121 related articles for article (PubMed ID: 6577313)
1. Congenital myopathy due to phosphorylase deficiency.
Cornelio F; Bresolin N; DiMauro S; Mora M; Balestrini MR
Neurology; 1983 Oct; 33(10):1383-5. PubMed ID: 6577313
[TBL] [Abstract][Full Text] [Related]
2. McArdle's disease: a study on the molecular basis of two different etiologies of myophosphorylase deficiency.
Koster JF; Slee RG; Jennekens FG; Wintzen AR; van Berkel TJ
Clin Chim Acta; 1979 Jun; 94(3):229-35. PubMed ID: 111879
[TBL] [Abstract][Full Text] [Related]
3. A new variant of late-onset myophosphorylase deficiency.
Kost GJ; Verity MA
Muscle Nerve; 1980; 3(3):195-201. PubMed ID: 6929403
[TBL] [Abstract][Full Text] [Related]
4. Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heart.
Miranda AF; Nette EG; Hartlage PL; DiMauro S
Neurology; 1979 Nov; 29(11):1538-41. PubMed ID: 291791
[TBL] [Abstract][Full Text] [Related]
5. [Glycogenosis type V of adults: muscle phosphorylase deficiency].
Coll Cantí J; Illa I; Beleta J; Anglada A; Pradas J; González Sastre F; Grau Veciana JM; Gella FJ
Med Clin (Barc); 1986 Mar; 86(8):335-8. PubMed ID: 3458989
[No Abstract] [Full Text] [Related]
6. Myophosphorylase deficiency: the course of an unusual congenital myopathy.
Abarbanel JM; Potashnik R; Frisher S; Moses SW; Osimani A; Herishanu Y
Neurology; 1987 Feb; 37(2):316-8. PubMed ID: 3808314
[TBL] [Abstract][Full Text] [Related]
7. Phosphorylation of McArdle phosphorylase induces activity.
Cerri CG; Willner JH
Proc Natl Acad Sci U S A; 1981 May; 78(5):2688-92. PubMed ID: 6265901
[TBL] [Abstract][Full Text] [Related]
8. McArdle's disease--what limit to the age of onset?
Hewlett RH; Gardner-Thorpe C
S Afr Med J; 1978 Jan; 53(2):60-3. PubMed ID: 273990
[TBL] [Abstract][Full Text] [Related]
9. Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease?
Preisler N; Orngreen MC; Echaniz-Laguna A; Laforet P; Lonsdorfer-Wolf E; Doutreleau S; Geny B; Akman HO; Dimauro S; Vissing J
Neurology; 2012 Jan; 78(4):265-8. PubMed ID: 22238410
[TBL] [Abstract][Full Text] [Related]
10. Peripheral nerve and vasculature involvement in myophosphorylase deficiency (McArdle's disease).
Byard RW; Lach B; Preston DN
Pathology; 1991 Jan; 23(1):62-5. PubMed ID: 2062570
[TBL] [Abstract][Full Text] [Related]
11. In McArdle disease, phosphorylase deficiency is the tip of an iceberg.
Willner JH; Cerri CG; Wood DS; Ponzetto-Zimmerman C; Reydel PM
Trans Am Neurol Assoc; 1981; 106():208-9. PubMed ID: 6294950
[No Abstract] [Full Text] [Related]
12. Research on molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). Use of new protein mapping and immunological techniques.
Daegelen-Proux D; Kahn A; Marie J; Dreyfus JC
Ann Hum Genet; 1981 May; 45(2):113-20. PubMed ID: 6797345
[TBL] [Abstract][Full Text] [Related]
13. McArdle disease: phosphorylase activity in regenerating muscle fibers.
Mitsumoto H
Neurology; 1979 Feb; 29(2):258-62. PubMed ID: 285339
[TBL] [Abstract][Full Text] [Related]
14. Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease.
Sato K; Imai F; Hatayama I; Roelofs RI
Biochem Biophys Res Commun; 1977 Sep; 78(2):663-8. PubMed ID: 269730
[No Abstract] [Full Text] [Related]
15. Myophosphorylase deficiency: two different molecular etiologies.
Feit H; Brooke MH
Neurology; 1976 Oct; 26(10):963-7. PubMed ID: 1066528
[TBL] [Abstract][Full Text] [Related]
16. Fatal infantile form of muscle phosphorylase deficiency.
DiMauro S; Hartlage PL
Neurology; 1978 Nov; 28(11):1124-9. PubMed ID: 101896
[TBL] [Abstract][Full Text] [Related]
17. [McArdle disease: report of four brothers with myophosphorylase deficiency].
López Martín A; Baños Madrid RI; García-Estañ Candela J; García Pérez B; Pérez Bautista FJ; Salmerón P
An Med Interna; 2001 Mar; 18(3):136-8. PubMed ID: 11594178
[TBL] [Abstract][Full Text] [Related]
18. McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
DiMauro S; Arnold S; Miranda A; Rowland LP
Trans Am Neurol Assoc; 1977; 102():112-5. PubMed ID: 278321
[No Abstract] [Full Text] [Related]
19. Histochemical and biochemical studies in a patient with myophosphorylase deficiency.
Tachi N; Sasaki K; Tachi M; Sugie H
Eur Neurol; 1990; 30(1):52-5. PubMed ID: 2298228
[TBL] [Abstract][Full Text] [Related]
20. Muscle accumulation of Tc-99m diphosphonate in myophosphorylase deficiency and other disorders of muscle glycogenolysis/glycolysis.
Brumback RA
Clin Nucl Med; 1983 Apr; 8(4):165-6. PubMed ID: 6573990
[No Abstract] [Full Text] [Related]
[Next] [New Search]
