133 related articles for article (PubMed ID: 5657039)
1. Phenotypic expression in chickens heterozygous for hereditary muscular dystrophy.
Farrell PM; Tureen LL
Proc Soc Exp Biol Med; 1968 Mar; 127(3):678-82. PubMed ID: 5657039
[No Abstract] [Full Text] [Related]
2. Structural changes in human and chicken muscular dystrophy.
Shafiq SA; Askanas V; Asiedu SA; Milhorat AT
Muscle Biol; 1972; 1():255-72. PubMed ID: 4270069
[No Abstract] [Full Text] [Related]
3. Comparison of plasma creatine phosphokinase changes in nutritional and genetic muscular dystrophy in the chicken.
Farrell PM; Eyerman EL; Tureen LL
Ann N Y Acad Sci; 1966 Sep; 138(1):102-12. PubMed ID: 5230204
[No Abstract] [Full Text] [Related]
4. Delay of hereditary muscular dystrophy of the chicken by oxygen therapy: histology.
Ashmore CR; Somes RG
Proc Soc Exp Biol Med; 1968 May; 128(1):103-7. PubMed ID: 5690464
[No Abstract] [Full Text] [Related]
5. Hereditary muscular dystrophy of the chicken. Quantitative histopathological findings of the Pectoralis at 6 weeks of age.
McMurtry SL; Julian LM; Asmundson VS
Arch Pathol; 1972 Sep; 94(3):217-24. PubMed ID: 4340660
[No Abstract] [Full Text] [Related]
6. Muscular dystrophy. Part II: Serum enzymes in relatives of cases of the Duchenne muscular dystrophy.
Narayanan I; Ramakrishna Rao P; Balakrishnan S; Subrahmanyam K
Indian J Med Res; 1974 Apr; 62(4):605-11. PubMed ID: 4435869
[No Abstract] [Full Text] [Related]
7. Benign sex-linked muscular dystrophy. Clinical and pathological features.
Markand ON; North RR; D'Agostino AN; Daly DD
Neurology; 1969 Jul; 19(7):617-33. PubMed ID: 5815127
[No Abstract] [Full Text] [Related]
8. Poikiloderma atrophicans vasculare associated with muscular dystrophy.
Woolfson H; McQueen A
Arch Dermatol; 1973 Jan; 107(1):115-7. PubMed ID: 4682534
[No Abstract] [Full Text] [Related]
9. Distal muscular dystrophy with autosomal recessive inheritance.
Scoppetta C; Vaccario ML; Casali C; Di Trapani G; Mennuni G
Muscle Nerve; 1984; 7(6):478-81. PubMed ID: 6543900
[TBL] [Abstract][Full Text] [Related]
10. Blood enzymes in Duchene's progressive muscular dystrophy and their correlation with the clinical and histological pictures.
Niebrój-Dobosz I; Jedrzejowska H; Hetnarska L
Acta Med Pol; 1970; 11(4):387-93. PubMed ID: 5493781
[No Abstract] [Full Text] [Related]
11. Plasma creatine phosphokinase activity of chickens with hereditary muscular dystrophy.
Holliday TA; Asmundson VS; Julian LM
Enzymol Biol Clin (Basel); 1965; 5(4):209-16. PubMed ID: 5864513
[No Abstract] [Full Text] [Related]
12. Carrier detection in X-linked Duchenne type muscular dystrophy. A pluridimensional investigation.
Radu H; Migea S; Török Z; Bordeianu L; Radu A
J Neurol Sci; 1968; 6(2):289-300. PubMed ID: 4179111
[No Abstract] [Full Text] [Related]
13. Serum and muscle creatine kinase isoenzymes and serum aspartate aminotransferase isoenzymes in progressive muscular dystrophy.
Cao A; De Virgiliis S; Lippi C; Coppa G
Enzyme; 1971; 12(1):49-62. PubMed ID: 5560399
[No Abstract] [Full Text] [Related]
14. The manifesting carrier in Duchenne muscular dystrophy.
Moser H; Emery AE
Clin Genet; 1974; 5(4):271-84. PubMed ID: 4854942
[No Abstract] [Full Text] [Related]
15. Pseudohypertrophic muscular dystrophy of Cuchenne with manifestations in the heterozygote.
Walker BA
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):108-9. PubMed ID: 5173116
[No Abstract] [Full Text] [Related]
16. Muscular dystrophy in young girls.
Penn AS; Lisak RP; Rowland LP
Neurology; 1970 Feb; 20(2):147-59. PubMed ID: 5460703
[No Abstract] [Full Text] [Related]
17. Inflammatory myopathy with facioscapulohumeral distribution.
Munsat TL; Piper D; Cancilla P; Mednick J
Neurology; 1972 Apr; 22(4):335-47. PubMed ID: 5062826
[No Abstract] [Full Text] [Related]
18. Benign congenital muscular dystrophy: a special form of congenital hypotonia.
Zellweger H; Afifi A; McCormick WF; Mergner W
Clin Pediatr (Phila); 1967 Nov; 6(11):655-63. PubMed ID: 6058423
[No Abstract] [Full Text] [Related]
19. Genetic counselling in X-linked muscular dystrophy.
Emery AE
J Neurol Sci; 1969; 8(3):579-87. PubMed ID: 4185251
[No Abstract] [Full Text] [Related]
20. The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndrome.
Bethlem J; van Wijngaarden GK; de Jong J
J Neurol Sci; 1973 Mar; 18(3):351-8. PubMed ID: 4698315
[No Abstract] [Full Text] [Related]
[Next] [New Search]