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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

198 related items for PubMed ID: 3903492

  • 21.
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  • 22. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M, Attia N, Chabouni H, Fardeau M.
    Rev Neurol (Paris); 1983; 139(4):289-97. PubMed ID: 6612142
    [Abstract] [Full Text] [Related]

  • 23. [A family of autosomal dominant facio-limb-girdle muscular dystrophy].
    Takao S, Kira J, Kohtake N, Yoshimura T, Goto I.
    Fukuoka Igaku Zasshi; 1996 Dec; 87(12):278-82. PubMed ID: 9011111
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  • 24. [A case of autoimmune polyglandular deficiency associated with progressive myopathy].
    Segawa F, Yamada H, Tomi H, Sunohara N, Nonaka I.
    Rinsho Shinkeigaku; 1992 May; 32(5):501-5. PubMed ID: 1458727
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  • 29. Quadriceps myopathy: report of a late onset sporadic case.
    Danielis R, Lazzarino LG, Nicolai A, Valassi F.
    Riv Neurol; 1991 May; 61(2):51-3. PubMed ID: 1887196
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  • 30.
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  • 31. Diagnostic criteria for the limb-girdle muscular dystrophies: report of the ENMC Consortium on Limb-Girdle Dystrophies.
    Bushby KM.
    Neuromuscul Disord; 1995 Jan; 5(1):71-4. PubMed ID: 7719146
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  • 32.
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  • 34. [The value of imaging procedures in myology].
    Nägele M, Reimers CD, Fenzl G, Witt TN, Götz AE, Reimers K, Pongratz DE, Hahn D.
    Bildgebung; 1995 Jan; 56(5):172-8. PubMed ID: 3078433
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  • 35. Congenital muscular dystrophy.
    Huang FL, Mak SC, Chi CS.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Feb; 63(2):165-9. PubMed ID: 10677931
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  • 36. [Progressive musclar dystrophy in the experience of the Pediatric Clinic of Florence. Longitudinal study of 43 subjects].
    Adami Lami Conti C, Calandi C, Nistri R, Aulisi A, Bucciolini MG, Vannelli G, Ragazzini F.
    Minerva Pediatr; 1981 May 15; 33(9):385-412. PubMed ID: 7019663
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  • 38. Detection of pathological change in dystrophic muscle with B-scan ultrasound imaging.
    Heckmatt JZ, Dubowitz V, Leeman S.
    Lancet; 1980 Jun 28; 1(8183):1389-90. PubMed ID: 6104175
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