Alcoholic neuropathy is clinicopathologically distinct from thiamine‐deficiency neuropathy

H Koike, M Iijima, M Sugiura, K Mori… - Annals of …, 2003 - Wiley Online Library
Characteristics of alcoholic neuropathy have been obscured by difficulty in isolating them
from features of thiamine‐deficiency neuropathy. We assessed 64 patients with alcoholic …

Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas

H Koike, F Tanaka, R Hashimoto, M Tomita… - Journal of Neurology …, 2012 - jnnp.bmj.com
Objective The objective of this study was to elucidate the natural history of late-onset
transthyretin Val30Met-associated familial amyloid polyneuropathy (FAP ATTR Val30Met) in non-…

The wide spectrum of clinical manifestations in Sjögren's syndrome-associated neuropathy

K Mori, M Iijima, H Koike, N Hattori, F Tanaka… - Brain, 2005 - academic.oup.com
We assessed the clinicopathological features of 92 patients with primary Sjögren's
syndrome-associated neuropathy (76 women, 16 men, 54.7 years, age at onset). The majority of …

Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease

D Adams, H Koike, M Slama, T Coelho - Nature Reviews Neurology, 2019 - nature.com
Hereditary amyloidogenic transthyretin (ATTRv) amyloidosis with polyneuropathy (also known
as familial amyloid polyneuropathy) is a condition with adult onset caused by mutation of …

Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early-vs late-onset form

H Koike, K Misu, S Ikeda, Y Ando… - Archives of …, 2002 - jamanetwork.com
Background Type I (transthyretin Met30) familial amyloid polyneuropathy (FAP TTR Met30)
occurs in 2 endemic foci in Japan. We have also reported late-onset Japanese cases …

Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of …

N Hattori, M Yamamoto, T Yoshihara, H Koike… - Brain, 2003 - academic.oup.com
Three genes commonly causing Charcot–Marie–Tooth disease (CMT) encode myelin‐related
proteins: peripheral myelin protein 22 (PMP22), myelin protein zero (MPZ) and connexin …

Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease

…, A Fujita, T Mizuguchi, K Hamanaka, K Mori, H Koike… - Nature …, 2019 - nature.com
Neuronal intranuclear inclusion disease (NIID) is a progressive neurodegenerative disease
that is characterized by eosinophilic hyaline intranuclear inclusions in neuronal and somatic …

Paranodal dissection in chronic inflammatory demyelinating polyneuropathy with anti-neurofascin-155 and anti-contactin-1 antibodies

H Koike, M Kadoya, K Kaida, S Ikeda… - Journal of Neurology …, 2017 - jnnp.bmj.com
Objective To investigate the morphological features of chronic inflammatory demyelinating
polyneuropathy (CIDP) with autoantibodies directed against paranodal junctional molecules, …

Diagnosis of sporadic transthyretin Val30Met familial amyloid polyneuropathy: a practical analysis

H Koike, R Hashimoto, M Tomita, Y Kawagashira… - Amyloid, 2011 - Taylor & Francis
Transthyretin (TTR) Val30Met-associated familial amyloid polyneuropathy (FAP ATTR
Val30Met) is the most common form of FAP and is now prevalent in areas other than those seen …

Clinicopathological features of adult-onset neuronal intranuclear inclusion disease

…, S Yokoi, K Araki, T Kato, T Nakamura, H Koike… - Brain, 2016 - academic.oup.com
Neuronal intranuclear inclusion disease (NIID) is a slowly progressive neurodegenerative
disease characterized by eosinophilic hyaline intranuclear inclusions in the central and …