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Items: 1 to 20 of 93

1.

A novel mutation in the albumin gene (c.1A>C) resulting in analbuminemia.

Caridi G, Dagnino M, Lugani F, Shalev SA, Campagnoli M, Galliano M, Spiegel R, Minchiotti L.

Eur J Clin Invest. 2013 Jan;43(1):72-8. doi: 10.1111/eci.12019. Epub 2012 Nov 26.

PMID:
23176518
2.

A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient.

Dagnino M, Caridi G, Marsciani M, Bettocchi I, Tassinari D, Bernardi F, Chiodo F, Campagnoli M, Galliano M, Minchiotti L.

Eur J Clin Invest. 2010 Mar;40(3):281-4. doi: 10.1111/j.1365-2362.2010.02256.x.

PMID:
20415703
3.

Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene.

Caridi G, Dagnino M, Erdeve O, Di Duca M, Yildiz D, Alan S, Atasay B, Arsan S, Campagnoli M, Galliano M, Minchiotti L.

Biochem Med (Zagreb). 2014 Feb 15;24(1):151-8. doi: 10.11613/BM.2014.017. eCollection 2014.

4.

Molecular diagnosis of analbuminemia: a new case caused by a nonsense mutation in the albumin gene.

Dagnino M, Caridi G, Haenni U, Duss A, Aregger F, Campagnoli M, Galliano M, Minchiotti L.

Int J Mol Sci. 2011;12(11):7314-22. doi: 10.3390/ijms12117314. Epub 2011 Oct 25.

5.

Analbuminemia produced by a novel splicing mutation.

Dolcini L, Caridi G, Dagnino M, Sala A, Gökçe S, Sökücü S, Campagnoli M, Galliano M, Minchiotti L.

Clin Chem. 2007 Aug;53(8):1549-52.

6.

A novel splicing mutation causes an undescribed type of analbuminemia.

Campagnoli M, Rossi A, Palmqvist L, Flisberg A, Niklasson A, Minchotti L, Galliano M.

Biochim Biophys Acta. 2002 Jan 2;1586(1):43-9.

7.

A novel splicing mutation causes analbuminemia in a Portuguese boy.

Caridi G, Dagnino M, Di Duca M, Pinto H, Espinheira Mdo C, Guerra A, Fernandes S, Campagnoli M, Galliano M, Minchiotti L.

Mol Genet Metab. 2012 Mar;105(3):479-83. doi: 10.1016/j.ymgme.2011.12.009. Epub 2011 Dec 16.

PMID:
22227324
8.

Analbuminemia in a Slovak Romany (gypsy) family: case report and mutational analysis.

Campagnoli M, Rosipal S, Debreová M, Rosipal R, Sala A, Romano A, Labò S, Galliano M, Minchiotti L.

Clin Chim Acta. 2006 Mar;365(1-2):188-93. Epub 2005 Sep 22.

PMID:
16183048
9.

Analbuminemia Zonguldak: case report and mutational analysis.

Caridi G, Dagnino M, Dalgic B, Egritas O, Sancak B, Campagnoli M, Dolcini L, Galliano M, Minchiotti L.

Clin Biochem. 2008 Mar;41(4-5):288-91. Epub 2007 Dec 5.

PMID:
18154732
10.

Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene.

Campagnoli M, Sala A, Labò S, Rossi A, Neuhaus TJ, Braegger CP, Minchiotti L, Galliano M.

Clin Biochem. 2005 Sep;38(9):819-23.

PMID:
15996651
11.

Analbuminemia in a Swedish male is caused by the Kayseri mutation (c228_229delAT).

Campagnoli M, Hansson P, Dolcini L, Caridi G, Dagnino M, Candiano G, Bruschi M, Palmqvist L, Galliano M, Minchiotti L.

Clin Chim Acta. 2008 Oct;396(1-2):89-92. doi: 10.1016/j.cca.2008.06.008. Epub 2008 Jun 12.

PMID:
18602380
12.

Albumin locust valley: a new case of analbuminemia.

Peters T Jr, Holowachuk EW, McIncrow R, Campagnoli M, Galliano M.

Clin Biochem. 2006 Sep;39(9):904-6. Epub 2006 Apr 21.

PMID:
16713595
13.

A nucleotide insertion and frameshift cause analbuminemia in an Italian family.

Watkins S, Madison J, Galliano M, Minchiotti L, Putnam FW.

Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2275-9.

14.

A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman.

Dagnino M, Caridi G, Aydin Z, Ozturk S, Karaali Z, Kazancioglu R, Cefle K, Gursu M, Campagnoli M, Galliano M, Minchiotti L.

Clin Chim Acta. 2010 Nov 11;411(21-22):1711-5. doi: 10.1016/j.cca.2010.07.009. Epub 2010 Jul 16.

PMID:
20638375
15.

A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family.

Caridi G, Gulec EY, Campagnoli M, Lugani F, Onal H, Kilic D, Galliano M, Minchiotti L.

Biochem Med (Zagreb). 2016;26(2):264-71. doi: 10.11613/BM.2016.031.

16.

Analbuminemia: three cases resulting from different point mutations in the albumin gene.

Watkins S, Madison J, Galliano M, Minchiotti L, Putnam FW.

Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9417-21.

17.

Molecular diagnosis of analbuminemia: a novel mutation identified in two Amerindian and two Turkish families.

Galliano M, Campagnoli M, Rossi A, Wirsing von König CH, Lyon AW, Cefle K, Yildiz A, Palanduz S, Ozturk S, Minchiotti L.

Clin Chem. 2002 Jun;48(6 Pt 1):844-9.

18.

Detection of a novel splicing mutation causing analbuminemia in a Libyan family.

Bibi A, Jouini L, Sahli CA, Hadj Fredj S, Abidi K, Gharsallah L, Mathlouthi S, Ouali F, Siala H, Belhaj R, Sammoud A, Messaoud T.

Clin Biochem. 2012 Oct;45(15):1183-6. doi: 10.1016/j.clinbiochem.2012.05.007. Epub 2012 May 18.

PMID:
22613267
19.

Location of the mutation site in the first two reported cases of analbuminemia.

Ruhoff MS, Greene MW, Peters T.

Clin Biochem. 2010 Mar;43(4-5):525-7. doi: 10.1016/j.clinbiochem.2009.12.002. Epub 2009 Dec 16.

PMID:
20025859
20.

Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene.

Campagna F, Fioretti F, Burattin M, Romeo S, Sentinelli F, Bifolco M, Sirinian MI, Del Ben M, Angelico F, Arca M.

Clin Chem. 2005 Jul;51(7):1256-8. No abstract available.

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