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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

148 related items for PubMed ID: 2030350

  • 21. [Pelizaeus-Metzbacher disease: clinical diagnosis].
    Förster C, Daschner F, Murken JD.
    Z Kinderheilkd; 1971; 110(3):248-60. PubMed ID: 5088756
    [No Abstract] [Full Text] [Related]

  • 22. The limb-girdle muscular dystrophies: diagnostic guidelines.
    Bushby KM.
    Eur J Paediatr Neurol; 1999; 3(2):53-8. PubMed ID: 10700539
    [Abstract] [Full Text] [Related]

  • 23. Severe muscular dystrophy in girls.
    Gardner-Medwin D, Johnston HM.
    J Neurol Sci; 1984 Apr; 64(1):79-87. PubMed ID: 6737006
    [Abstract] [Full Text] [Related]

  • 24. Carrier detection in X-linked muscular dystrophy.
    Walton JN.
    J Genet Hum; 1969 Oct; 17(3):497-510. PubMed ID: 5387424
    [No Abstract] [Full Text] [Related]

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  • 27. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
    Nakamura A, Yoshida K, Ikeda S.
    Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303
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  • 30. Possible neurogenic factor in muscular dystrophy: its similarity to denervation atrophy.
    Dastur DK, Razzak ZA.
    J Neurol Neurosurg Psychiatry; 1973 Jun; 36(3):399-410. PubMed ID: 4714102
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  • 31. Welander's distal myopathy: clinical, neurophysiological and muscle biopsy observations in young and middle aged adults with early symptoms.
    Borg K, Ahlberg G, Borg J, Edström L.
    J Neurol Neurosurg Psychiatry; 1991 Jun; 54(6):494-8. PubMed ID: 1652622
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  • 33. Congenital muscular dystrophy (non-Fukuyama type) in Turkey: a clinical and pathological evaluation.
    Topaloğlu H, Yalaz K, Renda Y, Kale G, Cağlar M, Göğüş S.
    Brain Dev; 1989 Jun; 11(5):341-4. PubMed ID: 2817300
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  • 36. [Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations].
    Gold R, Kress W, Meurers B, Müller CR, Reichmann H.
    Nervenarzt; 1991 Jun; 62(6):360-8. PubMed ID: 1876220
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  • 37. Congenital muscular dystrophy and cerebral dysgenesis in a Dutch family.
    Krijgsman JB, Barth PG, Stam FC, Slooff JL, Jaspar HH.
    Neuropadiatrie; 1980 May; 11(2):108-20. PubMed ID: 6893737
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  • 38. [Contribution to the question of diffuse infantile cerebral sclerosis with primary dystrophy of the suprarenal gland].
    Riedel H.
    Psychiatr Neurol Med Psychol (Leipz); 1968 Feb; 20(2):67-73. PubMed ID: 5304006
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  • 39. [Skeletal muscle MRI findings in autosomal recessive distal muscular dystrophy (Miyoshi)].
    Ohsuga H, Ohsuga S, Yamamoto M, Shinohara Y.
    Rinsho Shinkeigaku; 1988 Nov; 28(11):1304-11. PubMed ID: 3233830
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