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Prophylactic colchicine for familial Mediterranean fever: response rates revisited. Scand J Rheumatol. 2025 Sep; 54(5):362-365.
Wiener A, Shinar Y, Pras E. PMID: 40468897.
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PubMed Mentions: Fields:
Translation:
Humans
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Determining the origin of different variants associated with familial mediterranean fever by machine-learning. Sci Rep. 2022 09 08; 12(1):15206.
Adato O, Brenner R, Levy A, Shinar Y, Shemer A, Dvir S, Ben-Zvi I, Livneh A, Unger R, Kivity S. PMID: 36076017; PMCID: PMC9458679.
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PubMed Mentions:
2 Fields:
Translation:
Humans
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Clinical significance of E148Q heterozygous variant in paediatric familial Mediterranean fever. Rheumatology (Oxford). 2021 11 03; 60(11):5447-5451.
Tirosh I, Yacobi Y, Vivante A, Barel O, Ben-Moshe Y, Erez Granat O, Spielman S, Semo Oz R, Shinar Y, Gerstein M. PMID: 33560333.
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PubMed Mentions:
9 Fields:
Translation:
Humans
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Familial Mediterranean fever: Penetrance of the p.[Met694Val];[Glu148Gln] and p.[Met694Val];[=] genotypes. Hum Mutat. 2020 11; 41(11):1866-1870.
Eyal O, Shinar Y, Pras M, Pras E. PMID: 32741030.
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PubMed Mentions:
8 Fields:
Translation:
Humans
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ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era. Clin Chem. 2020 04 01; 66(4):525-536.
Shinar Y, Ceccherini I, Rowczenio D, Aksentijevich I, Arostegui J, Ben-Chétrit E, Boursier G, Gattorno M, Hayrapetyan H, Ida H, Kanazawa N, Lachmann HJ, Mensa-Vilaro A, Nishikomori R, Oberkanins C, Obici L, Ohara O, Ozen S, Sarkisian T, Sheils K, Wolstenholme N, Zonneveld-Huijssoon E, van Gijn ME, Touitou I. PMID: 32176780.
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PubMed Mentions:
34 Fields:
Translation:
Humans
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[A CLINICAL DISCUSSION: FEVER OF UNKNOWN ORIGIN IN THE MODERN ERA - MORE QUESTIONS THAN ANSWERS]. Harefuah. 2019 Dec; 158(12):787-788.
Druyan A, Shinar Y. PMID: 31823531.
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PubMed Mentions: Fields:
Translation:
Humans
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Current practices for the genetic diagnosis of autoinflammatory diseases: results of a European Molecular Genetics Quality Network Survey. Eur J Hum Genet. 2019 10; 27(10):1502-1508.
Rowczenio D, Shinar Y, Ceccherini I, Sheils K, Van Gijn M, Patton SJ, Touitou I. PMID: 31186541; PMCID: PMC6777449.
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PubMed Mentions:
7 Fields:
Translation:
HumansPHPublic Health
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Classification criteria for autoinflammatory recurrent fevers. Ann Rheum Dis. 2019 08; 78(8):1025-1032.
Gattorno M, Hofer M, Federici S, Vanoni F, Bovis F, Aksentijevich I, Anton J, Arostegui JI, Barron K, Ben-Cherit E, Brogan PA, Cantarini L, Ceccherini I, De Benedetti F, Dedeoglu F, Demirkaya E, Frenkel J, Goldbach-Mansky R, Gul A, Hentgen V, Hoffman H, Kallinich T, Kone-Paut I, Kuemmerle-Deschner J, Lachmann HJ, Laxer RM, Livneh A, Obici L, Ozen S, Rowczenio D, Russo R, Shinar Y, Simon A, Toplak N, Touitou I, Uziel Y, van Gijn M, Foell D, Garassino C, Kastner D, Martini A, Sormani MP, Ruperto N, Eurofever Registry and the Paediatric Rheumatology International Trials Organisation (PRINTO). PMID: 31018962.
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PubMed Mentions:
201 Fields:
Translation:
Humans
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Reply. Arthritis Rheumatol. 2018 07; 70(7):1167-1168.
Brenner R, Ben-Zvi I, Shinar Y, Livneh A, Liphshitz I, Silverman B, Peled N, Levy C, Ben-Chetrit E, Kivity S. PMID: 29569855.
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PubMed Mentions: Fields:
Translation:
Humans
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New workflow for classification of genetic variants' pathogenicity applied to hereditary recurrent fevers by the International Study Group for Systemic Autoinflammatory Diseases (INSAID). J Med Genet. 2018 08; 55(8):530-537.
Van Gijn ME, Ceccherini I, Shinar Y, Carbo EC, Slofstra M, Arostegui JI, Sarrabay G, Rowczenio D, Omoyimni E, Balci-Peynircioglu B, Hoffman HM, Milhavet F, Swertz MA, Touitou I. PMID: 29599418.
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PubMed Mentions:
67 Fields:
Translation:
Humans
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Familial Mediterranean Fever and Incidence of Cancer: An Analysis of 8,534 Israeli Patients With 258,803 Person-Years. Arthritis Rheumatol. 2018 01; 70(1):127-133.
Brenner R, Ben-Zvi I, Shinar Y, Liphshitz I, Silverman B, Peled N, Levy C, Ben-Chetrit E, Livneh A, Kivity S. PMID: 28992365.
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PubMed Mentions:
16 Fields:
Translation:
Humans
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A high and equal prevalence of the Q703K variant in NLRP3 patients with autoinflammatory symptoms and ethnically matched controls. Clin Exp Rheumatol. 2017 Nov-Dec; 35 Suppl 108(6):82-85.
Lidar M, Brantz Y, Shinar Y, Reznik-Wolf H, Livneh A, Ben Zvi I, Cohen R, Berkun Y, Hashkes PJ, Peleg H, Kessel A, Slobodin G, Rozenbaum M, Goldzweig O, Pras E. PMID: 29148409.
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PubMed Mentions:
4 Fields:
Translation:
Humans
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Carriage of Mediterranean Fever (MEFV) Mutations in Patients with Postpericardiotomy Syndrome (PPS). Isr Med Assoc J. 2017 Sep; 19(9):562-565.
Dechtman ID, Grossman C, Shinar Y, Cohen R, Nachum E, Raanani E, Livneh A, Ben-Zvi I. PMID: 28971640.
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PubMed Mentions: Fields:
Translation:
Humans
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Distressing Visions at the End of Life: Case Report and Review of the Literature. J Pastoral Care Counsel. 2015 Dec; 69(4):251-3.
Shinar YR, Marks AD. PMID: 26631525.
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PubMed Mentions:
4 Fields:
Translation:
Humans
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Acquired familial Mediterranean fever associated with a somatic MEFV mutation in a patient with JAK2 associated post-polycythemia myelofibrosis. Orphanet J Rare Dis. 2015 Jun 30; 10:86.
Shinar Y, Tohami T, Livneh A, Schiby G, Hirshberg A, Nagar M, Goldstein I, Cohen R, Kukuy O, Shubman O, Sharabi Y, Gonzalez-Roca E, Arostegui JI, Rechavi G, Amariglio N, Salomon O. PMID: 26123310; PMCID: PMC4506767.
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PubMed Mentions:
9 Fields:
Translation:
HumansCells
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Familial Mediterranean fever (FMF) with proteinuria: clinical features, histology, predictors, and prognosis in a cohort of 25 patients. J Rheumatol. 2013 Dec; 40(12):2083-7.
Kukuy O, Livneh A, Ben-David A, Kopolovic J, Volkov A, Shinar Y, Holtzman E, Dinour D, Ben-Zvi I. PMID: 24128782.
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PubMed Mentions:
12 Fields:
Translation:
Humans
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E148Q MEFV mutation carriage and longevity in individuals of Ashkenazi origin. Immunol Res. 2013 Jul; 56(2-3):371-5.
Lidar M, Shinar Y, Goldberg M, Ben-Zvi I, Langevitz P, Livneh A. PMID: 23592051.
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PubMed Mentions:
2 Fields:
Translation:
Humans
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T helper 17 polarization in familial Mediterranean fever. Genes Immun. 2013 Jun; 14(4):212-6.
Ovadia A, Livneh A, Feld O, Ben-Zvi I, Kukuy E, Kivity S, Lidar M, Barda-Saad M, Shinar Y. PMID: 23466494.
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PubMed Mentions:
8 Fields:
Translation:
HumansCells
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Guidelines for the genetic diagnosis of hereditary recurrent fevers. Ann Rheum Dis. 2012 Oct; 71(10):1599-605.
Shinar Y, Obici L, Aksentijevich I, Bennetts B, Austrup F, Ceccherini I, Costa JM, De Leener A, Gattorno M, Kania U, Kone-Paut I, Lezer S, Livneh A, Moix I, Nishikomori R, Ozen S, Phylactou L, Risom L, Rowczenio D, Sarkisian T, van Gijn ME, Witsch-Baumgartner M, Morris M, Hoffman HM, Touitou I, European Molecular Genetics Quality Network. PMID: 22661645; PMCID: PMC3500529.
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PubMed Mentions:
63 Fields:
Translation:
Humans
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Familial Mediterranean FeVer gene (MEFV) mutations as a modifier of systemic lupus erythematosus. Lupus. 2012 Aug; 21(9):993-8.
Shinar Y, Kosach E, Langevitz P, Zandman-Goddard G, Pauzner R, Rabinovich E, Livneh A, Lidar M. PMID: 22532615.
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PubMed Mentions:
8 Fields:
Translation:
Humans
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NOD2/CARD15 gene mutations in patients with familial Mediterranean fever. Semin Arthritis Rheum. 2012 Aug; 42(1):84-8.
Berkun Y, Karban A, Padeh S, Pras E, Shinar Y, Lidar M, Livneh A, Bujanover Y. PMID: 22244368.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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'Silent' carriage of two familial Mediterranean fever gene mutations in large families with only a single identified patient. Clin Genet. 2012 Sep; 82(3):288-91.
Camus D, Shinar Y, Aamar S, Langevitz P, Ben-Zvi I, Livneh A, Lidar M. PMID: 21995303.
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PubMed Mentions:
12 Fields:
Translation:
Humans
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Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean fever. Arthritis Care Res (Hoboken). 2010 Sep; 62(9):1294-8.
Marek-Yagel D, Berkun Y, Padeh S, Lidar M, Shinar Y, Bar-Joseph I, Reznik-Wolf H, Langevitz P, Livneh A, Pras E. PMID: 20506103.
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PubMed Mentions:
4 Fields:
Translation:
Humans
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Familial Mediterranean Fever in the first two years of life: a unique phenotype of disease in evolution. J Pediatr. 2010 Jun; 156(6):985-989.
Padeh S, Livneh A, Pras E, Shinar Y, Lidar M, Feld O, Berkun Y. PMID: 20227729.
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PubMed Mentions:
19 Fields:
Translation:
Humans
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Familial Mediterranean fever in children presenting with attacks of fever alone. J Rheumatol. 2010 Apr; 37(4):865-9.
Padeh S, Livneh A, Pras E, Shinar Y, Lidar M, Feld O, Berkun Y. PMID: 20194447.
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PubMed Mentions:
13 Fields:
Translation:
Humans
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MEFV mutation carriage in Israeli Jewish individuals from ethnicities with low risk for familial Mediterranean fever. J Hum Genet. 2009 Jun; 54(6):369-71.
Feld O, Livneh A, Shinar Y, Berkun Y, Lidar M. PMID: 19373257.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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An international external quality assessment for molecular diagnosis of hereditary recurrent fevers: a 3-year scheme demonstrates the need for improvement. Eur J Hum Genet. 2009 Jul; 17(7):890-6.
Touitou I, Rittore C, Philibert L, Yagüe J, Shinar Y, Aksentijevich I. PMID: 19172992; PMCID: PMC2986501.
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PubMed Mentions:
8 Fields:
Translation:
Humans
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Systemic lupus erythematosus and familial Mediterranean fever: a possible negative association between the two disease entities--report of four cases and review of the literature. Lupus. 2008 Jul; 17(7):663-9.
Lidar M, Zandman-Goddard G, Shinar Y, Zaks N, Livneh A, Langevitz P. PMID: 18625639.
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PubMed Mentions:
6 Fields:
Translation:
Humans
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Mutations in the familial Mediterranean fever gene of patients with IgA nephropathy and other forms of glomerulonephritis. Clin Genet. 2008 Feb; 73(2):146-51.
Kukuy OL, Kopolovic J, Blau A, Ben-David A, Lotan D, Shaked M, Shinar Y, Dinour D, Langevitz P, Livneh A. PMID: 18177471.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Unique spectrum of MEFV mutations in Iranian Jewish FMF patients--clinical and demographic significance. Rheumatology (Oxford). 2007 Nov; 46(11):1718-22.
Shinar Y, Kuchuk I, Menasherow S, Kolet M, Lidar M, Langevitz P, Livneh A. PMID: 17938136.
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PubMed Mentions:
3 Fields:
Translation:
HumansCells
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Transthyretin amyloidosis in a patient of Iranian-Jewish extraction: a second Israeli-Jewish case. Clin Chem Lab Med. 2007; 45(5):625-8.
Kaplan B, Shinar Y, Avisar C, Livneh A. PMID: 17484624.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis. Scand J Rheumatol. 2007 Jan-Feb; 36(1):48-52.
Rabinovich E, Shinar Y, Leiba M, Ehrenfeld M, Langevitz P, Livneh A. PMID: 17454935.
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PubMed Mentions:
24 Fields:
Translation:
Humans
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Long-term outcomes in difficult-to-treat patients with recurrent pericarditis. Am J Cardiol. 2006 Jul 15; 98(2):267-71.
Brucato A, Brambilla G, Moreo A, Alberti A, Munforti C, Ghirardello A, Doria A, Shinar Y, Livneh A, Adler Y, Shoenfeld Y, Mauri F, Palmieri G, Spodick DH. PMID: 16828606.
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PubMed Mentions:
30 Fields:
Translation:
Humans
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Role of the pyrin M694V (A2080G) allele in acute myocardial infarction and longevity: a study in the Sicilian population. J Leukoc Biol. 2006 Mar; 79(3):611-5.
Grimaldi MP, Candore G, Vasto S, Caruso M, Caimi G, Hoffmann E, Colonna-Romano G, Lio D, Shinar Y, Franceschi C, Caruso C. PMID: 16387839.
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PubMed Mentions:
18 Fields:
Translation:
Humans
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Evaluation of disease severity in familial Mediterranean fever. Semin Arthritis Rheum. 2005 Aug; 35(1):57-64.
Mor A, Shinar Y, Zaks N, Langevitz P, Chetrit A, Shtrasburg S, Rabinovitz E, Livneh A. PMID: 16084225.
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PubMed Mentions:
39 Fields:
Translation:
Humans
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Severe disease in patients with rheumatoid arthritis carrying a mutation in the Mediterranean fever gene. Ann Rheum Dis. 2005 Jul; 64(7):1009-14.
Rabinovich E, Livneh A, Langevitz P, Brezniak N, Shinar E, Pras M, Shinar Y. PMID: 15958759; PMCID: PMC1755576.
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PubMed Mentions:
34 Fields:
Translation:
Humans
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Idiopathic recurrent acute pericarditis: familial Mediterranean fever mutations and disease evolution in a large cohort of Caucasian patients. Lupus. 2005; 14(9):670-4.
Brucato A, Shinar Y, Brambilla G, Robbiolo L, Ferrioli G, Patrosso MC, Zanni D, Penco S, Boiani E, Ghirardello A, Caforio AL, Bergantin A, Tombini V, Moreo A, Ashtamkar L, Doria A, Shoenfeld Y, Livneh A. PMID: 16218464.
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PubMed Mentions:
12 Fields:
Translation:
Humans
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PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations. Neurology. 2004 Oct 26; 63(8):1482-5.
Hatano Y, Sato K, Elibol B, Yoshino H, Yamamura Y, Bonifati V, Shinotoh H, Asahina M, Kobayashi S, Ng AR, Rosales RL, Hassin-Baer S, Shinar Y, Lu CS, Chang HC, Wu-Chou YH, Ataç FB, Kobayashi T, Toda T, Mizuno Y, Hattori N. PMID: 15505170.
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PubMed Mentions:
15 Fields:
Translation:
HumansCells
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Colchicine nonresponsiveness in familial Mediterranean fever: clinical, genetic, pharmacokinetic, and socioeconomic characterization. Semin Arthritis Rheum. 2004 Feb; 33(4):273-82.
Lidar M, Scherrmann JM, Shinar Y, Chetrit A, Niel E, Gershoni-Baruch R, Langevitz P, Livneh A. PMID: 14978665.
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PubMed Mentions:
46 Fields:
Translation:
Humans
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Analysis of the three most common MEFV mutations in 412 patients with familial Mediterranean fever. Isr Med Assoc J. 2003 Aug; 5(8):585-8.
Zaks N, Shinar Y, Padeh S, Lidar M, Mor A, Tokov I, Pras M, Langevitz P, Pras E, Livneh A. PMID: 12929299.
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PubMed Mentions:
15 Fields:
Translation:
Humans
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Common mutations in the familial Mediterranean fever gene associate with rapid progression to disability in non-Ashkenazi Jewish multiple sclerosis patients. Genes Immun. 2003 Apr; 4(3):197-203.
Shinar Y, Livneh A, Villa Y, Pinhasov A, Zeitoun I, Kogan A, Achiron A. PMID: 12700594.
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PubMed Mentions:
10 Fields:
Translation:
Humans
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Clinical and diagnostic value of genetic testing in 216 Israeli children with Familial Mediterranean fever. J Rheumatol. 2003 Jan; 30(1):185-90.
Padeh S, Shinar Y, Pras E, Zemer D, Langevitz P, Pras M, Livneh A. PMID: 12508410.
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PubMed Mentions:
35 Fields:
Translation:
Humans
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Cranial nerve lesions and abnormal visually evoked potentials associated with the M694V mutation in familial Mediterranean fever. Clin Rheumatol. 2002 Aug; 21(4):317-21.
Finsterer J, Stöllberger C, Shinar Y. PMID: 12189462.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews. Hum Genet. 2002 Aug; 111(2):214-8.
Ben-Zeev B, Levy-Nissenbaum E, Lahat H, Anikster Y, Shinar Y, Brand N, Gross-Tzur V, MacGregor D, Sidi R, Kleta R, Frydman M, Pras E. PMID: 12189496.
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PubMed Mentions:
12 Fields:
Translation:
Humans
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A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cysts. J Med Genet. 2002 Jan; 39(1):54-7.
Shinar Y, Ben-Zeev B, Brand N, Lahat H, Gross-Zur V, MacGregor D, Bahan T, Kastner DL, Pras E. PMID: 11826027; PMCID: PMC1734951.
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PubMed Mentions: Fields:
Translation:
HumansCells
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Common MEFV mutations among Jewish ethnic groups in Israel: high frequency of carrier and phenotype III states and absence of a perceptible biological advantage for the carrier state. Am J Med Genet. 2001 Aug 15; 102(3):272-6.
Kogan A, Shinar Y, Lidar M, Revivo A, Langevitz P, Padeh S, Pras M, Livneh A. PMID: 11484206.
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PubMed Mentions:
31 Fields:
Translation:
Humans
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A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behçet's disease (FMF-BD). Eur J Hum Genet. 2001 Mar; 9(3):191-6.
Livneh A, Aksentijevich I, Langevitz P, Torosyan Y, G-Shoham N, Shinar Y, Pras E, Zaks N, Padeh S, Kastner DL, Pras M. PMID: 11313758.
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PubMed Mentions:
20 Fields:
Translation:
Humans
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Vacuolating megalencephalic leukoencephalopathy in 12 Israeli patients. J Child Neurol. 2001 Feb; 16(2):93-9.
Ben-Zeev B, Gross V, Kushnir T, Shalev R, Hoffman C, Shinar Y, Pras E, Brand N. PMID: 11292232.
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PubMed Mentions:
12 Fields:
Translation:
HumansCells
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Lack of evidence for an association between two genetic polymorphisms in the tumor necrosis factor receptor 1 gene and multiple sclerosis in Ashkenazi Jews. Eur Neurol. 2001; 46(3):153-5.
Pras E, Aksentijevich I, Shinar Y, Kastner DL, Achiron A. PMID: 11598334.
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PubMed Mentions:
1 Fields:
Translation:
Humans
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Genotype-phenotype assessment of common genotypes among patients with familial Mediterranean fever. J Rheumatol. 2000 Jul; 27(7):1703-7.
Shinar Y, Livneh A, Langevitz P, Zaks N, Aksentijevich I, Koziol DE, Kastner DL, Pras M, Pras E. PMID: 10914855.
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PubMed Mentions:
27 Fields:
Translation:
Humans
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Familial Mediterranean fever in two Bedouin families: mutation analysis and disease severity. Am J Med Genet. 2000 Jun 05; 92(4):247-9.
Press J, Shinar Y, Langevitz P, Livneh A, Pras M, Buskila D. PMID: 10842289.
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PubMed Mentions: Fields:
Translation:
Humans
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Protracted febrile myalgia of familial Mediterranean fever. Mutation analysis and clinical correlations. Scand J Rheumatol. 2000; 29(3):174-6.
Sidi G, Shinar Y, Livneh A, Langevitz P, Pras M, Pras E. PMID: 10898070.
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PubMed Mentions:
15 Fields:
Translation:
Humans
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Late-onset familial Mediterranean fever (FMF): a subset with distinct clinical, demographic, and molecular genetic characteristics. Am J Med Genet. 1999 Nov 05; 87(1):30-5.
Tamir N, Langevitz P, Zemer D, Pras E, Shinar Y, Padeh S, Zaks N, Pras M, Livneh A. PMID: 10528243.
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PubMed Mentions:
20 Fields:
Translation:
Humans
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Familial Mediterranean fever: new aspects and prospects at the end of the millenium. Isr Med Assoc J. 1999 Sep; 1(1):31-6.
Langevitz P, Livneh A, Padeh S, Zaks N, Shinar Y, Zemer D, Pras E, Pras M. PMID: 11370119.
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PubMed Mentions:
4 Fields:
Translation:
Humans
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MEFV mutation analysis in patients suffering from amyloidosis of familial Mediterranean fever. Amyloid. 1999 Mar; 6(1):1-6.
Livneh A, Langevitz P, Shinar Y, Zaks N, Kastner DL, Pras M, Pras E. PMID: 10211405.
View in:
PubMed Mentions:
38 Fields:
Translation:
HumansCells
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Analysis of allelic association between D6S461 marker and multiple sclerosis in Ashkenazi and Iraqi Jewish patients. J Mol Neurosci. 1998 Dec; 11(3):265-9.
Shinar Y, Pras E, Siev-Ner I, Gamus D, Brautbar C, Israel S, Achiron A. PMID: 10344796.
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PubMed Mentions:
2 Fields:
Translation:
Humans
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Developing oligodendroglia express mRNA for insulin-like growth factor-I, a regulator of oligodendrocyte development. J Neurosci Res. 1995 Nov 01; 42(4):516-27.
Shinar Y, McMorris FA. PMID: 8568938.
View in:
PubMed Mentions:
16 Fields:
Translation:
AnimalsCells
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Regulation of oligodendrocyte development and central nervous system myelination by insulin-like growth factors. Ann N Y Acad Sci. 1993 Aug 27; 692:321-34.
McMorris FA, Mozell RL, Carson MJ, Shinar Y, Meyer RD, Marchetti N. PMID: 8215042.
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PubMed Mentions:
18 Fields:
Translation:
AnimalsCells
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Temporal and spatial patterns of expression of laminin, chondroitin sulphate proteoglycan and HNK-1 immunoreactivity during regeneration in the goldfish optic nerve. J Neurocytol. 1992 Aug; 21(8):557-73.
Battisti WP, Shinar Y, Schwartz M, Levitt P, Murray M. PMID: 1380544.
View in:
PubMed Mentions:
4 Fields:
Translation:
Animals