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3. [Some data on the characteristics of myopathy in the Orenburg region]. Shtil' RG Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1461-5. PubMed ID: 4257931 [No Abstract] [Full Text] [Related]
4. [A case of Landouzy-Déjérine disease with ptosis]. Desvignes P; Blanck MF; Mougeot M; Cassan JL Bull Soc Ophtalmol Fr; 1971; 71(9):874-7. PubMed ID: 5151032 [No Abstract] [Full Text] [Related]
5. [Identification of primary and secondary forms of progressive muscular dystrophy, from data of clinico-genetic and biochemical studies]. Bondarenko ES; Tamarkina AD; Zakoshchikova LV Vestn Akad Med Nauk SSSR; 1973; 28(7):38-44. PubMed ID: 4786657 [No Abstract] [Full Text] [Related]
6. [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]
7. [Malate dehydrogenase activity in patients with different forms of progressive muscular dystrophy]. Gil'manov VKh Zh Nevropatol Psikhiatr Im S S Korsakova; 1970; 70(9):1309-12. PubMed ID: 5511109 [No Abstract] [Full Text] [Related]
8. Scoliosis in muscular dystrophy. Some comments about diagnosis, observations on prognosis, and suggestions for therapy. Siegel IM Clin Orthop Relat Res; 1973 Jun; (93):235-8. PubMed ID: 4722946 [No Abstract] [Full Text] [Related]
9. Reconstruction in Landouzy-Dejerine progressive muscular dystrophy. Case report. Cocke WM; Davis WG Plast Reconstr Surg; 1971 Jul; 48(1):77-9. PubMed ID: 5556722 [No Abstract] [Full Text] [Related]
10. [Variant of the facial-scapular-humeral-gluteal-femoral form of primary myopathy in children]. Grinio LP Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(10):1338-41. PubMed ID: 494906 [TBL] [Abstract][Full Text] [Related]
11. [Malate dehydrogenase activity in children with myopathy]. Gil'manov VKh Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):829-31. PubMed ID: 4753593 [No Abstract] [Full Text] [Related]
12. The facio-scapulo-limb (or the facioscapulohumeral) type of muscular dystrophy. Clinical and genetic study of 200 cases. Kazakov VM; Bogorodinsky DK; Znoyko ZV; Skorometz AA Eur Neurol; 1974; 11(4):236-60. PubMed ID: 4854830 [No Abstract] [Full Text] [Related]
13. [Muscle innervation in Werdnig-Hoffmann spinal amyotrophy and several other atrophies in children]. Olenev SN; Savel'eva-Vasil'eva ; Zav'ialova NS Zh Nevropatol Psikhiatr Im S S Korsakova; 1972; 72(10):1445-9. PubMed ID: 4660417 [No Abstract] [Full Text] [Related]
14. Early signs of Landouzy-Déjerine disease: wrist and finger weakness. Siegel IM JAMA; 1972 Jul; 221(3):302. PubMed ID: 5067800 [No Abstract] [Full Text] [Related]
15. [Thoraco-scapular arthrodesis in facioscapulohumeral dystrophy]. Toni A; Merlini L; Sudanese A; Baldini N; Granata C Chir Organi Mov; 1986; 71(2):127-31. PubMed ID: 3542419 [No Abstract] [Full Text] [Related]
16. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease. Jackson CE; Strehler DA Pediatrics; 1968 Feb; 41(2):495-502. PubMed ID: 5637795 [No Abstract] [Full Text] [Related]
17. [Landouzy-Dejerine syndrome. Evolution of the concept of facio-scapulo-humeral amyotrophia]. Schmitt J; Barrucand D; Schmidt C Rev Neurol (Paris); 1977 Apr; 133(4):279-82. PubMed ID: 929032 [TBL] [Abstract][Full Text] [Related]