135 related articles for article (PubMed ID: 1066528)
1. 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]
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. Absence of biochemical heterogeneity in McArdle's disease. A high resolution SDS-polyacrylamide gel electrophoresis study.
Mantle D; Lauffart B; Atack J; Lane RJ
J Neurol Sci; 1987 Mar; 78(1):63-70. PubMed ID: 3471865
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. [McArdle's disease (muscular phosphorylase deficiency)].
Schollmeyer P; Nolte J; Meisel D; Dichgans J; Jerusalem F
Verh Dtsch Ges Inn Med; 1977 Apr 17-21; 83():1277-80. PubMed ID: 274025
[No Abstract] [Full Text] [Related]
8. Low muscle levels of pyridoxine in McArdle's syndrome.
Haller RG; Dempsey WB; Feit H; Cook JD; Knochel JP
Am J Med; 1983 Feb; 74(2):217-20. PubMed ID: 6572033
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Angina in McArdle's disease.
Nicholls DP; Campbell NP; Stevenson HP; Patterson VH
Heart; 1996 Oct; 76(4):372-3. PubMed ID: 8983689
[TBL] [Abstract][Full Text] [Related]
11. Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.
Martinuzzi A; Vergani L; Carrozzo R; Fanin M; Bartoloni L; Angelini C; Askanas V; Engel WK
J Clin Invest; 1993 Oct; 92(4):1774-80. PubMed ID: 8408630
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. McArdle's syndrome. Fine structural changes in muscle.
Korényi-Both A; Smith BH; Baruah JK
Acta Neuropathol; 1977 Sep; 40(1):11-9. PubMed ID: 269622
[TBL] [Abstract][Full Text] [Related]
15. McArdle's disease presenting as treatment resistant polymyositis.
Higgs JB; Blaivas M; Albers JW
J Rheumatol; 1989 Dec; 16(12):1588-91. PubMed ID: 2625691
[TBL] [Abstract][Full Text] [Related]
16. Absence of functional messenger RNA for glycogen phosphorylase in the muscle of two patients with McArdle's disease.
Daegelen D; Munnich A; Levin MJ; Girault A; Goasguen J; Kahn A; Dreyfus JC
Ann Hum Genet; 1983 May; 47(2):107-15. PubMed ID: 6576726
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis.
Gautron S; Daegelen D; Mennecier F; Dubocq D; Kahn A; Dreyfus JC
J Clin Invest; 1987 Jan; 79(1):275-81. PubMed ID: 3466902
[TBL] [Abstract][Full Text] [Related]
20. A female case of glycogen storage myopathy due to phosphorylase kinase deficiency.
Ohtani Y; Matsuda I; Iwamasa T
J Inherit Metab Dis; 1982; 5(2):71-2. PubMed ID: 6820425
[No Abstract] [Full Text] [Related]
[Next] [New Search]