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23. [Familial ataxia with peroneal muscular atrophy and optic atrophy]. Bernabo' Brea G; Rathschüler R; Rasore-Quartino A Riv Otoneurooftalmol; 1966; 41(4):273-90. PubMed ID: 5991731 [No Abstract] [Full Text] [Related]
24. Lower limb muscle atrophy on MRI as a guide in the diagnosis of muscle diseases. Renard D; Thouvenot E Acta Neurol Belg; 2017 Sep; 117(3):635-636. PubMed ID: 28602008 [No Abstract] [Full Text] [Related]
25. [Histological and histochemical diagnosis of muscular diseases in childhood]. Minetti C Minerva Pediatr; 1982 Nov; 34(22):969-76. PubMed ID: 6759914 [No Abstract] [Full Text] [Related]
26. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy. Frajman M; Brilla E; Gutiérrez A; Hun L Rev Invest Clin; 1983; 35(4):305-8. PubMed ID: 6672928 [No Abstract] [Full Text] [Related]
27. Werdnig-Hoffman's disease in four members of a family. Paul FM; Chao Tzee Cheng J Singapore Paediatr Soc; 1966 Oct; 8(2):80-5. PubMed ID: 5954388 [No Abstract] [Full Text] [Related]
28. [Clinicoelectroneuromyographic characteristics of neuralgic amyotrophy]. Viatkina SIa; Novikova NP Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(11):1650-5. PubMed ID: 6275642 [TBL] [Abstract][Full Text] [Related]
29. [Morphometric quantification of spinal and cranial nerve roots in amyotrophic lateral sclerosis and adult onset X-linked recessive bulbo-spinal muscular atrophy (author's transl)]. Sobue G; Matsuoka Y; Mukai E; Takayanagi T; Sobue I Rinsho Shinkeigaku; 1981 Jun; 21(6):506-16. PubMed ID: 7296981 [No Abstract] [Full Text] [Related]
33. Vitamin E deficiency in Werdnig-Hoffmann disease. Shapira Y; Amit R; Rachmilewitz E Ann Neurol; 1981 Sep; 10(3):266-8. PubMed ID: 7294734 [TBL] [Abstract][Full Text] [Related]
34. [Classic neurogenic (Werdnig-Hoffman) and infantile pseudo-myopathic amyotrophy in siblings. (Discussion of the validity of the different forms of neurogenic amyotrophy)]. Martin-Sneessens L; Radermecker J J Genet Hum; 1965 Dec; 14(4):341-50. PubMed ID: 5862080 [No Abstract] [Full Text] [Related]
35. [A case of Parsonage-Turner syndrome in a child]. Frăţilă A; Suţu A; Părîu T Pediatria (Bucur); 1966; 15(1):73-7. PubMed ID: 5949753 [No Abstract] [Full Text] [Related]