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Journal Abstract Search
148 related items for PubMed ID: 709963
1. [A family with progressive neural muscular atrophy--with special reference to relation with allied diseases (author's transl)]. Hayashi Y, Tomita M, Shimizu K, Takamiya M, Watanabe H. Rinsho Shinkeigaku; 1978 Oct; 18(10):593-600. PubMed ID: 709963 [No Abstract] [Full Text] [Related]
2. [A case of peroneal muscular atrophy with cerebellar ataxia, pyramidal signs and loss of deep sensations]. Shinoda H, Kitaguchi T, Kobayashi T, Goto I, Kuroiwa Y. Rinsho Shinkeigaku; 1987 Mar; 27(3):356-9. PubMed ID: 3608327 [No Abstract] [Full Text] [Related]
3. [Nosology of Von Graefe-Lindenov syndrome. Study of mental disorders in this genetic neurosensory disease]. Nehlil J. Ann Med Psychol (Paris); 1981 Mar; 139(3):352-6. PubMed ID: 7325492 [No Abstract] [Full Text] [Related]
4. [Charcot-Marie-Tooth disease. Report of a family (author's transl)]. Alonso ME, Figueroa HH, Zermeño F, Escobar A, Flores T. Rev Invest Clin; 1981 Mar; 33(3):303-7. PubMed ID: 7330503 [No Abstract] [Full Text] [Related]
5. [Progressive cerebellar ataxia and distal amyotrophy of Charcot-Marie-Tooth type with hyperglutamataemia:two sibling cases]. Tanji H, Takeda A, Tateyama M, Mochizuki H, Itoyama Y. Rinsho Shinkeigaku; 1995 Jul; 35(7):793-7. PubMed ID: 8777805 [Abstract] [Full Text] [Related]
6. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy. McLeod JG, Low PA, Morgan JA. Proc Aust Assoc Neurol; 1975 Jul; 12():23-5. PubMed ID: 1215391 [Abstract] [Full Text] [Related]
7. [Latent hyperbilirubinemias elicited by nicotinic acid test among the family of a case of Gilbert's syndrome with a kind of muscle atrophy which is similar to Charcot-Marie-Tooth disease (author's transl)]. Mizoguchi Y, Okubo A, Imawari M, Itakura H, Miyagawa Y. Nihon Naika Gakkai Zasshi; 1975 Mar 10; 64(3):254-60. PubMed ID: 1171919 [No Abstract] [Full Text] [Related]
8. Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same family. Fernandez PG, Day JH, Simpson NE, Zachariah PK. Can Med Assoc J; 1978 Sep 09; 119(5):455-8. PubMed ID: 688147 [Abstract] [Full Text] [Related]
10. [Peroneal muscular atrophy associated with intellectual impairment and pyramidal signs]. Sobue G, Ibi T, Matsuoka Y, Takahashi A. Rinsho Shinkeigaku; 1985 Jul 09; 25(7):818-25. PubMed ID: 4075646 [No Abstract] [Full Text] [Related]
11. [Marie's ataxia with nuclear external ophthalmoplegia and muscle atrophy of lower extremities--report of an autopsy case and its family (author's transl)]. Kurachi M, Shibata T, Koyama Y, Isaki K, Yamaguchi N. Seishin Shinkeigaku Zasshi; 1977 Jul 09; 79(1):1-25. PubMed ID: 577311 [No Abstract] [Full Text] [Related]
12. Pathogenesis of pes cavus in Charcot-Marie-Tooth disease. Sabir M, Lyttle D. Clin Orthop Relat Res; 1983 May 09; (175):173-8. PubMed ID: 6839584 [Abstract] [Full Text] [Related]
13. Palmoplantar keratoderma and Charcot-Marie-Tooth disease. Rabbiosi G, Borroni G, Pinelli P, Cosi V. Arch Dermatol; 1980 Jul 09; 116(7):789-90. PubMed ID: 6446889 [Abstract] [Full Text] [Related]
14. Leber's optic neuropathy and Charcot-Marie-Tooth disease. Report of a case. McCluskey DJ, O'Connor PS, Sheehy JT. J Clin Neuroophthalmol; 1986 Jun 09; 6(2):76-81. PubMed ID: 2942573 [Abstract] [Full Text] [Related]
17. [Family with hereditary polyneuropthy assoicated with pyramidal signs]. Doi H, Shibasaki H, Goto I, Kuroiwa Y, Ohta M. Rinsho Shinkeigaku; 1976 Sep 16; 16(9):642-8. PubMed ID: 1034548 [No Abstract] [Full Text] [Related]
18. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness]. Murakami K, Sobue G, Takahashi A, Mitsuma T. Rinsho Shinkeigaku; 1986 Sep 16; 26(9):952-9. PubMed ID: 3791775 [No Abstract] [Full Text] [Related]
19. [Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results]. Fardin P, Micaglio GF, Angelini C, Negrin P, Siciliano G. Riv Neurobiol; 1984 Sep 16; 30(2-3):222-8. PubMed ID: 6544478 [No Abstract] [Full Text] [Related]
20. [Familial hypertrophic neuropathies. Conceptual and critical outline. Report of a family with Dyck and Lambert's type IV disease (author's transl)]. Sadaba Garay F, Franco Vicario R, Miguel de la Villa F, Ibarmia Lahuerta J, Bustamante Murga V. Med Clin (Barc); 1980 Oct 10; 75(6):240-6. PubMed ID: 7421358 [Abstract] [Full Text] [Related] Page: [Next] [New Search]