Lorenzo Minchiotti
Pavia, 27100, Italy
Last Updated: 09/26/2026
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Found 21 publications
Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects.
Journal: International journal of molecular sciences
Published: December 24, 2021
A novel nonsense variation in the albumin gene (c.1309 A>T) causing analbuminaemia.
Journal: British journal of biomedical science
Published: September 04, 2020
Recurrent Hypoglycemia in a Case of Congenital Analbuminemia.
Journal: Case reports in endocrinology
Published: October 20, 2019
Congenital analbuminemia in a patient affected by hypercholesterolemia: A case report.
Journal: World journal of clinical cases
Published: October 18, 2018
Diagnosis, Phenotype, and Molecular Genetics of Congenital Analbuminemia.
Journal: Frontiers in genetics
Published: September 18, 2018
A novel insertion (c.1098dupT) in the albumin gene causes analbuminemia in a consanguineous family.
Journal: European journal of medical genetics
Published: May 11, 2018
A novel splicing mutation in the ALB gene causing analbuminaemia in a Portuguese woman.
Journal: Pathology
Published: January 19, 2018
Clinical, Genetic, and Protein Structural Aspects of Familial Dysalbuminemic Hyperthyroxinemia and Hypertriiodothyroninemia.
Journal: Frontiers in endocrinology
Published: August 24, 2017
Congenital Analbuminemia in Unrelated Algerian and Turkish Families is Caused by the Same Molecular Defect in the Albumin Gene.
Journal: Annals of laboratory medicine
Published: June 30, 2017
A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family.
Journal: Biochemia medica
Published: January 26, 2016
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant.
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infant.
Journal: Annals of clinical biochemistry
Published: October 28, 2015
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.
Journal: Biochimica et biophysica acta
Published: October 09, 2015
Last Updated: 09/26/2026