Xiru R. Wu

Beijing, 100081, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 83 publications

Analysis of clinical characteristics and factors associated with mortality in hematological patients infected with Stenotrophomonas maltophilia

Analysis of clinical characteristics and factors associated with mortality in hematological patients infected with Stenotrophomonas maltophilia

Journal: Zhonghua yi xue za zhi

Published: March 08, 2026

Analysis of primary teeth crown dimensions and dental arch physiological data of individual normal occlusion children in 67 children of 3.5-4.5 years of age

Analysis of primary teeth crown dimensions and dental arch physiological data of individual normal occlusion children in 67 children of 3.5-4.5 years of age

Journal: Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology

Published: November 27, 2025

Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.

Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.

Journal: Orphanet journal of rare diseases

Published: May 07, 2021

Kenneth Swaiman and His Role in the Development of Child Neurology in China.

Kenneth Swaiman and His Role in the Development of Child Neurology in China.

Journal: Pediatric neurology

Published: April 26, 2021

Analysis of caries experience and the dental treatments under general anesthesia in 103 cases of children with autism spectrum disorders

Analysis of caries experience and the dental treatments under general anesthesia in 103 cases of children with autism spectrum disorders

Journal: Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology

Published: September 04, 2020

Clinical phenotypes of epilepsy associated with GABRA1 gene variants

Clinical phenotypes of epilepsy associated with GABRA1 gene variants

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: February 27, 2020

Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular Dystrophies.

Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular Dystrophies.

Journal: Biochemical genetics

Published: January 22, 2020

MECP2 mutation spectrum and its clinical characteristics in a Chinese cohort.

MECP2 mutation spectrum and its clinical characteristics in a Chinese cohort.

Journal: Clinical genetics

Published: December 27, 2019

Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients.

Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients.

Journal: Journal of medical genetics

Published: November 01, 2019

Clinical characteristics of PCDH19-female limited epilepsy

Clinical characteristics of PCDH19-female limited epilepsy

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: November 01, 2019

A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients.

A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients.

Journal: Clinical genetics

Published: October 30, 2019

CHD2-related epilepsy: novel mutations and new phenotypes.

CHD2-related epilepsy: novel mutations and new phenotypes.

Journal: Developmental medicine and child neurology

Published: August 21, 2019

Showing 1-12 of 83

Last Updated: 09/26/2026