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Zohar Argov

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Ilan Sela; Lena Yakovlev; Nurit Yanay; Hagit Yotvat; Zohar Argov; Michal Becker Cohen; Uri Ben Shlomo; Moran Elbaz; Yakov Fellig; Stella Mitrani-Rosenbaum
Variable phenotypes of knockin mice carrying the M712T Gne mutation.
Stella Mitrani-Rosenbaum; Zohar Argov; Michal Becker Cohen; Uri Ben Shlomo; Moran Elbaz; Yakov Fellig; Avi Harazi; Michal Telem; Lena Yakovlev; Nurit Yanay; Hagit Yotvat; Ilan Sela
Sustained expression and safety of human GNE in normal mice after gene transfer based on AAV8 systemic delivery.
Adir Shaulov; Boris Shichman; Maya Spiegel; Hagit Peleg; Misgav Rottenstreich; Zohar Argov
Myasthenia gravis appearing 18 years after resection of benign thymoma with subsequent limbic encephalitis.

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2013: Ilan Sela; Lena Yakovlev; Nurit Yanay; Hagit Yotvat; Zohar Argov; Michal Becker Cohen; Uri Ben Shlomo; Moran Elbaz; Yakov Fellig; Stella Mitrani-Rosenbaum
Variable phenotypes of knockin mice carrying the M712T Gne mutation.
Neuromolecular medicine 2013;15(1):180-91.
2012: Stella Mitrani-Rosenbaum; Zohar Argov; Michal Becker Cohen; Uri Ben Shlomo; Moran Elbaz; Yakov Fellig; Avi Harazi; Michal Telem; Lena Yakovlev; Nurit Yanay; Hagit Yotvat; Ilan Sela
Sustained expression and safety of human GNE in normal mice after gene transfer based on AAV8 systemic delivery.
Neuromuscular disorders : NMD 2012;22(11):1015-24.
2012: Adir Shaulov; Boris Shichman; Maya Spiegel; Hagit Peleg; Misgav Rottenstreich; Zohar Argov
Myasthenia gravis appearing 18 years after resection of benign thymoma with subsequent limbic encephalitis.
Journal of the neurological sciences 2012;317(1-2):146-7.
2011: Ilan Sela; Irit Milman Krentsis; Zipora Shlomai; Menachem Sadeh; Ron Dabby; Zohar Argov; Hannah Ben-Bassat; Stella Mitrani-Rosenbaum
The proteomic profile of hereditary inclusion body myopathy.
PloS one 2011;6(1):e16334.
2011: Zohar Argov
Current approach to seronegative myasthenia.
Journal of neurology 2011;258(1):14-8.
2009: Zohar Argov; Marianne de Visser
What we do not know about pregnancy in hereditary neuromuscular disorders.
Neuromuscular disorders : NMD 2009;19(10):675-9.
2009: Zohar Argov
Management of myasthenic conditions: nonimmune issues.
Current opinion in neurology 2009;22(5):493-7.
2008: Zohar Argov; Stella Mitrani-Rosenbaum
The hereditary inclusion body myopathy enigma and its future therapy.
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 2008;5(4):633-7.
2008: Israel Steiner; Marc Gotkine; Bettina Steiner-Birmanns; Iftah Biran; S Silverstein; D Abeliovich; Zohar Argov; Itzhak Wirguin
Increased severity over generations of Charcot-Marie-Tooth disease type 1A.
Journal of neurology 2008;255(6):813-9.
2008: Jon D Sussman; Zohar Argov; David McKee; Eli Hazum; Solli Brawer; Hermona Soreq
Antisense treatment for myasthenia gravis: experience with monarsen.
Annals of the New York Academy of Sciences 2008;1132():283-90.
2007: Esther Leshinsky-Silver; Zohar Argov; L Rozenboim; S Cohen; Z Tzofi; Y Cohen; Y Wirguin; Ron Dabby; Dorit Lev; Menachem Sadeh
Dysferlinopathy in the Jews of the Caucasus: a frequent mutation in the dysferlin gene.
Neuromuscular disorders : NMD 2007;17(11-12):950-4.
2007: Nizar Elleuch; Naima Bouslam; Sylvain Hanein; Alexander Lossos; Abdelmadjid Hamri; Stephan Klebe; Vardiella Meiner; Nazha Birouk; Israela Lerer; Djamel Grid; Delphine Bacq; Meriem Tazir; Diana Zelenika; Zohar Argov; Alexandra Durr; Mohamed Yahyaoui; Ali Benomar; Alexis Brice; Giovanni Stevanin
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families.
Neurogenetics 2007;8(4):307-15.
2007: Marc Gotkine; Zohar Argov
Clinical differentiation between primary lateral sclerosis and upper motor neuron predominant amyotrophic lateral sclerosis.
Archives of neurology 2007;64(10):1545; author reply 1545.
2007: Zohar Argov; D McKee; Samuel Agus; S Brawer; N Shlomowitz; O Ben Yoseph; Hermona Soreq; J D Sussman
Treatment of human myasthenia gravis with oral antisense suppression of acetylcholinesterase.
Neurology 2007;69(7):699-700.
2007: Sabine Krause; A Aleo; Stephan Hinderlich; Luciano Merlini; I Tournev; Maggie C Walter; Zohar Argov; Stella Mitrani-Rosenbaum; Hanns Lochmüller
GNE protein expression and subcellular distribution are unaltered in HIBM.
Neurology 2007;69(7):655-9.
2007: Frank L Mastaglia; Zohar Argov
Toxic and iatrogenic myopathies.
Handbook of clinical neurology 2007;86():321-41.
2007: Zohar Argov; Stella Mitrani-Rosenbaum
Hereditary inclusion body myopathy and other rimmed vacuolar myopathies.
Handbook of clinical neurology 2007;86():243-53.
2006: Alexander Lossos; Giovanni Stevanin; Vardiella Meiner; Zohar Argov; Naima Bouslam; Joel P Newman; John Moshe Gomori; Stephan Klebe; Israela Lerer; Nizar Elleuch; Shira Silverstein; Alexandra Durr; Oded Abramsky; Ziva Ben-Nariah; Alexis Brice
Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.
Archives of neurology 2006;63(5):756-60.
2006: Alexander Lossos; Moona Khoury; William B Rizzo; John Moshe Gomori; Eyal Banin; Abraham Zlotogorski; Saleh Jaber; Oded Abramsky; Zohar Argov; Hanna Rosenmann
Phenotypic variability among adult siblings with Sjögren-Larsson syndrome.
Archives of neurology 2006;63(2):278-80.
2005: Netta Levin; Oded Abramsky; Alexander Lossos; Dimitrios Karussis; Tali Siegal; Zohar Argov; Tamir Ben-Hur
Extrathymic malignancies in patients with myasthenia gravis.
Journal of the neurological sciences 2005;237(1-2):39-43.
2005: Alexander Lossos; Carol Dobson-Stone; Anthony P Monaco; Dov Soffer; Ezra Rahamim; Joel P Newman; Saidi Mohiddin; Lameh Fananapazir; Israela Lerer; Eduard Linetsky; Avinoam Reches; Zohar Argov; Oded Abramsky; Natan Gadoth; Menachem Sadeh; John Moshe Gomori; Moshe Boher; Vardiella Meiner
Early clinical heterogeneity in choreoacanthocytosis.
Archives of neurology 2005;62(4):611-4.
2005: Sabine Krause; Stephan Hinderlich; Shira Amsili; Rüdiger Horstkorte; Heinz Wiendl; Zohar Argov; Stella Mitrani-Rosenbaum; Hanns Lochmüller
Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex and the nucleus of mammalian cells.
Experimental cell research 2005;304(2):365-79.
2005: Ilan Salama; Stephan Hinderlich; Zipora Shlomai; Iris Eisenberg; Sabine Krause; Kevin J Yarema; Zohar Argov; Hanns Lochmuller; Werner Reutter; Ron Dabby; Menachem Sadeh; Hannah Ben-Bassat; Stella Mitrani-Rosenbaum
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation.
Biochemical and biophysical research communications 2005;328(1):221-6.
2005: Alexander Lossos; Dov Soffer; Bettina Steiner-Birmanns; Sharon Hassin-Baer; Menachem Sadeh; Michal Sagi; Eduard Linetski; Oded Abramsky; Zohar Argov; Hanna Rosenmann
Extended phenotype in the transthyretin Tyr77 familial amyloid polyneuropathy.
European neurology 2005;53(2):55-9.
2005: Alexander Lossos; Lekbir Baala; Dov Soffer; Lea Averbuch-Heller; Shlomo Dotan; Arnold Munnich; Stanislas LYONNET; John Moshe Gomori; Adnan Genem; Meir Neufeld; Oded Abramsky; Joël Zlotogora; Zohar Argov
A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12.
Brain : a journal of neurology 2005;128(Pt 1):42-51.
2004: Stephan Hinderlich; Ilan Salama; Iris Eisenberg; Tamara Potikha; Lars R Mantey; Kevin J Yarema; Rüdiger Horstkorte; Zohar Argov; Menachem Sadeh; Werner Reutter; Stella Mitrani-Rosenbaum
The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy.
FEBS letters 2004;566(1-3):105-9.
2003: Netta Levin; Zohar Argov
Painful eye movements in aseptic meningitis.
Journal of neurology 2003;250(10):1257-8.
2003: Reeval Segel; Shira Silverstein; Israela Lerer; Esther Kahana; Rachel Meir; Michal Sagi; Nelly Zilber; Amos D Korczyn; Yehuda Shapira; Zohar Argov; Dvorah Abeliovich
Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations.
American journal of medical genetics. Part A 2003;119A(3):273-8.
2003: Zohar Argov; Iris Eisenberg; Gil Grabov-Nardini; Menachem Sadeh; Itzhak Wirguin; Dov Soffer; Stella Mitrani-Rosenbaum
Hereditary inclusion body myopathy: the Middle Eastern genetic cluster.
Neurology 2003;60(9):1519-23.
2003: Iris Eisenberg; Gil Grabov-Nardini; Hagit Hochner; Mira Korner; Menachem Sadeh; Tulio Bertorini; Kate Bushby; Claudio Castellan; Kevin Felice; Jerry Mendell; Luciano Merlini; Christopher Shilling; Itzhak Wirguin; Zohar Argov; Stella Mitrani-Rosenbaum
Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps.
Human mutation 2003;21(1):99.
2002: isabelle korn-lubetzki; Zohar Argov; Annick Raas-Rothschild; Itzhak Wirguin; Israel Steiner
Family with inflammatory demyelinating polyneuropathy and the HNPP 17p12 deletion.
American journal of medical genetics 2002;113(3):275-8.
2002: Iris Eisenberg; Hagit Hochner; Menachem Sadeh; Zohar Argov; Stella Mitrani-Rosenbaum
Establishment of the genomic structure and identification of thirteen single-nucleotide polymorphisms in the human RECK gene.
Cytogenetic and genome research 2002;97(1-2):58-61.
2001: J T Chen; Tanja Taivassalo; Zohar Argov; Douglas L Arnold
Modeling in vivo recovery of intracellular pH in muscle to provide a novel index of proton handling: application to the diagnosis of mitochondrial myopathy.
Magnetic resonance in medicine : official journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine 2001;46(5):870-8.
2001: Iris Eisenberg; Nili Avidan; Tamara Potikha; Hagit Hochner; M Chen; Tsviya Olender; M Barash; Mordechai Shemesh; Menachem Sadeh; Gil Grabov-Nardini; I Shmilevich; A Friedmann; George Karpati; Walter G Bradley; Lisa Baumbach; Doron Lancet; E B Asher; Jacques Beckmann; Zohar Argov; Stella Mitrani-Rosenbaum
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
Nature genetics 2001;29(1):83-7.
2001: Iris Eisenberg; Hagit Hochner; Mordechai Shemesh; Tatjana Levi; Tamara Potikha; Menachem Sadeh; Zohar Argov; C L Jackson; Stella Mitrani-Rosenbaum
Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13.
European journal of human genetics : EJHG 2001;9(7):501-9.
2000: Louise V B Anderson; R M Harrison; R Pogue; E Vafiadaki; C Pollitt; K Davison; JA Moss; Sharon M Keers; Angela Pyle; Pamela J Shaw; Ibrahim Mahjneh; Zohar Argov; Cheryl R Greenberg; Klaus Wrogemann; Tulio Bertorini; H H Goebel; Jacques Beckmann; Rumaisa Bashir; K M D Bushby
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).
Neuromuscular disorders : NMD 2000;10(8):553-9.
2000: Zohar Argov; M Löfberg; Douglas L Arnold
Insights into muscle diseases gained by phosphorus magnetic resonance spectroscopy.
Muscle & nerve 2000;23(9):1316-34.
2000: Neli Boneva; Talma Brenner; Zohar Argov
Gabapentin may be hazardous in myasthenia gravis.
Muscle & nerve 2000;23(8):1204-8.
2000: Zohar Argov; Menachem Sadeh; K Mazor; Dov Soffer; Esther Kahana; Iris Eisenberg; Stella Mitrani-Rosenbaum; Isabelle Richard; Jacques Beckmann; Sharon M Keers; Rumaisa Bashir; Kate Bushby; Hanna Rosenmann
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features.
Brain : a journal of neurology 2000;123 ( Pt 6)():1229-37.
2000: Elizabeth McNally; CT Ly; Hanna Rosenmann; Stella Mitrani-Rosenbaum; W Jiang; Louise V B Anderson; Dov Soffer; Zohar Argov
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation.
American journal of medical genetics 2000;91(4):305-12.
2000: Zohar Argov; D L Arnold
MR spectroscopy and imaging in metabolic myopathies.
Neurologic clinics 2000;18(1):35-52.
2000: M Carmela Tartaglia; J T Chen; Zografos Caramanos; Tanja Taivassalo; Douglas L Arnold; Zohar Argov
Muscle phosphorus magnetic resonance spectroscopy oxidative indices correlate with physical activity.
Muscle & nerve 2000;23(2):175-81.
1999: Tanja Taivassalo; Nicola de Stefano; J Chen; George Karpati; Douglas L Arnold; Zohar Argov
Short-term aerobic training response in chronic myopathies.
Muscle & nerve 1999;22(9):1239-43.
1999: Louise V B Anderson; K Davison; JA Moss; C Young; M J Cullen; J Walsh; MA Johnson; Rumaisa Bashir; S Britton; Sharon M Keers; Zohar Argov; Ibrahim Mahjneh; Françoise Fougerousse; Jacques Beckmann; K M D Bushby
Dysferlin is a plasma membrane protein and is expressed early in human development.
Human molecular genetics 1999;8(5):855-61.
1999: A Ashkenazi; Sharon Freeman; Zohar Argov
Effects of cholinergic blockers on auditory brain-stem evoked potentials in rats.
Journal of the neurological sciences 1999;164(2):124-8.
1999: Iris Eisenberg; C Thiel; Tatjana Levi; Efrat Tiram; Zohar Argov; Menachem Sadeh; C L Jackson; Ludwig Thierfelder; Stella Mitrani-Rosenbaum
Fine-structure mapping of the hereditary inclusion body myopathy locus.
Genomics 1999;55(1):43-8.
1998: Alexander Lossos; Zeev Meiner; V Barash; Dov Soffer; I Schlesinger; Oded Abramsky; Zohar Argov; Shoshanna Shpitzen; Vardiella Meiner
Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme gene.
Annals of neurology 1998;44(6):867-72.
1998: Zohar Argov; Iris Eisenberg; Stella Mitrani-Rosenbaum
Genetics of inclusion body myopathies.
Current opinion in rheumatology 1998;10(6):543-7.
1998: Zohar Argov; Tanja Taivassalo; Nicola de Stefano; Angela Genge; George Karpati; Douglas L Arnold
Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy study.
Muscle & nerve 1998;21(11):1523-5.
1998: Rumaisa Bashir; S Britton; Tom Strachan; Sharon M Keers; E Vafiadaki; Majlinda Lako; Isabelle Richard; Sylvie Marchand; Nathalie Bourg; Zohar Argov; Menachem Sadeh; Ibrahim Mahjneh; Giampiero Marconi; M R Passos-Bueno; E de S Moreira; M Zatz; Jacques Beckmann; Kate Bushby
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B.
Nature genetics 1998;20(1):37-42.
1998: Zohar Argov; Menachem Sadeh; Iris Eisenberg; George Karpati; Stella Mitrani-Rosenbaum
Facial weakness in hereditary inclusion body myopathies.
Neurology 1998;50(6):1925-6.
1998: Tanja Taivassalo; Nicola de Stefano; Zohar Argov; Paul Matthews; J Chen; Angela Genge; George Karpati; Douglas L Arnold
Effects of aerobic training in patients with mitochondrial myopathies.
Neurology 1998;50(4):1055-60.
1998: O Cohen; I Steiner; Zohar Argov; A Ashkenazi; J Diment; Ann Saada (Reisch); Y River
Mitochondrial myopathy with atypical subacute presentation.
Journal of neurology, neurosurgery, and psychiatry 1998;64(3):410-1.
1998: Zohar Argov
Functional evaluation techniques in mitochondrial disorders.
European neurology 1998;39(2):65-71.
1997: Zohar Argov; Nicola de Stefano; D L Arnold
Muscle high-energy phosphates in central nervous system disorders. The phosphorus MRS experience.
Italian journal of neurological sciences 1997;18(6):353-7.
1997: M Sadeh; Y River; Zohar Argov
Stimulated single-fiber electromyography in Lambert-Eaton myasthenic syndrome before and after 3,4-diaminopyridine.
Muscle & nerve 1997;20(6):735-9.
1997: Zohar Argov; Efrat Tiram; Iris Eisenberg; Menachem Sadeh; C E Seidman; J G Seidman; George Karpati; Stella Mitrani-Rosenbaum
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1.
Annals of neurology 1997;41(4):548-51.
1997: Zohar Argov; Nicola de Stefano; Tanja Taivassalo; J Chen; George Karpati; Douglas L Arnold
Abnormal oxidative metabolism in exercise intolerance of undetermined origin.
Neuromuscular disorders : NMD 1997;7(2):99-104.
1997: I Steiner; Zohar Argov; Oded Abramsky
Epidural anesthesia.
Neurology 1997;48(1):293; author reply 294-5.
1996: Zohar Argov; Nicola de Stefano; Douglas L Arnold
ADP recovery after a brief ischemic exercise in normal and diseased human muscle--a 31P MRS study.
NMR in biomedicine 1996;9(4):165-72.
1996: Nicola de Stefano; Zohar Argov; Paul Matthews; George Karpati; Douglas L Arnold
Impairment of muscle mitochondrial oxidative metabolism in McArdles's disease.
Muscle & nerve 1996;19(6):764-9.
1996: Stella Mitrani-Rosenbaum; Zohar Argov; A Blumenfeld; Christine E Seidman; Jonathan G Seidman
Hereditary inclusion body myopathy maps to chromosome 9p1-q1.
Human molecular genetics 1996;5(1):159-163.
1996: I Schlesinger; D Soffer; Alexander Lossos; Zeev Meiner; Zohar Argov
Inclusion body myositis: atypical clinical presentations.
European neurology 1996;36(2):89-93.
1995: Zohar Argov; Y Shapira; L Averbuch-Heller; I Wirguin
Lambert-Eaton myasthenic syndrome (LEMS) in association with lymphoproliferative disorders.
Muscle & nerve 1995;18(7):715-9.
1995: Alexander Lossos; H Cooperman; D Soffer; Z Ben-Nariah; E Sagi; M Gomori; Oded Abramsky; Shmuel Shoshan; Zohar Argov
Hereditary leukoencephalopathy and palmoplantar keratoderma: a new disorder with increased skin collagen content.
Neurology 1995;45(2):331-7.
1995: Nina Raben; J B Sherman; E Adams; Zohar Argov; H Nakajima; Paul H Plotz
Various classes of mutations in patients with phosphofructokinase deficiency (Tarui's disease).
Muscle & nerve. Supplement 1995;(3):S35-8.
1995: Nina Raben; J B Sherman; E Adams; H Nakajima; Zohar Argov; Paul H Plotz
Various classes of mutations in patients with phosphofructokinase deficiency (Tarui's disease).
Muscle & nerve. Supplement 1995;3():S35-8.
1994: J B Sherman; Nina Raben; C Nicastri; Zohar Argov; H Nakajima; EM Adams; C M Eng; T M Cowan; Paul H Plotz
Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequency.
American journal of human genetics 1994;55(2):305-13.
1994: S L Kirshner; Y Katz-Levy; I Wirguin; Zohar Argov; Edna Mozes
Fine specificity of T cell lines and clones that are capable of inducing autoimmune manifestations in mice.
Cellular immunology 1994;157(1):11-28.
1994: Zohar Argov; V Barash; D Soffer; J Sherman; Nina Raben
Late-onset muscular weakness in phosphofructokinase deficiency due to exon 5/intron 5 junction point mutation: a unique disorder or the natural course of this glycolytic disorder?
Neurology 1994;44(6):1097-100.
1994: Y River; L Averbuch-Heller; M Weinberger; Zeev Meiner; D Mevorach; I Schlesinger; Zohar Argov
Antibiotic induced meningitis.
Journal of neurology, neurosurgery, and psychiatry 1994;57(6):705-8.
1994: I Wirguin; Talma Brenner; Camille Sicsic; Zohar Argov
Variable effect of calcium channel blockers on the decremental response in experimental autoimmune myasthenia gravis.
Muscle & nerve 1994;17(5):523-7.
1992: I Wirguin; Talma Brenner; Zohar Argov; Israel Steiner
Multifocal motor nerve conduction abnormalities in amyotrophic lateral sclerosis.
Journal of the neurological sciences 1992;112(1-2):199-203.
1991: Alexander Lossos; V Barash; D Soffer; Zohar Argov; M Gomori; Z Ben-Nariah; Oded Abramsky; Israel Steiner
Hereditary branching enzyme dysfunction in adult polyglucosan body disease: a possible metabolic cause in two patients.
Annals of neurology 1991;30(5):655-62.
1991: Alexander Lossos; Zohar Argov; Zvi Ackerman; O Abramsky
Peripheral neuropathy and folate deficiency as the first sign of Crohn's disease.
Journal of clinical gastroenterology 1991;13(4):442-4.
1991: Zohar Argov; W J Bank
Phosphorus magnetic resonance spectroscopy (31P MRS) in neuromuscular disorders.
Annals of neurology 1991;30(1):90-7.
1991: Alexander Lossos; Zohar Argov
Orthostatic hypotension induced by vitamin B12 deficiency.
Journal of the American Geriatrics Society 1991;39(6):601-2.
1991: V Barash; S Lilling; R Fischer; Zohar Argov
Apparent absence of glycogen branching enzyme activity in phosphofructokinase deficiency.
Journal of inherited metabolic disease 1991;14(6):902-7.
1990: S Eliashiv; I Wirguin; Talma Brenner; Zohar Argov
Aggravation of human and experimental myasthenia gravis by contrast media.
Neurology 1990;40(10):1623-5.
1990: I Wirguin; Talma Brenner; E Shinar; Zohar Argov
Citrate-induced impairment of neuromuscular transmission in human and experimental autoimmune myasthenia gravis.
Annals of neurology 1990;27(3):328-30.
1988: E Wertman; Zohar Argov; O Abrmasky
Chronic inflammatory demyelinating polyradiculoneuropathy: features and prognostic factors with corticosteroid therapy.
European neurology 1988;28(4):199-204.