Results 51 to 60 of about 1,552 (157)

Investigating the Mechanism of Conditioning Versus Postoperative Electrical Stimulation to Enhance Nerve Regeneration: One Therapy, Two Distinct Effects

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, Bonnie Y. Wang, K. Ming Chan, Christine A. Webber, Jenna‐Lynn B. Senger   +4 more
wiley   +1 more source

Botulinum toxin type A treatment for a parotid gland injury in two adult horses

Equine Veterinary Education, Volume 37, Issue 7, Page e119-e125, July 2025.
Summary The most common disorder affecting the salivary glands in horses is trauma to the parotid gland or duct. Several management techniques have been described, each with their own set of complications. The objective of this case report was to describe the direct injection of botulinum toxin type A into the parotid gland and its outcome in two ...
C. Jimenez, F. Comino, D. Gorvy
wiley   +1 more source

Demyelinating etiology as a possible cause of Parry–Romberg Syndrome (PP-14) [PDF]

Neurology Letters, 2023
Parry–Romberg syndrome (PRS) is a rare disease that causes hemiatrophy of the face. The pathophysiological mechanisms involved in its etiology are unknown, but several previous reports suggest the involvement of autoimmune factors.
K. Bahrami, Mohammad Ali Nahayati, Mohammad Shriati   +2 more
doaj  

Airway Ultrasound Findings in a Rare Case of Parry–Romberg Syndrome

Airway
Parry–Romberg syndrome (PRS) is a rare disorder characterised by progressive hemifacial atrophy, along with various neurological and ophthalmological manifestations.
Bhavna Gupta, Gaurav Jain, Ravi Chaudhary, Kajal Shrestha   +3 more
doaj   +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

The cerebellum in epilepsy

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, Rebecca Kerestes, Puneet Opal, Maria Marchese, Orrin Devinsky   +4 more
wiley   +1 more source

Diagnostic Utility of Clinical Neurophysiology in Jerky Movement Disorders: A Review from the MDS Clinical Neurophysiology Study Group

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, Christos Ganos, Masashi Hamada, Nicolas Phielipp, Lorenzo Rocchi, Shabbir Merchant, Marina A. Tijssen, Sterre van der Veen, Robert Chen   +8 more
wiley   +1 more source

Facial Myokymia With or Without Concurrent Neurological Deficits in Seven Dogs and Two Cats

Journal of Veterinary Internal Medicine, Volume 39, Issue 2, March/April 2025.
ABSTRACT Background Myokymia is a form of peripheral nerve hyperexcitability that can be focal or generalized. Information regarding focal myokymia in veterinary medicine is currently limited, resulting in a need for a better understanding of this clinical sign.
Tomás Elvira, Claudia Mallol, Abbe Crawford, Edward Ives, Anne R. Fraser, Lorenzo Mari, Anna Tauro, Patricia Alvarez, Victoria Indzhova, Giulia Corsini, Bruno Lopes, Josep Brocal   +11 more
wiley   +1 more source

Parry-romberg syndrome: about a case

The Pan African Medical Journal, 2017
A six-year-old girl presented with skin lesions on the left cheek at 5 years of age. On examination diffuse sclerosis on the left cheek was noted, hypoplasia of left half of the face and deviation of mouth and lips to left side were noted. Investigations
Hanane Oummad, Lalla Ouafae Cherkaoui
doaj   +1 more source

Congenital Partial Hypoplasia of the Lower Lip: A Rare Form of 28–29 Tessier Cleft? Report of a Case

Clinical Case Reports, Volume 13, Issue 2, February 2025.
ABSTRACTWe aim to describe a case of congenital partial hypoplasia of the lower lip in a 2‐year‐old child. The presence of a gingival notch, a mucosal bridle, and difficulties with tooth eruption raised the possibility of a modified 28–29 Tessier cleft.
Olina Rios, Virginie Lafontaine, Cyril Debortoli, Charles Savoldelli, Beatrice Morand   +4 more
wiley   +1 more source