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Clinical features and long-term outcomes of moyamoya disease: a single-center experience with 528 cases in China

Journal of neurosurgery, 2015-02, Vol.122 (2), p.392-399

2015

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Amino acid metabolism‐related gene expression‐based risk signature can better predict overall survival for glioma

Cancer science, 2019-01, Vol.110 (1), p.321-333

2019

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Associations of unintended pregnancy with autism spectrum disorders and the modification of folic acid supplements

Autism research, 2024-01, Vol.17 (1), p.172-181

2024

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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

PloS one, 2015-04, Vol.10 (4), p.e0124409-e0124409

2015

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MiR-155-5p exerts tumor-suppressing functions in Wilms tumor by targeting IGF2 via the PI3K signaling pathway

Biomedicine & pharmacotherapy, 2020-05, Vol.125, p.109880-109880, Article 109880

2020

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Evaluation of 99mTC-ECD SPECT/CT brain Imaging with NeuroGam analysis in Moyamoya disease after surgical revascularization

Medicine (Baltimore), 2019-11, Vol.98 (46), p.e16525-e16525

2019

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Expert consensus on multidisciplinary approach to the diagnosis and treatment of primary hyperparathyroidism in pregnancy in China

Endocrine, 2023-11, Vol.82 (2), p.282-295

2023

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ADAM9 Expression Is Associate with Glioma Tumor Grade and Histological Type, and Acts as a Prognostic Factor in Lower-Grade Gliomas

International journal of molecular sciences, 2016-08, Vol.17 (9), p.1276-1276

2016

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Clinical and prognostic analysis of 42 children with malignant rhabdoid tumor of the kidney: a 7-year retrospective multi-center study

BMC pediatrics, 2022-10, Vol.22 (1), p.591-591, Article 591

2022

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The tumor suppressor role of miR-124 in osteosarcoma

PloS one, 2014-06, Vol.9 (6), p.e91566-e91566

2014

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Surgical Outcomes of Trabeculotomy in Newborns with Primary Congenital Glaucoma

Chinese medical journal, 2016-09, Vol.129 (18), p.2178-2183

2016

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Relative transmissibility of shigellosis among male and female individuals: a modeling study in Hubei Province, China

Infectious diseases of poverty, 2020-04, Vol.9 (1), p.39-39, Article 39

2020

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Fasciotomy through multiple small skin incisions for the treatment of early acute osteofascial compartment syndrome in children

Journal of orthopaedic surgery and research, 2020-07, Vol.15 (1), p.269-269, Article 269

2020

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Anterior Subcutaneous Transposition of the Ulnar Nerve Affects Elbow Range of Motion: A Mean 13.5 Years of Follow-up

Chinese medical journal, 2018-02, Vol.131 (3), p.282-288

2018

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A novel GATA6 mutation associated with congenital ventricular septal defect

International journal of molecular medicine, 2012-06, Vol.29 (6), p.1065-1071

2012

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Increasing prevalence of myopia and the impact of education in primary-school students in Xi'an, north-western of China

Frontiers in public health, 2022-12, Vol.10, p.1070984-1070984

2022

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Cannulated screw and Kirschner fixation for the treatment of medial and lateral malleolar epiphyseal fractures in children: a retrospective study of 36 cases

Journal of orthopaedic surgery and research, 2019-08, Vol.14 (1), p.254-254, Article 254

2019

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A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect

Pediatric cardiology, 2015-03, Vol.36 (3), p.646-656

2015

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Prevalence and spectrum of GATA5 mutations associated with congenital heart disease

International journal of cardiology, 2013-05, Vol.165 (3), p.570-573

2013

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Palmar approach with Kirschner-wire fixation in the treatment of children's distal radius extension type fracture

Chinese journal of traumatology, 2018-10, Vol.21 (5), p.301-303

2018

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A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in a Chinese patient with non-familial nocturnal frontal lobe epilepsy

Epilepsy research, 2014-12, Vol.108 (10), p.1927-1931

2014

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Transarterial embolization in the management of intractable epistaxis: the angiographic findings and results based on etiologies

Acta oto-laryngologica, 2016-08, Vol.136 (8), p.864-868

2016

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A novel NKX2-5 mutation in familial ventricular septal defect

International journal of molecular medicine, 2011-03, Vol.27 (3), p.369-375

2011

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A Novel GATA4 Loss-of-Function Mutation Associated With Congenital Ventricular Septal Defect

Pediatric cardiology, 2012-04, Vol.33 (4), p.539-546

2012

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Prevalence and risk factors of child maltreatment among migrant families in China

Child abuse & neglect, 2017-03, Vol.65, p.171-181

2017

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Clinical features and long-term outcomes of moyamoya disease: a single-center experience with 528 cases in China

Amino acid metabolism‐related gene expression‐based risk signature can better predict overall survival for glioma

Associations of unintended pregnancy with autism spectrum disorders and the modification of folic acid supplements

PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

MiR-155-5p exerts tumor-suppressing functions in Wilms tumor by targeting IGF2 via the PI3K signaling pathway

Evaluation of 99mTC-ECD SPECT/CT brain Imaging with NeuroGam analysis in Moyamoya disease after surgical revascularization

Expert consensus on multidisciplinary approach to the diagnosis and treatment of primary hyperparathyroidism in pregnancy in China

ADAM9 Expression Is Associate with Glioma Tumor Grade and Histological Type, and Acts as a Prognostic Factor in Lower-Grade Gliomas

Clinical and prognostic analysis of 42 children with malignant rhabdoid tumor of the kidney: a 7-year retrospective multi-center study

The tumor suppressor role of miR-124 in osteosarcoma

Surgical Outcomes of Trabeculotomy in Newborns with Primary Congenital Glaucoma

Relative transmissibility of shigellosis among male and female individuals: a modeling study in Hubei Province, China

Fasciotomy through multiple small skin incisions for the treatment of early acute osteofascial compartment syndrome in children

Anterior Subcutaneous Transposition of the Ulnar Nerve Affects Elbow Range of Motion: A Mean 13.5 Years of Follow-up

A novel GATA6 mutation associated with congenital ventricular septal defect

Increasing prevalence of myopia and the impact of education in primary-school students in Xi'an, north-western of China

Cannulated screw and Kirschner fixation for the treatment of medial and lateral malleolar epiphyseal fractures in children: a retrospective study of 36 cases

A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect

Prevalence and spectrum of GATA5 mutations associated with congenital heart disease

Palmar approach with Kirschner-wire fixation in the treatment of children's distal radius extension type fracture

A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in a Chinese patient with non-familial nocturnal frontal lobe epilepsy

Transarterial embolization in the management of intractable epistaxis: the angiographic findings and results based on etiologies

A novel NKX2-5 mutation in familial ventricular septal defect

A Novel GATA4 Loss-of-Function Mutation Associated With Congenital Ventricular Septal Defect

Prevalence and risk factors of child maltreatment among migrant families in China

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