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PubPharm (21)
1
Comparison of Mental Health among Japanese Healthcare Workers at Two Points during the COVID-19 Pandemic
enthalten in:
Journal of Nippon Medical School = Nippon Ika Daigaku zasshi
| 2022
von
Awano, N.
|
Oyama, N.
|
Akiyama, K.
| +9
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2
Anxiety, Depression, and Resilience of Healthcare Workers in Japan During the Coronavirus Disease 2019 Outbreak
enthalten in:
Internal medicine (Tokyo, Japan)
| 2020
von
Awano, N.
|
Oyama, N.
|
Akiyama, K.
| +12
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3
A combination of 7-ketocholesterol, lysosphingomyelin and bile acid-408 to diagnose Niemann-Pick disease type C using LC-MS/MS
enthalten in:
PloS one
| 2020
von
Wu, C.
|
Iwamoto, T.
|
Hossain, M.
| +4
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4
Future clinical and biochemical predictions of Fabry disease in females by methylation studies of the GLA gene
enthalten in:
Molecular genetics and metabolism reports
| 2019
von
Hossain, M.
|
Wu, C.
|
Yanagisawa, H.
| +3
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5
A Case of Adult-onset Pompe Disease with Cerebral Stroke and Left Ventricular Hypertrophy
enthalten in:
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
| 2018
von
Hossain, M.
|
Miyajima, T.
|
Akiyama, K.
| +1
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6
Characteristics of PPT1 and TPP1 enzymes in neuronal ceroid lipofuscinosis (NCL) 1 and 2 by dried blood spots (DBS) and leukocytes and their application to newborn screening
enthalten in:
Molecular genetics and metabolism
| 2018
von
Itagaki, R.
|
Endo, M.
|
Yanagisawa, H.
| +13
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7
Ten-year-long enzyme replacement therapy shows a poor effect in alleviating giant leg ulcers in a male with Fabry disease
enthalten in:
Molecular genetics and metabolism reports
| 2018
von
Okada, J.
|
Hossain, M.
|
Wu, C.
| +4
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8
L-leucine and SPNS1 coordinately ameliorate dysfunction of autophagy in mouse and human Niemann-Pick type C disease
enthalten in:
Scientific reports
| 2017
von
Yanagisawa, H.
|
Ishii, T.
|
Endo, K.
| +8
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9
Application of a diagnostic methodology by quantification of 26:0 lysophosphatidylcholine in dried blood spots for Japanese newborn screening of X-linked adrenoleukodystrophy
enthalten in:
Molecular genetics and metabolism reports
| 2017
von
Wu, C.
|
Iwamoto, T.
|
Igarashi, J.
| +6
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10
The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome
enthalten in:
Molecular genetics and metabolism
| 2017
von
Hossain, M.
|
Yanagisawa, H.
|
Miyajima, T.
| +10
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Internal medicine (Tokyo, Japan)
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Research Support, Non-U.S. Gov't
2
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Gb3, globotriaosylceramide
2
Membrane Proteins
2
Methylation
2
anxiety
2
coronavirus disease 2019
2
depression
2
healthcare worker
2
resilience
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α-Galactosidase A
2
α-gal A, α-galactosidase A
1
10216-23-6
1
107-73-3
1
15FIX9V2JP
1
20:0 LysoPC, 20:0 lysophosphatidylcholine
1
24:0 LysoPC, 24:0 lysophosphatidylcholine
1
26:0 LysoPC, 26:0 lysophosphatidylcholine
1
26:0-d4 LysoPC, 26:0-d4 lysophosphatidylcholine
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