K. Murayama - Concepedia

Author

K. Murayama

National Center of Neurology and Psychiatry

Also Known As

K MURAYAMA, K Murayama, K. MURAYAMA, K. Murayama, Kodai MURAYAMA, Kohei Murayama

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

National Center of Neurology and Psychiatry Shimane University

About

K. Murayama is an author at National Center of Neurology and Psychiatry specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	406
2	Immunology	2	2	244
3	Engineering	1	1	51
4	Cell Biology	1	1	154
5	Molecular Genetics	1	1	37

K. Murayama

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
mtDNA polymorphism in East Asian Populations, with special reference to the peopling of Japan. Satoshi Horai, K. Murayama, Kenji Hayasaka, PubMed	1996	251
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy Ichizo Nishino, S. Noguchi, K. Murayama, Neurology	2002	240
Host range mutant of human immunodeficiency virus type 1: modification of cell tropism by a single point mutation at the neutralization epitope in the env gene Y Takeuchi, Mitsuaki Akutsu, K. Murayama, Journal of Virology Viral ReplicationImmunologySingle Point MutationT CellsImmunotherapy	1991	154
Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan Mari Okada, Genri Kawahara, S. Noguchi, Neurology	2007	112
Ullrich disease due to deficiency of collagen VI in the sarcolemma H. Ishikawa, Kazuma Sugie, K. Murayama, Neurology VasculitisImmunologyBasal LaminaPathologyDermatology	2004	90
Ullrich disease: Collagen VI deficiency: EM suggests a new basis for muscular weakness H. Ishikawa, Kazuma Sugie, K. Murayama, Neurology Rare DiseasesCollagen ViAutoimmune DiseaseCollagen Vi DeficiencyMuscular Weakness	2002	74
Molecular pathomechanism of distal myopathy with rimmed vacuoles. Ichizo Nishino, May Christine V. Malicdan, K. Murayama, PubMed MechanobiologyCardiomyopathyEngineeringMendelian DisorderGenetic Disorder	2005	51
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy Rim Amouri, Adel Driss, K. Murayama, Neuromuscular Disorders Allelic VariantMendelian DisorderGenetic DisorderMedicineGenetics	2005	37
A new diagnostic test for VLCAD deficiency using immunohistochemistry Yasushi Ohashi, Yuki Hasegawa, K. Murayama, Neurology	2004	36
A New Technology for Mutation Detection William H. Shackelford, Shao-lin Deng, K. Murayama, Annals of the New York Academy of Sciences	2004	22

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