These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 6596064)

  • 1. Familial myopathy associated with Marfanoid features and multicores.
    Joyce DA; Mastaglia FL; Ojeda VJ; Spagnolo DV
    Aust N Z J Med; 1984 Aug; 14(4):495-9. PubMed ID: 6596064
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Minicore myopathy with dominant inheritance.
    Paljärvi L; Kalimo H; Lang H; Savontaus ML; Sonninen V
    J Neurol Sci; 1987 Jan; 77(1):11-22. PubMed ID: 3806134
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial multicore disease with focal loss of cross-striations and ophthalmoplegia.
    Swash M; Schwartz MS
    J Neurol Sci; 1981 Oct; 52(1):1-10. PubMed ID: 7299413
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A fatal congenital myopathy with severe type I fibre atrophy, central nuclei and multicores.
    Lee YS; Yip WC
    J Neurol Sci; 1981 May; 50(2):277-90. PubMed ID: 7229670
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Muscle fibrillin deficiency in Marfan's syndrome myopathy.
    Behan WM; Longman C; Petty RK; Comeglio P; Child AH; Boxer M; Foskett P; Harriman DG
    J Neurol Neurosurg Psychiatry; 2003 May; 74(5):633-8. PubMed ID: 12700307
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Centronuclear myopathy with unusual clinical picture.
    Lovaste MG; Aldovini D; Ferrari G
    Eur Neurol; 1987; 26(3):153-60. PubMed ID: 3569369
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Centronuclear myopathy with type I fibre hypotrophy and "fingerprint" inclusions associated with Marfan's syndrome.
    Jadro-Santel D; Grcević N; Dogan S; Franjić J; Benc H
    J Neurol Sci; 1980 Feb; 45(1):43-56. PubMed ID: 6244371
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unclassified familial myopathy resembling Steinert disease, without myotonia.
    Telerman-Toppet N; Khoubesserian P; Bacq M; Durdu J; Lambelin D; Lousberg G; Coërs C
    Muscle Nerve; 1984; 7(6):439-41. PubMed ID: 6543897
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multicore myopathy--a case report.
    Myong NH; Kang YK; Chi JG; Suk SI
    J Korean Med Sci; 1993 Aug; 8(4):312-7. PubMed ID: 8198769
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal dominant multicore disease.
    Vanneste JA; Stam FC
    J Neurol Neurosurg Psychiatry; 1982 Apr; 45(4):360-5. PubMed ID: 7077346
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Myopathy associated with Marfan's syndrome. Fine structural and histochemical observations.
    Goebel HH; Muller J; DeMyer W
    Neurology; 1973 Dec; 23(12):1257-68. PubMed ID: 4357113
    [No Abstract]   [Full Text] [Related]  

  • 12. Familial "myotubular" myopathy.
    van Wijngaarden GK; Fleury P; Bethlem J; Meijer AE
    Neurology; 1969 Sep; 19(9):901-8. PubMed ID: 5816884
    [No Abstract]   [Full Text] [Related]  

  • 13. A dominantly inherited myopathy with excessive tubular aggregates.
    Rohkamm R; Boxler K; Ricker K; Jerusalem F
    Neurology; 1983 Mar; 33(3):331-6. PubMed ID: 6681878
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multicore disease. Report of a case with lack of fibre type differentiation.
    Taratuto AL; Sfaello ZM; Rezzonico C; Morales RC
    Neuropadiatrie; 1978 Aug; 9(3):285-97. PubMed ID: 213746
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multicore myopathy: not always a benign entity.
    Shuaib A; Martin JM; Mitchell LB; Brownell AK
    Can J Neurol Sci; 1988 Feb; 15(1):10-4. PubMed ID: 3345455
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expression.
    Dotti MT; Malandrini A; Bartolini S; Fabrizi GM; Federico A
    Brain Dev; 1993; 15(4):291-4. PubMed ID: 8250152
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sarcotubular myopathy. A newly recognized, benign, congenital, familial muscle disease.
    Jerusalem F; Engel AG; Gomez MR
    Neurology; 1973 Sep; 23(9):897-906. PubMed ID: 4269389
    [No Abstract]   [Full Text] [Related]  

  • 18. A study of a myopathy presenting as idiopathic scoliosis. Multicore disease or mitochondrial myopathy?
    Fitzsimons RB; Tyer HD
    J Neurol Sci; 1980 Apr; 46(1):33-48. PubMed ID: 7373343
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Familial form of centronuclear myopathy in the adult].
    Pépin B; Mikol J; Goldstein B; Haguenau M; Godlewski S
    Rev Neurol (Paris); 1976 Dec; 132(12):845-57. PubMed ID: 1013570
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial desminopathy: myopathy with accumulation of desmin-type intermediate filaments.
    Vajsar J; Becker LE; Freedom RM; Murphy EG
    J Neurol Neurosurg Psychiatry; 1993 Jun; 56(6):644-8. PubMed ID: 8509778
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.