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Journal Abstract Search
295 related items for PubMed ID: 615721
1. Chronic spinal muscular atrophy simulating facioscapulohumeral type and limb-girdle type of muscular dystrophy. Report of two cases. Kazakov VM, Kovalenko TM, Skorometz AA, Mikhailov EP. Eur Neurol; 1977; 16(1-6):90-8. PubMed ID: 615721 [Abstract] [Full Text] [Related]
2. Possible neurogenic factor in muscular dystrophy: its similarity to denervation atrophy. Dastur DK, Razzak ZA. J Neurol Neurosurg Psychiatry; 1973 Jun; 36(3):399-410. PubMed ID: 4714102 [Abstract] [Full Text] [Related]
3. Electrophysiological estimation of motor units in limb-girdle muscular dystrophy and chronic spinal muscular atrophy. Panayiotopoulos CP, Scarpalezos S. J Neurol Sci; 1975 Jan; 24(1):95-107. PubMed ID: 1110376 [No Abstract] [Full Text] [Related]
9. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood. Gamstorp I. Birth Defects Orig Artic Ser; 1971 Feb 22; 7(2):72-81. PubMed ID: 5173129 [Abstract] [Full Text] [Related]
10. [Spinal facioscapulo-peroneal (or facioscapulo-crural) muscular atrophy and facioscapulo-peroneal muscular dystrophy]. Kazakov VM, Skoromets AA, Mikhaĭlov EP, Barantsevich ER. Zh Nevropatol Psikhiatr Im S S Korsakova; 1986 Feb 22; 86(5):662-7. PubMed ID: 3739474 [Abstract] [Full Text] [Related]
14. The nosology of the spinal muscular atrophies. Emery AE. J Med Genet; 1971 Dec 22; 8(4):481-95. PubMed ID: 4948374 [No Abstract] [Full Text] [Related]
15. [Hereditary proximal neurogenic muscular atrophy (Wohlfart-Kugelberg-Welander disease). Electromyographic, anatomo-pathologic and clinical study in 3 brothers]. De Freitas MR, Nascimento OJ. Arq Neuropsiquiatr; 1976 Mar 22; 34(1):81-8. PubMed ID: 1259636 [Abstract] [Full Text] [Related]