Nathalie Lannoy

Brussels, BRU, Belgium

Last Updated: 09/26/2026

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Found 15 publications

Accessibility and visibility of genetic testing for haemophilia across Europe: Where do we stand?

Accessibility and visibility of genetic testing for haemophilia across Europe: Where do we stand?

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: February 23, 2022

Inhibitor epidemiology and genetic-related risk factors in people with haemophilia from Côte d'Ivoire.

Inhibitor epidemiology and genetic-related risk factors in people with haemophilia from Côte d'Ivoire.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: August 02, 2019

Genetic mosaicism in haemophilia: A practical review to help evaluate the risk of transmitting the disease.

Genetic mosaicism in haemophilia: A practical review to help evaluate the risk of transmitting the disease.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: July 10, 2019

Incidental finding of unreported large duplication in F8 gene during prenatal analysis: Which management for genetic counselling?

Incidental finding of unreported large duplication in F8 gene during prenatal analysis: Which management for genetic counselling?

Journal: Thrombosis research

Published: March 12, 2019

Review of molecular mechanisms at distal Xq28 leading to balanced or unbalanced genomic rearrangements and their phenotypic impacts on hemophilia.

Review of molecular mechanisms at distal Xq28 leading to balanced or unbalanced genomic rearrangements and their phenotypic impacts on hemophilia.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: June 09, 2018

Comparative study of the prevalence of clotting factor deficiency in carriers of haemophilia A and haemophilia B.

Comparative study of the prevalence of clotting factor deficiency in carriers of haemophilia A and haemophilia B.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: May 22, 2017

Usual and unusual mutations in a cohort of Belgian patients with hemophilia B.

Usual and unusual mutations in a cohort of Belgian patients with hemophilia B.

Journal: Thrombosis research

Published: October 12, 2016

Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene.

Five int22h homologous copies at the Xq28 locus identified in intron22 inversion type 3 of the Factor VIII gene.

Journal: Thrombosis research

Published: October 14, 2015

Principles of genetic variations and molecular diseases: applications in hemophilia A.

Principles of genetic variations and molecular diseases: applications in hemophilia A.

Journal: Critical reviews in oncology/hematology

Published: May 26, 2015

Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A.

Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: February 24, 2015

Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?

Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?

Journal: Thrombosis research

Published: December 15, 2014

Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene.

Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene.

Journal: European journal of human genetics : EJHG

Published: August 13, 2012

Showing 1-12 of 15

Last Updated: 09/26/2026