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PubPharm (16)
1
Clinical and genetic characterization of 47 Chinese pediatric patients with Pitt-Hopkins syndrome : a retrospective study
enthalten in:
Orphanet journal of rare diseases
| 2024
von
Zhao, T.
|
Wu, S.
|
Shen, Y.
| +4
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2
Clinical and genetic characterization of 47 Chinese pediatric patients with Pitt–Hopkins syndrome: a retrospective study
enthalten in:
Orphanet journal of rare diseases
| 2024
von
Zhao, T.
|
Wu, S.
|
Shen, Y.
| +4
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3
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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4
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...
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
Wird geladen...
6
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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7
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
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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
Wird geladen...
9
Correction to : Clinical features and treatment efficacy for IgG4-related thyroiditis
enthalten in:
Orphanet journal of rare diseases
| 2021
von
Han, X.
|
Zhang, P.
|
Li, J.
| +8
ErratumFor: Orphanet J Rare Dis. 2021 Jul 21;16(1):324. - PMID 34289855
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10
Correction to: Clinical features and treatment efficacy for IgG4-related thyroiditis
enthalten in:
Orphanet journal of rare diseases
| 2021
von
Han, X.
|
Zhang, P.
|
Li, J.
| +8
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Zeitschrift: Orphanet journal of rare diseases
Medienart
16
Aufsätze
16
E-Artikel
16
E-Ressourcen
Zeitschriftentitel
Orphanet journal of rare diseases
Thema
5
Journal Article
4
Rare disease
4
Research Support, Non-U.S. Gov't
4
Shanghai
3
C26: carnitine
3
Hexacosanoylcarnitine
3
Metabolomic signature
3
Newborn screening
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
t-SNE
2
China
2
Cost of illness
2
Developmental delay
2
Economic burden
Alle anzeigen ...
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Erscheinungszeitraum
14
2020-
2
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
16
Englisch
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