These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. [The clinical and genetic studes of muscular dystrophy in six young girls (author's transl)]. Hazama R; Mori K; Shibuya N; Nakazawa Y; Tsujihata M Rinsho Shinkeigaku; 1978 Aug; 18(8):462-9. PubMed ID: 699442 [No Abstract] [Full Text] [Related]
3. [Unusual sibling cases of Fukuyama type congenital muscular dystrophy (author's transl)]. Riku S; Konagaya M; Ibi T; Sobue I Rinsho Shinkeigaku; 1982 Mar; 22(3):216-22. PubMed ID: 7105594 [No Abstract] [Full Text] [Related]
4. [Prevention of duchenne's muscular dystrophy: methodological problems in the detection of carriers (author's transl)]. Scarlato G; Valli G; Meola G Riv Patol Nerv Ment; 1977; 98(3):133-50. PubMed ID: 616016 [TBL] [Abstract][Full Text] [Related]
5. [Particular aspects of cardiomyopathy in Landouzy-Déjérine's progressive muscular dystrophy. Study of a family (author's transl)]. Biancalana D; Simonetti C; Pina DD G Ital Cardiol; 1977; 7(3):240-7. PubMed ID: 870365 [TBL] [Abstract][Full Text] [Related]
6. [Identification of the carrier state in the severe recessive X-linked muscular dystrophy (Duchenne type). I. Assay of activated serum creatine kinase activity in serum (author's transl)]. Rotthauwe HW; Kowalewski S Z Kinderheilkd; 1973 Nov; 115(4):333-42. PubMed ID: 4591596 [No Abstract] [Full Text] [Related]
7. [Peculiar type of congenital muscular dystrophy (Fukuyama type) (author's transl)]. Itagaki Y; Sakamoto Y; Nishitani Y Rinsho Shinkeigaku; 1980 Nov; 20(11):897-903. PubMed ID: 7249470 [No Abstract] [Full Text] [Related]
8. [Myocardial affection in progressive muscular dystrophy. Review of the author's 5 cases]. Iversen VJ Ugeskr Laeger; 1969 Dec; 131(50):2195-200. PubMed ID: 5376321 [No Abstract] [Full Text] [Related]
9. [Cardiomyopathy in Heredofamilial Neuromyopathies (author's transl)]. Sekiguchi M; Numao Y; Hiroe M Kokyu To Junkan; 1975 Mar; 23(3):209-24. PubMed ID: 1093249 [No Abstract] [Full Text] [Related]
10. [Electron microscopic study of the T-system in progressive muscular dystrophy and other neuromuscular diseases (author's transl)]. Oguchi K; Tsukagoshi H Rinsho Shinkeigaku; 1978 May; 18(5):266-72. PubMed ID: 699433 [No Abstract] [Full Text] [Related]
12. A family of progressive muscular dystrophy with mental retardation. Clinical observations. Suga M; Yoshimuta S; Hayashi Y; Sakamoto F Jinrui Idengaku Zasshi; 1966 Mar; 10(4):189-92. PubMed ID: 6008646 [No Abstract] [Full Text] [Related]
13. The inheritance of progressive muscular dystrophy in Japan. Murakami U Jinrui Idengaku Zasshi; 1967 Dec; 12(3):150-69. PubMed ID: 5626875 [No Abstract] [Full Text] [Related]
18. [Erythrocyte membrane protein in Duchenne muscular dystrophy (author's transl)]. Herranz J; Mazo E; Arteaga R; Hermosa V; Zubizarreta A An Esp Pediatr; 1981 Nov; 15(5):433-42. PubMed ID: 7332144 [No Abstract] [Full Text] [Related]
19. [Pulmonary function in progressive muscular dystrophy. Follow-up study for 3 years (author's transl)]. Sato K; Shima K; Ando M; Fukuda Y; Ideta T Nihon Naika Gakkai Zasshi; 1975 May; 64(5):483-90. PubMed ID: 1171927 [No Abstract] [Full Text] [Related]
20. [A new kinship with X-chromosomal benign progressive muscular dystrophy and early contractures (Emery-Dreifuss)]. Cammann R; Vehreschild T; Ernst K Psychiatr Neurol Med Psychol (Leipz); 1974 Jul; 26(7):431-8. PubMed ID: 4449913 [No Abstract] [Full Text] [Related] [Next] [New Search]