Add to ORKGSIGLEAvailable from British Library Document Supply Centre- DSC:DX174020 / BLDSC - British Library Document Supply CentreGBUnited Kingdo
Initially it was believed that phosphorylase was responsible for both glycogen breakdown and synthes...
McArdle disease or Glycogen Storage Disease type V (GSD V; myophosphorylase deficiency; MIM 232600) ...
International audienceObjective: Glycogen storage diseases (GSDs) are severe human disorders resulti...
Six glycogen storage diseases (resulting from deficiencies of acid maltase, phosphorylase, phosphofr...
Human phosphofructokinase (PFK) exists in tetrameric isozy-mic forms, at least in vitro. Muscle and ...
Biochemical analysis of muscle in a 37-year-old man with exercise intolerance, myalgia, recurrent my...
We studied a group of 14 patients from Northern Italy with myophosphorylase deficiency. The disease ...
SIGLEAvailable from British Library Document Supply Centre- DSC:D94181 / BLDSC - British Library Doc...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN008749 / BLDSC - British Library D...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN017705 / BLDSC - British Library D...
Mutations in the PYGM gene encoding skeletal muscle glycogen phosphorylase (GP) cause a metabolic di...
Ten adult patients complained of exercise intolerance; five of them had cramps and three had recurre...
Muscular glycogenosis is a disease resulting from genetic abnormalities altering an enzyme which is ...
Phosphofructokinase (PFK) is the key regulatory enzyme of glycolysis. Patients lacking the muscular ...
patients with muscle phosphofructokinase (PFK; EC 2.7.1.11) deficiency (Glycogenosis type VII; Tarui...
Initially it was believed that phosphorylase was responsible for both glycogen breakdown and synthes...
McArdle disease or Glycogen Storage Disease type V (GSD V; myophosphorylase deficiency; MIM 232600) ...
International audienceObjective: Glycogen storage diseases (GSDs) are severe human disorders resulti...
Six glycogen storage diseases (resulting from deficiencies of acid maltase, phosphorylase, phosphofr...
Human phosphofructokinase (PFK) exists in tetrameric isozy-mic forms, at least in vitro. Muscle and ...
Biochemical analysis of muscle in a 37-year-old man with exercise intolerance, myalgia, recurrent my...
We studied a group of 14 patients from Northern Italy with myophosphorylase deficiency. The disease ...
SIGLEAvailable from British Library Document Supply Centre- DSC:D94181 / BLDSC - British Library Doc...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN008749 / BLDSC - British Library D...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN017705 / BLDSC - British Library D...
Mutations in the PYGM gene encoding skeletal muscle glycogen phosphorylase (GP) cause a metabolic di...
Ten adult patients complained of exercise intolerance; five of them had cramps and three had recurre...
Muscular glycogenosis is a disease resulting from genetic abnormalities altering an enzyme which is ...
Phosphofructokinase (PFK) is the key regulatory enzyme of glycolysis. Patients lacking the muscular ...
patients with muscle phosphofructokinase (PFK; EC 2.7.1.11) deficiency (Glycogenosis type VII; Tarui...
Initially it was believed that phosphorylase was responsible for both glycogen breakdown and synthes...
McArdle disease or Glycogen Storage Disease type V (GSD V; myophosphorylase deficiency; MIM 232600) ...
International audienceObjective: Glycogen storage diseases (GSDs) are severe human disorders resulti...