Results 111 to 120 of about 6,749 (232)

Chronic motor neuropathies: response to interferon-beta1a after failure of conventional therapies [PDF]

, 1999
OBJECTIVES: The effect of interferon-beta1a (INF-beta1a; Rebif) was studied in patients with chronic motor neuropathies not improving after conventional treatments such as immunoglobulins, steroids, cyclophosphamide or ...
Doorn, P.A. (Pieter) van, Martina, I.S., Meché, F.G.A. (Frans) van der, Meulstee, J. (Jan), Schmitz, P.I.M. (Paul)   +4 more
core  

Motor Nerve Conduction Studies in Patients with Chronic Renal failure

Journal of Rawalpindi Medical College, 2010
Background: Detection of frequency of neuropathy in patients with chronic renal failure by utilizing nerve conduction studies (NCS) Methods: In this cross sectional comparative study, thirty patients with chronic renal failure, of at least three months ...
Khadija Fatima
doaj   +2 more sources

The Anterior Tarsal Tunnel Syndrome [PDF]

, 1977
Krause, Klaus-Henning, Ross, A., Witt, T. N.   +2 more
core   +1 more source

Charcot–Marie–Tooth disease: Genetics, epidemiology and complications [PDF]

, 2017
Background and aims: Charcot Marie Tooth disease (CMT) is the most prevalent hereditary neuropathy and its frequency is 1 in 2500. CMT is a heterogeneous disease and has different clinical symptoms.
Ahmadinejad, Fereshteh., Jami, Mohammad-Saeid., Maghsoudi, Reza., Pourhadi, Masoumeh.   +3 more
core  

Common peroneal neuropathy

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

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  

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  

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

A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease [PDF]

, 2013

core   +1 more source

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