D. Hong

发表

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy.

Y. Liang, H. Lv, Wei Zhang, 2020, American journal of human genetics.

Bilateral striatal necrosis due to homoplasmic mitochondrial 3697G>A mutation presents with incomplete penetrance and sex bias

D. Hong, Xuguang Gao, Shanshan Zhong, 2019, Molecular genetics & genomic medicine.

Efficacy comparison between long-term high-dose praziquantel and surgical therapy for cerebral sparganosis: A multicenter retrospective cohort study

D. Hong, Jun Zhang, Chun-Hua Xu, 2018, PLoS neglected tropical diseases.

Repeat expansion scanning of the NOTCH2NLC gene in patients with multiple system atrophy

Tao Hong, Min Zhu, D. Hong, 2020, Annals of clinical and translational neurology.

Domoic acid induced spinal cord lesions in adult mice: evidence for the possible molecular pathways of excitatory amino acids in spinal cord lesions.

Renshi Xu, D. Hong, Chengsi Wu, 2008, Neurotoxicology.

The polyG diseases: a new disease entity

Zhaoxia Wang, Yun Yuan, Jianwen Deng, 2022, Acta Neuropathologica Communications.

TMEM151A phenotypic spectrum includes paroxysmal kinesigenic dyskinesia with infantile convulsions

Min Zhu, D. Hong, Xin Fang, 2022, Neurological Sciences.

Novel and Recurrent Mutations in a Cohort of Chinese Patients With Young-Onset Amyotrophic Lateral Sclerosis

H. Lv, Wei Zhang, Zhaoxia Wang, 2019, Front. Neurosci..

NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL

H. Lv, Wei Zhang, Zhaoxia Wang, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Juvenile-onset PSAT1-related neuropathy: A milder phenotype of serine deficiency disorder

Yun Peng, Jianwen Deng, Min Zhu, 2022, Frontiers in Genetics.

Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy

Jianwen Deng, Min Zhu, D. Hong, 2022, Annals of clinical and translational neurology.

TMEM151A phenotypic spectrum includes paroxysmal kinesigenic dyskinesia with infantile convulsions

Min Zhu, D. Hong, Xin Fang, 2022, Neurological Sciences.

MAPT as a predisposing gene for sporadic amyotrophic lateral sclerosis in the Chinese Han population

Wenyuan Xu, Min Zhu, D. Hong, 2013, Neural regeneration research.

FUS P525L mutation causing amyotrophic lateral sclerosis and movement disorders

Min Zhu, D. Hong, Yanyan Yu, 2020, Brain and behavior.

Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases

Zhaoxia Wang, M. Oulad-Abdelghani, P. Koebel, 2021, Neuron.

FUS Mutation Causes Disordered Lipid Metabolism in Skeletal Muscle Associated with ALS

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2022, Molecular Neurobiology.

Acute-onset multiple acyl-CoA dehydrogenase deficiency mimicking Guillain-Barré syndrome: two cases report

D. Hong, Yanyan Yu, Jun Zhang, 2018, BMC Neurology.

Long-read sequencing identified repeat expansions in the 5′UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease

Zhaoxia Wang, Yun Yuan, Yining Huang, 2019, Journal of Medical Genetics.

CGG repeat expansion in NOTCH2NLC causes mitochondrial dysfunction and progressive neurodegeneration in Drosophila model

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2022, Proceedings of the National Academy of Sciences of the United States of America.

A novel mutation in the PDZ‐like motif of ZASP causes distal ZASP‐related myofibrillar myopathy

Min Zhu, D. Hong, Shuyun Chen, 2017, Neuropathology : official journal of the Japanese Society of Neuropathology.

A novel CPT1C variant causes pure hereditary spastic paraplegia with benign clinical course

D. Hong, Shanshan Zhong, Jun Zhang, 2019, Annals of clinical and translational neurology.

Editorial: Current advances in genetic dementia and aging

Jun Liu, U. Gómez-Pinedo, D. Hong, 2022, Frontiers in Aging Neuroscience.

Increasing LRP4 diminishes neuromuscular deficits in a mouse model of Duchenne muscular dystrophy

Shunqi Wang, Suqi Zou, D. Hong, 2021, Human molecular genetics.

Risk factors of vestibular migraine-related brain white matter lesions.

D. Hong, Mengyao Hu, Qian Cao, 2022, Acta neurologica Belgica.

Risk factors for cancer‐associated myositis: A large‐scale multicenter cohort study

M. Miao, Jing He, D. Hong, 2020, International journal of rheumatic diseases.

Neutral lipid storage disease with myopathy in China: a large multicentric cohort study

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2019, Orphanet Journal of Rare Diseases.

A novel PNPLA2 mutation causes neutral lipid storage disease with myopathy (NLSDM) presenting muscular dystrophic features with lipid storage and rimmed vacuoles.

Y. Yuan, D. Hong, Z. Wang, 2010, Clinical neuropathology.

Novel ABCD1 Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum

Min Zhu, D. Hong, Yusen Qiu, 2018, Neurodegenerative Diseases.

A novel KIF5A gene variant causes spastic paraplegia and cerebellar ataxia

D. Hong, Xuguang Gao, Shanshan Zhong, 2018, Annals of clinical and translational neurology.

Chronic progressive external ophthalmoplegia coexistent with motor neuron disease in a patient with a novel large-scale mitochondrial DNA deletion

Dan-hua Zhao, Wei Zhang, Zhaoxia Wang, 2013, Clinical Neurology and Neurosurgery.

Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiency

Dan-hua Zhao, H. Lv, Wei Zhang, 2016, Neuromuscular Disorders.

Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patients

Xuan Zhu, Min Zhu, D. Hong, 2014, Journal of Human Genetics.

Induction of apoptosis and autosis in cardiomyocytes by the combination of homocysteine and copper via NOX-mediated p62 expression

Chun Xing Li, S. Lai, Ran Yin, 2022, Cell death discovery.

A novel heterozygous deletion–insertion mutation (2695–2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2010, Neuromuscular Disorders.

Sturge-Weber syndrome coexisting with episodes of rhabdomyolysis

Min Zhu, D. Hong, Hui Wan, 2013, BMC Neurology.

Phenotype variability and histopathological findings in patients with a novel DNM2 mutation

Ping Huang, Min Zhu, D. Hong, 2018, Neuropathology : official journal of the Japanese Society of Neuropathology.

Anti-dipeptidyl-peptidase-like protein 6 encephalitis with pure cerebellar ataxia: a case report

Min Zhu, D. Hong, Meihong Zhou, 2022, BMC Neurology.

Case report: Reversible encephalopathy associated with liposomal amphotericin B in a patient with cryptococcal meningitis

D. Hong, Meihong Zhou, Chen-Long Wu, 2022, Frontiers in Neurology.

Bent spine syndrome as an initial manifestation of late-onset multiple acyl-CoA dehydrogenase deficiency: a case report and literature review

Min Zhu, D. Hong, C. Wei, 2015, BMC Neurology.

A series of Chinese patients with desminopathy associated with six novel and one reported mutations in the desmin gene

Wei Zhang, X. Luan, J. Lu, 2011, Neuropathology and applied neurobiology.

Clinical and muscle magnetic resonance image findings in patients with late-onset multiple acyl-CoA dehydrogenase deficiency

Min Zhu, D. Hong, Shanshan Zhong, 2019, Chinese medical journal.

Familial IBGC caused by SLC20A2 mutation presenting as paroxysmal kinesigenic dyskinesia.

Xuan Zhu, Min Zhu, D. Hong, 2014, Parkinsonism & related disorders.

Widespread Mislocalization of FUS Is Associated With Mitochondrial Abnormalities in Skeletal Muscle in Amyotrophic Lateral Sclerosis With FUS Mutations.

Wei Zhang, Zhaoxia Wang, Jing Liu, 2022, Journal of neuropathology and experimental neurology.

GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy

H. Lv, Wei Zhang, Zhaoxia Wang, 2021, Annals of clinical and translational neurology.

Diverse myopathological features in the congenital myasthenia syndrome with GFPT1 mutation

Xiaorong Wu, Min Zhu, D. Hong, 2021, Brain and behavior.

Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathy

Dan-hua Zhao, Zhaoxia Wang, Jing Liu, 2017, Journal of the Neurological Sciences.

Cerebral sparganosis in mainland Chinese patients

Min Zhu, D. Hong, Ren-shi Xu, 2013, Journal of Clinical Neuroscience.

Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy

Dan-hua Zhao, Yun Yuan, C. Bonnemann, 2014, World Journal of Pediatrics.

The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4.

H. Lv, Wei Zhang, Zhaoxia Wang, 2022, American journal of human genetics.

The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3

H. Lv, Wei Zhang, Zhaoxia Wang, 2021, Brain : a journal of neurology.

Clonazepam improves the symptoms of two siblings with novel variants in the SYNJ1 gene.

D. Hong, Xuguang Gao, Shanshan Zhong, 2019, Parkinsonism & related disorders.

Human viral encephalitis associated with suid herpesvirus 1

D. Hong, Zunchun Xie, Meihong Zhou, 2021, Neurological Sciences.

Clinical phenotype of autosomal dominant progressive external ophthalmoplegia in a family with a novel mutation in the C10orf2 gene

Zhaoxia Wang, Yun Yuan, D. Hong, 2010, Muscle & nerve.

Mutational spectrum and clinical features in 35 unrelated mainland Chinese patients with GNE myopathy

H. Lv, Wei Zhang, Zhaoxia Wang, 2015, Journal of the Neurological Sciences.

Response to Eura et al.

H. Lv, Wei Zhang, Zhaoxia Wang, 2022, American journal of human genetics.

Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease

Wei Zhang, Zhaoxia Wang, Jing Liu, 2021, Journal of Medical Genetics.

Neuronal intranuclear inclusion disease: recognition and update

D. Hong, Xi Lu, 2021, Journal of Neural Transmission.

The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis

Laimin Luo, Min Zhu, D. Hong, 2015, BMC Neurology.

The clinical and genetic features in a cohort of ma inland Chinese patients with thyrotoxic periodic paralysis

Laimin Luo, Min Zhu, D. Hong, 2014 .

Diffuse leptomeningeal gliomatosis initially presenting with intraventricular hemorrhage: a case report and literature review

D. Hong, Yuanzhao Zhu, Hui Wan, 2015, BMC Neurology.

GGC Repeat Expansion in the NOTCH2NLC Gene Is Associated With a Phenotype of Predominant Motor–Sensory and Autonomic Neuropathy

H. Lv, Wei Zhang, Zhaoxia Wang, 2021, Frontiers in Genetics.

Subclinical peripheral neuropathy is common in neuronal intranuclear inclusion disease with dominant encephalopathy

Zhaoxia Wang, Yun Yuan, Jianwen Deng, 2022, European journal of neurology.

Urine cytological study in patients with clinicopathologically confirmed neuronal intranuclear inclusion disease

Zhaoxia Wang, Jianwen Deng, Min Zhu, 2022, Frontiers in Aging Neuroscience.

Asian patients with limb girdle muscular dystrophy 2I (LGMD2I)

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2011, Journal of Clinical Neuroscience.

Patients with MELAS with negative myopathology for characteristic ragged-red fibers

Dan-hua Zhao, Zhaoxia Wang, Yun Yuan, 2019, Journal of the Neurological Sciences.

Normokalemic periodic paralysis with involuntary movements and generalized epilepsy associated with two novel mutations in SCN4A gene

D. Hong, Xiaobing Li, Lingling Cao, 2015, Seizure.

Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Pathological changes of the sural nerve in patients with familial episodic pain syndrome

Min Zhu, D. Hong, Xin Fang, 2022, Neurological Sciences.

Variants in MME are associated with autosomal‐recessive distal hereditary motor neuropathy

H. Ouyang, D. Hong, Xuguang Gao, 2019, Annals of clinical and translational neurology.

Hot spot mutations in electron transfer flavoprotein dehydrogenase gene of riboflavin responsive lipid storage myopathy in 20 Chinese families

Dan-hua Zhao, Zhaoxia Wang, Yun Yuan, 2011 .

Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

Dan-hua Zhao, H. Lv, Wei Zhang, 2011, Journal of Human Genetics.

Clinical and muscular pathological characteristics of hypomyopathic dermatomyositis : an analysis of six cases

Yun Yuan, Xiao‐lei Zhang, D. Hong, 2016 .

Reversible splenial lesion syndrome associated with encephalitis/encephalopathy presenting with great clinical heterogeneity

Ling Zhang, Z. Zeng, Min Zhu, 2016, BMC Neurology.

Benign monomelic amyotrophy of lower limb in a cohort of chinese patients

Min Zhu, D. Hong, Meihong Zhou, 2020, Brain and behavior.

3,4-diaminopyridine treatment for Lambert-Eaton myasthenic syndrome in adults: a meta-analysis of randomized controlled trials

Meihua Li, Tao Hong, D. Hong, 2020, BMC Neurology.

The polyG diseases: a new disease entity

Zhaoxia Wang, Yun Yuan, Jianwen Deng, 2022, Acta neuropathologica communications.

Clinical, myopathological features and sodium channel α-subunit encoding gene mutation analysis in 17 patients with skeletal muscle sodium channelopathies

Wei Zhang, Zhaoxia Wang, D. Hong, 2014 .

Myocardial fibrosis in desmin-related hypertrophic cardiomyopathy

Zhao-qi Zhang, Yi He, D. Hong, 2010, Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance.

Background and roles: myosin in autoimmune diseases

J. Kou, Yanni Lv, D. Hong, 2023, Frontiers in cell and developmental biology.

Danon disease caused by two novel mutations of the LAMP2 gene: implications for two ends of the clinical spectrum.

Zhaoxia Wang, Yun Yuan, D. Hong, 2012, Clinical neuropathology.

Clinical and pathological features in adult-onset NIID patients with cortical enhancement

Zhaoxia Wang, Yun Yuan, Huiting Liang, 2020, Journal of Neurology.

Diagnostic indicators for adult-onset neuronal intranuclear inclusion disease.

Jiewen Zhang, J. Zhao, D. Hong, 2019, Clinical neuropathology.

Editorial: Current advances in genetic presentations of dementia and aging, volume II

Jun Liu, U. Gómez-Pinedo, D. Hong, 2023, Frontiers in Aging Neuroscience.