Suchergebnisse - "Xu, Xiaowei"

PubPharm (29)

1

Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region : a case report

enthalten in: Italian journal of pediatrics | 2022

von Wu, J. | Lei, M. | Wang, X. | +5

ErratumIn: Ital J Pediatr. 2023 Mar 20;49(1):32. - PMID 36941634

2

A de novo variant in CASK gene causing intellectual disability and brain hypoplasia : a case report and literature review

enthalten in: Italian journal of pediatrics | 2022

von Zhang, Y. | Nie, Y. | Mu, Y. | +5

3

Genetic analysis of 46,XY disorders of sex development in children caused by a new NR5A1 gene variant

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2021

von Gao, L. | Wang, P. | Zhang, M. | +6

4

Angiokeratoma-like purpuric palmar nodules following chemotherapy

enthalten in: Dermatology online journal | 2021

von Torre, E. | Kersh, A. | Fischer, A. | +3

5

Metastatic Melanoma With Features of Desmoplastic Melanoma in a Patient With Primary Cutaneous Superficial Spreading Melanoma With Epithelioid Features

enthalten in: The American Journal of dermatopathology | 2021

von Modi, M. | Moshiri, A. | Klein, W. | +3

6

A case of tumor-to-tumor metastasis of cutaneous malignant melanoma

enthalten in: Journal of cutaneous pathology | 2020

von Straker, R. | Modi, M. | Elder, D. | +4

7

Basal temporo-occipital mild malformation of cortical development with oligodendroglial hyperplasia : A multimodal investigation turning non-lesional to lesional epilepsy

enthalten in: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology | 2020

von Lin, Y. | Xu, X. | Aung, T. | +5

CommentIn: Clin Neurophysiol. 2021 Jan;132(1):154-156. - PMID 33278668

8

Clinical study using mesenchymal stem cells for the treatment of patients with severe COVID-19

enthalten in: Frontiers of medicine | 2020

von Tang, L. | Jiang, Y. | Zhu, M. | +16

9

A hydralazine-induced triumvirate : Lupus, cutaneous vasculitis, and cryptococcoid Sweet syndrome

enthalten in: JAAD case reports | 2019

von Skaljic, M. | Agarwal, A. | Smith, R. | +6

10

Mutation spectrum of MMACHC in Chinese pediatric patients with cobalamin C disease : A case series and literature review

enthalten in: European journal of medical genetics | 2019

von Wang, C. | Li, D. | Cai, F. | +9