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2. [Serum aldolase activity in patients with myopathies and in their close reltives]. Dzhuraev A Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(8):1159-63. PubMed ID: 5136820 [No Abstract] [Full Text] [Related]
3. [Rapidly progressing facio-scapulo-humero-femoro-peroneal muscular dystrophy with sensorineural deafness]. Badalian LO; Temin PA; Mukhin KIu; Nikanorova MIu; Bulaeva NV; Kret LA; Lysov VL Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(9):5-8. PubMed ID: 1664615 [TBL] [Abstract][Full Text] [Related]
6. [Articulation disorder as the initial manifestation of facioscapulohumeral muscular dystrophy in childhood]. Lischka A; Grisold W; Weninger M; Toifl K; Tatzer E Klin Padiatr; 1986; 198(2):119-21. PubMed ID: 3702273 [TBL] [Abstract][Full Text] [Related]
7. The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome. Ricker K; Mertens HG Eur Neurol; 1968; 1(5):275-307. PubMed ID: 5696602 [No Abstract] [Full Text] [Related]
8. [Neurogenic atrophy simulating facio-scapulo humaral dystrophy. On the facio-scapulo-humeral form of spibal atrophy in young adults]. Alberca R; Martínez-Matos JA; Acilona V; Montero C; Miranda-Nieves G Arch Neurobiol (Madr); 1974; 37(1):11-30. PubMed ID: 4838664 [No Abstract] [Full Text] [Related]
9. [Contribution to the pathogenesis of the scapuloperoneal syndrome]. Fotopulos D; Schulz H Psychiatr Neurol Med Psychol (Leipz); 1966 Apr; 18(4):129-36. PubMed ID: 5983161 [No Abstract] [Full Text] [Related]
11. [Case of facio-scapulo-humeral muscular dystrophy with mitochondrial inclusion bodies found in muscle and liver biopsy]. Wakayama Y; Takayanagi T; Mukoyama M; Sobue I Rinsho Shinkeigaku; 1976 Oct; 16(10):706-14. PubMed ID: 188583 [No Abstract] [Full Text] [Related]
12. Clinical variability of facioscapulohumeral muscular dystrophy in Russia. Kazakov VM; Rudenko DI Muscle Nerve Suppl; 1995; 2():S85-95. PubMed ID: 7739632 [TBL] [Abstract][Full Text] [Related]
13. [Distal myopathies: critical study and report on one case (author's transl)]. Serratrice G; Pellissier JF; Pouget J Ann Med Interne (Paris); 1982; 133(3):192-9. PubMed ID: 7103305 [TBL] [Abstract][Full Text] [Related]
14. [Clinical and genetic aspects of progressive muscular dystrophy. Genetic and clinical forms of myopathy; clinical, anatomical, and EMG study]. Voiculescu V; Pruskauer-Apostol B; Mărcuţiu V; Alecu C; Stănescu A Neurol Psihiatr Neurochir; 1973; 18(4):347-58. PubMed ID: 4752178 [No Abstract] [Full Text] [Related]
15. [Study of the kinetics of anion metabolism in the erythrocytes of patients with various forms of hereditary neuromuscular diseases]. Sitnikov VF; Khrennikov VIu; Sidorov EP Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(11):1617-20. PubMed ID: 3434056 [TBL] [Abstract][Full Text] [Related]
16. The myogenic scapulo-peroneal syndrome. Muscular dystrophy in the K. kindred: clinical study and genetics. Kazakov VM; Bogorodinsky DK; Skorometz AA Clin Genet; 1976 Jul; 10(1):41-50. PubMed ID: 949863 [TBL] [Abstract][Full Text] [Related]