BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

304 related articles for article (PubMed ID: 11989852)

  • 1. Nemaline myopathy: description of an adult onset case.
    Ginanneschi F; Mondelli M; Malandrini A; Gambelli S; Dotti MT; Federico A
    J Submicrosc Cytol Pathol; 2002 Jan; 34(1):105-8. PubMed ID: 11989852
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adult-onset nemaline myopathy: a case report and review of the literature.
    Gyure KA; Prayson RA; Estes ML
    Arch Pathol Lab Med; 1997 Nov; 121(11):1210-3. PubMed ID: 9372751
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Nemaline congenital myopathy:clinical features and histopathological findings in nine patients].
    Botelho CH; Carod-Artal FJ; Kalil RK
    Rev Neurol; 2001 Feb 16-28; 32(4):309-14. PubMed ID: 11333383
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Idiopathic adult-onset nemaline myopathy presenting with isolated respiratory failure.
    Whitaker J; Love S; Williams AP; Plummeridge M
    Muscle Nerve; 2009 Mar; 39(3):406-8. PubMed ID: 19208402
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Adult-onset nemaline myopathy with distal muscle atrophy--case report].
    Niwa F; Shiga K; Kimura M; Yamaguchi T; Kondo M; Nakagawa M
    Brain Nerve; 2009 Jun; 61(6):695-9. PubMed ID: 19526838
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2).
    Tajsharghi H; Ohlsson M; Lindberg C; Oldfors A
    Arch Neurol; 2007 Sep; 64(9):1334-8. PubMed ID: 17846275
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinical and pathological studies on nemaline myopathy in adulthood].
    Suzuki Y; Nonaka I; Akiyama C; Kuroiwa Y
    Rinsho Shinkeigaku; 1998 Sep; 38(9):791-5. PubMed ID: 10078028
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report].
    Oya Y; Segawa M; Ogawa M; Goto Y; Nonaka I; Kawai M
    Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1).
    Ohlsson M; Tajsharghi H; Darin N; Kyllerman M; Oldfors A
    Neuromuscul Disord; 2004 Sep; 14(8-9):471-5. PubMed ID: 15336687
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Sporadic adult form of nemaline myopathy--a difficult differential diagnosis].
    Klarl BA; Bornemann A; Demuth K; Zähringer M; Lindner A
    Fortschr Neurol Psychiatr; 2009 Mar; 77(3):166-8. PubMed ID: 19283652
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Adult-onset nemaline myopathy and monoclonal gammopathy.
    Keller CE; Hays AP; Rowland LP; Moghadaszadeh B; Beggs AH; Bhagat G
    Arch Neurol; 2006 Jan; 63(1):132-4. PubMed ID: 16401746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [An adulthood progressive case of congenital nemaline myopathy showing rimmed vacuoles in muscle biopsy and diffuse neurogenic changes on electromyography].
    Ikezoe K; Murai H; Kawajiri M; Ohyagi Y; Kira J
    Rinsho Shinkeigaku; 2004 Jul; 44(7):450-3. PubMed ID: 15384708
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sporadic late onset nemaline myopathy.
    Chahin N; Selcen D; Engel AG
    Neurology; 2005 Oct; 65(8):1158-64. PubMed ID: 16148261
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred.
    Hutchinson DO; Charlton A; Laing NG; Ilkovski B; North KN
    Neuromuscul Disord; 2006 Feb; 16(2):113-21. PubMed ID: 16427282
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominant nemaline myopathy: a new phenotype unlinked to previously known genetic loci.
    Jeannet PY; Mittaz L; Dunand M; Lobrinus JA; Bonafe L; Kuntzer T
    Neuromuscul Disord; 2007 Jan; 17(1):6-12. PubMed ID: 17157023
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A patient of late-onset nemaline myopathy with mononuclear cell infiltration].
    Miura H; Kannari K; Kashiwamura H; Nonaka I
    Rinsho Shinkeigaku; 1994 Oct; 34(10):1061-3. PubMed ID: 7834955
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Adult-onset nemaline myopathy presenting as respiratory failure.
    Kelly E; Farrell MA; McElvaney NG
    Respir Care; 2008 Nov; 53(11):1490-4. PubMed ID: 18957152
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H).
    Koy A; Ilkovski B; Laing N; North K; Weis J; Neuen-Jacob E; Mayatepek E; Voit T
    Neuropediatrics; 2007 Dec; 38(6):282-6. PubMed ID: 18461503
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A 22-year-old man with long-standing weakness and atrophy predominantly in the lower extremities].
    Mori H; Sato K; Hirasawa E; Kondo T; Mizuno Y
    No To Shinkei; 1996 Aug; 48(8):763-71. PubMed ID: 8797213
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 'Cap myopathy': case report of a family.
    Cuisset JM; Maurage CA; Pellissier JF; Barois A; Urtizberea JA; Laing N; Tajsharghi H; Vallée L
    Neuromuscul Disord; 2006 Apr; 16(4):277-81. PubMed ID: 16531045
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.