WN VALENTINE, KR TANAKA, DE PAGLIA - Annals of internal medicine, 1985 - annals.org.p.angrylapdog.com The human erythrocyte generates high-energy adenosine triphosphate by anaerobic
glycolysis and cycles oxidized and reduced nicotinamide adenine dinucleotide
phosphate by the aerobic pentose phosphate shunt pathway. Certain ... Cited by 25 - Related articles - All 4 versions
P Boulard-Heitzmann, M Boulard, C Tallineau, … - Scand J Haematol, 1984 - interscience.wiley.com A 40-year-old woman splenectomized 17 years previously for hereditary haemolytic
anaemia was investigated in our laboratory because of persistent conjunctival
subic-terus associated with compensated haemolysis. The results of the ... Cited by 4 - Related articles - All 3 versions
S Yamada, H Nakajima, MR Kuehn - Biochemical and Biophysical Research …, 2004 - Elsevier We have identified novel transcriptional isoforms of the human and mouse genes
encoding muscle type phosphofructokinase-1 (PFK-M). These isoforms are expressed
specifically in the testis and in the mid-gestation embryo, and have been ... Cited by 4 - Related articles - All 4 versions
[CITATION] Disorders of erythrocyte glycolysis and nucleotide metabolism
P de Atauri, A Repiso, B Oliva, J Lluis Vives- … - BBA-Molecular Basis of Disease, 2005 - Elsevier In a patient with clinical diagnosis of Hereditary Spherocytosis and partial
deficiency (50%) of red blood cell phosphoglycerate mutase (PGAM) activity, we
have recently reported [A. Repiso, P. Pérez de la Ossa, X. Avilés, B. ... Cited by 5 - Related articles - All 4 versions
