List of works - Francesca Lugani

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

scientific article published on 26 November 2012

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

scientific article published on January 2016

A retrotransposon insertion in the 5' regulatory domain of Ptf1a results in ectopic gene expression and multiple congenital defects in Danforth's short tail mouse.

scientific article

Comment on: Clinical application of best practice guidelines for genetic diagnosis of MODY2

scientific article published on 25 November 2011

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

scientific article

Genome-wide association study identifies susceptibility loci for IgA nephropathy

scientific article

Hyperglycaemia and β-cell antibodies: is it always pre-type 1 diabetes?

scientific article

Long-term home parenteral nutrition in children with chronic intestinal failure: A 15-year experience at a single Italian centre

article

Mutations in DSTYK and dominant urinary tract malformations

scientific article

Neonatal Diabetes Caused by Pancreatic Agenesia: Which other genes should be used for diagnosis?

article

Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy

article

Osteocalcin regulates murine and human fertility through a pancreas-bone-testis axis

scientific article

Osteocalcin regulates murine and human fertility through a pancreas-bone-testis axis

scientific article published on May 2015

Osteocalcin regulates murine and human fertility through a pancreas-bone-testis axis

article by Franck Oury et al published 1 December 2014 in Journal of Clinical Investigation

Recurrent Hypoglycemia in a Case of Congenital Analbuminemia

scientific article published on 27 February 2020

Strong association between time watching television and blood glucose control in children and adolescents with type 1 diabetes: response to Margeirsdottir et al.

scientific article published in December 2007

To the editor: Alcaligenes as a pathogen in airways chronic infection in cystic fibrosis

scientific article published in May 2003

Wolfram syndrome: new mutations, different phenotype

scientific article

List of works by Francesca Lugani

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

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

A retrotransposon insertion in the 5' regulatory domain of Ptf1a results in ectopic gene expression and multiple congenital defects in Danforth's short tail mouse.

Comment on: Clinical application of best practice guidelines for genetic diagnosis of MODY2

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

Genome-wide association study identifies susceptibility loci for IgA nephropathy

Hyperglycaemia and β-cell antibodies: is it always pre-type 1 diabetes?

Long-term home parenteral nutrition in children with chronic intestinal failure: A 15-year experience at a single Italian centre

Mutations in DSTYK and dominant urinary tract malformations

Neonatal Diabetes Caused by Pancreatic Agenesia: Which other genes should be used for diagnosis?

Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy

Osteocalcin regulates murine and human fertility through a pancreas-bone-testis axis

Osteocalcin regulates murine and human fertility through a pancreas-bone-testis axis

Osteocalcin regulates murine and human fertility through a pancreas-bone-testis axis

Recurrent Hypoglycemia in a Case of Congenital Analbuminemia

Strong association between time watching television and blood glucose control in children and adolescents with type 1 diabetes: response to Margeirsdottir et al.

To the editor: Alcaligenes as a pathogen in airways chronic infection in cystic fibrosis

Wolfram syndrome: new mutations, different phenotype