. 1971;2(4):203-9.

Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease)

K Fried et al. Clin Genet. 1971.

. 1971;2(4):203-9.

No abstract available

Cited by

Spinal muscular atrophy associated with HLA-B7.
Upstill-Goddard G, Gardner-Medwin D, Roberts DF, Wentzel J. Upstill-Goddard G, et al. Br Med J. 1979 Mar 17;1(6165):720-1. doi: 10.1136/bmj.1.6165.721. Br Med J. 1979. PMID: 435751 Free PMC article. No abstract available.
Motor nerve conduction velocity in spinal muscular atrophy of childhood.
Moosa A, Dubowitz V. Moosa A, et al. Arch Dis Child. 1976 Dec;51(12):974-7. doi: 10.1136/adc.51.12.974. Arch Dis Child. 1976. PMID: 1015851 Free PMC article.
Chronic proximal spinal muscular atrophy of childhood and adolescence: problems of classification and genetic counselling.
Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J. Hausmanowa-Petrusewicz I, et al. J Med Genet. 1985 Oct;22(5):350-3. doi: 10.1136/jmg.22.5.350. J Med Genet. 1985. PMID: 4078864 Free PMC article.
Expectations of the adolescent labelled as "muscular dystrophy".
Williams E, Nichols PJ. Williams E, et al. Proc R Soc Med. 1975 May;68(5):319-20. doi: 10.1177/003591577506800529. Proc R Soc Med. 1975. PMID: 129784 Free PMC article. No abstract available.
The nosology of the spinal muscular atrophies.
Emery AE. Emery AE. J Med Genet. 1971 Dec;8(4):481-95. doi: 10.1136/jmg.8.4.481. J Med Genet. 1971. PMID: 4948374 Free PMC article. Review. No abstract available.