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S W Eber

Showing results (41-50 of 47) with videos related to

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European Journal of Pediatrics|September 1, 1991
Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activityS W Eber, A Pekrun, A Bardosi, et al.
Annals of Hematology|December 22, 1999
Frequency of very late fatal sepsis after splenectomy for hereditary spherocytosis: impact of insufficient antibody response to pneumococcal infectionS W Eber, C M Langendörfer, M Ditzig, et al.
British Journal of Haematology|July 1, 1989
Hereditary stomatocytosis: consistent association with an integral membrane protein deficiencyS W Eber, W M Lande, T A Iarocci, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Progressive fatal pancytopenia, psychomotor retardation and muscle carnitine deficiency in a child with ethylmalonic aciduria and ethylmalonic acidaemiaG F Hoffmann, D H Hunneman, C Jakobs, et al.
British Journal of Haematology|May 1, 1996
Thrombo-embolic disease after splenectomy for hereditary stomatocytosisG W Stewart, J A Amess, S W Eber, et al.
Transfusion|September 30, 1999
Application of RHD and RHCE genotyping for correct blood group determination in chronically transfused patientsT J Legler, S W Eber, M Lakomek, et al.
Nature Genetics|June 1, 1996
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosisS W Eber, J M Gonzalez, M L Lux, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
European Journal of Pediatrics|September 1, 1991
Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activityS W Eber, A Pekrun, A Bardosi, et al.
Annals of Hematology|December 22, 1999
Frequency of very late fatal sepsis after splenectomy for hereditary spherocytosis: impact of insufficient antibody response to pneumococcal infectionS W Eber, C M Langendörfer, M Ditzig, et al.
British Journal of Haematology|July 1, 1989
Hereditary stomatocytosis: consistent association with an integral membrane protein deficiencyS W Eber, W M Lande, T A Iarocci, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Progressive fatal pancytopenia, psychomotor retardation and muscle carnitine deficiency in a child with ethylmalonic aciduria and ethylmalonic acidaemiaG F Hoffmann, D H Hunneman, C Jakobs, et al.
British Journal of Haematology|May 1, 1996
Thrombo-embolic disease after splenectomy for hereditary stomatocytosisG W Stewart, J A Amess, S W Eber, et al.
Transfusion|September 30, 1999
Application of RHD and RHCE genotyping for correct blood group determination in chronically transfused patientsT J Legler, S W Eber, M Lakomek, et al.
Nature Genetics|June 1, 1996
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosisS W Eber, J M Gonzalez, M L Lux, et al.
Pageof 5