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Biopolymer Materials Based Carboxymethyl Cellulose as a Proton Conducting Biopolymer Electrolyte for Application in Rechargeable Proton Battery

Electrochimica acta, 2014-05, Vol.129, p.1-13

2014

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Traumatic and spontaneous carotid and vertebral artery dissection in a level 1 trauma center

Journal of clinical neuroscience, 2012-08, Vol.19 (8), p.1112-1114

2012

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Guidelines and the use of inferior vena cava filters: a review of an institutional experience

Journal of thrombosis and haemostasis, 2009-01, Vol.7 (1), p.65-71

2009

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P22-20 Using multiple electrophysiological techniques for the differentiation of Parkinsonian syndromes

Clinical neurophysiology, 2010, Vol.121, p.S237-S237

2010

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Bioactive Compounds in Legumes and Their Germinated Products

Journal of agricultural and food chemistry, 2006-05, Vol.54 (11), p.3807-3814

2006

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Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event

Journal of human genetics, 2017-07, Vol.62 (7), p.711-715

2017

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A submicroscopic deletion involving part of the CREBBP gene detected by array-CGH in a patient with Rubinstein–Taybi syndrome

Gene, 2012-05, Vol.499 (1), p.182-185

2012

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Changes of property and morphology of cationic corn starches

Carbohydrate polymers, 2007-06, Vol.69 (3), p.544-553

2007

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Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disorders

Gene, 2020-03, Vol.731, p.144360-144360, Article 144360

2020

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Molecular and granular characteristics of corn starch modified by HCl-methanol at different temperatures

Carbohydrate polymers, 2006-03, Vol.63 (4), p.527-534

2006

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PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

Journal of medical genetics, 2018-02, Vol.55 (2), p.104-113

2018

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Novel phenotypic feature in a patient with a recurrent NOTCH2 nonsense mutation

American journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.2135-2138

2022

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Coffin-Siris Syndrome-1: Report of five cases from Asian populations with truncating mutations in the ARID1B gene

Journal of the neurological sciences, 2020-07, Vol.414, p.116819-116819, Article 116819

2020

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Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability

European journal of human genetics : EJHG, 2021-11, Vol.29 (11), p.1663-1668

2021

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Novel and recurrent variants in PAX6 in four patients with ocular phenotypes from Southeast Asia

Clinical dysmorphology, 2024-04, Vol.33 (2), p.63-68

2024

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Water status of cooked white salted noodles evaluated by MRI

Food research international, 2004, Vol.37 (10), p.957-966

2004

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Prenatal cerebral imaging features of a new syndromic entity related to KIAA1109 pathogenic variants mimicking tubulinopathy

Prenatal diagnosis, 2020-01, Vol.40 (2), p.276-281

2020

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Speckled brain lesions in Incontinentia Pigmenti patients with acquired brain syndromes

European journal of paediatric neurology, 2021-07, Vol.33, p.106-111

2021

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Properties and microstructure of plasticized zein films

Cereal chemistry, 1997-11, Vol.74 (6), p.771-775

1997

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Additional individuals with CHD7 variants in Chinese and other southeast Asian patients

American journal of medical genetics. Part A, 2020-10, Vol.182 (10), p.2461-2465

2020

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Acute lymphoblastic leukemia in a child with a de novo germline gnb1 mutation

American journal of medical genetics. Part A, 2017-02, Vol.173 (2), p.550-552

2017

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Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients

Human genomics, 2015-12, Vol.9 (1), p.33-33, Article 33

2015

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Aortic and pulmonary artery dilatation in Cantu syndrome: expanding the phenotype

Clinical dysmorphology, 2019-07, Vol.28 (3), p.167-167

2019

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The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome

Molecular genetics & genomic medicine, 2019-04, Vol.7 (4), p.e00581-n/a

2019

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Chromosome 12q24.31 microdeletion and congenital heart disease: a case report and review of the literature

Clinical dysmorphology, 2019-01, Vol.28 (1), p.53-56

2019

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Biopolymer Materials Based Carboxymethyl Cellulose as a Proton Conducting Biopolymer Electrolyte for Application in Rechargeable Proton Battery

Traumatic and spontaneous carotid and vertebral artery dissection in a level 1 trauma center

Guidelines and the use of inferior vena cava filters: a review of an institutional experience

P22-20 Using multiple electrophysiological techniques for the differentiation of Parkinsonian syndromes

Bioactive Compounds in Legumes and Their Germinated Products

Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event

A submicroscopic deletion involving part of the CREBBP gene detected by array-CGH in a patient with Rubinstein–Taybi syndrome

Changes of property and morphology of cationic corn starches

Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disorders

Molecular and granular characteristics of corn starch modified by HCl-methanol at different temperatures

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

Novel phenotypic feature in a patient with a recurrent NOTCH2 nonsense mutation

Coffin-Siris Syndrome-1: Report of five cases from Asian populations with truncating mutations in the ARID1B gene

Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability

Novel and recurrent variants in PAX6 in four patients with ocular phenotypes from Southeast Asia

Water status of cooked white salted noodles evaluated by MRI

Prenatal cerebral imaging features of a new syndromic entity related to KIAA1109 pathogenic variants mimicking tubulinopathy

Speckled brain lesions in Incontinentia Pigmenti patients with acquired brain syndromes

Properties and microstructure of plasticized zein films

Additional individuals with CHD7 variants in Chinese and other southeast Asian patients

Acute lymphoblastic leukemia in a child with a de novo germline gnb1 mutation

Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients

Aortic and pulmonary artery dilatation in Cantu syndrome: expanding the phenotype

The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome

Chromosome 12q24.31 microdeletion and congenital heart disease: a case report and review of the literature

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