Antonio Medina de Almeida


AuthID: R-000-T91

Confirmed Publications: 65



51
TITLE: Clinical management of gastrointestinal disturbances in patients with myelodysplastic syndromes receiving iron chelation treatment with deferasirox  Full Text
AUTHORS: Nolte, F; Angelucci, E; Beris, P; Macwhannell, A; Selleslag, D; Schumann, C; Xicoy, B; Almeida, A ; Guerci Bresler, A; Sliwa, T; Muus, P; Porter, J; Hofmann, WK;
PUBLISHED: 2011, SOURCE: Leukemia Research, VOLUME: 35, ISSUE: 9
INDEXED IN: Scopus CrossRef
IN MY: ORCID | CIÊNCIAVITAE
52
TITLE: Chapter 16 Inherited GPI deficiency
AUTHORS: Almeida, A ; Layton, M; Karadimitris, A;
PUBLISHED: 2009, SOURCE: Enzymes, VOLUME: 26, ISSUE: C
INDEXED IN: Scopus CrossRef
IN MY: ORCID | CIÊNCIAVITAE
53
TITLE: Inherited glycosylphosphatidyl inositol deficiency: A treatable CDG  Full Text
AUTHORS: Antonio Almeida ; Mark Layton; Anastasios Karadimitris;
PUBLISHED: 2009, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1792, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
54
TITLE: RECOMMENDATIONS FOR DIAGNOSIS, TREATMENT AND MONITORING OF CHRONIC MYELOID LEUKEMIA  Full Text
AUTHORS: Antonio Almeida ; Isabel Castro; Jorge Coutinho; Lurdes Guerra; Herlander Marques ; Ana Marques Pereira;
PUBLISHED: 2009, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 22, ISSUE: 5
INDEXED IN: Scopus WOS
IN MY: ORCID | CIÊNCIAVITAE
55
TITLE: Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency  Full Text
AUTHORS: Almeida, AM ; Murakami, Y; Layton, DM; Hillmen, P; Sellick, GS; Maeda, Y; Richards, S; Patterson, S; Kotsianidis, I; Mollica, L; Crawford, DH; Baker, A; Ferguson, M; Roberts, I; Houlston, R; Kinoshita, T; Karadimitris, A;
PUBLISHED: 2006, SOURCE: Nature Medicine, VOLUME: 12, ISSUE: 7
INDEXED IN: Scopus CrossRef
IN MY: ORCID | CIÊNCIAVITAE
56
TITLE: Bone involvement in sickle cell disease  Full Text
AUTHORS: Almeida, A ; Roberts, I;
PUBLISHED: 2005, SOURCE: British Journal of Haematology, VOLUME: 129, ISSUE: 4
INDEXED IN: Scopus CrossRef
IN MY: ORCID | CIÊNCIAVITAE
57
TITLE: Human invariant NKT cells are required for effective in vitro alloresponses
AUTHORS: Patterson, S; Kotsianidis, I; Almeida, A ; Politou, M; Rahemtulla, A; Matthew, B; Schmidt, RR; Cerundolo, V; Roberts, IAG; Karadimitris, A;
PUBLISHED: 2005, SOURCE: Journal of Immunology, VOLUME: 175, ISSUE: 8
INDEXED IN: Scopus CrossRef: 8
IN MY: ORCID | CIÊNCIAVITAE
58
TITLE: Automated computer result reporting for haemoglobinopathy screening  Full Text
AUTHORS: Daniel, Y; Witchlow, B; Almeida, A ;
PUBLISHED: 2004, SOURCE: Clinical and Laboratory Haematology, VOLUME: 26, ISSUE: 1
INDEXED IN: Scopus CrossRef
IN MY: ORCID | CIÊNCIAVITAE
59
TITLE: The use of recombinant factor VIIa in children with inherited platelet function disorders  Full Text
AUTHORS: Almeida, AM ; Khair, K; Hann, I; Liesner, R;
PUBLISHED: 2003, SOURCE: British Journal of Haematology, VOLUME: 121, ISSUE: 3
INDEXED IN: Scopus CrossRef
IN MY: ORCID | CIÊNCIAVITAE
60
TITLE: Therapeutic challenges in childhood sickle cell disease Part 1: Current and future treatment options  Full Text
AUTHORS: Amrolia, PJ; Almeida, A ; Halsey, C; Roberts, IAG; Davies, SC;
PUBLISHED: 2003, SOURCE: British Journal of Haematology, VOLUME: 120, ISSUE: 5
INDEXED IN: Scopus CrossRef
IN MY: ORCID | CIÊNCIAVITAE
Page 6 of 7. Total results: 65.

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