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Poland’s syndrome associated with chronic granulocytic leukaemia
Costa R, Afonso E, Benedito M, Maricato L
Sangre (Barc), 36(5):417-8
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Dominant b-thalassemia trait in a portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin gene.
Oner R, Oner C, Wilson JB, Tamagnini GP, Ribeiro ML, HuismanTJ
Br J Haematol. Oct;79(2):306-10
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Hb Coimbra or alpha 2 beta 299 (G1)Asp-Glu, a newly discovered high oxygen affinity variant
Tamagnini G, Ribeiro ML, Valente V, Ramachandran M, Wilson JB, Baysal E, Gu LH, Huisman THJ
Hemoglobin, 15(6):487-96
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Linfohistiocitose Hemofagocítica Familiar – a propósito de um caso clínico
M Benedito, F Maduro, F Heitor, R Maia, R Batista, L Maricato
, Rev Port Pediatr, 22:121-3
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Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin gene.
Zhao W, Wilson JB, Webber BB, Kutlar A, Tamagnini GP, Kuam B, Huisman TH
Hemoglobin, 14(6):627-35
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B-cell chronic lymphocytic leukaemia: prognostic value of the immunophenotype and the clinico-haematological features.
Orfão A, Gonzalez M, San Miguel JF, Rios A, Canizo MC, Hernandez J, Maricato ML, Lopez Borrasca A
Am J Haematol, 31(1):26-31
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Neoplasias malignas em crianças do Centro de Portugal (317 casos em 10 anos)
I Casal, ML Ribeiro, D Lopes, R Baptista
Rev Port Pediatr, 20:445-448.
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Linfoma de Burkitt experiência do Hospital Pediátrico de Coimbra
R Baptista, I Casal, L Maricato, ML Ribeiro, D Lopes
Rev Port Pediatr, 20:449-54.
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Estratégia para a detecção dos portadores de Talassemia na população portuguesa
G Tamagnini, ML Ribeiro
O Médico, 120:114-9
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Síndrome Mieldisplástico na criança – a propósito de 3 casos clínicos
I Pires, C Menezes, M Benedito, R Baptista, L Maricato
Ver Port Pediatr, 20:177-80
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