MS
Masahito Suehara

Highly Cited

57
Works
1,478
Citations
23
H-Index
Search Authors
Author Statistics
  • OpenAlex ID A5032141198
  • i10-Index 35
  • 2-Yr Mean Citedness 0.00
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Masahito Suehara

Also known as: M Suehara, M. Suehara, MASAHITO SUEHARA, Masahito SUEHARA, Masahito Suehara

57

Total Works

1,478

Citations

23

H-Index

35

i10-Index

Citation & Works Trend by Year
36 years active
Top Research Topics
Hereditary Neurological Disorders (16) Peripheral Neuropathies and Disorders (14) Muscle Physiology and Disorders (13) Genetic Neurodegenerative Diseases (9) T-cell and Retrovirus Studies (8)
Recent Publications
15 shown
Year Publication Title Citations Action
2024 Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications Acta Neuropathologica Communications 10
2023 Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation Frontiers in Neurology 5
2018 The natural history of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) in 97 Japanese patients Intractable & Rare Diseases Research 10
2017 Clinical course of hereditary motor and sensory neuropathy, Okinawa type Journal of the Neurological Sciences 0
2017 3-2-03. Does cervical radiculopathy complicate brachial plexopathy? An electrophysiological analysis Clinical Neurophysiology 0
2016 Clinical manifestations of 5 patients with idiopathic paroxysmal kinesigenic choreoathetosis Rinsho Shinkeigaku 0
2015 Ultrasound evaluation of tongue and trapezius muscles in advanced cases of hereditary motor and sensory neuropathy with proximal predominance Neurosonology 0
2014 Three‐tesla magnetic resonance neurography of the brachial plexus in cervical radiculopathy Muscle & Nerve 21
2014 Persistent Hiccups and Vomiting with Multiple Cranial Nerve Palsy in a Case of Zoster Sine Herpete Internal Medicine 10
2012 An autopsy case of coexisting Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyradiculoneuropathy, later associated with amyotrophic lateral sclerosis Rinsho Shinkeigaku 2
2011 Successful development of novel monoclonal antibodies against HTLV-1 bZIP factor and their applications in studying the pathogenesis of HAM/TSP Retrovirology 0
2009 Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan Journal of Human Genetics 15
2006 Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene Neurogenetics 29
2005 Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency Muscle & Nerve 13
2003 Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency Acta Neuropathologica 13

Data source: OpenAlex API