Hitoshi Warita
Overview
Explore the profile of Hitoshi Warita including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
82
Citations
996
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Ishizuka Y, Oe Y, Kinomura S, Kin S, Noguchi Y, Kikuchi K, et al.
Intern Med
. 2025 Feb;
PMID: 39924244
AA amyloidosis is a rare renal complication of Waldenström's macroglobulinemia/lymphoplasmacytic lymphoma (WM/LPL). A 66-year-old man with WM/LPL presented with nephrotic syndrome. A renal biopsy showed AA amyloidosis. Chemotherapy resulted in...
2.
Nishiyama A, Niihori T, Suzuki N, Izumi R, Akiyama T, Kato M, et al.
Neurol Genet
. 2024 Nov;
10(6):e200196.
PMID: 39502740
Background And Objectives: Amyotrophic lateral sclerosis (ALS) is an adult-onset progressive neurodegenerative disease. Approximately 10% of ALS cases are familial, and more than 20 causative genes have been identified. As...
3.
Okada K, Ito D, Morimoto S, Kato C, Oguma Y, Warita H, et al.
Brain
. 2024 Sep;
147(11):3933-3948.
PMID: 39312484
Advanced pathological and genetic approaches have revealed that mutations in fused in sarcoma/translated in liposarcoma (FUS/TLS), which is pivotal for DNA repair, alternative splicing, translation and RNA transport, cause familial...
4.
Kirikae H, Harada R, Hosaka T, Misu T, Ando D, Warita H, et al.
F1000Res
. 2024 Sep;
11:546.
PMID: 39281332
We report a rare case of a vertebro-vertebral arteriovenous fistula (VVAVF) manifesting as amyotrophic lateral sclerosis (ALS). A 76-year-old female patient presented with progressive weakness, muscle atrophy, fasciculation, and preserved...
5.
Suzuki N, Kanzaki M, Koide M, Izumi R, Fujita R, Takahashi T, et al.
PLoS One
. 2024 Aug;
19(8):e0306021.
PMID: 39088432
Sporadic inclusion body myositis (sIBM) is a muscle disease in older people and is characterized by inflammatory cell invasion into intact muscle fibers and rimmed vacuoles. The pathomechanism of sIBM...
6.
Suzuki N, Mori-Yoshimura M, Katsuno M, Takahashi M, Yamashita S, Oya Y, et al.
J Neurol Neurosurg Psychiatry
. 2024 Jun;
95(11):1093-1094.
PMID: 38839274
No abstract available.
7.
Urushitani M, Warita H, Atsuta N, Izumi Y, Kano O, Shimizu T, et al.
Rinsho Shinkeigaku
. 2024 Mar;
64(4):252-271.
PMID: 38522911
Amyotrophic lateral sclerosis (ALS) is an adult-onset intractable motor neuron disease characterized by selective degeneration of cortical neurons in the frontotemporal lobe and motor neurons in the brainstem and spinal...
8.
Izumi R, Warita H, Niihori T, Furusawa Y, Nakano M, Oya Y, et al.
Cerebellum
. 2024 Feb;
23(4):1498-1508.
PMID: 38324175
Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS) is an autosomal recessive multisystem neurologic disorder caused by biallelic intronic repeats in RFC1. Although the phenotype of CANVAS has been expanding...
9.
Yamashita S, Takahashi Y, Hashimoto J, Murakami A, Nakamura R, Katsuno M, et al.
Ann Clin Transl Neurol
. 2024 Jan;
11(4):938-945.
PMID: 38287512
Objective: Multisystem proteinopathy (MSP) is an inherited disorder in which protein aggregates with TAR DNA-binding protein of 43 kDa form in multiple organs. Mutations in VCP, HNRNPA2B1, HNRNPA1, SQSTM1, MATR3,...
10.
Izumi R, Ikeda K, Niihori T, Suzuki N, Shirota M, Funayama R, et al.
Ann Clin Transl Neurol
. 2023 Dec;
11(3):577-592.
PMID: 38158701
Objective: Multisystem proteinopathy type 3 (MSP3) is an inherited, pleiotropic degenerative disorder caused by a mutation in heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1), which can affect the muscle, bone, and/or nervous...