Results 111 to 120 of about 6,748 (229)

Detection of evolving injury to the brachial plexus during transaxillary robotic thyroidectomy. [PDF]

, 2012
OBJECTIVES/HYPOTHESIS: Continuous intraoperative neuromonitoring (IONM) of transcranial electric motor evoked potentials (tceMEPs) and somatosensory evoked potentials (SSEPs) has gained universal acceptance as an efficacious method for detecting emerging
Cognetti, David, Luginbuhl, Adam, Pribitkin, Edmund, Schwartz, Daniel M, Sestokas, Anthony K   +4 more
core   +1 more source

Common peroneal neuropathy

, 2021
Patrick Baird-Fraser, Rohit Sharma, Mostafa Elfeky   +2 more
openaire   +1 more source

Lowering the osteotomized level of fibular osteotomy reduces neuromuscular complications while maintaining clinical efficacy in treating medial compartment knee osteoarthritis: a retrospective comparative cohort study

European Journal of Medical Research
Background Partial fibular osteotomy (PFO) offers a minimally invasive strategy for treating medial compartment knee osteoarthritis (MKOA), yet its proximity to the peroneal nerve raises concern for postoperative neuropathy.
Ting-Yu Chang, Chih-Wei Chang, Yen-Nien Chen, Chyun-Yu Yang, Jou-Hua Wang   +4 more
doaj   +1 more source

Wartenberg’s migrant sensory neuritis: a prospective follow-up study [PDF]

, 2010
Abraham C. J. Stork, Marjon F. G. van der Meulen, W.-Ludo van der Pol, Alexander F. J. E. Vrancken, Hessel Franssen, Nicolette C. Notermans, AK Asbury, G Devigili, H Franssen, RWM Keunen, J Kimura, C Laterre, WB Matthews, MW Nicolle, E Nobile-Orazio, L Servioli, G Sobue, AF Vrancken, R Wartenberg, UA Zifko   +19 more
core   +1 more source

Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies [PDF]

, 2017
Hereditary neuropathies form a heterogeneous group of disorders for which over 40 causal genes have been identified to date. Recently, dominant mutations in the transient receptor potential vanilloid 4 gene were found to be associated with three distinct
Auer-Grumbach, Michaela, Baets, Jonathan, Barisic, Nina, Berciano, José, Boltshauser, Eugen, Crosby, Andrew H., Fischbeck, Kenneth H., Garcia, Antonio, Gaudet, Rachelle, Hilton-Jones, David, Houlden, Henry, Jonghe, Peter De, Jordanova, Albena, Landouré, Guida, Lopez-Laso, Eduardo, Ludlow, Christy L., McEntagart, Meriel, Merlini, Luciano, Reilly, Mary M., Shaw, Christopher E., Sumner, Charlotte J., Timmerman, Vincent, Zimoń, Magdalena   +22 more
core  

SIGMAR1 mutation associated with autosomal recessive Silver-like syndrome [PDF]

, 2016
OBJECTIVE: To describe the genetic and clinical features of a simplex patient with distal hereditary motor neuropathy (dHMN) and lower limb spasticity (Silver-like syndrome) due to a mutation in the sigma nonopioid intracellular receptor-1 gene (SIGMAR1)
Blake, JC, Gonzalez, MA, Hanna, MG, Horga, A, Houlden, H, Laurà, M, Manzur, AY, Muntoni, F, Reilly, MM, Tomaselli, PJ, Züchner, S   +10 more
core  

Joubert syndrome presenting bilateral peroneal neuropathies: A case report. [PDF]

Medicine (Baltimore)
Kim HM, Jo HS, Han JY, Choi IS, Song MK, Park HK.   +5 more
europepmc   +1 more source

Isolated Left Peroneal Neuropathy Following Total Laparoscopic Hysterectomy: A Case Report. [PDF]

Cureus
Hurtado Bravo HA, Bravo Rodriguez LM.
europepmc   +1 more source

Nerve conduction velocity in patients under longterm treatment with antiepileptic drugs [PDF]

, 1990
Berlit, Peter, Krause, Klaus-Henning
core  

Defining True Motor Conduction Block in Chronic Immune-Mediated Demyelinating Neuropathies: A Temporal Dispersion-Based Electrodiagnostic Approach. [PDF]

Eur J Neurol
Mercan M, Yayla V, Kurt A.
europepmc   +1 more source