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Results: 1 to 20 of 195

1.

Hepatic amyloidosis resulting from deposition of the apolipoprotein A-I variant Leu75Pro.

Coriu D, Dispenzieri A, Stevens FJ, Murphy CL, Wang S, Weiss DT, Solomon A.

Amyloid. 2003 Dec;10(4):215-23.

PMID:
14986480
[PubMed - indexed for MEDLINE]
2.

Renal apolipoprotein A-I amyloidosis associated with a novel mutant Leu64Pro.

Murphy CL, Wang S, Weaver K, Gertz MA, Weiss DT, Solomon A.

Am J Kidney Dis. 2004 Dec;44(6):1103-9.

PMID:
15558533
[PubMed - indexed for MEDLINE]
3.

Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.

Booth DR, Tan SY, Booth SE, Tennent GA, Hutchinson WL, Hsuan JJ, Totty NF, Truong O, Soutar AK, Hawkins PN, Bruguera M, Caballería J, Solé M, Campistol JM, Pepys MB.

J Clin Invest. 1996 Jun 15;97(12):2714-21.

PMID:
8675681
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families.

Obici L, Palladini G, Giorgetti S, Bellotti V, Gregorini G, Arbustini E, Verga L, Marciano S, Donadei S, Perfetti V, Calabresi L, Bergonzi C, Scolari F, Merlini G.

Gastroenterology. 2004 May;126(5):1416-22.

PMID:
15131802
[PubMed - indexed for MEDLINE]
5.

A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosis.

Hamidi Asl K, Liepnieks JJ, Nakamura M, Parker F, Benson MD.

Biochem Biophys Res Commun. 1999 Apr 13;257(2):584-8.

PMID:
10198255
[PubMed - indexed for MEDLINE]
6.

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.

Soutar AK, Hawkins PN, Vigushin DM, Tennent GA, Booth SE, Hutton T, Nguyen O, Totty NF, Feest TG, Hsuan JJ, et al.

Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7389-93.

PMID:
1502149
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1.

Hamidi Asl L, Liepnieks JJ, Hamidi Asl K, Uemichi T, Moulin G, Desjoyaux E, Loire R, Delpech M, Grateau G, Benson MD.

Am J Pathol. 1999 Jan;154(1):221-7.

PMID:
9916936
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis.

Booth DR, Tan SY, Booth SE, Hsuan JJ, Totty NF, Nguyen O, Hutton T, Vigushin DM, Tennent GA, Hutchinson WL, et al.

QJM. 1995 Oct;88(10):695-702. Review.

PMID:
7493166
[PubMed - indexed for MEDLINE]
9.

Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26Arg.

Gillmore JD, Stangou AJ, Tennent GA, Booth DR, O'Grady J, Rela M, Heaton ND, Wall CA, Keogh JA, Hawkins PN.

Transplantation. 2001 Apr 15;71(7):986-92.

PMID:
11349736
[PubMed - indexed for MEDLINE]
10.

A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII gene.

Benson MD, Liepnieks JJ, Yazaki M, Yamashita T, Hamidi Asl K, Guenther B, Kluve-Beckerman B.

Genomics. 2001 Mar 15;72(3):272-7.

PMID:
11401442
[PubMed - indexed for MEDLINE]
11.

The intracellular quality control system down-regulates the secretion of amyloidogenic apolipoprotein A-I variants: a possible impact on the natural history of the disease.

Marchesi M, Parolini C, Valetti C, Mangione P, Obici L, Giorgetti S, Raimondi S, Donadei S, Gregorini G, Merlini G, Stoppini M, Chiesa G, Bellotti V.

Biochim Biophys Acta. 2011 Jan;1812(1):87-93. doi: 10.1016/j.bbadis.2010.07.002. Epub 2010 Jul 15.

PMID:
20637862
[PubMed - indexed for MEDLINE]
Free Article
12.

Renal apolipoprotein A-I amyloidosis: a rare and usually ignored cause of hereditary tubulointerstitial nephritis.

Gregorini G, Izzi C, Obici L, Tardanico R, Röcken C, Viola BF, Capistrano M, Donadei S, Biasi L, Scalvini T, Merlini G, Scolari F.

J Am Soc Nephrol. 2005 Dec;16(12):3680-6. Epub 2005 Oct 12.

PMID:
16221867
[PubMed - indexed for MEDLINE]
Free Article
13.

The new apolipoprotein A-I variant leu(174) --> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide.

Obici L, Bellotti V, Mangione P, Stoppini M, Arbustini E, Verga L, Zorzoli I, Anesi E, Zanotti G, Campana C, Viganò M, Merlini G.

Am J Pathol. 1999 Sep;155(3):695-702.

PMID:
10487826
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

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

Yazaki M, Varga J, Dyck PJ, Benson MD.

Amyloid. 2002 Dec;9(4):268-71.

PMID:
12557757
[PubMed - indexed for MEDLINE]
15.

Hepatic familial amyloidosis caused by a new mutation in the apolipoprotein AI gene: clinical and pathological features.

Caballería J, Bruguera M, Solé M, Campistol JM, Rodés J.

Am J Gastroenterol. 2001 Jun;96(6):1872-6.

PMID:
11419842
[PubMed - indexed for MEDLINE]
16.

Two different types of amyloid deposits--apolipoprotein A-IV and transthyretin--in a patient with systemic amyloidosis.

Bergström J, Murphy CL, Weiss DT, Solomon A, Sletten K, Hellman U, Westermark P.

Lab Invest. 2004 Aug;84(8):981-8.

PMID:
15146166
[PubMed - indexed for MEDLINE]
Free Article
17.

Light chain-associated amyloid deposits comprised of a novel kappa constant domain.

Solomon A, Weiss DT, Murphy CL, Hrncic R, Wall JS, Schell M.

Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9547-51.

PMID:
9689117
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain.

Benson MD, Liepnieks J, Uemichi T, Wheeler G, Correa R.

Nat Genet. 1993 Mar;3(3):252-5.

PMID:
8097946
[PubMed - indexed for MEDLINE]
19.

Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis.

Wallace MR, Dwulet FE, Conneally PM, Benson MD.

J Clin Invest. 1986 Jul;78(1):6-12.

PMID:
3722385
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Amyloid contained in the knee joint meniscus is formed from apolipoprotein A-I.

Solomon A, Murphy CL, Kestler D, Coriu D, Weiss DT, Makovitzky J, Westermark P.

Arthritis Rheum. 2006 Nov;54(11):3545-50.

PMID:
17075859
[PubMed - indexed for MEDLINE]
Free Article

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