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/vufind/Search/Results?lookfor=%22Tian%2C+Guoli%22&type=Person&sort=year
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PubPharm (20)
1
Clinical analysis and genetic diagnosis of three children with Isoleucine metabolic disorders due to variants of HSD17B10 and ACAT1 genes
enthalten in:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
| 2024
von
Ji, W.
|
Tian, G.
|
Zhang, X.
| +4
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2
Comparative analysis of inherited metabolic diseases in normal newborns and high-risk children : Insights from a 10-year study in Shanghai
enthalten in:
Clinica chimica acta; international journal of clinical chemistry
| 2024
von
Zhang, X.
|
Ji, W.
|
Wang, Y.
| +3
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3
CD276-dependent efferocytosis by tumor-associated macrophages promotes immune evasion in bladder cancer
enthalten in:
Nature communications
| 2024
von
Cheng, M.
|
Chen, S.
|
Li, K.
| +19
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4
A prognostic model based on Scissor+ cancer associated fibroblasts identified from bulk and single cell RNA sequencing data in head and neck squamous cell carcinoma
enthalten in:
Cellular signalling
| 2024
von
Tian, G.
|
Zhang, J.
|
Bao, Y.
| +2
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5
Correction : Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Zhu, Z.
|
Genchev, G.
|
Wang, Y.
| +5
ErratumFor: Orphanet J Rare Dis. 2023 May 2;18(1):102. - PMID 37189159
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6
Correction: Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Zhu, Z.
|
Genchev, G.
|
Wang, Y.
| +5
Wird geladen...
7
Correction: Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Zhu, Z.
|
Genchev, G.
|
Wang, Y.
| +5
Wird geladen...
8
Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Zhu, Z.
|
Genchev, G.
|
Wang, Y.
| +5
ErratumIn: Orphanet J Rare Dis. 2023 Jun 15;18(1):150. - PMID 37322480
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9
Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Zhu, Z.
|
Genchev, G.
|
Wang, Y.
| +5
Wird geladen...
10
Multivariate analysis and model building for classifying patients in the peroxisomal disorders X-linked adrenoleukodystrophy and Zellweger syndrome in Chinese pediatric patients
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Zhu, Z.
|
Genchev, G.
|
Wang, Y.
| +5
Wird geladen...
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Zeitschriftentitel
6
Orphanet journal of rare diseases
3
Neurological sciences
2
Clinical biochemistry
1
Cellular signalling
1
Clinica chimica acta; international journal of ...
1
Frontiers in molecular biosciences
1
Nature communications
1
Neurological sciences : official journal of the...
1
The Journal of Dermatology
1
The Journal of dermatology
1
Zhejiang da xue xue bao. Yi xue ban = Journal o...
1
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Thema
9
Journal Article
4
L-2-hydroxyglutaric aciduria
4
Mutation
4
Newborn screening
4
Whole-exome sequencing
3
C26: carnitine
3
Case Reports
3
Hexacosanoylcarnitine
3
Metabolomic signature
3
PCA
3
PLS-DA
3
Sparse PLS-DA
3
Very long chain fatty acids
3
X-ALD
3
X-linked adrenoleukodystrophy
3
Zellweger syndrome
3
gene
3
t-SNE
2
Carnitine
2
Research Support, Non-U.S. Gov't
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Erscheinungszeitraum
14
2020-
6
2010-2019
Erscheinungsjahr(e)
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Sprache
17
Englisch
1
Chinesisch
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