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High FGF‐21 level in a cohort of 22 patients with Dravet Syndrome—Possible relationship with the disease outcomes

Epilepsia open, 2021-12, Vol.6 (4), p.685-693

2021

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My 30-year roadmap for pediatric myasthenia gravis in Hong Kong: Searching for international collaboration

Clinical & experimental neuroimmunology, 2015-02, Vol.6 (1), p.13-20

Wong, Virginia Chun-Nei

2015

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Gene panel analysis for nonsyndromic cryptogenic neonatal/infantile epileptic encephalopathy

Epilepsia open, 2017-06, Vol.2 (2), p.236-243

2017

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Anti-N-methyl-d-aspartate receptor encephalitis in children: Incidence and experience in Hong Kong

Brain & development (Tokyo. 1979), 2018-06, Vol.40 (6), p.473-479

2018

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Analysis of mutations in 7 genes associated with neuronal excitability and synaptic transmission in a cohort of children with non-syndromic infantile epileptic encephalopathy

PloS one, 2015-05, Vol.10 (5), p.e0126446-e0126446

2015

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CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothers

Molecular genetics and metabolism reports, 2024-03, Vol.38, p.101023, Article 101023

2024

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Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome

PloS one, 2012-07, Vol.7 (7), p.e41802-e41802

2012

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CDKL5 variant in a boy with Infantile Epileptic Encephalopathy: Case report

Brain & development (Tokyo. 1979), 2015-04, Vol.37 (4), p.446-448

2015

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Prevalence and Characteristics of Vaccination triggered Seizures in Dravet syndrome in Hong Kong: A retrospective study

Pediatric neurology, 2016-05, Vol.58, p.41-47

2016

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Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10

Molecular autism, 2017-06, Vol.8 (1), p.31-31, Article 31

2017

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Review of evolution of clinical, training and educational services and research program for autism spectrum disorders in Hong Kong

Science China. Life sciences, 2015-10, Vol.58 (10), p.991-1009

2015

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Spinal Muscular Atrophy With Respiratory Distress Type 1—A Child With Atypical Presentation

Child neurology open, 2018, Vol.5, p.2329048X18769811

2018

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Randomized control trial of using tongue acupuncture in autism spectrum disorder

Journal of Traditional Chinese Medical Sciences, 2014-07, Vol.1 (1), p.62-72

2014

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My 30‐year roadmap for pediatric myasthenia gravis in H ong K ong: Searching for international collaboration

Clinical & experimental neuroimmunology, 2015-02, Vol.6 (1), p.13-20

Wong, Virginia Chun‐Nei

2015

Volltextzugriff (PDF)

Randomized controlled trial of acupuncture versus sham acupuncture in autism spectrum disorder

The journal of alternative and complementary medicine (New York, N.Y.), 2010-05, Vol.16 (5), p.545

2010

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Analysis of Mutations in 7 Genes Associated with Neuronal Excitability and Synaptic Transmission in a Cohort of Children with Non-Syndromic Infantile Epileptic Encephalopathy: e0126446

PloS one, 2015-05, Vol.10 (5)

2015

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Clinical manifestations of neurofibromatosis-1 in Chinese children

Pediatric neurology, 1994-11, Vol.11 (4), p.301-307

Wong, Virginia Chun-Nei

1994

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CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothers

Molecular genetics and metabolism reports, 2024, Vol.38, p.101023-101023

2024

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Spinal Muscular Atrophy With Respiratory Distress Type 1-A Child With Atypical Presentation

Child neurology open, 2018, Vol.5, p.2329048X18769811-2329048X18769811

2018

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High FGF‐21 level in a cohort of 22 patients with Dravet Syndrome—Possible relationship with the disease outcomes

My 30-year roadmap for pediatric myasthenia gravis in Hong Kong: Searching for international collaboration

Gene panel analysis for nonsyndromic cryptogenic neonatal/infantile epileptic encephalopathy

Anti-N-methyl-d-aspartate receptor encephalitis in children: Incidence and experience in Hong Kong

Analysis of mutations in 7 genes associated with neuronal excitability and synaptic transmission in a cohort of children with non-syndromic infantile epileptic encephalopathy

CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothers

Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome

CDKL5 variant in a boy with Infantile Epileptic Encephalopathy: Case report

Prevalence and Characteristics of Vaccination triggered Seizures in Dravet syndrome in Hong Kong: A retrospective study

Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10

Review of evolution of clinical, training and educational services and research program for autism spectrum disorders in Hong Kong

Spinal Muscular Atrophy With Respiratory Distress Type 1—A Child With Atypical Presentation

Randomized control trial of using tongue acupuncture in autism spectrum disorder

My 30‐year roadmap for pediatric myasthenia gravis in H ong K ong: Searching for international collaboration

Randomized controlled trial of acupuncture versus sham acupuncture in autism spectrum disorder

Analysis of Mutations in 7 Genes Associated with Neuronal Excitability and Synaptic Transmission in a Cohort of Children with Non-Syndromic Infantile Epileptic Encephalopathy: e0126446

Clinical manifestations of neurofibromatosis-1 in Chinese children

CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothers

Spinal Muscular Atrophy With Respiratory Distress Type 1-A Child With Atypical Presentation

Guillain–Barré syndrome and Fisher syndrome: Case definitions and guidelines for collection, analysis, and presentation of immunization safety data

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