Z Argov
Overview
Explore the profile of Z Argov including associated specialties, affiliations and a list of published articles.
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Articles
111
Citations
1509
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Recent Articles
1.
Argov Z
Eur J Neurol
. 2014 Dec;
22(1):31-6.
PMID: 25495398
Statins intolerance is mainly due to their side effects on the neuromuscular system (primarily muscle). It has become an important issue because of the major cardiovascular risk reduction of this...
2.
Kerty E, Elsais A, Argov Z, Evoli A, Gilhus N
Eur J Neurol
. 2014 Jan;
21(5):687-93.
PMID: 24471489
Background And Purpose: The symptoms of acquired autoimmune ocular myasthenia are restricted to the extrinsic eye muscles, causing double vision and drooping eyelids. These guidelines are designed to provide advice...
3.
Steiner I, Gotkine M, Steiner-Birmanns B, Biran I, Silverstein S, Abeliovich D, et al.
J Neurol
. 2008 Apr;
255(6):813-9.
PMID: 18438698
Background: Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene. This mutation is not modified during...
4.
Leshinsky-Silver E, Argov Z, Rozenboim L, Cohen S, Tzofi Z, Cohen Y, et al.
Neuromuscul Disord
. 2007 Sep;
17(11-12):950-4.
PMID: 17825554
Dysferlin encoding gene (DYS) is mutated in the autosomal recessive disorders Miyoshi myopathy, Limb Girdle Muscular Dystrophy type 2B (LGMD2B) and distal anterior compartment myopathy, causing dysferlin deficiency in muscle...
5.
Argov Z, McKee D, Agus S, Brawer S, Shlomowitz N, Yoseph O, et al.
Neurology
. 2007 Aug;
69(7):699-700.
PMID: 17698793
No abstract available.
6.
Krause S, Aleo A, Hinderlich S, Merlini L, Tournev I, Walter M, et al.
Neurology
. 2007 Aug;
69(7):655-9.
PMID: 17698786
Mutations in GNE encoding UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) cause hereditary inclusion body myopathy (HIBM). To define the role of GNE mutations in HIBM pathogenesis, GNE protein expression was analyzed. GNE...
7.
Miller F, Rider L, Plotz P, Rutkove S, Pestronk A, Wortmann R, et al.
Neurology
. 2004 Jul;
63(2):402.
PMID: 15277657
No abstract available.
8.
Argov Z, Eisenberg I, Grabov-Nardini G, Sadeh M, Wirguin I, Soffer D, et al.
Neurology
. 2003 May;
60(9):1519-23.
PMID: 12743242
Background: Recessively inherited hereditary inclusion body myopathy (HIBM) with quadriceps sparing was initially described only in Jews originating from the region of Persia. The recent identification of the gene responsible...
9.
Eisenberg I, Hochner H, Sadeh M, Argov Z, Mitrani-Rosenbaum S
Cytogenet Genome Res
. 2002 Nov;
97(1-2):58-61.
PMID: 12438739
The human RECK gene, mapped at 9p13-->p12, is known as a tumor suppressor gene and as a key regulator of extracellular matrix integrity and angiogenesis. We have established the entire...
10.
Chen J, Taivassalo T, Argov Z, Arnold D
Magn Reson Med
. 2001 Oct;
46(5):870-8.
PMID: 11675637
Post-exercise recovery of intracellular pH (pH(i)) assessed using phosphorus magnetic resonance spectroscopy has not been previously evaluated in its entirety due to its complex time-course and missing data points resulting...