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Journal of Internal Medicine|January 1, 1994
Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuriaM F McMullin, P Hillmen, J Jackson, et al.Blood|December 15, 1995
Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift typeK Nafa, P J Mason, P Hillmen, et al.Human Molecular Genetics|May 1, 1994
Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21M Bessler, P Hillmen, L Longo, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 9, 1982
Pyruvate kinase deficiency: characterization of two new genetic variantsL Dente, M D'Urso, S Di Maio, et al.The Journal of Laboratory and Clinical Medicine|May 1, 1979
Genetically determined deficiency of glucose 6-phosphate dehydrogenase (type-A-) is expressed in the liverO A Oluboyede, G J Esan, T I Francis, et al.British Journal of Haematology|November 13, 2001
Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuriaD J Araten, D Swirsky, A Karadimitris, et al.Blood Cells, Molecules & Diseases|October 29, 1998
The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplicationsK Nafa, M Bessler, H Castro-Malaspina, et al.Haematologica|March 1, 1997
Small bowel infarction by AspergillusL Catalano, M Picardi, D Anzivino, et al.Genomics|April 10, 1995
Genomic structure and sequence of the Fugu rubripes glucose-6-phosphate dehydrogenase gene (G6PD)P J Mason, D J Stevens, L Luzzatto, et al.Human Heredity|May 1, 1996
Molecular characterization of G6PD deficiency in OmanS Daar, T J Vulliamy, J Kaeda, et al.Pageof 20