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Journal of Clinical Pathology|August 1, 1977
Serial plasmapheresis in a haemophiliac with antibodies to FVIIIR Cobcroft, G Tamagnini, K M DormandyActa Medica Portuguesa|September 11, 1999
[Type-II dyserythropoietic anemia. A partial form of the glycoprotein degradation syndrome?]J M Marques, G Tamagnini, J HumbertoBritish Journal of Haematology|June 3, 1999
PK-LR gene mutations in pyruvate kinase deficient Portuguese patientsL Manco, M L Ribeiro, H Almeida, et al.Expert Review of Medical Devices|February 15, 2021
Device profile of the Inspiris Resilia valve for aortic valve replacement: overview of its safety and efficacyG Tamagnini, T Bourguignon, F Rega, et al.British Journal of Haematology|November 1, 1994
A variant of spectrin low-expression allele alpha LELY carrying a hereditary elliptocytosis mutation in codon 28J Randon, L Boulanger, J Marechal, et al.Blood|July 29, 1998
Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiencyJ H McVey, E J Boswell, O Takamiya, et al.Human Genetics|March 1, 1992
Molecular heterogeneity underlying the G6PD Mediterranean phenotypeC M Corcoran, V Calabrò, G Tamagnini, et al.British Journal of Haematology|October 29, 2000
A new PKLR gene mutation in the R-type promoter region affects the gene transcription causing pyruvate kinase deficiencyL Manco, M L Ribeiro, V Máximo, et al.Anales Espanoles De Pediatria|September 15, 1984
[Immunologic and enzymatic markers of acute infantile lymphoblastic leukemias]M González, G Tamagnini, J F San Miguel, et al.Blood|February 26, 2000
Elliptocytosis in patients with C-terminal domain mutations of protein 4.1 correlates with encoded messenger RNA levels rather than with alterations in primary protein structureM Morinière, L Ribeiro, N Dalla Venezia, et al.Pageof 2