166 related articles for article (PubMed ID: 6988001)
1. Inherited muscle disease.
Ellis FR
Br J Anaesth; 1980 Feb; 52(2):153-64. PubMed ID: 6988001
[No Abstract] [Full Text] [Related]
2. [Hreditary myopathies].
Kuhn E
Ergeb Inn Med Kinderheilkd; 1969; 28():188-290. PubMed ID: 4897097
[No Abstract] [Full Text] [Related]
3. Genetic approaches to the nosology of muscular disease: myotonias and similar diseases.
Becker PE
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):52-62. PubMed ID: 5293617
[TBL] [Abstract][Full Text] [Related]
4. Pathology of muscle.
Buxton PH
Br J Anaesth; 1980 Feb; 52(2):139-51. PubMed ID: 6988000
[No Abstract] [Full Text] [Related]
5. The myotonias: their diagnosis and treatment.
Moxley RT
Compr Ther; 1996 Jan; 22(1):8-21. PubMed ID: 8654027
[No Abstract] [Full Text] [Related]
6. 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]
7. Channelopathies: the nondystrophic myotonias and periodic paralyses.
Lehmann-Horn F; Rüdel R
Semin Pediatr Neurol; 1996 Jun; 3(2):122-39. PubMed ID: 8795846
[TBL] [Abstract][Full Text] [Related]
8. Anesthesia and neuromuscular diseases.
Mehta MP; Gergis SD; Sokoll MD
Middle East J Anaesthesiol; 1985 Feb; 8(1):49-63. PubMed ID: 3892237
[TBL] [Abstract][Full Text] [Related]
9. [Myopathy--with reference to hereditary myopathy].
Araki S
Saishin Igaku; 1966 Apr; 21(4):732-45. PubMed ID: 5340851
[No Abstract] [Full Text] [Related]
10. Duchenne-Becker muscular dystrophy and the nondystrophic myotonias. Paradigms for loss of function and change of function of gene products.
Hoffman EP; Wang J
Arch Neurol; 1993 Nov; 50(11):1227-37. PubMed ID: 8215981
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Hereditary myopathies.
Emery AE
Clin Orthop Relat Res; 1964; 33():164-73. PubMed ID: 5889019
[No Abstract] [Full Text] [Related]
13. The diagnosis and orthopaedic treatment of inherited muscular diseases of childhood.
Shapiro F; Specht L
J Bone Joint Surg Am; 1993 Mar; 75(3):439-54. PubMed ID: 8444925
[No Abstract] [Full Text] [Related]
14. Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations.
Plassart E; Reboul J; Rime CS; Recan D; Millasseau P; Eymard B; Pelletier J; Thomas C; Chapon F; Desnuelle C
Eur J Hum Genet; 1994; 2(2):110-24. PubMed ID: 8044656
[TBL] [Abstract][Full Text] [Related]
15. [VALUE OF MUSCLE BIOPSY IN MUSCULAR AND NERVOUS SYSTEM DISEASES].
CHRISTENSEN E
Nord Med; 1965 Apr; 73():340-2. PubMed ID: 14265343
[No Abstract] [Full Text] [Related]
16. Ion channel mutations in periodic paralysis and related myotonic diseases.
Brown RH
Ann N Y Acad Sci; 1993 Dec; 707():305-16. PubMed ID: 9137561
[No Abstract] [Full Text] [Related]
17. Paramyotonia congenita (von Eulenburg) in Denmark.
Johnsen T; Friis ML
Acta Neurol Scand; 1980 Feb; 61(2):78-87. PubMed ID: 7395457
[TBL] [Abstract][Full Text] [Related]
18. Genetic counselling.
Bundey S
Br J Hosp Med; 1977 Apr; 17(4):342, 345-9. PubMed ID: 851686
[No Abstract] [Full Text] [Related]
19. Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis.
Ptáĉek LJ; Tawil R; Griggs RC; Meola G; McManis P; Barohn RJ; Mendell JR; Harris C; Spitzer R; Santiago F
Neurology; 1994 Aug; 44(8):1500-3. PubMed ID: 8058156
[TBL] [Abstract][Full Text] [Related]
20. [Anesthesia in hereditary peripheral muscular disease].
Islander G; Jungner M
Lakartidningen; 2005 Feb 21-27; 102(8):566-71. PubMed ID: 15786909
[No Abstract] [Full Text] [Related]
[Next] [New Search]
