Kinuko Suzuki, MD

Affiliations: 
Pathology University of North Carolina, Chapel Hill, Chapel Hill, NC 
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"Kinuko Suzuki"
Bio:

http://journals.lww.com/jneuropath/Citation/2008/12000/2008_Award_Recipients_Kinuko_Suzuki,_MD,_by_James.10.aspx


TAKANAWA MINATO KU
TOKYO, Japan

Mean distance: 15.77 (cluster 32)
 
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Publications

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Uchino A, Nagai M, Kanazawa N, et al. (2020) An autopsy case of G gangliosidosis type II in a patient who survived a long duration with artificial respiratory support. Neuropathology : Official Journal of the Japanese Society of Neuropathology
Miyoshi Y, Yoshioka Y, Suzuki K, et al. (2014) A new mouse allele of glutamate receptor delta 2 with cerebellar atrophy and progressive ataxia. Plos One. 9: e107867
Yoneshige A, Suzuki K, Suzuki K, et al. (2010) A mutation in the saposin C domain of the sphingolipid activator protein (Prosaposin) gene causes neurodegenerative disease in mice. Journal of Neuroscience Research. 88: 2118-34
Fritchie K, Siintola E, Armao D, et al. (2009) Novel mutation and the first prenatal screening of cathepsin D deficiency (CLN10). Acta Neuropathologica. 117: 201-8
Hiremath MM, Chen VS, Suzuki K, et al. (2008) MHC class II exacerbates demyelination in vivo independently of T cells. Journal of Neuroimmunology. 203: 23-32
Kagitani-Shimono K, Mohri I, Yagi T, et al. (2008) Peripheral neuropathy in the twitcher mouse: accumulation of extracellular matrix in the endoneurium and aberrant expression of ion channels. Acta Neuropathologica. 115: 577-87
Takao M, Mori T, Orikasa H, et al. (2007) Postmortem diagnosis of Fabry disease with acromegaly and a unique vasculopathy. Virchows Archiv : An International Journal of Pathology. 451: 721-7
Mohri I, Kadoyama K, Kanekiyo T, et al. (2007) Hematopoietic prostaglandin D synthase and DP1 receptor are selectively upregulated in microglia and astrocytes within senile plaques from human patients and in a mouse model of Alzheimer disease. Journal of Neuropathology and Experimental Neurology. 66: 469-80
Langmade SJ, Gale SE, Frolov A, et al. (2006) Pregnane X receptor (PXR) activation: a mechanism for neuroprotection in a mouse model of Niemann-Pick C disease. Proceedings of the National Academy of Sciences of the United States of America. 103: 13807-12
Tsai YS, Pendse A, Moy SS, et al. (2006) A de novo deafwaddler mutation of Pmca2 arising in ES cells and hitchhiking with a targeted modification of the Pparg gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 716-22
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