Results 171 to 180 of about 11,788 (205)
Some of the next articles are maybe not open access.
Fiber density in acute and chronic inflammatory demyelinating polyneuropathy
Muscle & Nerve, 1992AbstractThe fiber density in the deltoid, extensor digitorum communis, and first dorsal interosseous muscles was measured using SFEMG in 11 patients with acute and chronic inflammatory demyelinating polyneuropathy. The fiber density was increased in 58% of the muscles studied. The deltoid muscle was the most abnormal of the 3 muscles studied. There was
M, Gantayat, M, Swash, M S, Schwartz
openaire +2 more sources
Concurrent transverse myelitis and acute inflammatory demyelinating polyneuropathy
BMJ Case ReportsA woman in her 40s presented with thoracic banding dysaesthesia and lower motor neuron weakness. Spinal imaging revealed a short segment of transverse myelitis and neurophysiology was suggestive of concurrent acute inflammatory demyelinating polyneuropathy.
Matthew Shrimpton, Cameron Shaw
openaire +2 more sources
Acute Inflammatory Demyelinating Polyneuropathy (Guillain-Barré Syndrome)
2013Acute inflammatory demyelinating polyneuropathy (AIDP), also known as Guillain-Barré syndrome (GBS), is a common acute neurological presentation encountered in both the outpatient setting and hospital wards. The hallmark of the disorder is the development of ascending motor paralysis with loss of deep tendon reflexes.
Aaron E. Miller, Teresa M. DeAngelis
openaire +1 more source
Journal of the Neurological Sciences, 2014
Inflammatory neuropathies have been reported to occur in association with nephrotic syndrome. Their underlying immuno-pathogenic mechanisms remain unknown. A 50-year-old woman concurrently presented with acute-onset chronic inflammatory demyelinating polyneuropathy and nephrotic syndrome secondary to focal segmental glomerulosclerosis.
Amy May Lin, Quek +4 more
openaire +2 more sources
Inflammatory neuropathies have been reported to occur in association with nephrotic syndrome. Their underlying immuno-pathogenic mechanisms remain unknown. A 50-year-old woman concurrently presented with acute-onset chronic inflammatory demyelinating polyneuropathy and nephrotic syndrome secondary to focal segmental glomerulosclerosis.
Amy May Lin, Quek +4 more
openaire +2 more sources
Chronic inflammatory demyelinating polyneuropathy mimicking an acute painful diabetic neuropathy
Neurological Sciences, 2015Acute diabetic painful neuropathy associated with weight loss, also known as ‘‘diabetic neuropathic cachexia’’, presents with severe burning pain, particularly in the feet and the onset is associated with weight loss. Clinical features are the presence of allodynia and hyperalgesia, as well as depression and erectile dysfunction.
TOPA, ANTONIETTA +4 more
openaire +2 more sources
Acute inflammatory demyelinating polyneuropathy as the initial presentation of lupus
The American Journal of Emergency Medicine, 2009A 28-year-old woman presented at the emergency department (ED) with acute bilateral leg weakness and lost the ability to walk 1 day after noticing bilateral leg numbness and intermittent pleuritic pain for 3 weeks. Physical examination revealed bilateral decreased muscle strength with score 4 symmetrically in the legs and decreased deep tendon reflex ...
Tai-Yi, Hsu +4 more
openaire +2 more sources
Perineurium contributes to axonal damage in acute inflammatory demyelinating polyneuropathy
Neurology, 2000To assess if axonal damage in severe acute inflammatory demyelinating polyneuropathy (AIDP) correlates with the appearance of epiperineurium in nerve trunks.Increase of endoneurial fluid pressure in nerve trunks possessing epiperineurium may be an important mechanism of axonal damage in AIDP.A 79-year-old man had a 2-day history of acroparesthesias and
J, Berciano +5 more
openaire +2 more sources
[Autonomic dysfunction in acute inflammatory demyelinating polyneuropathy].
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 2005Acute inflammatory demyelinating polyneuropathy (AIDP) is an autoimmune process that is characterized by progressive weakness, mild sensory changes and autonomic dysfunction. It is a rare disorder, afflicting about 1 person in 100,000. Yet, since the decline in the number of polio cases, it represents the most common cause of acute neuromuscular ...
D, Cuciureanu, Rodica, Prodan
openaire +1 more source
Acute inflammatory demyelinating polyneuropathy following Ciguatera poisoning
Muscle & Nerve, 2022Katsumi Kurokawa +6 more
openaire +2 more sources
Acute inflammatory demyelinating polyneuropathy following bone marrow transplantation.
Bone marrow transplantation, 1992Acute inflammatory demyelinating polyneuropathy (AIDP) appeared in two patients following allogeneic bone marrow transplantation (BMT). In one transplanted patient (but not in the donor) T cells were sensitized against peripheral nervous system myelin. This could reflect a change in the T cell repertoire in a different milieu.
S, Eliashiv +6 more
openaire +1 more source

