Results 111 to 120 of about 31,200 (259)

Dynamics of Nerve Conduction Studies in Patients With Guillain–Barré Syndrome

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims The value of electrodiagnostic subtyping of Guillain–Barré syndrome (GBS) is still debated. This study aimed to determine the diagnostic yield, timing, and changes of the electrodiagnostic subtyping in patients with GBS in serial nerve conduction studies (NCS).
Samuel Arends   +181 more
wiley   +1 more source

Pyridostigmine Treatment for Pediatric Axonal Guillain–Barré Syndrome

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims Direct involvement of the neuromuscular junction (NMJ) in the inflammatory process of Guillain–Barré syndrome (GBS) has been described. Despite this, the NMJ very rarely serves as a target for direct medical intervention in GBS.
E. Zohar‐Dayan   +3 more
wiley   +1 more source

Autoimmune mechanisms in Guillain-Barré syndrome subtypes: a systematic review

open access: yesBulletin of Faculty of Physical Therapy
Guillain-Barré syndrome (GBS) is a complex autoimmune disorder characterized by acute onset of motor weakness, often following an infectious illness. The pathophysiology of GBS involves a multifaceted interplay between immune mechanisms and environmental
O. I. Oshomoji   +4 more
doaj   +1 more source

NMDA Receptors Coordinate Metabolic Reprogramming and Mitophagy in Schwann Cells to Promote Peripheral Nerve Regeneration

open access: yesResearch
Schwann cells (SCs) are indispensable for peripheral nerve regeneration, yet the mechanisms enabling their metabolic adaptation to meet the energetic demands of axonal repair remain elusive.
Fangzhen Shan   +7 more
doaj   +1 more source

290 surgical procedures for ulnar nerve entrapment at the elbow: Physiopathology, clinical experience and results [PDF]

open access: yes, 2000
Ulnar nerve entrapment at the elbow is an important and relatively frequent pathological condition that may be related to diffent causes depending on individual or external factors. The cause of the nerve lesion is also idiopathic in about one-quarter to
Artico, M   +3 more
core   +1 more source

Ultrasonographic evaluation of ulnar innervated muscles in ulnar neuropathy at the elbow

open access: yesPM&R, EarlyView.
Abstract Background Quantitative muscle ultrasound (qMUS) provides morphological measurements that can support clinical observation of muscle atrophy and weakness. As the use of qMUS continues to expand, and its potential for broader implementation in neuromuscular evaluation grows, there is a clear need for further validation, particularly in ...
Emmanuel Ogalo   +7 more
wiley   +1 more source

An unusual presentation of gbs: case report and literature review [PDF]

open access: yes, 2016
Guillain-Barre syndrome (GBS), also known as Landry paralysis is an acute idiopathic polyneuritis, believed to be immunologically mediated. It usually presents as a demyelinating neuropathy with ascending weakness, however, many clinical variants have ...
Badshah, Mazhar   +3 more
core   +1 more source

Hyperreflexia in acute motor axonal neuropathy

open access: yesTürkiye Fiziksel Tıp ve Rehabilitasyon Dergisi, 2016
We observed hyperreflexia in the course of the motor axonal neuropathy form of Guillain-Barre syndrome (GBS). Herein, we would like comment on a rare case. Acute motor axonal neuropathy (AMAN) is a type of GBS accompanied by peripheral axonal involvement where acute motor paralysis, loss of reflex or hyporeflexia, insignificant sensory loss, and ...
openaire   +2 more sources

Differentiating lower motor neuron syndromes [PDF]

open access: yes, 2017
Lower motor neuron (LMN) syndromes typically present with muscle wasting and weakness and may arise from pathology affecting the distal motor nerve up to the level of the anterior horn cell. A variety of hereditary causes are recognised, including spinal
Cornblath, DR   +12 more
core  

The differential diagnosis of chorea [PDF]

open access: yes, 2007
Chorea is a hyperkinetic movement disorder characterised by excessive spontaneous movements that are irregularly timed, randomly distributed and abrupt. In this article, the authors discuss the causes of chorea, particularly Huntington's disease and the ...
Tabrizi, SJ, Wild, EJ
core   +1 more source

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