Ji Yoon Han
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Explore the profile of Ji Yoon Han including associated specialties, affiliations and a list of published articles.
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48
Citations
234
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Recent Articles
1.
Han J, Kim T, Park J
Biomedicines
. 2025 Jan;
12(12.
PMID: 39767570
Objectives: This study investigated the characteristics of adolescent-onset epilepsy (AOE) and conducted genetic tests on a cohort of 76 Korean patients to identify variants and expand the spectrum of mutations...
2.
Park E, Eom T, Han J, Bin J, Oh J, Kim Y, et al.
Transl Pediatr
. 2024 Nov;
13(10):1737-1746.
PMID: 39524385
Background: Syncope is common among children and adolescents. Although it is most commonly caused by vasovagal syncope, it can also be due to undiagnosed, potentially serious, or even life-threatening conditions....
3.
Han S, Kim J, Park E, Han J, Lee J
Medicina (Kaunas)
. 2024 Oct;
60(10).
PMID: 39459412
: Brain imaging studies in pediatric patients with headaches often reveal inflammation of the sphenoid sinus. When we encounter patients presenting with headaches without respiratory symptoms, determining the causal relationship...
4.
Park E, Han S, Lee J, Kim J, Han J
Brain Sci
. 2024 Oct;
14(10).
PMID: 39451966
Background: Headache is a common complaint during childhood and adolescence. It is important to be aware of the characteristics of pediatric headaches in order to make a precise and timely...
5.
Han J, Kim T, Gwack J, Park J
Int J Mol Sci
. 2024 Oct;
25(19).
PMID: 39408661
The mutations encompass a nearly continuous spectrum of neurodevelopmental disorders (NDDs), ranging from lissencephaly to Proud syndrome, as well as infantile spasms without brain malformations, and including both syndromic and...
6.
Han J, Gwack J, Kim T, Park J
Int J Mol Sci
. 2024 Sep;
25(18).
PMID: 39337310
Maturity-onset diabetes of the young (MODY; OMIM # 606391) comprises a cluster of inherited disorders within non-autoimmune diabetes mellitus (DM), typically emerging during adolescence or young adulthood. We report a...
7.
Rhim J, Kim D, Han J, Park J
Heliyon
. 2024 Sep;
10(17):e36717.
PMID: 39296067
Background: Autosomal recessive non-syndromic deafness-28 (DFNB28; OMIM #609823) specifically refers to prelingual sensorineural hearing loss (SNHL) resulting from homozygous or compound heterozygous mutations in the TRIO- and F-actin-binding protein, gene....
8.
Han J, Park J
Genes (Basel)
. 2024 Apr;
15(4).
PMID: 38674380
Background: Noonan syndrome (NS)/Noonan syndrome with multiple lentigines (NSML) is commonly characterized by distinct facial features, a short stature, cardiac problems, and a developmental delay of variable degrees. However, as...
9.
Kim K, Han J, Park J, Cho J
Int J Mol Sci
. 2024 Apr;
25(7).
PMID: 38612512
-related disorders represent some of the rarest inherited disorders, exhibiting clinical features that overlap with cardiac, facial, and digital anomalies with developmental delay (CAFDADD) syndrome, as well as blepharophimosis-mental retardation...
10.
Han J, Park J
Heliyon
. 2024 Apr;
10(7):e28684.
PMID: 38571618
Background: mutations account for a diverse array of clinical manifestations, encompassing periodic paralysis, myotonia, and newly recognized symptoms like classical congenital myopathy or congenital myasthenic syndromes. We describe the initial...