Benson MD - Search Results

1

A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.

Magy N, Liepnieks JJ, Gil H, Kantelip B, Dupond JL, Kluve-Beckerman B, Benson MD. Magy N, et al. Among authors: benson md. Amyloid. 2003 Mar;10(1):29-33. doi: 10.3109/13506120308995254. Amyloid. 2003. PMID: 12762139

2

Production and functional analysis of normal and variant recombinant human transthyretin proteins.

Murrell JR, Schoner RG, Liepnieks JJ, Rosen HN, Moses AC, Benson MD. Murrell JR, et al. Among authors: benson md. J Biol Chem. 1992 Aug 15;267(23):16595-600. J Biol Chem. 1992. PMID: 1644839 Free article.

3

Characterization of an isoelectric focusing variant of SAA1 (ASP-72) in a family of Turkish origin.

Kluve-Beckerman B, Malle E, Vitt H, Pfeiffer C, Benson M, Steinmetz A. Kluve-Beckerman B, et al. Biochem Biophys Res Commun. 1991 Dec 31;181(3):1097-102. doi: 10.1016/0006-291x(91)92051-k. Biochem Biophys Res Commun. 1991. PMID: 1764061

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: benson md. 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: benson md. 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

Rapidly progressive amyloid polyneuropathy associated with a novel variant transthyretin serine 25.

Yazaki M, Yamashita T, Kincaid JC, Scott JR, Auger RG, Dyck PJ, Benson MD. Yazaki M, et al. Among authors: benson md. Muscle Nerve. 2002 Feb;25(2):244-50. doi: 10.1002/mus.10032. Muscle Nerve. 2002. PMID: 11870693

7

Laboratory assessment of transthyretin amyloidosis.

Benson MD, Yazaki M, Magy N. Benson MD, et al. Clin Chem Lab Med. 2002 Dec;40(12):1262-5. doi: 10.1515/CCLM.2002.218. Clin Chem Lab Med. 2002. PMID: 12553428 Review.

8

Transthyretin amyloidosis associated with a novel variant (Trp41Leu) presenting with vitreous opacities.

Yazaki M, Connors LH, Eagle RC Jr, Leff SR, Skinner M, Benson MD. Yazaki M, et al. Among authors: benson md. Amyloid. 2002 Dec;9(4):263-7. doi: 10.3109/13506120209114104. Amyloid. 2002. PMID: 12557756

9

A new transthyretin variant Leu55Gln in a patient with systemic amyloidosis.

Yazaki M, Varga J, Dyck PJ, Benson MD. Yazaki M, et al. Among authors: benson md. Amyloid. 2002 Dec;9(4):268-71. doi: 10.3109/13506120209114105. Amyloid. 2002. PMID: 12557757

10

A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis.

Yazaki M, Farrell SA, Benson MD. Yazaki M, et al. Among authors: benson md. Kidney Int. 2003 May;63(5):1652-7. doi: 10.1046/j.1523-1755.2003.00904.x. Kidney Int. 2003. PMID: 12675840 Free article.

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