Monica Galliano Selected Research

Familial Dysalbuminemic Hyperthyroxinemia

1/2017	Clinical, Genetic, and Protein Structural Aspects of Familial Dysalbuminemic Hyperthyroxinemia and Hypertriiodothyroninemia.
4/2016	Mutants and molecular dockings reveal that the primary L-thyroxine binding site in human serum albumin is not the one which can cause familial dysalbuminemic hyperthyroxinemia.

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Monica Galliano Research Topics

Disease

2	Neoplasms (Cancer) 01/2020 - 05/2013
2	Familial Dysalbuminemic Hyperthyroxinemia 01/2017 - 04/2016
2	Edema (Dropsy) 11/2010 - 08/2008
1	Alzheimer Disease (Alzheimer's Disease) 01/2019
1	Fatigue 01/2019
1	Hyperlipidemias (Hyperlipidemia) 01/2019
1	Neurodegenerative Diseases (Neurodegenerative Disease) 01/2019
1	Hyperthyroxinemia 01/2017
1	Hypoalbuminemia 09/2016
1	Hypercholesterolemia 03/2012
1	Liver Diseases (Liver Disease) 01/2011
1	Chronic Kidney Failure (Chronic Renal Failure) 03/2007
1	Focal Segmental Glomerulosclerosis (Glomerulosclerosis, Focal) 03/2007
1	Uremia 12/2004

Drug/Important Bio-Agent (IBA)

6	AlbuminsIBA 01/2019 - 08/2008
6	Proteins (Proteins, Gene)FDA Link 01/2019 - 12/2004
2	LectinsIBA 01/2020 - 05/2013
2	Tryptophan (L-Tryptophan)FDA Link 01/2019 - 12/2004
1	3-hydroxykynurenineIBA 01/2019
1	Thyroid HormonesIBA 01/2017
1	Thyroxine (Levothyroxine)FDA LinkGeneric 04/2016
1	Human Serum Albumin FDA LinkGeneric 04/2016
1	Antineoplastic Agents (Antineoplastics)IBA 05/2013
1	Nonsense Codon (Nonsense Mutation)IBA 08/2008
1	Serum AlbuminIBA 03/2007
1	KynurenineIBA 12/2004

Therapy/Procedure

1	Transplantation 03/2007
1	Renal Dialysis (Hemodialysis) 12/2004