Guanghuan Pi

Chengdu, China

Last Updated: 09/26/2026

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Found 10 publications

Efficacy and safety of inhaled ambroxol hydrochloride solution in Chinese pediatric patients with acute lower respiratory tract infections: a real-world, multicenter, open-label, single-arm study.

Efficacy and safety of inhaled ambroxol hydrochloride solution in Chinese pediatric patients with acute lower respiratory tract infections: a real-world, multicenter, open-label, single-arm study.

Journal: Translational pediatrics

Published: February 26, 2026

Genetic analysis of partial duplication of the long arm of chromosome 16.

Genetic analysis of partial duplication of the long arm of chromosome 16.

Journal: BMC medical genomics

Published: September 10, 2024

Clinical characterization and genetic analysis of transient abnormal myelopoiesis without the down syndrome phenotype.

Clinical characterization and genetic analysis of transient abnormal myelopoiesis without the down syndrome phenotype.

Journal: Molecular genetics and metabolism reports

Published: August 21, 2024

Genotype-phenotype correlation of ODLURO syndrome comorbid epilepsy associated with KMT2E variations: Report on a novel case and systematic literature review.

Genotype-phenotype correlation of ODLURO syndrome comorbid epilepsy associated with KMT2E variations: Report on a novel case and systematic literature review.

Journal: Epilepsy & behavior : E&B

Published: August 11, 2024

Prenatal diagnosis of monozygotic twins with phenotypic differences in chromosome 17q12 deletion syndrome.

Prenatal diagnosis of monozygotic twins with phenotypic differences in chromosome 17q12 deletion syndrome.

Journal: Journal of clinical ultrasound : JCU

Published: July 08, 2024

The impact of the COVID-19 pandemic on RSV outbreaks in children: A multicenter study from China.

The impact of the COVID-19 pandemic on RSV outbreaks in children: A multicenter study from China.

Journal: Respiratory medicine

Published: March 18, 2024

Genetic Analysis of De Novo Variants in KMT2A mixed-lineage leukemia Identified in a Family of Wiedermann-Steiner Syndromes.

Genetic Analysis of De Novo Variants in KMT2A mixed-lineage leukemia Identified in a Family of Wiedermann-Steiner Syndromes.

Journal: Annals of Indian Academy of Neurology

Published: February 14, 2024

Rubinstein-Taybi syndrome with ganglioneuroblastoma: a case report and literature review.

Rubinstein-Taybi syndrome with ganglioneuroblastoma: a case report and literature review.

Journal: BMC pediatrics

Published: February 09, 2024

Proximal 4p Deletion Syndrome in an Infant With Multiple Systemic Anomalies.

Proximal 4p Deletion Syndrome in an Infant With Multiple Systemic Anomalies.

Journal: Molecular genetics & genomic medicine

Published: December 07, 2023

Effect of intrauterine infection on brain development and injury.

Effect of intrauterine infection on brain development and injury.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: May 31, 2013

Showing 1-10 of 10

Last Updated: 09/26/2026