Takashi Matsukawa
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Explore the profile of Takashi Matsukawa including associated specialties, affiliations and a list of published articles.
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Articles
178
Citations
1413
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Recent Articles
1.
Sugiyama A, Nakagawa Y, Mukai H, Yokota H, Oda F, Yamaguchi A, et al.
J Neurol Sci
. 2025 Mar;
472:123444.
PMID: 40056872
No abstract available.
2.
Matsukawa T, Sudo A, Kakumoto T, Hao A, Kainaga M, Chang H, et al.
Hum Genome Var
. 2025 Feb;
12(1):5.
PMID: 40021620
Adrenoleukodystrophy (ALD), an X-linked leukodystrophy caused by pathogenic variants in ABCD1, exhibits a broad range of phenotypes from childhood-onset cerebral forms to adult-onset adrenomyeloneuropathy (AMN). We report a rare in-frame...
3.
Mitsutake A, Matsukawa T, Hino R, Fujino G, Sakai Y, Mitsui J, et al.
Intern Med
. 2025 Feb;
PMID: 39894496
Objective Spastic paraplegia 7 (SPG7) is an autosomal recessive neurodegenerative disorder caused by biallelic pathogenic variants in SPG7. It is predominantly characterized by adult-onset slowly progressive spastic paraparesis. While SPG7...
4.
Okubo S, Orimo K, Matsukawa T, Hamada M, Satake W, Mitsui J, et al.
J Neurol Sci
. 2025 Jan;
469():123391.
PMID: 39793471
Introduction: Patients with neurodegenerative disorders resulting in progressive dysphagia often require gastrostomy. Pulmonary function tests (PFTs) are crucial in presurgical evaluation; however, reports on pulmonary function in multiple system atrophy...
5.
Mitsutake A, Kawai M, Orimo K, Matsukawa T, Ishiura H, Mitsui J, et al.
Cerebellum
. 2024 Dec;
24(1):20.
PMID: 39730866
Variants in KIF1A are associated with hereditary spastic paraplegia (SPG30), which can manifest in both pure and complex forms. We describe a Japanese family with a novel KIF1A variant presenting...
6.
Kotoda Y, Hishiyama S, Shim J, Kobayashi H, Takamino A, Abe M, et al.
Drug Des Devel Ther
. 2024 Dec;
18:6199-6208.
PMID: 39722682
Purpose: Corneal pain is one of the most common eye symptoms caused by various types of epithelial injuries, including traumatic abrasion, chemical injury, ulcers, ultraviolet exposure, and infection. However, current...
7.
Okubo S, Naruse H, Ishiura H, Sudo A, Esaki K, Mitsui J, et al.
J Neurol
. 2024 Dec;
272(1):36.
PMID: 39666121
Introduction: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder of the motor system. Pathogenic variants in SPTLC1, encoding a subunit of serine palmitoyltransferase, cause hereditary sensory and autonomic neuropathy...
8.
Miyano R, Mitsutake A, Matsukawa T, Obata S, Koyama H, Nakai Y, et al.
Intern Med
. 2024 Dec;
PMID: 39662915
We herein report a 26-year-old man diagnosed with Wilson's disease (WD), initially treated for schizophrenia for 11 years. At 26 years old, he was admitted because of status epilepticus. Brain...
9.
Yamada M, Nakadate Y, Omiya K, Oguchi T, Abe M, Matsukawa T
Steroids
. 2024 Nov;
213:109542.
PMID: 39613131
Purpose: S-equol, an isoflavone metabolite with high estrogenic activity, exhibits organ-protective effects via the phosphatidylinositol 3-kinase/protein kinase B (PI3K/Akt) signaling pathway. While estrogen has cardioprotective effects against ischemia-reperfusion injury, whether...
10.
Kakumoto T, Orimo K, Matsukawa T, Mitsui J, Ishihara T, Onodera O, et al.
Eur J Hum Genet
. 2024 Nov;
33(3):325-333.
PMID: 39604554
Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic nervous system dysfunction and cerebellar ataxia or parkinsonism. Recently, expanded GAA repeats (≥250 repeat units) in intron 1 of...