Phenotypic Spectrum and Chromosomal Discordance in Alobar Holoprosencephaly: A Comparative Case Series from a Tertiary Referral Center. [PDF]
Caropeboka MFA +4 more
europepmc +1 more source
Abstract Objective SCN2A pathogenic mutations, such as the recurrent heterozygous Nav1.2‐L1342P, are monogenic causes of epilepsy. In this human‐induced pluripotent stem cell–derived model system, we aim to investigate the molecular and cellular mechanisms underlying SCN2A‐L1342P‐associated pathology. Methods Using a human male induced pluripotent stem
Maria I. Olivero‐Acosta +26 more
wiley +1 more source
<i>Tectum opticum</i> development in embryonic quail <i>(Coturnix japonica)</i> and the role of HSP70 in the developmental process. [PDF]
Ermutlu DG +5 more
europepmc +1 more source
Embryological development and comparative analysis of Anguis colchica (Nordmann, 1840): Insights into ossification and morphological traits in anguimorph lizards. [PDF]
Yıldırım Caynak E +5 more
europepmc +1 more source
Epileptic Seizures in a Pediatric Patient With Vein of Galen Aneurysmal Malformation and Obstructive Hydrocephalus: A Rare Case Report. [PDF]
Ivanov K +4 more
europepmc +1 more source
Ophthalmologic Findings in an Induced Model of Holoprosencephaly in Zebrafish. [PDF]
Bulk J, Kyrychenko V, Heermann S.
europepmc +1 more source
Mapping of uterine-related neurons in central nervous system of mice by <i>trans</i>-synaptic tracing with pseudorabies virus. [PDF]
Wang H +10 more
europepmc +1 more source
Visualizing α‐synuclein pathology in live brain: A new platform for Parkinson's disease research
Clinical and Translational Medicine, Volume 16, Issue 10, October 2026.
Minhui Yu, Peng Cao
wiley +1 more source
A cortical pathway to sleep: Role of long‐range inhibition
Clinical and Translational Medicine, Volume 16, Issue 10, October 2026.
Geoffrey Terral, Renata Batista‐Brito
wiley +1 more source

