[PDF][PDF] Tc-99m pyrophosphate muscle labeling in McArdle syndrome
TR Swift, M Brown - Journal of Nuclear Medicine, 1978 - Soc Nuclear Med
This paper reports the findings on two patients with McArdle syndrome (myophoaphorylase
deficiency) in whom conventional bone scans with Tc. 99m pyrophosphate revealed Intense …
deficiency) in whom conventional bone scans with Tc. 99m pyrophosphate revealed Intense …
McArdle's disease presenting as convulsion and rhabdomyolysis
SE Salmon, CE Turner - The American Journal of Medicine, 1965 - Elsevier
A case of myophosphorylase deficiency (McArdle's disease) is presented in which a grand
mal seizure occurred and was followed by myoglobinuria. Muscle biopsy disclosed severe …
mal seizure occurred and was followed by myoglobinuria. Muscle biopsy disclosed severe …
Examination of a Case of Suspected McArdle's Syndrome by 31P Nuclear Magnetic Resonance
BD Ross, GK Radda, DG Gadian… - … England Journal of …, 1981 - Mass Medical Soc
McARDLE'S syndrome, 1 an inborn error of metabolism caused by a lack of glycogen
phosphorylase activity in skeletal muscle, is a recessive condition of some rarity. 2 …
phosphorylase activity in skeletal muscle, is a recessive condition of some rarity. 2 …
[CITATION][C] McArdle's syndrome (myophosphorylase deficiency): a study of a family
RH Salter, DG Adamson… - QJM: An International …, 1967 - academic.oup.com
THE energy for muscle contraction is generally considered to be mediated via adenosine
triphosphate (ATP). This compound is formed and is utilized both during the anaerobic …
triphosphate (ATP). This compound is formed and is utilized both during the anaerobic …
McArdle's syndrome. Fine structural changes in muscle
A Korenyi-Both, BH Smith, JK Baruah - Acta Neuropathologica, 1977 - Springer
Two cases of McArdle's syndrome are reported. One is a “classical” exaple; the other is
unusual because of the in vitro presence of muscle phosphorylase activity. In the latter case …
unusual because of the in vitro presence of muscle phosphorylase activity. In the latter case …
McArdle's disease: lack of muscle phosphorylase
DM DAWSON, FL SPONG… - Annals of Internal …, 1968 - acpjournals.org
In a family with McArdle's syndrome, four siblings all had frequent muscle cramps caused by
exercise and had episodes of myoglobinuria. The absence of phosphorylase activity was …
exercise and had episodes of myoglobinuria. The absence of phosphorylase activity was …
Dominant inheritance of McArdle syndrome
LA Chui, TL Munsat - Archives of Neurology, 1976 - jamanetwork.com
• Myophosphorylase deficiency (McArdle syndrome) is an uncommon condition
characterized by exercise intolerance, muscle cramping, and myoglobinuria. Although the …
characterized by exercise intolerance, muscle cramping, and myoglobinuria. Although the …
Acute renal failure in McArdle's disease: Report of two cases
JP Grünfeld, D Ganeval, J Chanard… - … England Journal of …, 1972 - Mass Medical Soc
Two patients with McArdle's disease had acute renal failure associated with acute
rhabdomyolysis. Both patients had only mild muscular symptoms before the onset of acute …
rhabdomyolysis. Both patients had only mild muscular symptoms before the onset of acute …
McArdle's disease: a review
MM Lubran - Annals of Clinical & Laboratory Science, 1975 - Assoc Clin Scientists
The clinical features of McArdle's disease (inherited deficiency of skeletal muscle
phosphorylase) and the histological and biochemical changes are described. Their possible …
phosphorylase) and the histological and biochemical changes are described. Their possible …
McArdle's disease: Metabolic studies in a patient and review of the syndrome
SM Fattah, A Rubulis, WW Faloon - The American Journal of Medicine, 1970 - Elsevier
A twenty-two year old man with recurrent stiffness following exercise was found to have
chemical and histologic changes consistent with partial deficiency of myopnosphorylase …
chemical and histologic changes consistent with partial deficiency of myopnosphorylase …