Results 21 to 30 of about 43,338 (304)

Mixed Connective Tissue Disease with Severe Axonal Polyneuropathy: A Case Report

open access: yesOman Medical Journal, 2022
Mixed connective tissue disease (MCTD) is a unique disorder characterized by the presence of a high titer of anti-U1 ribonucloprotein antibody with overlapping features of various connective tissue disorders including systemic lupus erythematosus ...
Talal Al Lawati, Batool Hassan
doaj   +1 more source

Inflammatory demyelinating polyneuropathies and patient management during the COVID-19 pandemic. Literature review

open access: yesNeurologijos seminarai, 2020
Inflammatory demyelinating polyneuropathies are rare but potentially treatable disorders. They can cause a lot of difficulties in daily practice due to their clinical heterogeneity and long term immunosuppressive treatment.
R. Bunevičiūtė , A. Klimašauskienė
doaj   +1 more source

Contemporary management of pain in cirrhosis: Toward precision therapy for pain

open access: yesHepatology, EarlyView., 2022
Abstract Chronic pain is highly prevalent in patients with cirrhosis and is associated with poor health‐related quality of life and poor functional status. However, there is limited guidance on appropriate pain management in this population, and pharmacologic treatment can be harmful, leading to adverse outcomes, such as gastrointestinal bleeding ...
Alexis Holman   +4 more
wiley   +1 more source

Pulmonary and Physical Rehabilitation in Critically Ill Patients [PDF]

open access: yesAcute and Critical Care, 2019
Some patients admitted to the intensive care unit (ICU) because of an acute illness, complicated surgery, or multiple traumas develop muscle weakness affecting the limbs and respiratory muscles during acute care in the ICU.
Myung Hun Jang   +2 more
doaj   +1 more source

Genome-Wide Association Study of 2,093 Cases With Idiopathic Polyneuropathy and 445,256 Controls Identifies First Susceptibility Loci

open access: yesFrontiers in Neurology, 2021
Background: About one third of patients with chronic polyneuropathy have no obvious underlying etiology and are classified as having idiopathic polyneuropathy. The lack of knowledge about pathomechanisms and predisposing factors limits the development of
Bendik S. Winsvold   +16 more
doaj   +1 more source

DIABETIC POLYNEUROPATHY: PATHOGENESIS, CLINICAL PRESETATION AND NEW APPROACHES TO PERSONALIZED TREATMENT

open access: yesМедицинский совет, 2017
In summary, this review provides complex presentation of the most contemporary concepts of pathogenesis, clinical presentation and therapy of diabetic polyneuropathies.
M. M. Tanashyan   +2 more
doaj   +1 more source

Deciphering immune mechanisms in chronic inflammatory demyelinating polyneuropathies.

open access: yesJCI Insight, 2020
Chronic inflammatory demyelinating polyneuropathy (CIDP) is an autoimmune disease of the peripheral nerves that presents with either chronic progression or relapsing disease.
Jolien Wolbert   +3 more
semanticscholar   +1 more source

Disulfiram-induced polyneurophaty [PDF]

open access: yesVojnosanitetski Pregled, 2012
Introduction. Disulfiram is used in the treatment of chronic alcoholism, because of the unpleasant symptoms produced after ethanol intake. Although it is well tolerated in most patients, one in 15,000 patients will develop peripheral neuropathy every ...
Vujisić Slavica   +5 more
doaj   +1 more source

The Coexistence of Antibodies to Neuronal Cell and Synaptic Receptor Proteins, Gangliosides and Selected Neurotropic Pathogens in Neurologic Disorders in Children

open access: yesDiagnostics, 2023
Various primarily non-autoimmune neurological disorders occur synchronously with autoantibodies against tissues in the nervous system. We aimed to assess serum and cerebrospinal fluid (CSF) autoantibodies in children with neurologic disorders.
Karol Lubarski   +5 more
doaj   +1 more source

Leprosy mimicking lupus erythematosus

open access: yesDermatologica Sinica, 2014
Leprosy, a contagious and chronic granulomatous disease caused by Mycobacterium leprae, is classically known to have cutaneous and neurologic sequelae. Leprosy usually has a long incubation period and may manifest with a variety of autoimmune phenomena ...
Tsung-Ting Hsieh, Yu-Hung Wu
doaj   +1 more source

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