Results 61 to 70 of about 10,838 (199)
Background The intrauterine ultrasound phenotype, genotype, pregnancy outcome, and neonatal prognosis of fetuses with 1p36 deletion syndrome were retrospectively analyzed, as previous reports are limited.
Meiying Cai +6 more
doaj +1 more source
Background: Recent studies suggest that clinically sound ventriculomegaly in dogs could be a preliminary form of the clinically significant hydrocephalus.
Eva Gunde +8 more
doaj +1 more source
OC002: Mild ventriculomegaly?has the prognosis of isolated ventriculomegaly changed? [PDF]
n ...
openaire +1 more source
Unilateral Freezing of Gait in Normal Pressure Hydrocephalus after Stroke
Movement Disorders Clinical Practice, EarlyView.
Jose Portales +2 more
wiley +1 more source
Inborn errors of immunity in children with neuroinflammation
Abstract Inborn errors of immunity (IEIs), an expanding group of monogenic disorders with diverse clinical manifestations, are increasingly recognized to include neuroinflammatory disease. Examples of diseases included under this umbrella are Aicardi–Goutières syndrome, deficiency of adenosine deaminase 2, familial haemophagocytic lymphohistiocytosis ...
Eppie M Yiu +5 more
wiley +1 more source
Ventricular Anatomy Across CT and MRI in Hydrocephalus: A Retrospective Study
Background/Objectives: Hydrocephalus is a complex neurological disorder marked by abnormal cerebrospinal fluid dynamics and ventricular enlargement. Despite breakthroughs in neuroimaging, diagnosis and longitudinal the application of imaging markers for ...
Andrada-Iasmina Roşu +7 more
doaj +1 more source
Abstract This study investigated Theory of Mind (ToM) deficits in patients with suspected idiopathic normal pressure hydrocephalus (iNPH), a condition affecting motor, cognitive and autonomic functions. Given the overlap between ToM‐related neural networks and those affected in iNPH, we examined whether ToM impairments are a feature of the disease ...
Akrivi Vatsi +9 more
wiley +1 more source
Fetal ventriculomegaly (VM) is a condition characterized by abnormal enlargement of the cerebral ventricles of the fetus brain that often causes developmental disorders in children.
Mannam Subbarao +6 more
doaj +1 more source
Meier-Gorlin syndrome (MGS) or ear-patella-short stature syndrome (MIM 224690) is a rarely reported autosomal recessive disorder having characteristic triad of microtia, short stature and aplastic or hypoplastic patella. Only 67 cases are reported.
Nabanita Kora +3 more
doaj +1 more source
Objectives To describe the clinical and electroencephalographic findings associated with absence seizures in a population of Cavalier King Charles Spaniels. Materials and Methods This was a retrospective descriptive case series of Cavalier King Charles Spaniels diagnosed with absence seizures at two veterinary referral hospitals between 2016 and 2025 ...
R. Paterson +10 more
wiley +1 more source

