245 related articles for article (PubMed ID: 5790554)
1. [Karyologic studies in muscle diseases].
Badurska B; Prot J
Pol Tyg Lek; 1969 Mar; 24(13):476-8. PubMed ID: 5790554
[No Abstract] [Full Text] [Related]
2. [Genetic counseling in myotonia and muscular dystrophy].
Becker PE
Internist (Berl); 1978 Aug; 19(8):475-81. PubMed ID: 357337
[No Abstract] [Full Text] [Related]
3. [Carbohydrate metabolism disorders in hereditary forms of neuromuscular diseases].
Golubeva VV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(8):1153-9. PubMed ID: 5136819
[No Abstract] [Full Text] [Related]
4. Hereditary myopathies.
Emery AE
Clin Orthop Relat Res; 1964; 33():164-73. PubMed ID: 5889019
[No Abstract] [Full Text] [Related]
5. [Hreditary myopathies].
Kuhn E
Ergeb Inn Med Kinderheilkd; 1969; 28():188-290. PubMed ID: 4897097
[No Abstract] [Full Text] [Related]
6. [Serum aldolase activity in patients with myopathies and in their close reltives].
Dzhuraev A
Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(8):1159-63. PubMed ID: 5136820
[No Abstract] [Full Text] [Related]
7. [Clinical polymorphism of X-linked myopathies].
Grinio LP
Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(3):321-9. PubMed ID: 4466264
[No Abstract] [Full Text] [Related]
8. Disabilities of genetic origin.
Sterling HM
Arch Phys Med Rehabil; 1970 May; 51(5):291-6 passim. PubMed ID: 4246188
[No Abstract] [Full Text] [Related]
9. Chromosome abnormalities in neurological diseases.
Vassilopoulos D
Eur Neurol; 1976; 14(5):328-39. PubMed ID: 181256
[TBL] [Abstract][Full Text] [Related]
10. [Genetics of myopathies].
Becker PE
Verh Dtsch Ges Inn Med; 1965; 71():171-83. PubMed ID: 5877617
[No Abstract] [Full Text] [Related]
11. [Malate dehydrogenase activity in children with myopathy].
Gil'manov VKh
Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):829-31. PubMed ID: 4753593
[No Abstract] [Full Text] [Related]
12. [Various epidemiologic and genetic aspects of the basic neurohereditary diseases].
Skudarnova ZA; Sakharov LN; Makeenkova LI; Torbochkina MD; Filonova AV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):848-53. PubMed ID: 4270984
[No Abstract] [Full Text] [Related]
13. [Genetic problems in neurologic diseases--consulting aspects].
Berg K
Nord Med; 1971 May; 85(21):670-1. PubMed ID: 5581420
[No Abstract] [Full Text] [Related]
14. [Myotonia congenital (Thomsen) and recessive generalized myotonia (Becker)].
Kuhn E
Nervenarzt; 1993 Dec; 64(12):766-9. PubMed ID: 8114977
[TBL] [Abstract][Full Text] [Related]
15. Approach to diagnosis in the child with muscle weakness.
Spiro AJ
Pediatr Ann; 1977 Mar; 6(3):149-61. PubMed ID: 322047
[No Abstract] [Full Text] [Related]
16. [Muscle innervation in Werdnig-Hoffmann spinal amyotrophy and several other atrophies in children].
Olenev SN; Savel'eva-Vasil'eva ; Zav'ialova NS
Zh Nevropatol Psikhiatr Im S S Korsakova; 1972; 72(10):1445-9. PubMed ID: 4660417
[No Abstract] [Full Text] [Related]
17. [Cardiological studies on patients with autosomal dominant and autosomal recessive hereditary myotonia congenital and myotonia dystrophica].
Bodem R; Boikhan MS; Kuhn E
Verh Dtsch Ges Inn Med; 1971; 77():1289-90. PubMed ID: 5156008
[No Abstract] [Full Text] [Related]
18. Electromyographic characteristics of congenital and early onset motor unit diseases.
Fowler WM; Taylor RG; Munsat TL
Arch Phys Med Rehabil; 1971 Aug; 52(8):343-61. PubMed ID: 5284447
[No Abstract] [Full Text] [Related]
19. A study of Duchenne's muscular dystrophy in females. A clinical, biochemical, pathological and chromosomal study of two families.
Reddy MV; Prabhakar V; Sadasivan G; Ebenezer LN
Neurol India; 1968; 16(2):41-5. PubMed ID: 5682570
[No Abstract] [Full Text] [Related]
20. Inherited muscle disease.
Ellis FR
Br J Anaesth; 1980 Feb; 52(2):153-64. PubMed ID: 6988001
[No Abstract] [Full Text] [Related]
[Next] [New Search]