Zeldenrust S - Search Results

1

Clinical characteristics in a kindred with early-onset Alzheimer's disease and their linkage to a G-->T change at position 2149 of the amyloid precursor protein gene.

Farlow M, Murrell J, Ghetti B, Unverzagt F, Zeldenrust S, Benson M. Farlow M, et al. Among authors: zeldenrust s. Neurology. 1994 Jan;44(1):105-11. doi: 10.1212/wnl.44.1.105. Neurology. 1994. PMID: 8290042

2

RFLP analysis for APP 717 mutations associated with Alzheimer's disease.

Zeldenrust SR, Murrell J, Farlow M, Ghetti B, Roses AD, Benson MD. Zeldenrust SR, et al. J Med Genet. 1993 Jun;30(6):476-8. doi: 10.1136/jmg.30.6.476. J Med Genet. 1993. PMID: 7686976 Free PMC article.

3

A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy.

Uemichi T, Murrell JR, Zeldenrust S, Benson MD. Uemichi T, et al. Among authors: zeldenrust s. J Med Genet. 1992 Dec;29(12):888-91. doi: 10.1136/jmg.29.12.888. J Med Genet. 1992. PMID: 1362222 Free PMC article.

4

A transthyretin variant (alanine 49) associated with familial amyloidotic polyneuropathy in a French family.

Benson MD 2nd, Julien J, Liepnieks J, Zeldenrust S, Benson MD. Benson MD 2nd, et al. Among authors: zeldenrust s. J Med Genet. 1993 Feb;30(2):117-9. doi: 10.1136/jmg.30.2.117. J Med Genet. 1993. PMID: 8095301 Free PMC article.

5

A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French family.

Benson MD 2nd, Turpin JC, Lucotte G, Zeldenrust S, LeChevalier B, Benson MD. Benson MD 2nd, et al. Among authors: zeldenrust s. J Med Genet. 1993 Feb;30(2):120-2. doi: 10.1136/jmg.30.2.120. J Med Genet. 1993. PMID: 8095302 Free PMC article.

6

Targeted suppression of an amyloidogenic transthyretin with antisense oligonucleotides.

Benson MD, Kluve-Beckerman B, Zeldenrust SR, Siesky AM, Bodenmiller DM, Showalter AD, Sloop KW. Benson MD, et al. Muscle Nerve. 2006 May;33(5):609-18. doi: 10.1002/mus.20503. Muscle Nerve. 2006. PMID: 16421881

7

Mass spectrometric-based proteomic analysis of amyloid neuropathy type in nerve tissue.

Klein CJ, Vrana JA, Theis JD, Dyck PJ, Dyck PJ, Spinner RJ, Mauermann ML, Bergen HR 3rd, Zeldenrust SR, Dogan A. Klein CJ, et al. Arch Neurol. 2011 Feb;68(2):195-9. doi: 10.1001/archneurol.2010.261. Epub 2010 Oct 11. Arch Neurol. 2011. PMID: 20937937 Free PMC article.

8

Orthotopic liver transplantation for hereditary fibrinogen amyloidosis.

Zeldenrust S, Gertz M, Uemichi T, Björnsson J, Wiesner R, Schwab T, Benson M. Zeldenrust S, et al. Transplantation. 2003 Feb 27;75(4):560-1. doi: 10.1097/01.TP.0000046526.10003.EC. Transplantation. 2003. PMID: 12605128

9

Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study.

Adams D, Polydefkis M, González-Duarte A, Wixner J, Kristen AV, Schmidt HH, Berk JL, Losada López IA, Dispenzieri A, Quan D, Conceição IM, Slama MS, Gillmore JD, Kyriakides T, Ajroud-Driss S, Waddington-Cruz M, Mezei MM, Planté-Bordeneuve V, Attarian S, Mauricio E, Brannagan TH 3rd, Ueda M, Aldinc E, Wang JJ, White MT, Vest J, Berber E, Sweetser MT, Coelho T; patisiran Global OLE study group. Adams D, et al. Lancet Neurol. 2021 Jan;20(1):49-59. doi: 10.1016/S1474-4422(20)30368-9. Epub 2020 Nov 16. Lancet Neurol. 2021. PMID: 33212063 Clinical Trial.

10

Solid organ transplantation for non-TTR hereditary amyloidosis: report from the 1st International Workshop on the Hereditary Renal Amyloidoses.

Stangou AJ, Lobato L, Zeldenrust S, Rela M, Portmann B, Linke RP, Conceicao I, Otto G, Wilczek H, Suhr O, Azoulay D, Grateau G, Picken M, O'Grady J, Heaton N, Ericzon BG, Benson MD. Stangou AJ, et al. Among authors: zeldenrust s. Amyloid. 2012 Jun;19 Suppl 1:81-4. doi: 10.3109/13506129.2012.668503. Epub 2012 Apr 27. Amyloid. 2012. PMID: 22540225

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