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Profil bibliographique

Zhenhua Xie

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

6Publications signalées
54Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Cardiac electrophysiology and arrhythmiasHydrology and Watershed Management StudiesGroundwater and Isotope GeochemistryIon channel regulation and functionCardiomyopathy and Myosin Studies

Les publications récentes

Accès ouvert 2025 article OpenAlex

The deletion of the EP402R and MGF505/360 genes attenuates a genotype I/II recombinant ASFV but fails to confer complete protection against homologous or genotype II challenge in pigs

Yao Li, Yingnan Liu, Zhuyun Sun, Zhenhua Xie et autres

African swine fever (ASF), a pig disease caused by ASFV, is highly contagious and often lethal. The recent emergence of novel ASFV with I/II genomic recombination has posed significant challenges to global ASF prevention and control. In this study, we used the …

cn, gb (code pays fourni par la source)

5 citations Emerging Microbes & Infections
Accès ouvert 2024 article OpenAlex

Cardiomyopathy in children: a single-centre, retrospective study of genetic and clinical characteristics

Qiqing Sun, Jun Feng Guo, Yaodong Zhang, Ruili Zheng et autres

Objectives This study aimed to describe the genetic and clinical characteristics of paediatric cardiomyopathy in a cohort of Chinese patients. Methods We retrospectively reviewed the clinical history and mutation spectrum of 75 unrelated Chinese paediatric patients who were diagnosed with cardiomyopathy and …

cn (code pays fourni par la source)

6 citations BMJ Paediatrics Open
Accès ouvert 2023 article OpenAlex

Case report of a child with long QT syndrome type 14 caused by CALM1 gene mutation and literature review

Qiqing Sun, Zhenhua Xie, Fangjie Wang, Jun Guo et autres

OBJECTIVE: To analyze the clinical and genetic characteristics of a patient with long QT syndrome type 14 (long QT syndrome-14, LQT14, OMIM # 616247) caused by a de novo CALM1 mutation. METHODS: The clinical data of the patient were collected, next-generation sequencing …

cn (code pays fourni par la source)

2 citations Molecular Genetics & Genomic Medicine
2023 article OpenAlex

[Clinical characteristics and genetic analysis of a child with Galactosemia due to compound heterozygous variants of GALT gene].

Zhenhua Xie, Jing Liu, Xian Li, Mengjun Xiao et autres

OBJECTIVE: To explore the clinical features and genetic basis of a child with Galactosemia. METHODS: A child who had presented at the Children's Hospital Affiliated to Zhengzhou University on November 20, 2019 was selected as the study subject. Clinical data of the …

cn (code pays fourni par la source)

0 citations PubMed

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