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5. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy]. Guízar Vázquez J; Navarrete Cadena C; Rico R; Mora G; Zavala C Bol Med Hosp Infant Mex; 1981; 38(1):23-33. PubMed ID: 7284070 [TBL] [Abstract][Full Text] [Related]
6. [Cardiocirculatory findings in the progressive muscular dystrophy of Duchenne du Boulogne]. Castellani A; Ippoliti B; Tezzele A Folia Cardiol; 1969; 28():11-33. PubMed ID: 5409240 [No Abstract] [Full Text] [Related]
7. [Study of urinary creatinine and creatine in progressive muscular dystrophy]. Sato N; Kanno M; Annaka S Iryo; 1968 Dec; 22(12):1372-8. PubMed ID: 5717703 [No Abstract] [Full Text] [Related]
8. Catecholamines and indoleamines in patients with Duchenne muscular dystrophy. Mendell JR; Murphy DL; Engel WK; Chase TN; Gordon E Arch Neurol; 1972 Dec; 27(6):518-20. PubMed ID: 5083869 [No Abstract] [Full Text] [Related]
10. [Significance of electro-vectorcardiographic changes in patients and carriers of Duchenne muscular dystrophy]. Wu SC; Secchi MB; Obbiassi M; Mancarella S; Vitolo E; Folli G Boll Soc Ital Cardiol; 1981; 26(1):29-39. PubMed ID: 7340857 [No Abstract] [Full Text] [Related]
11. Clinical studies in progressive muscular dystrophy. Prot J Pol Med J; 1972; 11(4):1004-12. PubMed ID: 5078704 [No Abstract] [Full Text] [Related]
12. Biochemical studies on muscular dystrophy. Serum and urine creatine, creatinine and aminoacids. el-Nabawy M; Sakr R; el-Hawary MF J Egypt Med Assoc; 1968; 51(11):949-63. PubMed ID: 5714513 [No Abstract] [Full Text] [Related]
13. [Nursing process/nursing of patients with muscular dystrophy. A case study and nursing of a patient with Duchenne type muscular dystrophy]. Watanabe Y; Higashiyama K; Fukuda S Kurinikaru Sutadi; 1981 Sep; 2(9):1050-68. PubMed ID: 6915321 [No Abstract] [Full Text] [Related]
14. Increased rates of myofibrillar protein breakdown in muscle-wasting diseases. Warnes DM; Tomas FM; Ballard FJ Muscle Nerve; 1981; 4(1):62-6. PubMed ID: 7231447 [TBL] [Abstract][Full Text] [Related]
15. Clinical symptoms in a female carrier of Duchenne muscular dystrophy. Zatz M; Levisky RB; Levy JA; Valente BO; Gianotti M; Frota-Pessoa O J Genet Hum; 1973 Dec; 21(4):297-305. PubMed ID: 4792239 [No Abstract] [Full Text] [Related]
16. 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]
17. Two families with late onset pseudohypertrophic muscular dystrophy (Becker type). Lee WL; Wong HB J Singapore Paediatr Soc; 1981; 23(3-4):159-63. PubMed ID: 7052857 [No Abstract] [Full Text] [Related]
18. [Electrocardiographic findings in the Duchenne-type of progressive muscular dystrophy]. Nakagawa K; Okamoto S; Goto H; Kato T; Yamamoto K Iryo; 1968 Dec; 22(12):1425-38. PubMed ID: 5717711 [No Abstract] [Full Text] [Related]
19. Genotype and electroretinal heterogeneity in Duchenne muscular dystrophy. Ino-ue M; Honda S; Nishio H; Matsuo M; Nakamura H; Yamamoto M Exp Eye Res; 1997 Dec; 65(6):861-4. PubMed ID: 9441711 [No Abstract] [Full Text] [Related]
20. Motor nerve conduction in Duchenne type of muscular dystrophy. Jayam AV; Raju TN; Pandya SS; Desai AD Neurol India; 1970 Mar; 18(1):8-12. PubMed ID: 5439386 [No Abstract] [Full Text] [Related] [Next] [New Search]