37 related articles for article (PubMed ID: 4227064)
1. A protein anomaly in erythrocyte membranes of patients with Duchenne muscular dystrophy.
Wallach DF; Verma SP; Singer WE
J Exp Med; 1983 Jun; 157(6):2017-28. PubMed ID: 6854213
[TBL] [Abstract][Full Text] [Related]
2. Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.
Moser H
Hum Genet; 1984; 66(1):17-40. PubMed ID: 6365739
[TBL] [Abstract][Full Text] [Related]
3. The distribution of inside-out and right-side-out erythrocyte membrane vesicles in Duchenne progressive muscular dystrophy.
Niebrój-Dobosz I
J Neurol; 1982; 228(3):195-9. PubMed ID: 6186793
[TBL] [Abstract][Full Text] [Related]
4. Osmotic fragility of erythrocytes in myopathies.
Korczyn AD; Nadler E; Falewski de Leon G
J Neurol; 1981; 224(4):253-5. PubMed ID: 6162926
[TBL] [Abstract][Full Text] [Related]
5. Erythrocyte-ghost Ca2+-stimulated Mg2+-dependent adenosine triphosphatase in Duchenne muscular dystrophy.
Dunn MJ; Burghes AH; Dubowitz V
Biochem J; 1982 Mar; 201(3):445-53. PubMed ID: 6124239
[TBL] [Abstract][Full Text] [Related]
6. Protein kinase activity in erythrocyte ghosts of patients with myotonic muscular dystrophy.
Roses AD; Appel SH
Proc Natl Acad Sci U S A; 1973 Jun; 70(6):1855-9. PubMed ID: 4352659
[TBL] [Abstract][Full Text] [Related]
7. Detection of Duchenne muscular dystrophy carriers: quantitative echography and creatine kinasemia.
Schapira G; Laugier P; Rochette J; Berger G; Katz P; Perrin J
Hum Genet; 1987 Jan; 75(1):19-23. PubMed ID: 3542803
[TBL] [Abstract][Full Text] [Related]
8. Increased concentration of spectrin is observed in avian dystrophic muscle.
Repasky EA; Pollina CM; Menold MM; Hudecki MS
Proc Natl Acad Sci U S A; 1986 Feb; 83(3):802-6. PubMed ID: 2935877
[TBL] [Abstract][Full Text] [Related]
9. Activity of creatine kinase isoenzyme MB in serum and red cell acetylcholinesterase variants in patients with Duchenne muscular dystrophy.
Goedde HW; Benkmann HG; Das PK; Agarwal DP
Klin Wochenschr; 1977 Mar; 55(5):215-7. PubMed ID: 846181
[TBL] [Abstract][Full Text] [Related]
10. Skeletal-muscle sarcolemma from normal and dystrophic mice. Isolation, characterization and lipid composition.
de Kretser TA; Livett BG
Biochem J; 1977 Nov; 168(2):229-37. PubMed ID: 597270
[TBL] [Abstract][Full Text] [Related]
11. The pattern of urinary catecholamines and their metabolites in Duchenne myopathy, in relation to disease evolution.
Dalmaz Y; Peyrin L; Mamelle JC; Tuil D; Gilly R; Cier JF
J Neural Transm; 1979; 46(1):17-34. PubMed ID: 501348
[TBL] [Abstract][Full Text] [Related]
12. Role of intracellular calcium in promoting muscle damage: a strategy for controlling the dystrophic condition.
Duncan CJ
Experientia; 1978 Dec; 34(12):1531-5. PubMed ID: 365566
[TBL] [Abstract][Full Text] [Related]
13. Erythrocyte membrane abnormalities in Duchenne muscular dystrophy monitored by saturation transfer electron paramagnetic resonance spectroscopy.
Wilkerson LS; Perkins RC; Roelofs R; Swift L; Dalton LR; Park JH
Proc Natl Acad Sci U S A; 1978 Feb; 75(2):838-41. PubMed ID: 204936
[TBL] [Abstract][Full Text] [Related]
14. Stoichiometry of sodium and potassium transport in erythrocytes from patients with myotonic muscular dystrophy.
Hull KL; Roses AD
J Physiol; 1976 Jan; 254(1):169-81. PubMed ID: 129563
[TBL] [Abstract][Full Text] [Related]
15. The sodium pump of erythrocytes from patients with Duchenne muscular dystrophy: effect of ouabain on the active sodium flux and on (Na+, K+)ATPase.
Souweine G; Bernard JC; Lasne Y; Lachanat J
J Neurol; 1978 Mar; 217(4):287-94. PubMed ID: 75965
[TBL] [Abstract][Full Text] [Related]
16. Erythrocyte ghost (Na+ + K+) ATPase activity in mice with hereditary muscular dystrophy (strain C57 BL/64J/dy).
Souweine G; Rolland MO; Maire I; Donas MC
J Neurol; 1978 Feb; 217(3):183-9. PubMed ID: 75952
[TBL] [Abstract][Full Text] [Related]
17. Erythrocyte abnormality in human myopathy.
Brown HD; Chattopadhyay SK; Patel AB
Science; 1967 Sep; 157(3796):1577-8. PubMed ID: 4227064
[TBL] [Abstract][Full Text] [Related]
18. Erythrocyte ghosts (Na+ + K+) ATPase activity in Duchenne's dystrophy and myotonia.
Niebrój-Dobosz I
J Neurol; 1976 Nov; 214(1):61-9. PubMed ID: 62828
[TBL] [Abstract][Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]