Ying-mai Yang

发表

THAP1/DYT6 sequence variants in non-DYT1 early-onset primary dystonia in China and their effects on RNA expression

L. Ozelius, J. Feng, Lin Wang, 2012, Journal of Neurology.

Pallidal Deep Brain Stimulation in Patients With Chorea‐Acanthocytosis

Renzhi Wang, Yu Wang, Wenbin Ma, 2018, Neuromodulation : journal of the International Neuromodulation Society.

Novel SERAC1 mutations in a Chinese patient presenting with parkinsonism and dystonia

Jun Ma, C. Mao, Lin Wang, 2018, Neurological Sciences.

Identification of TH Variants in Chinese Dopa-Responsive Dystonia Patients and Long-Term Outcomes

Meng-yu Zhang, Lin Wang, Jie Wang, 2021, Frontiers in Neurology.

ANO3 Mutations in Chinese Dystonia: A Genetic Screening Study Using Next-Generation Sequencing

Jun Ma, S. Li, Lin Wang, 2020, Frontiers in Neurology.

Identification of Novel KMT2B Variants in Chinese Dystonia Patients via Whole-Exome Sequencing

Jun Ma, S. Li, Lin Wang, 2019, Front. Neurol..

Dystonia‐Deafness Syndrome Response to Subthalamic Nucleus Stimulation

Yi Guo, Lin Wang, Mengyu Zhang, 2022, Movement disorders clinical practice.

Pain and numbness of left upper limb for five months, weakness for three months, aggravating with pain and weakness of other limbs for one month

L. Cui, B. Peng, H. Guan, 2017 .

Subcellular distribution of THAP1 and alterations in the microstructure of brain white matter in DYT6 dystonia.

F. Feng, B. Hou, J. Feng, 2012, Parkinsonism & related disorders.

Mutations in ANO3 and GNAL gene in thirty‐three isolated dystonia families

T. Feng, Lin Wang, X. Wan, 2015, Movement disorders : official journal of the Movement Disorder Society.

1.261 THAP1/DYT6 SEQUENCE VARIANTS IN NON-DYT1 EARLY ONSET PRIMARY DYSTONIA IN CHINA AND THEIR EFFECTS ON RNA EXPRESSION

L. Ozelius, Jiachun Feng, Lin Wang, 2012 .

Chromosome 1q loss of heterozygosity frequently occurs in sporadic insulinomas and is associated with tumor malignancy

Xin Lu, X. Sang, Jie Gao, 2005, International journal of cancer.

Clinical implications of microsatellite instability and MLH1 gene inactivation in sporadic insulinomas.

Xin Lu, X. Sang, D. Deng, 2009, The Journal of clinical endocrinology and metabolism.

No mutations in CIZ1 in twelve adult‐onset primary cervical dystonia families

Lin Wang, X. Wan, Ling-yan Ma, 2013, Movement disorders : official journal of the Movement Disorder Society.

Dissociative Tremor Response with Pallidal Deep Brain Stimulation in Parkinson’s Disease

J. Pilitsis, E. Molho, A. Ramirez-Zamora, 2020, Tremor and other hyperkinetic movements.

Targeted gene capture sequencing in diagnosis of dystonia patients

Jun Ma, Lin Wang, X. Wan, 2018, Journal of the Neurological Sciences.

Subthalamic Nuclei Stimulation in Patients With Pantothenate Kinase‐Associated Neurodegeneration (PKAN)

Renzhi Wang, Yu Wang, Wenbin Ma, 2017, Neuromodulation : journal of the International Neuromodulation Society.

Brain-derived neurotrophic factor Val66Met polymorphism is not associated with primary dystonia in a Chinese population

Lin Wang, Yuan Tian, Yi Chen, 2013, Neuroscience Letters.

Mutations in ANO3 and GNAL gene in thirty‐three isolated dystonia families

T. Feng, Lin Wang, X. Wan, 2015, Movement disorders : official journal of the Movement Disorder Society.

Mutations in GNAL gene in 214 cases with isolated dystonia.

Lin Wang, X. Wan, Ling-yan Ma, 2015, Parkinsonism & related disorders.