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Items: 1 to 20 of 25

1.
Alterations in the Plasma Protein Expression Pattern in Congenital Analbuminemia—A Systematic Review
Bailey M. Foster, Afsoun Abdollahi, Gregory C. Henderson
Biomolecules. 2023 Mar; 13(3): 407. Published online 2023 Feb 22. doi: 10.3390/biom13030407
PMCID:
PMC10046341
AbstractArticlePDF–819K
2.
Oxidative stress mediated platelet activation in patients with congenital analbuminemia: Effect of albumin infusion
Francesco Baratta, Simona Bartimoccia, Roberto Carnevale, Lucia Stefanini, Francesco Angelico, Maria Del Ben
J Thromb Haemost. 2021 Dec; 19(12): 3090–3094. Published online 2021 Oct 16. doi: 10.1111/jth.15545
PMCID:
PMC9293470
AbstractArticlePDF–1.0M
3.
Recurrent Hypoglycemia in a Case of Congenital Analbuminemia
Martin Litzel, Gianluca Caridi, Francesca Lugani, Monica Campagnoli, Lorenzo Minchiotti, Stefan Fischli
Case Rep Endocrinol. 2020; 2020: 8452564. Published online 2020 Feb 27. doi: 10.1155/2020/8452564
PMCID:
PMC7063871
AbstractArticlePDF–1.2M
4.
Congenital Analbuminemia in a Korean Male Diagnosed with Single Nucleotide Polymorphism in the ALB Gene: The First Case Reported in Korea
Youngji Kim, Ye Seul Yang, Sung Sup Park, Man Jin Kim, Cheol Min Shin, Sung Hee Choi
Yonsei Med J. 2019 Jul 1; 60(7): 700–703. Published online 2019 Jun 24. doi: 10.3349/ymj.2019.60.7.700
PMCID:
PMC6597461
AbstractArticlePDF–1.0M
5.
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia
Lorenzo Minchiotti, Gianluca Caridi, Monica Campagnoli, Francesca Lugani, Monica Galliano, Ulrich Kragh-Hansen
Front Genet. 2019; 10: 336. Published online 2019 Apr 17. doi: 10.3389/fgene.2019.00336
PMCID:
PMC6478806
AbstractArticlePDF–1.9M
6.
Congenital analbuminemia in a patient affected by hypercholesterolemia: A case report
Patrizia Suppressa, Concetta Carbonara, Francesca Lugani, Monica Campagnoli, Teresa Troiano, Lorenzo Minchiotti, Carlo Sabbà
World J Clin Cases. 2019 Feb 26; 7(4): 466–472. Published online 2019 Feb 26. doi: 10.12998/wjcc.v7.i4.466
PMCID:
PMC6397822
AbstractArticlePDF–1.5M
7.
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family
Gianluca Caridi, Elif Yilmaz Gulec, Monica Campagnoli, Francesca Lugani, Hasan Onal, Duzgun Kilic, Monica Galliano, Lorenzo Minchiotti
Biochem Med (Zagreb) 2016 Jun 10; 26(2): 264–271. Published online 2016 Jun 10. doi: 10.11613/BM.2016.031
PMCID:
PMC4910280
AbstractArticlePDF–811K
8.
Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene
Gianluca Caridi, Monica Dagnino, Omer Erdeve, Marco Di Duca, Duran Yildiz, Serdar Alan, Begum Atasay, Saadet Arsan, Monica Campagnoli, Monica Galliano, Lorenzo Minchiotti
Biochem Med (Zagreb) 2014 Feb; 24(1): 151–158. Published online 2014 Feb 15. doi: 10.11613/BM.2014.017
PMCID:
PMC3936982
AbstractArticlePDF–369K
9.
Treatment of a patient with congenital analbuminemia with atorvastatin and albumin infusion
Maria Del Ben, Francesco Angelico, Lorenzo Loffredo, Francesco Violi
World J Clin Cases. 2013 Apr 16; 1(1): 44–48. Published online 2013 Apr 16. doi: 10.12998/wjcc.v1.i1.44
PMCID:
PMC3845927
AbstractArticlePDF–695K
10.
Perinatal and childhood morbidity and mortality in congenital analbuminemia
Jennifer M Toye, Edmond G Lemire, Krista L Baerg
Paediatr Child Health. 2012 Jun-Jul; 17(6): e20–e23.
PMCID:
PMC3380755
AbstractArticlePDF–777K
11.
Molecular Diagnosis of Analbuminemia: A New Case Caused by a Nonsense Mutation in the Albumin Gene
Monica Dagnino, Gianluca Caridi, Ueli Haenni, Adrian Duss, Fabienne Aregger, Monica Campagnoli, Monica Galliano, Lorenzo Minchiotti
Int J Mol Sci. 2011; 12(11): 7314–7322. Published online 2011 Oct 25. doi: 10.3390/ijms12117314
PMCID:
PMC3233406
AbstractArticlePDF–478K
12.
Coronary Artery Bypass Surgery in a Patient with Analbuminemia
Ergun Demirsoy, Gokce Sirin, Emre Ozker
Tex Heart Inst J. 2011; 38(1): 85–87.
PMCID:
PMC3060746
AbstractArticlePDF–196K
13.
Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.
J C Murray, C M Demopulos, R M Lawn, A G Motulsky
Proc Natl Acad Sci U S A. 1983 Oct; 80(19): 5951–5955. doi: 10.1073/pnas.80.19.5951
PMCID:
PMC390195
SummaryPage BrowsePDF–1.1M
14.
Restriction fragment length polymorphism of the rat albumin gene in Sprague-Dawley rats and its application in genetic study of analbuminemia.
H Esumi, Y Takahashi, S Sato, T Sugimura
Nucleic Acids Res. 1982 Jul 24; 10(14): 4247–4257. doi: 10.1093/nar/10.14.4247
PMCID:
PMC320797
SummaryPage BrowsePDF–1.2M
15.
Splicing mutation in human hereditary analbuminemia.
D E Ruffner, A Dugaiczyk
Proc Natl Acad Sci U S A. 1988 Apr; 85(7): 2125–2129. doi: 10.1073/pnas.85.7.2125
PMCID:
PMC279941
SummaryPage BrowsePDF–1.0M
16.
Analbuminemia: three cases resulting from different point mutations in the albumin gene.
S Watkins, J Madison, M Galliano, L Minchiotti, F W Putnam
Proc Natl Acad Sci U S A. 1994 Sep 27; 91(20): 9417–9421. doi: 10.1073/pnas.91.20.9417
PMCID:
PMC44823
SummaryPage BrowsePDF–1.3M
17.
A nucleotide insertion and frameshift cause analbuminemia in an Italian family.
S Watkins, J Madison, M Galliano, L Minchiotti, F W Putnam
Proc Natl Acad Sci U S A. 1994 Mar 15; 91(6): 2275–2279. doi: 10.1073/pnas.91.6.2275
PMCID:
PMC43353
SummaryPage BrowsePDF–1.3M
18.
Albumin knockout mice exhibit reduced plasma free fatty acid concentration and enhanced insulin sensitivity
Afsoun Abdollahi, Brianna N. Dowden, Kimberly K. Buhman, Alyssa S. Zembroski, Gregory C. Henderson
Physiol Rep. 2022 Mar; 10(5): e15161. Published online 2022 Mar 3. doi: 10.14814/phy2.15161
PMCID:
PMC8892599
AbstractArticlePDF–2.0M
19.
Albumin-deficient mouse models for studying metabolism of human albumin and pharmacokinetics of albumin-based drugs
Derry C Roopenian, Benjamin E Low, Gregory J Christianson, Gabriele Proetzel, Thomas J Sproule, Michael V Wiles
MAbs. 2015 Mar-Apr; 7(2): 344–351. Published online 2015 Feb 5. doi: 10.1080/19420862.2015.1008345
PMCID:
PMC4623309
AbstractArticlePDF–314K
20.
Original domain for the serum albumin family arose from repeated sequences.
S Ohno
Proc Natl Acad Sci U S A. 1981 Dec; 78(12): 7657–7661. doi: 10.1073/pnas.78.12.7657
PMCID:
PMC349328
SummaryPage BrowsePDF–961K

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