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3. [The dystrophic type of scapuloperoneal syndrome]. Steidl L; Urbánek K Cesk Neurol; 1973 May; 36(3):147-50. PubMed ID: 4704112 [No Abstract] [Full Text] [Related]
4. [A case of Emery-Dreifuss muscular dystrophy--scapuloperoneal muscular atrophy with disturbance of heart conduction]. Terauchi A; Kuroda I; Mori T; Matsuoka T No To Hattatsu; 1985 Sep; 17(5):443-7. PubMed ID: 4074564 [No Abstract] [Full Text] [Related]
6. [Late scapuloperoneal form of progressive muscular dystrophy]. Stamatoiu I; Florea G; Vasilescu C Neurol Psihiatr Neurochir; 1965; 10(1):21-7. PubMed ID: 5827299 [No Abstract] [Full Text] [Related]
7. Myogenic scapuloperoneal syndrome - muscular dystrophy in the K. kindred. Reexamination of the K. family described for the first time by Oransky in 1927. Kazakov VM; Bogorodinsky DK; Skorometz AA Eur Neurol; 1975; 13(4):350-9. PubMed ID: 1149755 [TBL] [Abstract][Full Text] [Related]
8. [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; 86(5):662-7. PubMed ID: 3739474 [TBL] [Abstract][Full Text] [Related]
16. [Emery-Dreifuss muscular dystrophy--reported a family with 5 cases]. Luo D Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1991 Dec; 24(6):330-1, 382. PubMed ID: 1800056 [TBL] [Abstract][Full Text] [Related]
17. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Wilhelmsen KC; Blake DM; Lynch T; Mabutas J; De Vera M; Neystat M; Bernstein M; Hirano M; Gilliam TC; Murphy PL; Sola MD; Bonilla E; Schotland DL; Hays AP; Rowland LP Ann Neurol; 1996 Apr; 39(4):507-20. PubMed ID: 8619529 [TBL] [Abstract][Full Text] [Related]
18. Congenital muscular dystrophy: case reports and reappraisal. Lazaro RP; Fenichel GM; Kilroy AW Muscle Nerve; 1979; 2(5):349-55. PubMed ID: 492211 [TBL] [Abstract][Full Text] [Related]
19. Lower extremity involvement in Duchenne's muscular dystrophy. Reinherz R; Mann I J Am Podiatry Assoc; 1977 Nov; 67(11):796-801. PubMed ID: 915190 [No Abstract] [Full Text] [Related]
20. 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; 7(2):72-81. PubMed ID: 5173129 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]