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.
9. Juvenile spinal muscular atrophy--a new hexosaminidase deficiency phenotype. Johnson WG; Wigger HJ; Karp HR; Glaubiger LM; Rowland LP Trans Am Neurol Assoc; 1981; 106():215-8. PubMed ID: 7348998 [No Abstract] [Full Text] [Related]
10. [Multiple symmetrical and multistructural arthropathies in a patient with syringomyelia]. Markiewicz M; Kawiak W; Warpechowska M; Hasiec T Wiad Lek; 1984 Mar; 37(6):466-9. PubMed ID: 6485330 [No Abstract] [Full Text] [Related]
11. [HLA system in spinal injury patients with neurogenic para-osteo-arthropathies]. Minaire P; Betuel H; Pilonchery G Nouv Presse Med; 1978 Oct; 7(34):3044. PubMed ID: 364410 [No Abstract] [Full Text] [Related]
13. [Chronic spinal muscular atrophy with predominant affection of distal muscles and muscular hypertrophy (author's transl)]. Fujimori N; Hanyu N; Oguchi K; Yanagisawa N; Tsukagoshi H Rinsho Shinkeigaku; 1980 Jun; 20(6):423-9. PubMed ID: 7408341 [No Abstract] [Full Text] [Related]
14. [Familial male hypogonadism in spinal and bulbar muscular atrophy of late onset (Kennedy's disease). A new cause of hypogonadism]. Gómez JM; Arbizu T; Santamaría J; Quilez A; Soler J; Peres J Arch Esp Urol; 1984; 37(1):49-55. PubMed ID: 6721595 [No Abstract] [Full Text] [Related]
16. [A sporadic case of the pareto-amyotrophic form of ulcero-mutilating acropathy]. Pragier G; Galmiche P Rev Rhum Mal Osteoartic; 1966; 33(7):440-4. PubMed ID: 5957358 [No Abstract] [Full Text] [Related]
17. [Chronic progressive external ophthalmoplegia, deafness, neurogenic muscular atrophy and hypergonadotropic hypogonadism (author's transl)]. Hazama R; Tsujihata M; Mori M; Takamori M; Egami T Rinsho Shinkeigaku; 1981 Apr; 21(4):304-10. PubMed ID: 7273535 [No Abstract] [Full Text] [Related]
18. [Swallowing disturbances in Werdning-Hoffman disease]. Nutman J; Nitzan M; Grünebaum M Harefuah; 1981 Dec; 101(11):301-3. PubMed ID: 7341358 [No Abstract] [Full Text] [Related]
19. [Severe oligophrenia with amyotrophia in two brothers one of whom presents poikilodermatomyositis with corneal changes (its place among the neuro-cutaneous dystrophies)]. Martin L; Hariga J J Genet Hum; 1968 Jan; 16(3):71-82. PubMed ID: 5710714 [No Abstract] [Full Text] [Related]