166 related articles for article (PubMed ID: 5815127)
1. 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]
2. 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]
3. [On Becker's benign muscular dystrophy: study of a family with 10 affected members in 6 generations].
Caruso G; Campanella G
Acta Neurol (Napoli); 1968; 23(4):709-31. PubMed ID: 5747395
[No Abstract] [Full Text] [Related]
4. 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]
5. 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]
6. [Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy].
Radu H; Stenzel K
Dtsch Z Nervenheilkd; 1969; 196(2):92-115. PubMed ID: 5800957
[No Abstract] [Full Text] [Related]
7. [Enzymatic activity of the serum in the family of a progressive muscular dystrophy patient].
Esaki K; Tokoro T; Yamamoto K; Kato T; Asano B
Iryo; 1969 Oct; 23(10):1306-11. PubMed ID: 5364982
[No Abstract] [Full Text] [Related]
8. 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]
9. [Contribution on the study of pseudohypertrophic muscular dystrophies. II. Pseudohypertrophic muscular dystrophies in females].
Radu H; Stenzel K
Dtsch Z Nervenheilkd; 1969; 196(2):116-35. PubMed ID: 5800953
[No Abstract] [Full Text] [Related]
10. The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy.
Thomson WH
Clin Chim Acta; 1969 Nov; 26(2):207-21. PubMed ID: 5352692
[No Abstract] [Full Text] [Related]
11. The diagnostic significance of serum enzymes and electrocardiogram in various muscular dystrophies.
Zellweger H; Durnin R; Simpson J
Acta Neurol Scand; 1972; 48(1):87-101. PubMed ID: 5019834
[No Abstract] [Full Text] [Related]
12. 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]
13. Serum enzyme studies in inherited disease of skeletal muscle.
Thomson WH
Clin Chim Acta; 1971 Nov; 35(1):183-91. PubMed ID: 5126991
[No Abstract] [Full Text] [Related]
14. Serum enzyme alterations in neuromuscular disorders.
Munsat TL; Baloh R; Pearson CM; Fowler W
JAMA; 1973 Dec; 226(13):1536-43. PubMed ID: 4800933
[No Abstract] [Full Text] [Related]
15. Serum enzymes in sex-linked (Duchenne) muscular dystrophy.
Shaw RF; Pearson CM; Chowdhury SR; Dreifuss FE
Arch Neurol; 1967 Feb; 16(2):115-22. PubMed ID: 6018043
[No Abstract] [Full Text] [Related]
16. Evidence against the existence of a subclinical form of X-linked Duchenne muscular dystrophy.
Emery AE; Spikesman A
J Neurol Sci; 1970 Jun; 10(6):523-33. PubMed ID: 5422556
[No Abstract] [Full Text] [Related]
17. A serum isozyme study in muscular dystrophy. Particular reference to creatine kinase, aspartate aminotransferase, and lactic acid dehydrogenase isozymes.
Somer H; Donner M; Murros J; Konttinen A
Arch Neurol; 1973 Nov; 29(5):343-5. PubMed ID: 4743886
[No Abstract] [Full Text] [Related]
18. [X-linked myotubular myopathy].
Il'ina NA; Aver'ianov IuN; Potomskaia LZ; Ivanchenko OV; Biriukov VB
Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(10):1334-8. PubMed ID: 573945
[No Abstract] [Full Text] [Related]
19. [Progressive muscular dystrophy: CPK, LDH, ALD (aldolase)--EMG, ECG in patients and their families].
Diotallevi P; Bargilli E; Danni M; Dellantonio R; Tocchini M; Milani-Comparetti M
Boll Soc Ital Biol Sper; 1988 Jun; 64(6):523-30. PubMed ID: 3190905
[No Abstract] [Full Text] [Related]
20. [Changes in the activity of blood serum enzymes in relatives of children with myopathy].
Grinio LP
Vopr Med Khim; 1966; 12(6):600-3. PubMed ID: 6000902
[No Abstract] [Full Text] [Related]
[Next] [New Search]
