PubMed (OMIM) for id: 4069

Year	Number of Results
1973	1
1974	2
1975	2
1981	1
1982	2
1985	1
1987	1
1988	1
1989	1
1990	1
1991	2
1993	2
1994	1
1996	2
1997	1
1999	2
2002	4
2003	2
2005	1
2006	1
2010	1
2012	1
2024	0

1

Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin.

Valleix S, Gillmore JD, Bridoux F, Mangione PP, Dogan A, Nedelec B, Boimard M, Touchard G, Goujon JM, Lacombe C, Lozeron P, Adams D, Lacroix C, Maisonobe T, Planté-Bordeneuve V, Vrana JA, Theis JD, Giorgetti S, Porcari R, Ricagno S, Bolognesi M, Stoppini M, Delpech M, Pepys MB, Hawkins PN, Bellotti V. Valleix S, et al. N Engl J Med. 2012 Jun 14;366(24):2276-83. doi: 10.1056/NEJMoa1201356. N Engl J Med. 2012. PMID: 22693999 Free article.

2

Antibodies to human serum amyloid P component eliminate visceral amyloid deposits.

Bodin K, Ellmerich S, Kahan MC, Tennent GA, Loesch A, Gilbertson JA, Hutchinson WL, Mangione PP, Gallimore JR, Millar DJ, Minogue S, Dhillon AP, Taylor GW, Bradwell AR, Petrie A, Gillmore JD, Bellotti V, Botto M, Hawkins PN, Pepys MB. Bodin K, et al. Nature. 2010 Nov 4;468(7320):93-7. doi: 10.1038/nature09494. Epub 2010 Oct 20. Nature. 2010. PMID: 20962779 Free PMC article.

3

Lysozyme amyloidosis: report of 4 cases and a review of the literature.

Granel B, Valleix S, Serratrice J, Chérin P, Texeira A, Disdier P, Weiller PJ, Grateau G. Granel B, et al. Medicine (Baltimore). 2006 Jan;85(1):66-73. doi: 10.1097/01.md.0000200467.51816.6d. Medicine (Baltimore). 2006. PMID: 16523055 Free article. Review.

4

Underdiagnosed amyloidosis: amyloidosis of lysozyme variant.

Granel B, Serratrice J, Disdier P, Weiller PJ, Valleix S, Grateau G, Droz D. Granel B, et al. Am J Med. 2005 Mar;118(3):321-2. doi: 10.1016/j.amjmed.2004.10.022. Am J Med. 2005. PMID: 15745733 No abstract available.

5

A camelid antibody fragment inhibits the formation of amyloid fibrils by human lysozyme.

Dumoulin M, Last AM, Desmyter A, Decanniere K, Canet D, Larsson G, Spencer A, Archer DB, Sasse J, Muyldermans S, Wyns L, Redfield C, Matagne A, Robinson CV, Dobson CM. Dumoulin M, et al. Nature. 2003 Aug 14;424(6950):783-8. doi: 10.1038/nature01870. Nature. 2003. PMID: 12917687 Free article.

6

A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis.

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

7

A family with gastrointestinal amyloidosis associated with variant lysozyme.

Granel B, Serratrice J, Valleix S, Grateau G, Droz D, Lafon J, Sault MC, Chaudier B, Disdier P, Laugier R, Delpech M, Weiller PJ. Granel B, et al. Gastroenterology. 2002 Oct;123(4):1346-9. doi: 10.1053/gast.2002.36022. Gastroenterology. 2002. PMID: 12360495

8

Glaucoma in primary amyloidosis: a fortuitous or causative association?

Vella FS, Simone B, Giannelli G, Sisto D, Sborgia C, Antonaci S. Vella FS, et al. Am J Med. 2002 Aug 15;113(3):252-4. doi: 10.1016/s0002-9343(02)01153-1. Am J Med. 2002. PMID: 12208391 No abstract available.

9

Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.

Lachmann HJ, Booth DR, Booth SE, Bybee A, Gilbertson JA, Gillmore JD, Pepys MB, Hawkins PN. Lachmann HJ, et al. N Engl J Med. 2002 Jun 6;346(23):1786-91. doi: 10.1056/NEJMoa013354. N Engl J Med. 2002. PMID: 12050338 Free article.

10

Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family.

Valleix S, Drunat S, Philit JB, Adoue D, Piette JC, Droz D, MacGregor B, Canet D, Delpech M, Grateau G. Valleix S, et al. Kidney Int. 2002 Mar;61(3):907-12. doi: 10.1046/j.1523-1755.2002.00205.x. Kidney Int. 2002. PMID: 11849445 Free article.

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