Glycogenosis type II: The infantile- and late-onset acid maltase deficiency observed in one family
- 1 August 1978
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 87 (3) , 451-453
- https://doi.org/10.1016/0009-8981(78)90191-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Residual acid maltase activity in late‐onset acid maltase deficiencyNeurology, 1977
- Physico-chemical and immunological properties of acid α-glucosidase from various human tissues in relation to glycogenosis type II (pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Acid maltase deficiency in non-identical adult twinsZeitschrift für Neurologie, 1976
- The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- The spectrum and diagnosis of acid maltase deficiencyNeurology, 1973
- The Use of Leucocytes as an Aid in the Diagnosis of a Variant of Glycogen Storage Disease Type II (Pompe's Disease)European Journal of Clinical Investigation, 1972
- Comparative Study of Acid Maltase DeficiencyArchives of Neurology, 1972
- Choice of leucocyte preparation in the diagnosis of glycogen storage disease type II (pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1971
- A rapid enzymic method for glycogen estimation in very small tissue samplesClinica Chimica Acta; International Journal of Clinical Chemistry, 1970