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Books
Lūk kæ čhǭmkōng / Chang Ji-Yoon ; Han Mi-æ [illustrator] ; Nitikǭn Ritthikhōt [plǣ].
Author / Creator:Chang, Ji-Yoon.
Publisher:Krung Thēp : Drīm Phapblitching, [2012?].
Edition:Phim khrang thī 1.
Date:[2012?].
Call Numbers:THA/J/00166
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ArticlesPeer ReviewedFull Text
Seasonal epidemiological and clinical characteristics of pediatric patients with human parainfluenza virus infection by serotype: a retrospective study
Author / Creator:Han, Ji Yoon ; Suh, Woosuck ; Han, Seung Beom
Publisher:London: BioMed Central Ltd
Journal title:Virology journal, 2022-09, Vol.19 (1), p.141-141, Article 141
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ArticlesPeer ReviewedFull Text
Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review
Author / Creator:Han, Ji Yoon ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-03, Vol.15 (4), p.445
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ArticlesPeer ReviewedFull Text
Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability
Author / Creator:Han, Ji Yoon ; Lee, In Goo
Publisher:Korea (South): Clinical and Experimental Pediatics / Korean Pediatric Society
Journal title:Clinical and Experimental Pediatrics, 2020, 63(6), , pp.195-202
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ArticlesPeer ReviewedFull Text
Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability
Author / Creator:Han, Ji Yoon ; Lee, In Goo
Journal title:Clinical and experimental pediatrics, 2020, Vol.63 (6), p.195-202
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ArticlesPeer ReviewedFull Text
Genetic Alterations in Atypical Cerebral Palsy Identified Through Chromosomal Microarray and Exome Sequencing
Author / Creator:Han, Ji Yoon ; Gwack, Jin ; Kim, Jong Hun ; Park, Min Kyu ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2025-03, Vol.26 (7), p.2929
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ArticlesPeer ReviewedFull Text
A Korean Family Presenting with Renal Cysts and Maturity-Onset Diabetes of the Young Caused by a Novel In-Frame Deletion of HNF1B
Author / Creator:Han, Ji Yoon ; Gwack, Jin ; Kim, Tae Yun ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-09, Vol.25 (18), p.9823
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ArticlesPeer ReviewedFull Text
The Aggravation of Neuropsychiatric Symptoms in the Offspring of a Korean Family with Intellectual Disability and Developmental Delay Caused by a Novel ARX p.Lys385Ter Variant
Author / Creator:Han, Ji Yoon ; Kim, Tae Yun ; Gwack, Jin ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-10, Vol.25 (19), p.10327
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ArticlesPeer ReviewedFull Text
Intergenerational Influence of Gender and the DM1 Phenotype of the Transmitting Parent in Korean Myotonic Dystrophy Type 1
Author / Creator:Han, Ji Yoon ; Jang, Woori ; Park, Joonhong
Publisher:Basel: MDPI AG
Journal title:Genes, 2022-08, Vol.13 (8), p.1465
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ArticlesPeer ReviewedFull Text
The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant
Author / Creator:Kim, Kyung Hee ; Han, Ji Yoon ; Park, Joonhong ; Cho, Jung Sun
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-04, Vol.25 (7), p.3701
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ArticlesPeer ReviewedFull Text
Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome
Author / Creator:Han, Ji Yoon ; Cho, Yong Gon ; Jo, Dae Sun ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2023-12, Vol.25 (1), p.253
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ArticlesPeer ReviewedFull Text
Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33–p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review
Author / Creator:Han, Ji Yoon ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2021-06, Vol.12 (7), p.1001
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ArticlesPeer ReviewedFull Text
A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A...
Author / Creator:Han, Ji Yoon ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2021-09, Vol.12 (9), p.1388
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ArticlesPeer ReviewedFull Text
Seizures Related to Influenza in Pediatric Patients: A Comparison with Seizures Associated with Other Respiratory Viral Infections
Author / Creator:Han, Ji Yoon ; Han, Seung Beom
Publisher:Basel: MDPI AG
Journal title:Journal of clinical medicine, 2021-07, Vol.10 (14), p.3088
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ArticlesPeer ReviewedFull Text
Clinical and Genetic Characterization of Adolescent-Onset Epilepsy: A Single-Center Experience in Republic of Korea
Author / Creator:Han, Ji Yoon ; Kim, Tae Yun ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:Biomedicines, 2024-12, Vol.12 (12), p.2663
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ArticlesPeer ReviewedFull Text
Pathogenetic and etiologic considerations of febrile seizures
Author / Creator:Han, Ji Yoon ; Han, Seung Beom
Publisher:Korea (South): Clinical and Experimental Pediatics / Korean Pediatric Society
Journal title:Clinical and experimental pediatrics, 2023-02, Vol.66 (2), p.46-53
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ArticlesPeer ReviewedFull Text
Clinical Significance of Isolated Sphenoid Sinusitis Identified in Pediatric Patients Presenting with Headache
Author / Creator:Han, Seung Beom ; Kim, Jee Min ; Park, Eu Gene ; Han, Ji Yoon ; Lee, Jin
Publisher:Switzerland: MDPI AG
Journal title:Medicina (Kaunas, Lithuania), 2024-10, Vol.60 (10), p.1625
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ArticlesPeer ReviewedFull Text
Phenotypic Diversity of 15q11.2 BP1–BP2 Deletion in Three Korean Families with Development Delay and/or Intellectual Disability: A Case Series and Literature Review
Author / Creator:Han, Ji Yoon ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:Diagnostics (Basel), 2021-04, Vol.11 (4), p.722
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ArticlesPeer ReviewedFull Text
Evaluation of the Analytical Performance of Oncomine Lung cfDNA Assay for Detection of Plasma EGFR Mutations
Author / Creator:Cho, Yong Gon ; Park, Joonhong ; Han, Ji Yoon ; Kim, Tae Yun
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2023-06, Vol.14 (6), p.1219
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ArticlesPeer ReviewedFull Text
Seizure duration may increase thyroid-stimulating hormone levels in children experiencing a seizure
Author / Creator:Han, Ji Yoon ; Lee, In Goo ; Shin, Soyoung ; Park, Joonhong
Publisher:London, England: SAGE Publications
Journal title:Journal of international medical research, 2020-05, Vol.48 (5), p.300060519888401-300060519888401
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Lūk kæ čhǭmkōng / Chang Ji-Yoon ; Han Mi-æ [illustrator] ; Nitikǭn Ritthikhōt [plǣ].

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Seasonal epidemiological and clinical characteristics of pediatric patients with human parainfluenza virus infection by serotype: a retrospective study

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Paternally Inherited Noonan Syndrome Caused by a PTPN11 Variant May Exhibit Mild Symptoms: A Case Report and Literature Review

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Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability

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Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability

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Genetic Alterations in Atypical Cerebral Palsy Identified Through Chromosomal Microarray and Exome Sequencing

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A Korean Family Presenting with Renal Cysts and Maturity-Onset Diabetes of the Young Caused by a Novel In-Frame Deletion of HNF1B

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The Aggravation of Neuropsychiatric Symptoms in the Offspring of a Korean Family with Intellectual Disability and Developmental Delay Caused by a Novel ARX p.Lys385Ter Variant

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Intergenerational Influence of Gender and the DM1 Phenotype of the Transmitting Parent in Korean Myotonic Dystrophy Type 1

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The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant

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Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome

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Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33–p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review

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A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A...

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Seizures Related to Influenza in Pediatric Patients: A Comparison with Seizures Associated with Other Respiratory Viral Infections

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Clinical and Genetic Characterization of Adolescent-Onset Epilepsy: A Single-Center Experience in Republic of Korea

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Pathogenetic and etiologic considerations of febrile seizures

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Clinical Significance of Isolated Sphenoid Sinusitis Identified in Pediatric Patients Presenting with Headache

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Phenotypic Diversity of 15q11.2 BP1–BP2 Deletion in Three Korean Families with Development Delay and/or Intellectual Disability: A Case Series and Literature Review

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Evaluation of the Analytical Performance of Oncomine Lung cfDNA Assay for Detection of Plasma EGFR Mutations

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Seizure duration may increase thyroid-stimulating hormone levels in children experiencing a seizure

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