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 *

120 related articles for article (PubMed ID: 3556789)

  • 21. A sporadic case of central core disease.
    Mrozek K; Strugalska M; Fidziańska A
    J Neurol Sci; 1970 Apr; 10(4):339-48. PubMed ID: 5444889
    [No Abstract]   [Full Text] [Related]  

  • 22. Fingerprint body myopathy, a newly recognized congenital muscle disease.
    Engel AG; Angelini C; Gomez MR
    Mayo Clin Proc; 1972 Jun; 47(6):377-88. PubMed ID: 4339422
    [No Abstract]   [Full Text] [Related]  

  • 23. [Nemaline myopathy. General review apropos of 3 cases].
    Pagès M; Ramos J; Pagès AM; Echenne B
    Ann Pathol; 1987; 7(3):216-22. PubMed ID: 3325069
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Surgical correction of spinal deformity in patients with congenital muscular dystrophy.
    Takaso M; Nakazawa T; Imura T; Okada T; Ueno M; Saito W; Takahashi K; Yamazaki M; Ohtori S
    J Orthop Sci; 2010 Jul; 15(4):493-501. PubMed ID: 20721717
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A case of congenital myopathy without specific features.
    Tachi N; Hosoya S; Watanabe M; Wakai S; Minami R
    Acta Paediatr Jpn; 1987 Jun; 29(3):455-60. PubMed ID: 3144876
    [No Abstract]   [Full Text] [Related]  

  • 26. Central core disease or not? Observations on a family with a non-progressive myopathy.
    Morgan-Hughes JA; Brett EM; Lake BD; Tomé FM
    Brain; 1973 Sep; 96(3):527-36. PubMed ID: 4743931
    [No Abstract]   [Full Text] [Related]  

  • 27. A case report of severe kyphoscoliosis and autofusion of the posterior elements in two siblings with central core disease.
    Sestero AM; Perra JH
    Spine (Phila Pa 1976); 2005 Jan; 30(2):E50-5. PubMed ID: 15644748
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction.
    Colamaria V; Zanetti R; Simeone M; Tomelleri G; Orrico D; Dordi B; Dalla Bernardina B
    Brain Dev; 1991 Sep; 13(5):358-62. PubMed ID: 1785661
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fatal nemaline myopathy in infancy.
    McMenamin JB; Curry B; Taylor GP; Becker LE; Murphy EG
    Can J Neurol Sci; 1984 May; 11(2):305-9. PubMed ID: 6733612
    [TBL] [Abstract][Full Text] [Related]  

  • 30. ["Central core" myopathy: report of a case].
    Werneck LC; Silvado CE
    Arq Neuropsiquiatr; 1981 Jun; 39(2):230-6. PubMed ID: 7283803
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ventilator weaning after staged anteroposterior spine fusion in a ventilator-dependent patient with congenital scoliosis: a case report.
    Lim M; Wazeka A; Boachie-Adjei O
    Spine (Phila Pa 1976); 2003 Jul; 28(13):E256-9. PubMed ID: 12838115
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Myopathy of congenital fiber type disproportion. Description of a clinical case].
    Millefiorini E; Paolella P; Antonini G; Millefiorini M
    Riv Neurol; 1984; 54(6):383-9. PubMed ID: 6528207
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Rigid spinal muscular dystrophy and rigid spine syndrome: report of 7 children.
    Koul R; Al-Yarubi S; Al-Kindy H; Al-Futaisi A; Al-Thihli K; Chacko PA; Sankhla D
    J Child Neurol; 2014 Nov; 29(11):1436-40. PubMed ID: 23481446
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Neonatal nemaline myopathy presenting with multiple joint contractures.
    Bucher HU; Boltshauser E; Briner J
    Eur J Pediatr; 1985 Sep; 144(3):288-90. PubMed ID: 2414108
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Centronuclear myopathy with unusual mitochondrial abnormalities.
    Canal N; Comi GC; Comola M; Testa D; Mora M; Cornelio F
    Clin Neuropathol; 1985; 4(1):23-7. PubMed ID: 2983917
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The cytoplasmic bodies in a congenital myopathy can be stained with antibodies to desmin, the muscle-specific intermediate filament protein.
    Osborn M; Goebel HH
    Acta Neuropathol; 1983; 62(1-2):149-52. PubMed ID: 6318501
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [An unusual myopathy: the so-called congenital fiber-type disproportion].
    Lössner J; Ziegan J; Oertel G
    Z Gesamte Inn Med; 1979 Nov; 34(22):685-7. PubMed ID: 549303
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A unique case of reducing body myopathy.
    Nomizu S; Person DA; Saito C; Lockett LJ
    Muscle Nerve; 1992 Apr; 15(4):463-6. PubMed ID: 1314327
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [A case of severe infantile form of congenital nemaline myopathy with extensive fatty replacement of the skeletal muscles].
    Shimizu J; Matsumura K; Noguchi H
    Rinsho Shinkeigaku; 1990 Oct; 30(10):1123-7. PubMed ID: 2177691
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Spheroid-cytoplasmic complexes in a congenital myopathy.
    Halbig L; Goebel HH; Hopf HC; Moll R
    Rev Neurol (Paris); 1991; 147(4):300-7. PubMed ID: 1648255
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.