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10. Duchenne muscular dystrophy and idiopathic hyperCKemia in a family causing confusion in genetic counselling. Bushby K; Goodship J; Haggerty D; Heald A; Walls T Am J Med Genet; 1996 Dec; 66(2):237-8. PubMed ID: 8958338 [No Abstract] [Full Text] [Related]
11. Change of serum creatine phosphokinase activity after exercise in Duchenne type of progressive muscular dystrophy. Nakane K Nagoya Med J; 1972 Feb; 17(3):203-16. PubMed ID: 5050757 [No Abstract] [Full Text] [Related]
12. Tabulation of findings in the muscular dystrophies and in myotonia dystrophica. Danowski TS; Wissinger HA; Hohmann TC; Gerneth JA; Folkers K; Vester JW; Fisher ER Arch Phys Med Rehabil; 1971 May; 52(5):193-200. PubMed ID: 4931852 [No Abstract] [Full Text] [Related]
13. Genetic counseling in Becker type X-linked muscular dystrophy. II: Practical considerations. Grimm T Am J Med Genet; 1984 Aug; 18(4):719-23. PubMed ID: 6486170 [TBL] [Abstract][Full Text] [Related]
14. Carrier detection and genetic counselling in Duchenne dystrophy. Dubowitz V Dev Med Child Neurol; 1975 Jun; 17(3):352-6. PubMed ID: 1107098 [No Abstract] [Full Text] [Related]
15. Genetic counselling in neuromuscular diseases in Western Australia. Hurse PV; Kakulas BA Proc Aust Assoc Neurol; 1974; 11():145-53. PubMed ID: 4469625 [No Abstract] [Full Text] [Related]
16. [Renewed interest in muscular dystrophy]. Eymard B Rev Prat; 2001 Feb; 51(3):262-9. PubMed ID: 11265422 [TBL] [Abstract][Full Text] [Related]