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Pin Fee Chong
Observed names:
CHONG PIN FEE,
Chong Pin Fee,
P.F. Chong,
Pin Chong,
Pin F Chong,
Pin F. Chong
show all 6
Institution:
Kyushu University
Observed institutions:
Kyushu University,
Kyushu University Hospital,
Fukuoka Children's Hospital and Medical Center for Infectious Diseases
ORCID:
0000-0002-2046-1360
Observed ORCID:
0000-0002-2046-1360
OpenAlex ID:
A5035876536
Acute flaccid myelitis: cause, diagnosis, and management
2020
·
Olwen C Murphy
, Kevin Messacar
, et al.
·
The Lancet
·
183
PDF
Clinical Features of Acute Flaccid Myelitis Temporally Associated With an Enterovirus D68 Outbreak: Results of a Nationwide Survey of Acute Flaccid Paralysis in Japan, August–December 2015
2017
·
Pin Fee Chong
, Ryutaro Kira
, et al.
·
Clinical Infectious Diseases
·
126
PDF
Ineffective quinidine therapy in early onset epileptic encephalopathy with KCNT 1 mutation
2016
·
Pin Fee Chong
, Ryoko Nakamura
, et al.
·
Annals of Neurology
·
74
Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders
2019
·
Toshiyuki Yamamoto
, Taichi Imaizumi
, et al.
·
Brain and Development
·
52
Challenges in detecting genomic copy number aberrations using next-generation sequencing data and the eXome Hidden Markov Model: a clinical exome-first diagnostic approach
2016
·
Toshiyuki Yamamoto
, Keiko Shimojima
, et al.
·
Human Genome Variation
·
49
PDF
Serial MRI findings of acute flaccid myelitis during an outbreak of enterovirus D68 infection in Japan
2018
·
Akihisa Okumura
, Harushi Mori
, et al.
·
Brain and Development
·
34
Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0
2019
·
Kenichi Maeda
, Pin Fee Chong
, et al.
·
Annals of Neurology
·
19
Leucine-rich alpha-2 glycoprotein in the cerebrospinal fluid is a potential inflammatory biomarker for meningitis
2018
·
Pin Fee Chong
, Yasunari Sakai
, et al.
·
Journal of the Neurological Sciences
·
19
Living-Donor Liver Transplantation From a Heterozygous Parent for Infantile Refsum Disease
2016
·
Masatoshi Matsunami
, Nobuyuki Shimozawa
, et al.
·
PEDIATRICS
·
19
Early onset of moyamoya syndrome in a Down syndrome patient with the genetic variant RNF213 p.R4810K
2014
·
Pin Fee Chong
, Reina Ogata
, et al.
·
Brain and Development
·
18
Clinical and genetic characteristics of patients with Doose syndrome
2020
·
Nodoka Hinokuma
, Mitsuko Nakashima
, et al.
·
Epilepsia Open
·
17
PDF
Progressive myoclonic epilepsy as an expanding phenotype of NGLY1-associated congenital deglycosylation disorder: A case report and review of the literature
2023
·
Yuri Sonoda
, Atsushi Fujita
, et al.
·
European Journal of Medical Genetics
·
16
Critical vitamin deficiencies in autism spectrum disorder: Reversible and irreversible outcomes
2022
·
Pin Fee Chong
, Michiko Torio
, et al.
·
European Journal of Clinical Nutrition
·
16
A case of pontine tegmental cap dysplasia with comorbidity of oculoauriculovertebral spectrum
2014
·
Pin Fee Chong
, Kohei Haraguchi
, et al.
·
Brain and Development
·
15
PDF
Clinical characteristics of SARS-CoV-2-associated encephalopathy in children: Nationwide epidemiological study
2024
·
Mariko Kasai
, Hiroshi Sakuma
, et al.
·
Journal of the Neurological Sciences
·
14
PDF
Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies
2021
·
Sachiko Miyamoto
, Mitsuhiro Kato
, et al.
·
Journal of Human Genetics
·
14
The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotype
2019
·
Gökhan Yigit
, Ken Saida
, et al.
·
Human Mutation
·
14
PDF
Deletions of SCN2A and SCN3A genes in a patient with West syndrome and autistic spectrum disorder
2018
·
Pin Fee Chong
, Hirotomo Saitsu
, et al.
·
Seizure
·
14
Isolated cranial neuritis of the oculomotor nerve: Expanding the MOG phenotype?
2020
·
Saori Kawakami
, Satoshi Akamine
, et al.
·
Multiple Sclerosis and Related Disorders
·
11
Long surviving classical Menkes disease treated with weekly intravenous copper therapy
2019
·
Reina Ogata
, Pin Fee Chong
, et al.
·
Journal of Trace Elements in Medicine and Biology
·
11
Three-Year Longitudinal Motor Function and Disability Level of Acute Flaccid Myelitis
2020
·
Pin Fee Chong
, Ryutaro Kira
, et al.
·
Pediatric Neurology
·
10
Mutations in NSD1 and NFIX in Three Patients with Clinical Features of Sotos Syndrome and Malan Syndrome
2017
·
Yongping Lu
, Pin Chong
, et al.
·
Journal of Pediatric Genetics
·
10
Rapid and long‐lasting efficacy of high‐dose ambroxol therapy for neuronopathic Gaucher disease: A case report and literature review
2024
·
Kanako Higashi
, Yuri Sonoda
, et al.
·
Molecular Genetics & Genomic Medicine
·
9
PDF
West Syndrome in an Infant With Vitamin B12 Deficiency Born to Autoantibodies Positive Mother
2019
·
Pin Fee Chong
, Masaru Matsukura
, et al.
·
Frontiers in Pediatrics
·
9
PDF
Monogenic causes of pigmentary mosaicism
2022
·
Ken Saida
, Pin Fee Chong
, et al.
·
Human Genetics
·
8
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Works count:
65
Citation count:
887
H-index:
14
I10-index:
22
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