Results 101 to 110 of about 22,853,154 (251)
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen +5 more
wiley +1 more source
Central nervous system parasites
When parasitic infections of the Central Nervous System (CNS) are examined, we encounter quite a lot of parasites. Among protozoans, especially free-living amoebae (such as Naegleria, Acanthamoeba, Balamuthia, and Sappinia) have attracted attention in ...
Aydinli, A.
core
Diffuse capillary-malformation-like cutaneous lesions are uncommon during pregnancy, and their clinical implications become more complex when they coexist with focal neurological symptoms or cerebrovascular malformation.
ZhiGao Pei, YanFang He, ShuBo Zhang
doaj +1 more source
In our research, KOA rat models were established and treated with ADSC injection into the KI10 acupoint. Pain relief, behavioral function, and joint structural improvements were systematically assessed using ethological tests, imaging, histopathological staining, transmission electron microscopy, and molecular analyses.
Mengwei Dong +7 more
wiley +1 more source
Ultrasound Super‐Resolution Imaging of Neonatal Cerebral Vascular Reorganization
During the first days of neonatal growth, the central nervous system (CNS) develops self‐regulatory mechanisms to ensure constant cerebral perfusion.
Simone Schwarz +19 more
doaj +1 more source
A rhesus macaque model of α‐dystroglycanopathy caused by a POMT1 splice altering variant
Rhesus macaques homozygous for a naturally occurring spice altering variant in the POMT1 gene develop lissencephaly, microphthalmia, and muscular contracture. The presentation models severe presentation of the human Walker‐Warburg syndrome. Abstract Background Biallelic mutations in genes associated with α‐dystroglycan glycosylation manifest in a ...
Anya Nordlund +7 more
wiley +1 more source
STUDY OF CONGENITAL MALFORMATIONS IN CENTRAL NERVOUS SYSTEM & GASTRO- INTESTINAL TRACT
Introduction: Congenital malformations comprise 8% of the perinatal mortality in India. They rank fifth as a cause of perinatal mortality, after asphyxia, respiratory problems, infections and cerebral trauma. However, the pattern is changing rapidly with
Saiyad SS, Jadav Hrishikesh
core
This review redefines the carotid bulb (CB) as a variable geometric dilation shaped by hemodynamics and the carotid sinus (CS) as a conserved neurohistological baroreceptor field. Distinguishing these entities clarifies a century of anatomical confusion and links geometry, neurohistology, and clinical interpretation within a unified framework ...
Răzvan Costin Tudose +2 more
wiley +1 more source
Rupture of a Basilar Aneurysm Secondary to Wyburn-Mason Syndrome: A Case Report
Wyburn-Mason syndrome (WMS) is an extremely rare, non-hereditary congenital disorder characterized by arteriovenous malformations (AVMs) that primarily affect the retina and central nervous system and, less commonly, other structures.
Nelson Antonio Milanés-González +4 more
doaj +1 more source
The petrotympanic canal (Huguier canal): Evolutionary, anatomical, and medical perspectives
Abstract The petrotympanic canal, traditionally referred to as Civinini's or Huguier's canal, represents an anatomical passage connecting the middle ear and temporomandibular joint (TMJ). Despite its early description, its structural complexity and functional significance have often been underestimated. In this study, we combined historical, anatomical,
Andrea Papini +8 more
wiley +1 more source

