Hiroko Yanagisawa
Overview
Explore the profile of Hiroko Yanagisawa including associated specialties, affiliations and a list of published articles.
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Articles
22
Citations
234
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Recent Articles
1.
Miyajima T, Saito R, Yanagisawa H, Igarashi M, Wu C, Iwamoto T, et al.
J Inherit Metab Dis
. 2022 Oct;
46(1):143-152.
PMID: 36220782
Fabry disease (FD) is an X-linked inherited lysosomal metabolism disorder in which globotriaosylceramide (Gb3) accumulates in various organs resulting from a deficiency in alpha-galactosidase A. The clinical features of FD...
2.
Miyabayashi T, Sato R, Okubo Y, Endo W, Inui T, Togashi N, et al.
Brain Dev
. 2022 Jul;
44(8):592-593.
PMID: 35864002
No abstract available.
3.
Hossain M, Wu C, Yanagisawa H, Miyajima T, Akiyama K, Eto Y
Mol Genet Metab Rep
. 2019 Aug;
20:100497.
PMID: 31372342
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of α-galactosidase A (α-gal A). The clinical variability of the phenotypes of Fabry disease in females is still...
4.
Yanagisawa H, Hossain M, Miyajima T, Nagao K, Miyashita T, Eto Y
Mol Genet Metab
. 2019 Mar;
126(4):460-465.
PMID: 30871880
Lysosomes are an essential organ for cellular metabolism and play an important role in autophagy. We examined the association between methylation and autophagy in a severely affected female patient with...
5.
Itagaki R, Endo M, Yanagisawa H, Hossain M, Akiyama K, Yaginuma K, et al.
Mol Genet Metab
. 2018 Mar;
124(1):64-70.
PMID: 29599076
We first characterized PPT1 and TPP1 enzymes in dried blood spots (DBS), plasma/serum, and leukocytes/lymphocytes using neuronal ceroid lipofuscinosis (NCL) 1 and 2 patients and control subjects. PPT1 enzyme had...
6.
Okada J, Hossain M, Wu C, Miyajima T, Yanagisawa H, Akiyama K, et al.
Mol Genet Metab Rep
. 2018 Jan;
14:68-72.
PMID: 29326878
Fabry disease is an X-linked lysosomal storage disorder caused by a deficiency of α-galactosidase A (α-gal A), leading to the progressive accumulation of glycosphingolipids. Classical hemizygous males usually present symptoms,...
7.
Yanagisawa H, Ishii T, Endo K, Kawakami E, Nagao K, Miyashita T, et al.
Sci Rep
. 2017 Nov;
7(1):15944.
PMID: 29162837
Lysosomal storage disorders are characterized by progressive accumulation of undigested macromolecules within the cell due to lysosomal dysfunction. 573C10 is a Schwann cell line derived from a mouse model of...
8.
Wu C, Iwamoto T, Igarashi J, Miyajima T, Hossain M, Yanagisawa H, et al.
Mol Genet Metab Rep
. 2017 Jul;
12:115-118.
PMID: 28725571
X-linked adrenoleukodystrophy (X-ALD) is a rare inherited metabolic disease that results in the accumulation of very long chain fatty acids (VLCFA) in plasma and all tissues. Recent studies regarding cerebral...
9.
Hossain M, Yanagisawa H, Miyajima T, Wu C, Takamura A, Akiyama K, et al.
Mol Genet Metab
. 2017 Jan;
120(3):173-179.
PMID: 28087245
Heterozygous Fabry females usually have an attenuated form of Fabry disease, causing them to be symptomatic; however, in rare cases, they can present with a severe phenotype. In this study,...
10.
Kimura-Kuroda J, Nishito Y, Yanagisawa H, Kuroda Y, Komuta Y, Kawano H, et al.
Int J Environ Res Public Health
. 2016 Oct;
13(10).
PMID: 27782041
Neonicotinoids are considered safe because of their low affinities to mammalian nicotinic acetylcholine receptors (nAChRs) relative to insect nAChRs. However, because of importance of nAChRs in mammalian brain development, there...