Results 41 to 50 of about 9,800 (213)
Motoric Automatisms of the Maxillofacial Region: a Lecture
Вестник восстановительной медицины, 2022 INTRODUCTION. Effective kinesitherapy of peripheral and central paralysis of the mimic, masticatory, lingual and pharyngeal muscles requires in-depth study of the features of the cooperative work of these muscles in the norm and in pathology. AIM.
Konstantin B. Petrov +2 more
doaj +1 more source
A practical approach to the patient presenting with dropped head [PDF]
, 2016 Head drop, or having a dropped head, is an uncommon condition in which patients present with a disabling inability to lift their head. It may arise in many neurological conditions that can be divided into those with neuromuscular weakness of neck ...
Demicoli, Marija, Marsh, Eleanor A.
core +1 more source
A Variant Guillain-Barré Syndrome with Anti-Ganglioside Complex Antibody [PDF]
Journal of Neurocritical Care, 2018 Background Recently, anti-ganglioside complex (GSC) antibodies were discovered among the various subtypes of Guillain-Barré syndrome. GSC is the novel glycoepitopes formed by two individual ganglioside molecules.
So-Young Huh +6 more
doaj +1 more source
Fatal subarachnoid hemorrhage following ischemia in vertebrobasilar dolichoectasia. [PDF]
, 2016 Vertebrobasilar dolichoectasia (VBD) is a chronic disorder with various cerebrovascular and compressive manifestations, involving subarachnoid hemorrhage (SAH).
Caso, V. +10 more
core +3 more sources
Motor Neurone Disease (MND/ALS) among Maltese in Malta and Australia : many sporadic cases were related [PDF]
, 2014 Objective: to look for genetic links between cases of MND. Method: to search for ancestors of Maltese cases dying in Malta and Australia and to record dispensations for consanguineous marriages.
Wyatt, H. V.
core
Neurotrophic keratitis in a patient with disseminated lymphangiomatosis. [PDF]
, 2009 INTRODUCTION: Neurotrophic keratitis, a degenerative corneal disease caused by trigeminal nerve impairment, has many etiologies and remains very difficult to treat.
Charukamnoetkanok, Puwat +2 more
core +2 more sources
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Introduction Progressive Supranuclear Palsy (PSP) is a neurodegenerative ‘tauopathy’ with predominating pathology in the basal ganglia and midbrain. Caudal tau spread frequently implicates the cerebellum; however, the pattern of atrophy remains equivocal.
Chloe Spiegel +8 more
wiley +1 more source
Bulbar Muscle Weakness in the Setting of Therapeutic Botulinum Injections
Clinical Practice and Cases in Emergency Medicine, 2018 We present a case of new-onset bulbar muscle weakness in the setting of therapeutic botulinum injections for spasticity in a teenaged patient with cerebral palsy. Through a careful history, a systemic effect of the local injections was suspected, and the
Jacob Lentz, Daniel Weingrow
doaj +1 more source
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family [PDF]
, 2018 Riboflavin transporter deficiency (formerly known as Brown-Vialetto-Van Laere [BVVL] or Fazio-Londe syndrome) is a neurodegenerative disorder characterized by progressive bulbar palsy with sensorineural deafness or bulbar hereditary neuropathy.1 It is ...
Bras, J +3 more
core +1 more source
Clinical Validation of Plasma p‐217tau in Neurological Diseases
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.
Takeshi Kawarabayashi +13 more
wiley +1 more source