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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes

Frontiers in genetics, 2021-05, Vol.12

2021

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Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients

Frontiers in genetics, 2020-03, Vol.11, p.126

2020

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Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid Lipofuscinosis

Frontiers in genetics, 2019-04, Vol.10, p.370

2019

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Neurological Abnormality Could be the First and Only Symptom of Familial Hemophagocytic Lymphohistiocytosis: Report of Two Families

Chinese medical journal, 2018-12, Vol.131 (24), p.3004-3006

2018

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Clinical Characteristics and Outcome Analysis of 94 Children With Brain Abscess in Beijing: A Single-center Retrospective Study

The Pediatric infectious disease journal, 2021-02, Vol.40 (2), p.109-115

2021

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Adrenocorticotropic hormone combined with magnesium sulfate therapy for infantile epileptic spasms syndrome: a real-world study

World journal of pediatrics : WJP, 2023-12

2023

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Epileptic seizure, as the first symptom of hypoparathyroidism in children, does not require antiepileptic drugs

Child's nervous system, 2017-02, Vol.33 (2), p.297-305

2017

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Risk Factors for Arterial Ischemic and Hemorrhagic Stroke in Childhood

Pediatric neurology, 2009-04, Vol.40 (4), p.277-281

2009

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Arterial Ischemic Stroke: Experience in Chinese Children

Pediatric neurology, 2008-03, Vol.38 (3), p.186-190

2008

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A Centralized Report on Pediatric Japanese Encephalitis Cases from Beijing Children's Hospital, 2013

Biomedical and environmental sciences, 2016-12, Vol.29 (12), p.902-908

2016

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Anti-N-methyl-D-aspartate receptor encephalitis in seven children

Zhonghua er ke za zhi, 2012-12, Vol.50 (12), p.885

2012

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Minor injury and basal ganglia calcification may be the risk factors of children's stroke

Zhonghua er ke za zhi, 2008-06, Vol.46 (6), p.475

2008

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Identification of the risk of breast cancer in patients suffering from endometriosis: A meta-analysis

Medical Theory and Hypothesis, 2023, Vol.6 (1), p.3

2023

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Association of three single nucleotide polymorphisms of ESR1 with breast cancer susceptibility：a meta-analysis

Journal of biomedical research, 2017, Vol.31 (3), p.213-225

2017

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Association of three single nucleotide polymorphisms of ESR1 with breast cancer susceptibility:a meta-analysis

生物医学研究杂志：英文版, 2017 (3), p.213-225

Xu Hu Linfei Jiang Chenhui Tang Yuehong Ju Li Jiu Yongyue Wei Li Guo Yang Zhao

2017

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Clinical effect of tacrolimus in the treatment of myasthenia gravis in children

Zhongguo dang dai er ke za zhi, 2020-09, Vol.22 (9), p.964

2020

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Scutellaria barbata D.Don Inhibits Colorectal Cancer Growth via Suppression of Wnt/β-Catenin Signaling Pathway

中国结合医学杂志：英文版, 2017, Vol.23 (11), p.858-863

2017

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A Centralized Report on Pediatric Japanese Encephalitis Cases from Beijing Children＇s Hospital, 2013

生物医学与环境科学：英文版, 2016, Vol.29 (12), p.902-908

LI Jiu Wei GAO Xiao Yan WU Yun FU Shi Hong TAN Xiao Juan CAO Yu Xi ZHANG Wei Hua YIN Zun Dongs HE Ying LI Yi Xing LIANG Guo Dong XU Wen Bo FANG Fang WANG Huan Yu

2016

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Predictive factors for postoperative visual function of primary chronic rhegmatogenous retinal detachment after scleral buckling

International journal of ophthalmology, 2016-07

2016

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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes

Frontiers in genetics, 2021, Vol.12, p.605778-605778

2021

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Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients

Frontiers in genetics, 2020, Vol.11, p.126-126

2020

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Neurological Abnormality Could be the First and Only Symptom of Familial Hemophagocytic Lymphohistiocytosis: Report of Two Families

Chinese medical journal, 2018, Vol.131 (24), p.3004-3006

2018

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Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid Lipofuscinosis

Frontiers in genetics, 2019, Vol.10, p.370-370

2019

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Effect of N Fertilization on Grain Yield of Winter Wheat and Apparent N Losses

Pedosphere, 2006-12, Vol.16 (6), p.806-812

2006

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Causes of Interannual and Interdecadal Variations of the Summertime Pacific–Japan-Like Pattern over East Asia

Journal of climate, 2017-11, Vol.30 (22), p.8845-8864

2017

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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes

Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients

Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid Lipofuscinosis

Neurological Abnormality Could be the First and Only Symptom of Familial Hemophagocytic Lymphohistiocytosis: Report of Two Families

Clinical Characteristics and Outcome Analysis of 94 Children With Brain Abscess in Beijing: A Single-center Retrospective Study

Adrenocorticotropic hormone combined with magnesium sulfate therapy for infantile epileptic spasms syndrome: a real-world study

Epileptic seizure, as the first symptom of hypoparathyroidism in children, does not require antiepileptic drugs

Risk Factors for Arterial Ischemic and Hemorrhagic Stroke in Childhood

Arterial Ischemic Stroke: Experience in Chinese Children

A Centralized Report on Pediatric Japanese Encephalitis Cases from Beijing Children's Hospital, 2013

Anti-N-methyl-D-aspartate receptor encephalitis in seven children

Minor injury and basal ganglia calcification may be the risk factors of children's stroke

Identification of the risk of breast cancer in patients suffering from endometriosis: A meta-analysis

Association of three single nucleotide polymorphisms of ESR1 with breast cancer susceptibility：a meta-analysis

Association of three single nucleotide polymorphisms of ESR1 with breast cancer susceptibility:a meta-analysis

Clinical effect of tacrolimus in the treatment of myasthenia gravis in children

Scutellaria barbata D.Don Inhibits Colorectal Cancer Growth via Suppression of Wnt/β-Catenin Signaling Pathway

A Centralized Report on Pediatric Japanese Encephalitis Cases from Beijing Children＇s Hospital, 2013

Predictive factors for postoperative visual function of primary chronic rhegmatogenous retinal detachment after scleral buckling

Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes

Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients

Neurological Abnormality Could be the First and Only Symptom of Familial Hemophagocytic Lymphohistiocytosis: Report of Two Families

Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid Lipofuscinosis

Effect of N Fertilization on Grain Yield of Winter Wheat and Apparent N Losses

Causes of Interannual and Interdecadal Variations of the Summertime Pacific–Japan-Like Pattern over East Asia

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