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View article: The role risk of cigarette smoking, alcohol consumption, sleeping disorder, and mental health with hearing loss among stroke patients
The role risk of cigarette smoking, alcohol consumption, sleeping disorder, and mental health with hearing loss among stroke patients Open
This study puts forward that smoking cigarettes along with factors like hypertension, obesity, vitamin D deficiency, and sleepiness, serve as notable danger element for loosing hearing ability among stroke patients. There is increasing evi…
View article: DRP2 Mutation in Familial Autism Spectrum Disorder: A Case Report of 2 Consanguineous Patients
DRP2 Mutation in Familial Autism Spectrum Disorder: A Case Report of 2 Consanguineous Patients Open
Autism spectrum disorder (ASD) is a complex neurodevelopmental condition with a strong genetic basis, and rare X-linked variants may contribute to its pathogenesis, particularly in consanguineous families. We present 2 pediatric cases from…
View article: Knowledge Attitude and practice about E-cigarettes among University Students: A comparative study between Afghanistan, Netherlands, and Turkey
Knowledge Attitude and practice about E-cigarettes among University Students: A comparative study between Afghanistan, Netherlands, and Turkey Open
Background The rise in electronic cigarette (e-cigarette) use among young adults has raised significant public health concerns. Initially introduced as a harm-reduction tool, e-cigarettes have increasingly become a popular alternative to t…
View article: Impact of Maternal Age on the Repairing Capacity of Oocytes on Paternal DNA Damage
Impact of Maternal Age on the Repairing Capacity of Oocytes on Paternal DNA Damage Open
Sperm DNA fragmentation is a primary cause of male infertility, affecting ART outcomes and success rates. Sperm has no DNA repair mechanisms because it is transcriptionally quiet. Oocytes’ repairing capacity is one of the suggested methods…
View article: Genetic and clinical characterization of Niemann-Pick disease type C with homozygous NPC1 gene mutation: insights from whole exome sequencing and advanced neuroimaging of two familial cases
Genetic and clinical characterization of Niemann-Pick disease type C with homozygous NPC1 gene mutation: insights from whole exome sequencing and advanced neuroimaging of two familial cases Open
Background: Niemann-Pick disease Type C (NPC) is a rare genetic lipid storage disorder characterized by heterogeneous clinical presentations primarily affecting the neurological and visceral systems. This study aims to elucidate the clinic…