Results 41 to 50 of about 1,012 (146)
Facial contouring with parascapular free flap: A case series of 22 cases
Indian Journal of Plastic Surgery, 2013 Background: The facial asymmetry correction in complex craniofacial malformations presents a challenging problem for reconstructive surgeons. Progressive hemifacial atrophy (HFA) and hemifacial microsomia (HFM) can manifest in different grades of ...
Guru Dayal Singh Kalra +1 more
doaj +1 more source
Epileptic Disorders, Volume 27, Issue 5, Page 745-802, October 2025.Abstract Although inborn errors of metabolism (IEM) are a rare cause of epilepsy, seizures are a common presentation in these disorders. Seizures in IEM are frequently refractory to conventional anti‐seizure medication and might warrant initiation of specific treatments based on vitamins or dietary modifications or provision of alternative substrates ...
D. Kapoor +7 more
wiley +1 more source
Computer Vision Technologies in Movement Disorders: A Systematic Review
Movement Disorders Clinical Practice, Volume 12, Issue 9, Page 1229-1243, September 2025.Abstract Background Evaluation of movement disorders primarily relies on phenomenology. Despite refinements in diagnostic criteria, the accuracy remains suboptimal. Such a gap may be bridged by machine learning and video technology, which permit objective, quantitative, non‐invasive motor analysis.
Pasquale Maria Pecoraro +4 more
wiley +1 more source
Muscle &Nerve, Volume 72, Issue 1, Page 15-33, July 2025.ABSTRACT Regeneration after peripheral nerve injury is often insufficient for functional recovery. Postoperative electrical stimulation (PES) following injury and repair significantly improves clinical outcomes; recently, conditioning electrical stimulation (CES), delivered before nerve injury, has been introduced as a candidate for clinical ...
Paige B. Hardy +4 more
wiley +1 more source
Journal of Cosmetic MedicineHemifacial atrophy, including Parry-Romberg syndrome, is a rare, progressive disorder characterized by unilateral loss of facial soft tissue, with or without neurologic and/or ocular manifestations.
Al Farabi Lee Jaafar +2 more
doaj +1 more source
Epilepsia, Volume 66, Issue 6, Page 1773-1792, June 2025.Abstract The cerebellum, a subcortical structure, is traditionally linked to sensorimotor integration and coordination, although its role in cognition and affective behavior, as well as epilepsy, is increasingly recognized. Cerebellar dysfunction in patients with epilepsy can result from genetic disorders, antiseizure medications, seizures, and seizure‐
Christopher Elder +4 more
wiley +1 more source
Parry–Romberg Syndrome with Uhthoff’s Phenomena: A Spectrum of Autoimmune Disease?
Case Reports in Immunology, 2019 Parry–Romberg syndrome (PRS) is a rare disorder characterized by unilateral facial atrophy. Currently, the pathogenesis of PRS is poorly understood and no definitive treatment is available.
Samuel Asanad
doaj +1 more source
Movement Disorders Clinical Practice, Volume 12, Issue 3, Page 272-284, March 2025.Abstract Background Myoclonus and other jerky movement disorders are hyperkinetic disorders, the diagnosis of which heavily relies on clinical neurophysiological testing. However, formal diagnostic criteria are lacking, and recently the utility and reliability of these tests have been questioned.
Anna Latorre +8 more
wiley +1 more source
Comparison of 3D facial photographs and clinical documentation in patients with craniofacial morphea
Skin Health and Disease, Volume 4, Issue 6, December 2024.Craniofacial morphea (CM) is a rare autoimmune disease characterised by progressive atrophy of the skin and soft tissue of the face, resulting in facial asymmetry. With the involvement of varying practices in the care of patients with CM, consistent documentation of disease location and severity lack standardized evaluation.
Tyler T. Nguyen +5 more
wiley +1 more source