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/vufind/Search/Results?lookfor=%22Song%2C+Deyu%22&type=Person&sort=year
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PubPharm (14)
1
Unilateral heliotrope rash : A call for recognizing its warning significance in anti-MDA5 antibody-associated dermatomyositis
enthalten in:
The Journal of dermatology
| 2024
von
Song, D.
|
Yi, Q.
|
Zhuang, K.
| +3
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2
A Child with Hoarseness and Recurrent Cheek Erosions : A Quiz
enthalten in:
Acta dermato-venereologica
| 2024
von
Song, D.
|
Wang, S.
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3
Epidermolytic ichthyosis caused by KRT10 parental cutaneous-gonadal mosaicism : a call for prospective genetic diagnosis
enthalten in:
International journal of dermatology
| 2023
von
Song, D.
|
Zhang, F.
|
Chen, Y.
| +2
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4
A retrospective study on VISIA of telangiectasia network in 378 cases of rosacea of the upper eyelid
enthalten in:
Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI)
| 2023
von
Yang, F.
|
Song, D.
|
Wang, L.
| +1
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5
One recurrent heterozygous mutation of the PLCD1 gene in a Chinese family with hereditary leukonychia : A case report and genotype-phenotype correlation analysis
enthalten in:
The Journal of dermatology
| 2023
von
Zhang, F.
|
Chen, Y.
|
Song, D.
| +1
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6
Clinical use of zinc in viral warts : a systematic review of the clinical trials
enthalten in:
The Journal of dermatological treatment
| 2022
von
Song, D.
|
Pan, L.
|
Zhang, M.
| +1
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7
A Cross-Sectional Study on the Relationship Between Rosacea Severity and Quality of Life or Psychological State
enthalten in:
Clinical, cosmetic and investigational dermatology
| 2022
von
Yang, F.
|
Zhang, Q.
|
Song, D.
| +3
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8
Novel deletion of the POFUT1 gene associated with multiple seborrheic keratosis Dowling-Degos disease
enthalten in:
The Journal of dermatology
| 2021
von
Chen, Y.
|
Li, Z.
|
Song, D.
| +1
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9
Recurrent c.459 C>A mutation of the PERP gene results in severe Olmsted syndrome with congenital hypotrichosis, atopic dermatitis, and growth retardation
enthalten in:
The Journal of dermatology
| 2021
von
Song, D.
|
Ran, X.
|
Chen, Y.
| +4
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10
Recurrent c.459 C>A mutation of the PERP gene results in severe Olmsted syndrome with congenital hypotrichosis, atopic dermatitis, and growth retardation
enthalten in:
The Journal of Dermatology
| 2021
von
Song, D.
|
Ran, X.
|
Chen, Y.
| +4
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