Results 81 to 90 of about 735,247 (179)
Protein Biomarkers in Risk and Prognosis of Amyotrophic Lateral Sclerosis
ABSTRACT Background Plasma and cerebrospinal fluid (CSF) protein biomarkers in amyotrophic lateral sclerosis (ALS) may provide insight into disease mechanisms and yield clinically useful biomarkers. Methods Overall, 363 proteins in plasma and CSF from 198 patients with ALS and 125 matched controls were profiled using Olink assays.
Lu Pan +23 more
wiley +1 more source
Introduction: Motor neuron diseases (MND), characterized by amyotrophic lateral sclerosis (ALS) and progressive bulbar palsy (PBP), is defined by progressive, irreversible and incapacitating motor paralysis with survival from two to five years after ...
Pimentel, Renata Martins [UNIFESP]
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Summary A 2‐year‐old Arabian filly presented with acute onset grade 4/5 (AAEP) right forelimb lameness and hindlimb ataxia following a collision with another horse and subsequent fall. The right forelimb lameness was associated with marked scapulohumeral joint instability.
O. E. Newman, B. Dunkel, M. Perrier
wiley +1 more source
Adult-onset bulbar ptosis in Joubert syndrome [PDF]
Benjamin Burt, Johanan Levine, Kim LeTexas Tech University, Department of Ophthalmology, Paul L Foster School of Medicine, El Paso, TexasAbstract: In this case report, we describe a case of adult-onset bulbar ptosis in a patient with Joubert syndrome ...
Le K, Burt B, Levine J
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Surgical interventions for the early management of Bell's palsy [PDF]
Background: Bell's palsy is an acute paralysis of one side of the face of unknown aetiology. Bell's palsy should only be used as a diagnosis in the absence of all other pathology.
McAllister, Kerrie +7 more
core +1 more source
VRK1‐Related Motor Neuropathy With Upper Motor Neuron Signs and Selective Muscle Involvement
ABSTRACT Introduction Hereditary motor neuropathies (HMN) represent a heterogeneous group of disorders with wide clinical and genetic variability. Despite advances in molecular diagnostics, approximately 50% of cases remain genetically unresolved, particularly those where distinguishing length‐dependent motor neuropathy from motor neuron disorder with ...
Manoella Guerra de Albuquerque Bueno +11 more
wiley +1 more source
A Quarter Century of EHD Protein Research: From Endosomal Recycling to Ciliopathies
Human EHD protein subcellular localization. ABSTRACT Eps15 homology domain‐containing proteins comprise a conserved family of membrane‐remodeling ATPases that regulate endocytic trafficking, membrane fission, receptor recycling, primary ciliogenesis and membrane dynamics across eukaryotes. Since the initial identification of EHD1 and its Caenorhabditis
Devin Frisby +3 more
wiley +1 more source
ABSTRACT This case report describes the clinical presentation and successful surgical management of a combined dorsal entropion‐ectropion macroblepharon with an elongated and folded nictitating membrane in a 2‐year‐old male giant rabbit. The rabbit initially presented with bilateral chronic, recurrent corneal erosions secondary to abnormal eyelid and ...
Anja Suter +4 more
wiley +1 more source
Zolpidem in Progressive Supranuclear Palsy [PDF]
Progressive supranuclear palsy (PSP) is a progressive neurodegenerative disorder, characterized by motor symptoms, postural instability, personality changes, and cognitive impairment. There is no effective treatment for this disorder.
Sandip K. Dash, Sandip K. Dash
core +1 more source
GUILLAIN-BARRÉ SYNDROME ASSOCIATED WITH ACUTE HEV HEPATITIS
Guillain-Barré Syndrome (GBS) otherwise known as Acute Inflammatory Polyneuritis, characterized by acute progressive limb weakness and aretlexia, is the prototype of a post infectious autoimmune disease.
Rawshan Ara Khanam +3 more
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