Q. Gang

发表

Genetic defects are common in myopathies with tubular aggregates

Zhaoxia Wang, Yun Yuan, J. Holton, 2021, Annals of clinical and translational neurology.

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

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

Cerebral microbleeds and postthrombolysis intracerebral hemorrhage risk

D. Werring, H. Jäger, A. Charidimou, 2015, Neurology.

Plasma level of miR-93 is associated with higher risk to develop type 2 diabetic retinopathy

Ying Zhang, Q. Gang, H. Zou, 2017, Graefe's Archive for Clinical and Experimental Ophthalmology.

Ongoing Developments in Sporadic Inclusion Body Myositis

L. Greensmith, J. Holton, H. Houlden, 2014, Current Rheumatology Reports.

First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-Sarcoglycanopathy

H. Lv, Zhaoxia Wang, Yun Yuan, 2022, Frontiers in Pediatrics.

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..

Tubular Aggregates and Cylindrical Spirals Have Distinct Immunohistochemical Signatures

S. Al-Sarraj, J. Holton, H. Houlden, 2016, Journal of neuropathology and experimental neurology.

Perimysial microarteriopathy in dermatomyositis with anti‐nuclear matrix protein‐2 antibodies

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2020, European journal of neurology.

Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing

H. Lv, Wei Zhang, Zhaoxia Wang, 2017, PLoS ONE.

Improvement on mantle cell culture and technique for large nucleated pearl producing in Hyriopsis cumingii

Q. Gang, 2011 .

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.

Sporadic cerebral amyloid angiopathy revisited: recent insights into pathophysiology and clinical spectrum

D. Werring, A. Charidimou, Q. Gang, 2011, Journal of Neurology, Neurosurgery & Psychiatry.

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.

Genetic Investigations of Sporadic Inclusion Body Myositis and Myopathies with Structural Abnormalities and Protein Aggregates in Muscle

Q. Gang, 2016 .

Response to Eura et al.

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

Genetic advances in sporadic inclusion body myositis

H. Houlden, M. Hanna, C. Bettencourt, 2015, Current opinion in rheumatology.

KNOWN GENES ASSOCIATED WITH FAMILIAL INCLUSION BODY MYOSITIS AND HEREDITARY INCLUSION BODY MYOPATHIES

H. Houlden, M. Hanna, C. Bettencourt, 2015 .

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis

H. Houlden, P. Machado, M. Hanna, 2014, Orphanet Journal of Rare Diseases.

Sural nerve pathology in TFG‐associated motor neuron disease with sensory neuropathy

Rui Wu, Wei Zhang, Zhaoxia Wang, 2019, Neuropathology : official journal of the Japanese Society of Neuropathology.

Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centre

J. Holton, H. Houlden, M. Reilly, 2019, Neuromuscular Disorders.

GJA1 Gene Polymorphisms and Topographic Distribution of Cranial MRI Lesions in Cerebral Small Vessel Disease

Haiqiang Jin, Yining Huang, Wei Zhang, 2020, Frontiers in Neurology.

Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

A. Singleton, J. Lamb, F. Mastaglia, 2016, Neurobiology of Aging.

Rare variants in SQSTM 1 and VCP genes and risk of sporadic inclusion body myositis

A. Singleton, D. Hughes, J. Holton, 2016 .

Subsarcolemmal and cytoplasmic p62 positivity and rimmed vacuoles are distinctive for PLIN4 ‐myopathy

H. Lv, Wei Zhang, Zhaoxia Wang, 2022, Annals of clinical and translational neurology.

The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis

J. Holton, H. Houlden, R. Barohn, 2015, Neurobiology of Aging.

Novel variants, muscle imaging, and myopathological changes in Chinese patients with VCP‐related multisystem proteinopathy

Zhaoxia Wang, Yun Yuan, Yi-ming Zheng, 2023, Molecular genetics & genomic medicine.

Negative results The effects of an intronic polymorphism in TOMM 40 and APOE genotypes in sporadic inclusion body myositis

J. Holton, H. Houlden, R. Barohn, 2015 .

Sporadic cerebral amyloid angiopathy revisited: recent insights into pathophysiology and clinical spectrum

D. Werring, A. Charidimou, Q. Gang, 2011, Journal of Neurology, Neurosurgery & Psychiatry.