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Journal Abstract Search
159 related items for PubMed ID: 3791775
1. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness]. Murakami K, Sobue G, Takahashi A, Mitsuma T. Rinsho Shinkeigaku; 1986 Sep; 26(9):952-9. PubMed ID: 3791775 [No Abstract] [Full Text] [Related]
10. [A case of hereditary motor and sensory neuropathy with vocal cords palsy and diaphragmatic weakness]. Fukuda H, Kitani M, Imaoka K. Rinsho Shinkeigaku; 1993 Feb; 33(2):175-81. PubMed ID: 8319389 [Abstract] [Full Text] [Related]
11. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers. Billinghurst JR. Afr J Med Med Sci; 1976 Dec; 5(4):269-72. PubMed ID: 829740 [Abstract] [Full Text] [Related]
12. Homozygous expression of a dominant gene for Charcot-Marie-Tooth neuropathy. Killian JM, Kloepfer HW. Ann Neurol; 1979 Jun; 5(6):515-22. PubMed ID: 475348 [Abstract] [Full Text] [Related]
15. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy. Frajman M, Brilla E, Gutiérrez A, Hun L. Rev Invest Clin; 1983 Jun; 35(4):305-8. PubMed ID: 6672928 [No Abstract] [Full Text] [Related]
16. [A case of neurogenic scapuloperoneal muscle atrophy with retinitis pigmentosa and neural deafness]. Eguchi K, Yamane K, Shibagaki Y, Hashimoto S, Shibata K. Rinsho Shinkeigaku; 1987 Nov; 27(11):1367-71. PubMed ID: 3447794 [No Abstract] [Full Text] [Related]