182 related articles for article (PubMed ID: 13115647)
1. Osseous changes in myopathy.
WALTON JN; WARRICK CK
Br J Radiol; 1954 Jan; 27(313):1-15. PubMed ID: 13115647
[No Abstract] [Full Text] [Related]
2. [Glutamic-oxalacetic transaminase activity in patients with myopathy].
MARANDOLA G
Cervello G Nevrol; 1962 Sep; 38():374-80. PubMed ID: 13932755
[No Abstract] [Full Text] [Related]
3. SOFT TISSUE RADIOGRAPHY OF EXTREMITIES IN NEUROMUSCULAR DISEASE WITH HISTOLOGICAL CORRELATIONS.
DICHIRO G; NELSON KB
Acta Radiol Diagn (Stockh); 1965 Jan; 3():65-88. PubMed ID: 14247270
[No Abstract] [Full Text] [Related]
4. [Muscular dystrophies and myotonias].
Karli P
Duodecim; 1979; 95(21):1412-21. PubMed ID: 575091
[No Abstract] [Full Text] [Related]
5. [ELECTROPHYSIOLOGICAL ASPECTS OF MUSCULAR DISEASES].
FUSTER B
Rev Neuropsiquiatr; 1964 Jun; 27():158-201. PubMed ID: 14320625
[No Abstract] [Full Text] [Related]
6. [BIOCHEMICAL AND PHYSIOCHEMICAL ASPECTS OF MUSCULAR DISEASES].
VAZQUEZDENEGROTTO O; RODRIGUEZ B; BALEA E; DAVILA L; PUPPO A
Rev Neuropsiquiatr; 1964 Jun; 27():105-32. PubMed ID: 14320622
[No Abstract] [Full Text] [Related]
7. [EEG FINDINGS AND TEST RESULTS IN MYOPATHY AND DENERVATION ATROPHY IN CHILDREN].
GAMSTORP I; SMITH M
Nord Med; 1964 Aug; 72():998-1000. PubMed ID: 14172485
[No Abstract] [Full Text] [Related]
8. [Muscular dystrophies].
MONCADA LORENZO E
Rev Clin Esp; 1958 Jan; 68(2):71-9. PubMed ID: 13542921
[No Abstract] [Full Text] [Related]
9. [CLASSIFICATION AND GENETICS OF MYOPATHIES].
LAPLANE D
Rev Prat; 1964 Feb; 14():557-65. PubMed ID: 14142229
[No Abstract] [Full Text] [Related]
10. GENETICS AND DISEASES OF MUSCLE.
BOYER SH; FAINER DC
Am J Med; 1963 Nov; 35():622-31. PubMed ID: 14076016
[No Abstract] [Full Text] [Related]
11. Cytotoxicity of lectins toward skin fibroblasts from patients with Duchenne muscular dystrophy and myotonic dystrophy.
Ohno K; Nakano C; Ishii S; Takeshita K
Jinrui Idengaku Zasshi; 1986 Jun; 31(2):85-91. PubMed ID: 3820771
[No Abstract] [Full Text] [Related]
12. THE SIGNIFICANCE OF LACTATE DEHYDROGENASE ISOZYMES IN ABNORMAL HUMAN SKELETAL MUSCLE.
BRODY IA
Neurology; 1964 Dec; 14():1091-100. PubMed ID: 14239095
[No Abstract] [Full Text] [Related]
13. [Adrenal cortex function in patients with various myopathies].
MARANDOLA G; IANNIRUBERTO A
Rass Int Clin Ter; 1962 Jun; 42():616-20. PubMed ID: 14469538
[No Abstract] [Full Text] [Related]
14. Muscular dystrophies and other genetic myopathies.
Shieh PB
Neurol Clin; 2013 Nov; 31(4):1009-29. PubMed ID: 24176421
[TBL] [Abstract][Full Text] [Related]
15. Muscle wasting in muscular dystrophy: decreased protein synthesis or increased degradation?
Griggs RC; Rennie MJ
Ann Neurol; 1983 Feb; 13(2):125-32. PubMed ID: 6338807
[No Abstract] [Full Text] [Related]
16. MUSCULAR ATROPHIES AND DYSTROPHIES IN MIDDLE LIFE.
AIRD RB
Geriatrics; 1964 Sep; 19():689-700. PubMed ID: 14221889
[No Abstract] [Full Text] [Related]
17. Variants of myotonia atrophica; report of three cases.
NIELSEN JM; MARVIN SL
Bull Los Angel Neuro Soc; 1957 Dec; 22(4):183-7. PubMed ID: 13489411
[No Abstract] [Full Text] [Related]
18. The heart in myotonia atrophica.
RINZLER SH
N Y State J Med; 1949 May; 49(9):1048-50. PubMed ID: 18118041
[No Abstract] [Full Text] [Related]
19. [Myopathies with ocular symptoms].
Neundörfer B
Ber Zusammenkunft Dtsch Ophthalmol Ges; 1980; 78():785-96. PubMed ID: 7039608
[No Abstract] [Full Text] [Related]
20. Qualitative study of aminoaciduria in muscular dystrophy and myotonia dystrophica.
BLAHD WH; BLOOM A; DRELL W
Proc Soc Exp Biol Med; 1955 Dec; 90(3):704-6. PubMed ID: 13289881
[No Abstract] [Full Text] [Related]
[Next] [New Search]