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 *

100 related articles for article (PubMed ID: 15337262)

  • 1. Inflammatory glial activation in the brain of a patient with hereditary sensory neuropathy type 1 with deafness and dementia.
    Hojo K; Kawamata T; Tanaka C; Maeda K
    Neurosci Lett; 2004 Sep; 367(3):340-3. PubMed ID: 15337262
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary sensory neuropathy with deafness and dementia: a clinical and neuroimaging study.
    Hojo K; Imamura T; Takanashi M; Ishii K; Sasaki M; Imura S; Ozono R; Takatsuki Y; Takauchi S; Mori E
    Eur J Neurol; 1999 May; 6(3):357-61. PubMed ID: 10210919
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary sensory neuropathy with deafness: a familial multisystem atrophy.
    Horoupian DS
    Neurology; 1989 Feb; 39(2 Pt 1):244-8. PubMed ID: 2915797
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findings.
    Lindahl AJ; Lhatoo SD; Campbell MJ; Nicholson G; Love S
    Clin Neurol Neurosurg; 2006 Dec; 108(8):780-3. PubMed ID: 16271825
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.
    Spring PJ; Kok C; Nicholson GA; Ing AJ; Spies JM; Bassett ML; Cameron J; Kerlin P; Bowler S; Tuck R; Pollard JD
    Brain; 2005 Dec; 128(Pt 12):2797-810. PubMed ID: 16311270
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aberrant neuronal-glial differentiation in Taylor-type focal cortical dysplasia (type IIA/B).
    Englund C; Folkerth RD; Born D; Lacy JM; Hevner RF
    Acta Neuropathol; 2005 May; 109(5):519-33. PubMed ID: 15877232
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of alpha-synuclein immunoreactivity with inflammatory activity in multiple sclerosis lesions.
    Lu JQ; Fan Y; Mitha AP; Bell R; Metz L; Moore GR; Yong VW
    J Neuropathol Exp Neurol; 2009 Feb; 68(2):179-89. PubMed ID: 19151622
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinico-pathological investigation of two patients with dementia with motor neuron disease].
    Yamamoto R; Iseki E; Murayama N; Minegishi M; Kimura M; Eto K; Arai H; Ohbu S; Hatanaka D; Hino H; Fujisawa K
    Brain Nerve; 2007 Mar; 59(3):263-9. PubMed ID: 17370652
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frontotemporal dementia with co-occurrence of astrocytic plaques and tufted astrocytes, and severe degeneration of the cerebral white matter: a variant of corticobasal degeneration?
    Tan CF; Piao YS; Kakita A; Yamada M; Takano H; Tanaka M; Mano A; Makino K; Nishizawa M; Wakabayashi K; Takahashi H
    Acta Neuropathol; 2005 Mar; 109(3):329-38. PubMed ID: 15841415
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Late onset neurodegeneration in the Cln3-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation.
    Pontikis CC; Cella CV; Parihar N; Lim MJ; Chakrabarti S; Mitchison HM; Mobley WC; Rezaie P; Pearce DA; Cooper JD
    Brain Res; 2004 Oct; 1023(2):231-42. PubMed ID: 15374749
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal dominant leukodystrophy with axonal spheroids and pigmented glia: clinical and neuropathological characteristics.
    Itoh K; Shiga K; Shimizu K; Muranishi M; Nakagawa M; Fushiki S
    Acta Neuropathol; 2006 Jan; 111(1):39-45. PubMed ID: 16328511
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Less neurogenesis and inflammation in the immature than in the juvenile brain after cerebral hypoxia-ischemia.
    Qiu L; Zhu C; Wang X; Xu F; Eriksson PS; Nilsson M; Cooper-Kuhn CM; Kuhn HG; Blomgren K
    J Cereb Blood Flow Metab; 2007 Apr; 27(4):785-94. PubMed ID: 16926844
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adult onset leukodystrophy with neuroaxonal spheroids and pigmented glia: report of a family, historical perspective, and review of the literature.
    Marotti JD; Tobias S; Fratkin JD; Powers JM; Rhodes CH
    Acta Neuropathol; 2004 Jun; 107(6):481-8. PubMed ID: 15067553
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hippocampal CA1 cell loss in a non-human primate model of transient global ischemia: a pilot study.
    Hara K; Yasuhara T; Matsukawa N; Maki M; Masuda T; Yu G; Xu L; Tambrallo L; Rodriguez NA; Stern DM; Kawase T; Yamashima T; Buccafusco JJ; Hess DC; Borlongan CV
    Brain Res Bull; 2007 Sep; 74(1-3):164-71. PubMed ID: 17683803
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A sporadic case of hereditary sensory neuropathy with tonic pupil, ichthyosis vulgaris, deafness and atypical retinitis pigmentosa (author's transl)].
    Saito T; Kowa H; Torii J; Yokoi F; Tazaki Y
    Rinsho Shinkeigaku; 1980 Mar; 20(3):201-8. PubMed ID: 6929748
    [No Abstract]   [Full Text] [Related]  

  • 16. Triple fluorescence labelling of neuronal, glial and vascular markers revealing pathological alterations in various animal models.
    Härtig W; Reichenbach A; Voigt C; Boltze J; Bulavina L; Schuhmann MU; Seeger J; Schusser GF; Freytag C; Grosche J
    J Chem Neuroanat; 2009 Mar; 37(2):128-38. PubMed ID: 19028564
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frontotemporal lobar degeneration without lobar atrophy.
    Josephs KA; Whitwell JL; Jack CR; Parisi JE; Dickson DW
    Arch Neurol; 2006 Nov; 63(11):1632-8. PubMed ID: 17101834
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation.
    Shi J; Shaw CL; Du Plessis D; Richardson AM; Bailey KL; Julien C; Stopford C; Thompson J; Varma A; Craufurd D; Tian J; Pickering-Brown S; Neary D; Snowden JS; Mann DM
    Acta Neuropathol; 2005 Nov; 110(5):501-12. PubMed ID: 16222525
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary sensory autonomic neuropathy--type II in siblings.
    Balachandran C; Sabitha L; Kantharaj GR
    Indian J Lepr; 1996; 68(4):373-4. PubMed ID: 9001907
    [No Abstract]   [Full Text] [Related]  

  • 20. Neuropathology of brain death in the modern transplant era.
    Wijdicks EF; Pfeifer EA
    Neurology; 2008 Apr; 70(15):1234-7. PubMed ID: 18256368
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.