p-methoxy-n-methylphenethylamine and Anemia, Hemolytic, Congenital

p-methoxy-n-methylphenethylamine has been researched along with Anemia, Hemolytic, Congenital in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ronquist, G; Sabina, RL; Waldenström, A	1

Other Studies

1 other study(ies) available for p-methoxy-n-methylphenethylamine and Anemia, Hemolytic, Congenital

Article	Year
The contribution of Ca+ calmodulin activation of human erythrocyte AMP deaminase (isoform E) to the erythrocyte metabolic dysregulation of familial phosphofructokinase deficiency. Haematologica, 2006, Volume: 91, Issue:5 Topics: Adenosine Triphosphate; AMP Deaminase; Anemia, Hemolytic, Congenital; Calcium; Calcium-Transporting ATPases; Calmodulin; Cell Membrane Permeability; Enzyme Activation; Erythrocyte Deformability; Erythrocytes; Glycogen Storage Disease Type VII; Glycolysis; Humans; Hypoxanthine; Inosine Monophosphate; Isoenzymes; Models, Biological; p-Methoxy-N-methylphenethylamine	2006

Article

Year

The contribution of Ca+ calmodulin activation of human erythrocyte AMP deaminase (isoform E) to the erythrocyte metabolic dysregulation of familial phosphofructokinase deficiency.

Haematologica, 2006, Volume: 91, Issue:5

Topics: Adenosine Triphosphate; AMP Deaminase; Anemia, Hemolytic, Congenital; Calcium; Calcium-Transporting ATPases; Calmodulin; Cell Membrane Permeability; Enzyme Activation; Erythrocyte Deformability; Erythrocytes; Glycogen Storage Disease Type VII; Glycolysis; Humans; Hypoxanthine; Inosine Monophosphate; Isoenzymes; Models, Biological; p-Methoxy-N-methylphenethylamine

2006