Timeline

Sabine Duchatelet

Post-doc

15 Jul 2017

publication

The Microbiological Landscape of Anaerobic Infections in Hidradenitis Suppurativa: A Prospective Metagenomic Study

01 Oct 2015

publication

Deciphering the microbiology of hidradenitis suppurativa: a step forward towards understanding an enigmatic inflammatory skin disease

31 Aug 2015

publication

A. First Nicastrin mutation in PASH syndrome Br

01 Jun 2015

publication

Erythrokeratodermia variabilis et progressiva allelic to oculo-dento-digital dysplasia

11 May 2015

team

Ecology and Emergence of Arthropod-borne Pathogens

17 Mar 2015

publication

Olmsted syndrome: clinical, molecular and therapeutic aspects

02 Nov 2014

publication

Familial pachyonychia congenita with steatocystoma multiplex and multiple abscesses of the scalp due to the p.Asn92Ser mutation in keratin 17

04 Aug 2014

publication

Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations

01 Mar 2014

publication

A new TRPV3 missense mutation in a patient with Olmsted syndrome and erythromelalgia

01 Mar 2014

publication

Genetics of atopic dermatitis: beyond filaggrin-the role of thymic stromal lymphopoietin in disease persistence

25 Feb 2014

publication

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation

15 Jul 2013

publication

Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome

17 Oct 2011

publication

Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencing

17 Sep 2010

publication

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

08 Oct 2007

publication

FCRL3 -169CT functional polymorphism in type 1 diabetes and autoimmunity traits

01 Feb 2007

publication

PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits

21 May 2006

publication

Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism

03 Nov 2004

publication

A little guide for advanced search:

Timeline

The Microbiological Landscape of Anaerobic Infections in Hidradenitis Suppurativa: A Prospective Metagenomic Study

Deciphering the microbiology of hidradenitis suppurativa: a step forward towards understanding an enigmatic inflammatory skin disease

A. First Nicastrin mutation in PASH syndrome Br

Erythrokeratodermia variabilis et progressiva allelic to oculo-dento-digital dysplasia

Ecology and Emergence of Arthropod-borne Pathogens

Olmsted syndrome: clinical, molecular and therapeutic aspects

Familial pachyonychia congenita with steatocystoma multiplex and multiple abscesses of the scalp due to the p.Asn92Ser mutation in keratin 17

Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations

A new TRPV3 missense mutation in a patient with Olmsted syndrome and erythromelalgia

Genetics of atopic dermatitis: beyond filaggrin-the role of thymic stromal lymphopoietin in disease persistence

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation

Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome

Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencing

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

FCRL3 -169CT functional polymorphism in type 1 diabetes and autoimmunity traits

PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits

Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism

Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes