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Ginsenoside Rg3 inhibits pulmonary fibrosis by preventing HIF-1α nuclear localisation

BMC pulmonary medicine, 2021-02, Vol.21 (1), p.70-70, Article 70

2021

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Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida

Human mutation, 2020-04, Vol.41 (4), p.786-799

2020

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Retraction Note: Immune characteristics of children with autoimmune encephalitis and the correlation with a short-term prognosis

Italian journal of pediatrics, 2023-12, Vol.49 (1), p.163-163, Article 163

2023

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Immune characteristics of children with autoimmune encephalitis and the correlation with a short-term prognosis

Italian journal of pediatrics, 2022-06, Vol.48 (1), p.94-94

2022

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Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway

Italian journal of pediatrics, 2019-03, Vol.45 (1), p.37-37, Article 37

2019

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Discovery of specific mutations in spinal muscular atrophy patients by next-generation sequencing

Neurological sciences, 2021-05, Vol.42 (5), p.1827-1833

2021

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A Novel Two-Nucleotide Deletion of MMADHC Gene Causing cblD Disease in a Chinese Family

Chinese medical journal, 2018-10, Vol.131 (20), p.2477-2479

2018

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A unique methylation pattern co-segregates with neural tube defect statuses in Han Chinese pedigrees

Neurological sciences, 2017-12, Vol.38 (12), p.2153-2164

2017

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Identification of novel rare mutations of DACT1 in human neural tube defects

Human mutation, 2012-10, Vol.33 (10), p.1450-1455

2012

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Choroid Plexus Papilloma of Bilateral Lateral Ventricle in an Infant Conceived by in vitro Fertilization

Pediatric neurosurgery, 2018-01, Vol.53 (6), p.401-406

2018

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The Clinical and Imaging Characteristics Associated With Neurological Sequelae of Pediatric Patients With Acute Necrotizing Encephalopathy

Frontiers in pediatrics, 2021-05, Vol.9, p.655074-655074

2021

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Vein of Galen Aneurysmal Malformation: An Updated Review

Journal of pediatric neurology, 2019-04, Vol.17 (2), p.45-56

2019

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RETRACTED ARTICLE: Immune characteristics of children with autoimmune encephalitis and the correlation with a short-term prognosis

Italian journal of pediatrics, 2022-06, Vol.48 (1), p.1-8, Article 94

2022

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Intracranial Medulloepithelioma in a Child: A Case Report

Turkish neurosurgery, 2019-01, Vol.29 (6), p.957-960

2019

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A novel mutation in a common pathogenic gene (SETD5) associated with intellectual disability: A case report

Experimental and therapeutic medicine, 2019-11

2019

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Polymorphisms in FZD3 and FZD6 genes and risk of neural tube defects in a northern Han Chinese population

Neurological sciences, 2014-11, Vol.35 (11), p.1701-1706

2014

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Immature teratoma of the posterior fossa in an infant: case report

Turk Pediatri Arsivi, 2019

Cai, Chun-Quan

2019

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Accessory Penis and Scrotum in a Male Infant

Journal of child science, 2017-01, Vol.7 (1), p.e24-e26

2017

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Clinical phenotype, gene mutation and application of targeted next generation sequencing in patients with early-onset epileptic encephalopathy

Zhongguo xian dai shen jing ji bing za zhi, 2018-06, Vol.18 (6), p.428

2018

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Neuroimages of persistent falcine sinus in children

World journal of pediatrics : WJP, 2009-02, Vol.5 (1), p.63-64

2009

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Primary intraspinal primitive neuroectodermal tumor: A case report and review of literature

Journal of pediatric neurosciences, 2008-07, Vol.3 (2), p.154

2008

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Ginsenoside Rg3 inhibits pulmonary fibrosis by preventing HIF-1[alpha] nuclear localisation

BMC pulmonary medicine, 2021-02, Vol.21 (1)

2021

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Importance of endomyocardial biopsy in unexplained cardiomyopathy in China： a report of 53 consecutive patients

Chinese medical journal, 2010-04, Vol.123 (7), p.864-870

2010

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Clinical phenotype, gene mutation and application of targeted next generation sequencing in patients with early-onset epileptic encephalopathy

Zhongguo xian dai shen jing ji bing za zhi, 2018-06, Vol.18 (6), p.428-437

2018

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The Author reply

World journal of pediatrics : WJP, 2009-08, Vol.5 (3), p.234-234

2009

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Ginsenoside Rg3 inhibits pulmonary fibrosis by preventing HIF-1α nuclear localisation

Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida

Retraction Note: Immune characteristics of children with autoimmune encephalitis and the correlation with a short-term prognosis

Immune characteristics of children with autoimmune encephalitis and the correlation with a short-term prognosis

Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway

Discovery of specific mutations in spinal muscular atrophy patients by next-generation sequencing

A Novel Two-Nucleotide Deletion of MMADHC Gene Causing cblD Disease in a Chinese Family

A unique methylation pattern co-segregates with neural tube defect statuses in Han Chinese pedigrees

Identification of novel rare mutations of DACT1 in human neural tube defects

Choroid Plexus Papilloma of Bilateral Lateral Ventricle in an Infant Conceived by in vitro Fertilization

The Clinical and Imaging Characteristics Associated With Neurological Sequelae of Pediatric Patients With Acute Necrotizing Encephalopathy

Vein of Galen Aneurysmal Malformation: An Updated Review

RETRACTED ARTICLE: Immune characteristics of children with autoimmune encephalitis and the correlation with a short-term prognosis

Intracranial Medulloepithelioma in a Child: A Case Report

A novel mutation in a common pathogenic gene (SETD5) associated with intellectual disability: A case report

Polymorphisms in FZD3 and FZD6 genes and risk of neural tube defects in a northern Han Chinese population

Immature teratoma of the posterior fossa in an infant: case report

Accessory Penis and Scrotum in a Male Infant

Clinical phenotype, gene mutation and application of targeted next generation sequencing in patients with early-onset epileptic encephalopathy

Neuroimages of persistent falcine sinus in children

Primary intraspinal primitive neuroectodermal tumor: A case report and review of literature

Ginsenoside Rg3 inhibits pulmonary fibrosis by preventing HIF-1[alpha] nuclear localisation

Importance of endomyocardial biopsy in unexplained cardiomyopathy in China： a report of 53 consecutive patients

Clinical phenotype, gene mutation and application of targeted next generation sequencing in patients with early-onset epileptic encephalopathy

The Author reply

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