Publications by authors named "Albert Iron"

Claim this Profile
T
The importance of functional tests to assess the effect of a new variant when genotype-phenotype correlation is not possible.
Alexandre Hinzpeter, Marie-Pierre Reboul, Isabelle Callebaut, Cécile Zordan, Bruno Costes, Albert Iron

Clin Case Rep· May 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders.
Christel Thauvin-Robinet, Anne Munck, Frédéric Huet, Alix de Becdelièvre, Clément Jimenez, Raphaël Chiron, Albert Iron

J Med Genet· April 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study.
Céline René, Damien Paulet, Emmanuelle Girodon, Catherine Costa, Guy Lalau, Albert Iron

Eur J Hum Genet· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.
Isabelle Sermet-Gaudelus, Emanuelle Girodon, Dorota Sands, Nathalie Stremmler, Vera Vavrova, Albert Iron

Am J Respir Crit Care Med· October 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Renal impairment in children with cystic fibrosis.
Annick Andrieux, Jérôme Harambat, Stéphanie Bui, Fabienne Nacka, Albert Iron

J Cyst Fibros· July 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis.
Isabelle Sermet-Gaudelus, Emmanuelle Girodon, Delphine Roussel, Eric Deneuville, Stéphanie Bui, Albert Iron

Thorax· June 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Influence of the duplication of CFTR exon 9 and its flanking sequences on diagnosis of cystic fibrosis mutations.
Ayman El-Seedy, Tony Dudognon, Frédéric Bilan, Marie-Claude Pasquet, Marie-Pierre Reboul, Albert Iron

J Mol Diagn· September 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening.
Phillis Lakeman, Johan J P Gille, Jeannette E Dankert-Roelse, Harry G M Heijerman, Anne Munck, Albert Iron

Genet Test· March 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rapid and accurate detection of the CFTR gene mutation 1811+1.6 kbA>G by real-time fluorescence resonance energy transfer PCR.
Marie-Pierre Reboul, Laurent Higueret, Nicolas Biteau, Albert Iron

Mol Cell Probes· October 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Isolated idiopathic chronic pancreatitis associated with a compound heterozygosity for two mutations of the CFTR gene.
Marie-Pierre Reboul, David Laharie, Michel Amouretti, Didier Lacombe, Albert Iron

Gastroenterol Clin Biol· January 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CFTR genotypes in patients with normal or borderline sweat chloride levels.
Delphine Feldmann, Remy Couderc, Marie-Pierre Audrezet, Claude Ferec, Thierry Bienvenu, Albert Iron

Hum Mutat· October 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis