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Biomedical Chromatography : BMC
|
December 23, 1998
Porphyrins in urine, plasma, erythrocytes, bile and faeces in a case of congenital erythropoietic porphyria (Gunther's disease) treated with blood transfusion and iron chelation: lack of benefit from oral charcoal
A Gorchein, R Guo, C K Lim, et al.
Scandinavian Journal of Haematology
|
April 1, 1983
Haemoglobin concentration and serum erythropoietin in renal dialysis and transplant patients
G P Summerfield, O H Gyde, A M Forbes, et al.
Annals of Clinical Biochemistry
|
January 1, 1989
Glycated fibrinogen: a new index of short-term diabetic control
M R Hammer, P N John, M D Flynn, et al.
Blood
|
October 15, 1996
Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemia
J Manabe, R Arya, H Sumimoto, et al.
Journal of Clinical Pathology
|
April 1, 1990
Lead poisoning: clinical, biochemical, and haematological aspects of a recent outbreak
A Pagliuca, G J Mufti, D Baldwin, et al.
Journal of Applied Physiology
|
June 1, 1971
Adaptation to exercise: role of hemoglobin affinity for oxygen and 2,3-diphosphoglycerate
S D Shappell, J A Murray, A J Bellingham, et al.
British Medical Journal (Clinical Research Ed.)
|
July 25, 1987
Gall stones in sickle cell disease in the United Kingdom
L R Bond, S R Hatty, M E Horn, et al.
British Journal of Haematology
|
October 1, 1990
Clinicopathological features of acute undifferentiated leukaemia with a stem cell phenotype
F Brito-Babapulle, H Pullon, D M Layton, et al.
British Medical Journal (Clinical Research Ed.)
|
March 15, 1986
Neonatal screening for sickle cell diseases in Camberwell: results and recommendations of a two year pilot study
M E Horn, M C Dick, B Frost, et al.
Blood
|
November 11, 1999
Reversal of metabolic block in glycolysis by enzyme replacement in triosephosphate isomerase-deficient cells
A Ationu, A Humphries, M R Lalloz, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 82) with videos related to
Sort By:
Page
of 9
Biomedical Chromatography : BMC
|
December 23, 1998
Porphyrins in urine, plasma, erythrocytes, bile and faeces in a case of congenital erythropoietic porphyria (Gunther's disease) treated with blood transfusion and iron chelation: lack of benefit from oral charcoal
A Gorchein, R Guo, C K Lim, et al.
Scandinavian Journal of Haematology
|
April 1, 1983
Haemoglobin concentration and serum erythropoietin in renal dialysis and transplant patients
G P Summerfield, O H Gyde, A M Forbes, et al.
Annals of Clinical Biochemistry
|
January 1, 1989
Glycated fibrinogen: a new index of short-term diabetic control
M R Hammer, P N John, M D Flynn, et al.
Blood
|
October 15, 1996
Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemia
J Manabe, R Arya, H Sumimoto, et al.
Journal of Clinical Pathology
|
April 1, 1990
Lead poisoning: clinical, biochemical, and haematological aspects of a recent outbreak
A Pagliuca, G J Mufti, D Baldwin, et al.
Journal of Applied Physiology
|
June 1, 1971
Adaptation to exercise: role of hemoglobin affinity for oxygen and 2,3-diphosphoglycerate
S D Shappell, J A Murray, A J Bellingham, et al.
British Medical Journal (Clinical Research Ed.)
|
July 25, 1987
Gall stones in sickle cell disease in the United Kingdom
L R Bond, S R Hatty, M E Horn, et al.
British Journal of Haematology
|
October 1, 1990
Clinicopathological features of acute undifferentiated leukaemia with a stem cell phenotype
F Brito-Babapulle, H Pullon, D M Layton, et al.
British Medical Journal (Clinical Research Ed.)
|
March 15, 1986
Neonatal screening for sickle cell diseases in Camberwell: results and recommendations of a two year pilot study
M E Horn, M C Dick, B Frost, et al.
Blood
|
November 11, 1999
Reversal of metabolic block in glycolysis by enzyme replacement in triosephosphate isomerase-deficient cells
A Ationu, A Humphries, M R Lalloz, et al.
Page
of 9