N. Sasagasako

发表

Relationship between tongue pressure and functional oral intake scale diet type in patients with neurological and neuromuscular disorders

H. Furuya, Y. Tsuboi, N. Sakae, 2020, Clinical Neurology and Neurosurgery.

The synthetic pathway for glucosylsphingosine in cultured fibroblasts.

I. Goto, Y. Yamaguchi, T. Kobayashi, 1994, Journal of biochemistry.

PCBP2 Is Downregulated in Degenerating Neurons and Rarely Observed in TDP-43-Positive Inclusions in Sporadic Amyotrophic Lateral Sclerosis.

Satoshi O. Suzuki, T. Iwaki, J. Kira, 2020, Journal of neuropathology and experimental neurology.

Amyotrophic lateral sclerosis with TDP‐43 abnormalities exhibiting globular glial tau inclusions in frontotemporal lobes and pallido‐nigral system

H. Honda, H. Noguchi, Sachiko Koyama, 2022, Neuropathology : official journal of the Japanese Society of Neuropathology.

Transactivation response DNA‐binding protein of 43 kDa proteinopathy and lysosomal abnormalities in spastic paraplegia type 11

Satoshi O. Suzuki, T. Iwaki, T. Taniwaki, 2021, Neuropathology : official journal of the Japanese Society of Neuropathology.

Chronological Changes in the Expression Pattern of Hippocampal Prion Proteins During Disease Progression in Sporadic Creutzfeldt-Jakob Disease MM1 Subtype.

T. Ninomiya, Y. Oda, S. Aishima, 2022, Journal of neuropathology and experimental neurology.

[An autopsy case of amyotrophic lateral sclerosis with ampulla cardiomyopathy].

T. Iwaki, J. Kira, T. Koga, 2008, Rinsho shinkeigaku = Clinical neurology.

Frequent Detection of Pituitary-Derived PrPres in Human Prion Diseases.

Satoshi O. Suzuki, T. Iwaki, K. Nakayama, 2019, Journal of neuropathology and experimental neurology.

Neuropathology of classic myotonic dystrophy type 1 is characterized by both early initiation of primary age-related tauopathy of the hippocampus and unique 3-repeat tauopathy of the brainstem.

T. Iwaki, H. Honda, H. Arahata, 2022, Journal of neuropathology and experimental neurology.

DCTN1 F52L mutation case of Perry syndrome with progressive supranuclear palsy-like tauopathy.

Satoshi O. Suzuki, T. Iwaki, Y. Tsuboi, 2018, Parkinsonism & related disorders.

Four‐repeat tau dominant pathology in a congenital myotonic dystrophy type 1 patient with mental retardation

T. Iwaki, H. Honda, N. Fujii, 2018, Brain pathology.

Evidence for Regulation of Myelin Protein Synthesis by Contact between Adjacent Schwann Cell Plasma Membranes

R. Quarles, N. Sasagasako, Masaharu Ohno, 2000, Developmental Neuroscience.

Myelin Gene Expression in Immortalized Schwann Cells: Relationship to Cell Density and Proliferation

R. Quarles, K. Toda, N. Sasagasako, 1996, Journal of neurochemistry.

Early and extensive alterations of glial connexins, distal oligodendrogliopathy type demyelination, and nodal/paranodal pathology are characteristic of multiple system atrophy

T. Iwaki, J. Kira, R. Yamasaki, 2022, Brain pathology.

A CASE OF STIFF-MAN SYNDROME IN A MAN WITH BREAST CANCER

T. Ezaki, E. Mori, A. Matsukuma, 2007 .

Glucosylceramide and glucosylsphingosine metabolism in cultured fibroblasts deficient in acid beta-glucosidase activity.

I. Goto, Y. Yamaguchi, N. Shinnoh, 1994, Journal of biochemistry.

Novel missense mutations in the human lysosomal sialidase gene in sialidosis patients and prediction of structural alterations of mutant enzymes

A. Pshezhetsky, H. Doi, J. Kira, 2002, Journal of Human Genetics.

Mutated FUS in familial amyotrophic lateral sclerosis involves multiple hnRNPs in the formation of neuronal cytoplasmic inclusions.

H. Honda, H. Arahata, H. Noguchi, 2023, Journal of neuropathology and experimental neurology.

Expanded polyglutamine impairs normal nuclear distribution of fused in sarcoma and poly (rC)‐binding protein 1 in Huntington's disease

Satoshi O. Suzuki, T. Iwaki, T. Taniwaki, 2019, Neuropathology : official journal of the Japanese Society of Neuropathology.

Symmetrical glial hyperplasia in the brainstem of fibrodysplasia ossificans progressiva

Satoshi O. Suzuki, T. Iwaki, H. Furuya, 2021, Neuropathology : official journal of the Japanese Society of Neuropathology.

Echocardiography versus (201)Tl semi-quantitative gated single photon emission tomography for the evaluation of cardiac disease associated with late stage Duchenne muscular dystrophy.

A. Watanabe, N. Fujii, H. Arahata, 2016, Hellenic journal of nuclear medicine.

Abnormal prion protein deposits with high seeding activities in the skeletal muscle, femoral nerve, and scalp of an autopsied case of sporadic Creutzfeldt–Jakob disease

T. Iwaki, A. Watanabe, K. Satoh, 2021, Neuropathology : official journal of the Japanese Society of Neuropathology.

Characteristic distribution and molecular properties of normal cellular prion protein in human endocrine and exocrine tissues

H. Honda, H. Noguchi, Hideomi Hamasaki, 2022, Scientific Reports.

Dynactin is involved in Lewy body pathology

Satoshi O. Suzuki, T. Iwaki, H. Honda, 2018, Neuropathology : official journal of the Japanese Society of Neuropathology.

P.11 Percutaneous endoscopic gastrostomy in patients with Duchenne muscular dystrophy compared with amyotrophic lateral sclerosis and Parkinson syndrome

N. Fujii, H. Arahata, A. Miyoshi, 2017, Neuromuscular Disorders.

Silence of resident microglia in GPI anchorless prion disease and activation of microglia in Gerstmann-Sträussler-Scheinker disease and sporadic Creutzfeldt-Jakob disease.

S. Aishima, K. Kai, H. Honda, 2022, Journal of neuropathology and experimental neurology.

Echocardiography versus Tl semi-quantitative gated single photon emission tomography for the evaluation of cardiac disease associated with late stage Duchenne muscular dystrophy

A. Watanabe, N. Fujii, H. Arahata, 2016 .

Ribosomal protein SA is a common component of neuronal intranuclear inclusions in polyglutamine diseases and Marinesco bodies.

H. Honda, H. Noguchi, Hideomi Hamasaki, 2023, Neuropathology : official journal of the Japanese Society of Neuropathology.

Prenatal diagnosis of congenital sialidosis

N. Shinnoh, T. Kobayashi, N. Sasagasako, 1993, Clinical genetics.

Increased expression of human antiviral protein MxA in FUS proteinopathy in amyotrophic lateral sclerosis.

H. Honda, H. Arahata, H. Noguchi, 2023, Brain pathology.

Longitudinal Changes of Tongue Thickness and Tongue Pressure in Neuromuscular Disorders

H. Furuya, Y. Tsuboi, N. Sakae, 2020, BMC Neurology.