamy;
Aalfs;
McMahon;
Richmond;
Jones;
Hennekam;
Poustka;
Mason;
Dokal;
Dokal, Inderjeet

Publication type:

Article

Three major G6PD-deficient polymorphic variants identified among the Mauritian population.

Published in:

British Journal of Haematology, 1999, v. 104, n. 4, p. 849, doi. 10.1046/j.1365-2141.1999.01230.x

By:

Kotea;
Kaeda;
Yan;
Sem Fa;
Beesoon;
Jankee;
Ramasawmy;
Vulliamy;
Bradnock;
Bautista;
Luzzatto;
Krishnamoorthy;
Mason;
Kaeda

Publication type:

Article

Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia.

Published in:

British Journal of Haematology, 1998, v. 101, n. 4, p. 670, doi. 10.1046/j.1365-2141.1998.00763.x

By:

Vulliamy, Tom J.;
Kaeda, Jaspal S.;
Ait-Chafa, Dahlila;
Mangerini, Rosa;
Roper, David;
Barbot, Jose;
Mehta, Athul B.;
Athanassiou-Metaxa, M.;
Luzzatto, Lucio;
Mason, Philip J.

Publication type:

Article

A mutation in a functional Sp1 binding site of the telomerase RNA gene (hTERC) promoter in a patient with Paroxysmal Nocturnal Haemoglobinuria.

Published in:

BMC Blood Disorders, 2004, v. 4, p. 1

By:

Keith, W. Nicol;
Vulliamy, Tom;
Jiangqin Zhao;
Ar, Cem;
Erzik, Can;
Bilsland, Alan;
Ulku, Birsen;
Marrone, Anna;
Mason, Philip J.;
Bessler, Monica;
Serakinci, Nedime;
Dokal, Inderjeet

Publication type:

Article

THE ONSLOW FAMILY.

Published in:

1953

By:

Pennington, D. H.

Publication type:

Book Review

ROMAN BRITAIN/THE STORY OF MAN'S WORK/OUR PREHISTORIC FORERUNNERS/MAN BEFORE HISTORY (Book).

Published in:

1926

By:

J. H. H.

Publication type:

Book Review

Generation or birth cohort effect on cancer risk in Li–Fraumeni syndrome.

Published in:

Human Genetics, 2005, v. 118, n. 3/4, p. 489, doi. 10.1007/s00439-005-0016-x

By:

Brown, Barry W.;
Costello, Tracy J.;
Shih-Jen Hwang;
Strong, Louise C.

Publication type:

Article