Publications by authors named "A Daoudi"

Hydranencephaly (HE) is a severe and isolated malformation affecting the cerebral mantle. In this condition, the cerebral hemispheres are entirely or almost entirely absent, replaced by a membranous sac filled with cerebrospinal fluid, while the midbrain is usually preserved. Although HE is a relatively rare brain disorder, the differential diagnosis must include conditions such as severe hydrocephalus, porencephalic cysts, and alobar holoprosencephaly.

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Background: Patients with bipolar disorder (BD) are at increased risk of dementia. The underlying mechanisms are debated. FDG-PET elucidates glucose metabolic reductions due to altered neuronal activity in the cerebral cortex, allowing detection and identification of neurodegenerative processes.

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Holoprosencephaly (HPE) is a severe and complex congenital brain malformation caused by a defect in the midline cleavage of the prosencephalon during early embryonic development. It is the most common prosencephalic malformation in humans and is categorized into three classical forms based on the severity of this cleavage defect: alobar, semilobar, and lobar HPE. A milder interhemispheric variant, called syntelencephaly, is also considered a form of HPE.

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π-Conjugated systems are the key to the charge transport properties of organic semiconductors. Four multifunctional mesogenic materials were designed and synthesised from 2-amino anthracene and -hydroxybenzaldehyde. Each material contains a central, rigid phenyl-anthracene core and one flexible alkyloxy chain with different lengths based on the concept of combining liquid crystal (LC) materials featuring facile processability, highly ordered alignment, and effective charge transport.

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Article Synopsis
  • Juvenile Dermatomyositis (JDM) is an autoimmune condition in children that causes inflammation in muscles and skin, and identifying specific autoantibodies can help classify its subtypes and predict outcomes.
  • A case study describes a 5-year-old Moroccan boy with JDM who exhibited symptoms such as dysphagia, facial erythema, muscle weakness, and characteristic skin rashes, along with positive anti-SAE antibodies, a rare finding.
  • Treatment involved high-dose methylprednisolone followed by a tapering dose of oral prednisone, highlighting the need for targeted therapies based on specific antibody presence in JDM.
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