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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

190 related items for PubMed ID: 6737006

  • 21.
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  • 23. Autosomal recessive distal muscular dystrophy as a new type of progressive muscular dystrophy. Seventeen cases in eight families including an autopsied case.
    Miyoshi K, Kawai H, Iwasa M, Kusaka K, Nishino H.
    Brain; 1986 Feb; 109 ( Pt 1)():31-54. PubMed ID: 3942856
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  • 26. Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.
    Romero NB, Tomé FM, Leturcq F, el Kerch FE, Azibi K, Bachner L, Anderson RD, Roberds SL, Campbell KP, Fardeau M.
    C R Acad Sci III; 1994 Jan; 317(1):70-6. PubMed ID: 7987694
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  • 27. Benign congenital muscular dystrophy: a special form of congenital hypotonia.
    Zellweger H, Afifi A, McCormick WF, Mergner W.
    Clin Pediatr (Phila); 1967 Nov; 6(11):655-63. PubMed ID: 6058423
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  • 28. [New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias].
    Rotthauwe HW, Mortier W, Beyer H.
    Humangenetik; 1972 Nov; 16(3):181-200. PubMed ID: 5082100
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  • 29. The detection of female carriers of pseudohypertrophic muscular dystrophy.
    Kakulas BA, Knight JO, Gubbay SS, Mastaglia FL.
    Proc Aust Assoc Neurol; 1968 Nov; 5(3):545-51. PubMed ID: 5709982
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  • 30. [Trisomy 21 in a boy with progressive muscular dystrophy (Duchenne)].
    Moser H.
    Z Kinderheilkd; 1971 Nov; 109(4):318-25. PubMed ID: 4252123
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  • 31. Poikiloderma atrophicans vasculare associated with muscular dystrophy.
    Woolfson H, McQueen A.
    Arch Dermatol; 1973 Jan; 107(1):115-7. PubMed ID: 4682534
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  • 34. Quantitative electromyography: carrier detection in Duchenne type muscular dystrophy using a new automatic technique.
    Moosa A, Brown BH, Dubowitz V.
    J Neurol Neurosurg Psychiatry; 1972 Dec; 35(6):841-4. PubMed ID: 4647857
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  • 37. Diagnostic advantage of needle muscle biopsy and ultrasound imaging in the detection of focal pathology in a girl with limb girdle dystrophy.
    Heckmatt JZ, Dubowitz V.
    Muscle Nerve; 1985 Oct; 8(8):705-9. PubMed ID: 3903492
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