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 *

125 related articles for article (PubMed ID: 8887956)

  • 21. Bcl-2 and Bax protein expression in human myopathies.
    Olivé M; Ferrer I
    J Neurol Sci; 1999 Mar; 164(1):76-81. PubMed ID: 10385052
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ultrastructural analysis and TUNEL demonstrate motor neuron apoptosis in Werdnig-Hoffmann disease.
    Simic G; Seso-Simic D; Lucassen PJ; Islam A; Krsnik Z; Cviko A; Jelasic D; Barisic N; Winblad B; Kostovic I; Kruslin B
    J Neuropathol Exp Neurol; 2000 May; 59(5):398-407. PubMed ID: 10888370
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Clinical study of 83 cases with spinal muscular atrophy in children].
    Li H; Wang HL; Shan CM
    Zhonghua Er Ke Za Zhi; 2004 Oct; 42(10):762-4. PubMed ID: 16221347
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Apoptosis in atrophic skeletal muscle induced by brachial plexus injury in rats].
    Tian T; Wu Z; Jin H
    Zhonghua Yi Xue Za Zhi; 2000 Jul; 80(7):530-3. PubMed ID: 11798813
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism.
    Fidziańska A; Goebel HH; Warlo I
    Brain; 1990 Apr; 113 ( Pt 2)():433-45. PubMed ID: 2328412
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1.
    Pitt M; Houlden H; Jacobs J; Mok Q; Harding B; Reilly M; Surtees R
    Brain; 2003 Dec; 126(Pt 12):2682-92. PubMed ID: 14506069
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Synaptic defects in type I spinal muscular atrophy in human development.
    Martínez-Hernández R; Bernal S; Also-Rallo E; Alías L; Barceló MJ; Hereu M; Esquerda JE; Tizzano EF
    J Pathol; 2013 Jan; 229(1):49-61. PubMed ID: 22847626
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Transient cytoplasmic bodies in muscle of three infants with Werdnig-Hoffmann disease.
    Buchino JJ; Bove KE; Iannaccone ST
    Pediatr Pathol; 1990; 10(4):563-73. PubMed ID: 2164661
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Bcl-2 and bax immunohistochemistry in denervation-reinnervation and necrosis-regeneration of rat skeletal muscles.
    Olivé M; Ferrer I
    Muscle Nerve; 2000 Dec; 23(12):1862-7. PubMed ID: 11102910
    [TBL] [Abstract][Full Text] [Related]  

  • 30. MR findings of Werdnig-Hoffmann disease in two infants.
    Hsu CF; Chen CY; Yuh YS; Chen YH; Hsu YT; Zimmerman RA
    AJNR Am J Neuroradiol; 1998 Mar; 19(3):550-2. PubMed ID: 9541317
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Apoptosis-associated markers in oral lichen planus.
    Dekker NP; Lozada-Nur F; Lagenaur LA; MacPhail LA; Bloom CY; Regezi JA
    J Oral Pathol Med; 1997 Apr; 26(4):170-5. PubMed ID: 9176791
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Enzyme-and immuno-histochemistry of muscle biopsies in severe infantile spinal muscular atrophy].
    Chen BF
    Zhonghua Bing Li Xue Za Zhi; 1991 Mar; 20(1):38-40. PubMed ID: 2065375
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Expression of the apoptosis-effector gene, Bax, is up-regulated in vulnerable hippocampal CA1 neurons following global ischemia.
    Chen J; Zhu RL; Nakayama M; Kawaguchi K; Jin K; Stetler RA; Simon RP; Graham SH
    J Neurochem; 1996 Jul; 67(1):64-71. PubMed ID: 8667027
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Immunohistochemical analysis of the distribution of MyoD1 in muscle biopsies of primary myopathies and neurogenic atrophy.
    Parham DM; Dias P; Bertorini T; von Wronski MA; Horner L; Houghton P
    Acta Neuropathol; 1994; 87(6):605-11. PubMed ID: 7522388
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Expression of Bcl-2 in inclusion body myositis.
    Fyhr IM; Lindberg C; Oldfors A
    Acta Neurol Scand; 2002 May; 105(5):403-7. PubMed ID: 11982494
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Spectrum of neuropathophysiology in spinal muscular atrophy type I.
    Harding BN; Kariya S; Monani UR; Chung WK; Benton M; Yum SW; Tennekoon G; Finkel RS
    J Neuropathol Exp Neurol; 2015 Jan; 74(1):15-24. PubMed ID: 25470343
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tenascin in denervated human muscle.
    Schoser BG; Goebel HH
    J Neurol Sci; 1996 Aug; 139(2):203-9. PubMed ID: 8856654
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Apoptosis is suspended in muscle of mitochondrial encephalomyopathies.
    Ikezoe K; Nakagawa M; Yan C; Kira J; Goto Y; Nonaka I
    Acta Neuropathol; 2002 Jun; 103(6):531-40. PubMed ID: 12012084
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Selective type II muscle fiber hypertrophy in severe infantile spinal muscular atrophy.
    Kingma DW; Feeback DL; Marks WA; Bobele GB; Leech RW; Brumback RA
    J Child Neurol; 1991 Oct; 6(4):329-34. PubMed ID: 1940135
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Type I spinal muscular atrophy can mimic sensory-motor axonal neuropathy.
    Anagnostou E; Miller SP; Guiot MC; Karpati G; Simard L; Dilenge ME; Shevell MI
    J Child Neurol; 2005 Feb; 20(2):147-50. PubMed ID: 15794183
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.