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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 1
2006 4
2007 1
2008 1
2009 3
2010 2
2011 2
2013 2
2014 2
2017 2
2024 0

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21 results

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Page 1
Cyclopia and proboscis - the extreme end of holoprosencephaly.
Măluţan AM, Dudea M, Ciortea R, Mureşan M, Bucuri CE, Mihu C, Mihu D. Măluţan AM, et al. Among authors: muresan m. Rom J Morphol Embryol. 2017;58(4):1555-1559. Rom J Morphol Embryol. 2017. PMID: 29556657 Free article.
Mutations in NR5A1 associated with ovarian insufficiency.
Lourenço D, Brauner R, Lin L, De Perdigo A, Weryha G, Muresan M, Boudjenah R, Guerra-Junior G, Maciel-Guerra AT, Achermann JC, McElreavey K, Bashamboo A. Lourenço D, et al. Among authors: muresan m. N Engl J Med. 2009 Mar 19;360(12):1200-10. doi: 10.1056/NEJMoa0806228. Epub 2009 Feb 25. N Engl J Med. 2009. PMID: 19246354 Free PMC article.
Recombinant human thyrotropin stimulates thyroid angiogenesis in vivo.
Klein M, Brunaud L, Muresan M, Barbé F, Marie B, Sapin R, Vignaud JM, Chatelin J, Angioï-Duprez K, Zarnegar R, Weryha G, Duprez A. Klein M, et al. Among authors: muresan m. Thyroid. 2006 Jun;16(6):531-6. doi: 10.1089/thy.2006.16.531. Thyroid. 2006. PMID: 16839254
Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10.
Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková S, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HP; International RET Exon 10 Consortium. Frank-Raue K, et al. Among authors: muresan m. Hum Mutat. 2011 Jan;32(1):51-8. doi: 10.1002/humu.21385. Hum Mutat. 2011. PMID: 20979234
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
Neumann HP, Pawlu C, Peczkowska M, Bausch B, McWhinney SR, Muresan M, Buchta M, Franke G, Klisch J, Bley TA, Hoegerle S, Boedeker CC, Opocher G, Schipper J, Januszewicz A, Eng C; European-American Paraganglioma Study Group. Neumann HP, et al. Among authors: muresan m. JAMA. 2004 Aug 25;292(8):943-51. doi: 10.1001/jama.292.8.943. JAMA. 2004. PMID: 15328326
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene.
Schiavi F, Boedeker CC, Bausch B, Peçzkowska M, Gomez CF, Strassburg T, Pawlu C, Buchta M, Salzmann M, Hoffmann MM, Berlis A, Brink I, Cybulla M, Muresan M, Walter MA, Forrer F, Välimäki M, Kawecki A, Szutkowski Z, Schipper J, Walz MK, Pigny P, Bauters C, Willet-Brozick JE, Baysal BE, Januszewicz A, Eng C, Opocher G, Neumann HP; European-American Paraganglioma Study Group. Schiavi F, et al. Among authors: muresan m. JAMA. 2005 Oct 26;294(16):2057-63. doi: 10.1001/jama.294.16.2057. JAMA. 2005. PMID: 16249420
21 results