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Journal Abstract Search
248 related items for PubMed ID: 4722946
21. Neuromuscular scoliosis: causes of deformity and principles for evaluation and management. Berven S, Bradford DS. Semin Neurol; 2002 Jun; 22(2):167-78. PubMed ID: 12524562 [Abstract] [Full Text] [Related]
22. Permanent paralysis of the atrium in a patient with facioscapulohumeral muscular dystrophy. Baldwin BJ, Talley RC, Johnson C, Nutter DO. Am J Cardiol; 1973 May; 31(5):649-53. PubMed ID: 4698137 [No Abstract] [Full Text] [Related]
23. 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 May; 11(4):236-60. PubMed ID: 4854830 [No Abstract] [Full Text] [Related]
24. [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 May; 18(4):347-58. PubMed ID: 4752178 [No Abstract] [Full Text] [Related]
26. Orthopedic correction of musculoskeletal deformity in muscular dystrophy. Siegel IM. Adv Neurol; 1977 Feb; 17():343-64. PubMed ID: 888741 [Abstract] [Full Text] [Related]
27. The genetics of muscular dystrophies. Harper PS. Prog Med Genet; 1985 Feb; 6():53-90. PubMed ID: 3915367 [No Abstract] [Full Text] [Related]
28. [Variant of the facial-scapular-humeral-gluteal-femoral form of primary myopathy in children]. Grinio LP. Zh Nevropatol Psikhiatr Im S S Korsakova; 1979 Feb; 79(10):1338-41. PubMed ID: 494906 [Abstract] [Full Text] [Related]
30. [Inner ear deafness in dystrophia myotonica and progressive muscular dystrophy]. Kuhn E, Ey W. Dtsch Med Wochenschr; 1966 May 20; 91(20):947-51. PubMed ID: 5930205 [No Abstract] [Full Text] [Related]
31. Assessing functional outcomes of children with muscular dystrophy and scoliosis: the Muscular Dystrophy Spine Questionnaire. Wright JG, Smith PL, Owen JL, Fehlings D. J Pediatr Orthop; 2008 Dec 20; 28(8):840-5. PubMed ID: 19034175 [Abstract] [Full Text] [Related]
32. Early signs of Landouzy-Déjerine disease: wrist and finger weakness. Siegel IM. JAMA; 1972 Jul 17; 221(3):302. PubMed ID: 5067800 [No Abstract] [Full Text] [Related]
33. Reconstruction in Landouzy-Dejerine progressive muscular dystrophy. Case report. Cocke WM, Davis WG. Plast Reconstr Surg; 1971 Jul 17; 48(1):77-9. PubMed ID: 5556722 [No Abstract] [Full Text] [Related]
34. Severity of scoliosis in patients with Duchenne muscular dystrophy at the time of referral to an orthopedic clinic. Galasko CS, Delaney CM. Muscle Nerve; 1993 Apr 17; 16(4):433-4. PubMed ID: 8455661 [No Abstract] [Full Text] [Related]
35. Gait and posture changes in the Duchenne muscular dystrophy child. Hsu JD, Furumasu J. Clin Orthop Relat Res; 1993 Mar 17; (288):122-5. PubMed ID: 8458124 [Abstract] [Full Text] [Related]
36. Creatine phosphokinase in facioscapulohumeral muscular dystrophy. Hughes BP. Br Med J; 1971 Aug 17; 3(5772):464-5. PubMed ID: 5567771 [Abstract] [Full Text] [Related]
37. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness. Korf BR, Bresnan MJ, Shapiro F, Sotrel A, Abroms IF. Ann Neurol; 1985 May 17; 17(5):513-6. PubMed ID: 4004175 [Abstract] [Full Text] [Related]
38. Diagnosis, management, and orthopaedic treatment of muscular dystrophy. Siegel IM. Instr Course Lect; 1981 May 17; 30():3-35. PubMed ID: 7052832 [No Abstract] [Full Text] [Related]
39. The treatment of scoliosis in childhood. James JI. Dev Med Child Neurol; 1971 Dec 17; 13(6):809-12. PubMed ID: 5138640 [No Abstract] [Full Text] [Related]