Francoise Bergametti

Francoise Bergametti

UNVERIFIED PROFILE

Are you Francoise Bergametti?   Register this Author

Register author
Francoise Bergametti

Francoise Bergametti

Publications by authors named "Francoise Bergametti"

Are you Francoise Bergametti?   Register this Author

14Publications

422Reads

23Profile Views

Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.

Brain 2015 Aug 10;138(Pt 8):2347-58. Epub 2015 Jun 10.

1 INSERM UMR 1161, Génétique et Physiopathologie des Maladies Cérébro-vasculaires, Paris, France 2 Université Paris Diderot, Sorbonne Paris Cité, UMR-S1161, Paris, France 5 AP-HP, Groupe Hospitalier Saint-Louis Lariboisière-Fernand-Widal, Service de Génétique Moléculaire Neurovasculaire, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), Paris, France

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/awv155DOI Listing
August 2015

Loss of α1β1 soluble guanylate cyclase, the major nitric oxide receptor, leads to moyamoya and achalasia.

Am J Hum Genet 2014 Mar 27;94(3):385-94. Epub 2014 Feb 27.

Institut National de la Santé et de la Recherche Médicale U1161, 75010 Paris, France; UMR-S1161, Génétique des Maladies Vasculaires, Université Paris Diderot, Sorbonne Paris Cité, 75010 Paris, France; Service de Génétique Moléculaire Neurovasculaire, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'Oeil, Groupe Hospitalier Saint-Louis Lariboisière-Fernand-Widal, Assistance Publique - Hôpitaux de Paris, 75010 Paris, France. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajhg.2014.01.018DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951937PMC
March 2014

Loss of BRCC3 deubiquitinating enzyme leads to abnormal angiogenesis and is associated with syndromic moyamoya.

Am J Hum Genet 2011 Jun 19;88(6):718-728. Epub 2011 May 19.

INSERM UMR-S-740; Université Paris, 7 Denis Diderot, 10 Avenue de Verdun, 75010 Paris, France; Assistance Publique des Hôpitaux de Paris, Groupe Hospitalier Lariboisière-Saint-Louis, Laboratoire de Génétique, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'Oeil, F-75010 Paris, France. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajhg.2011.04.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113251PMC
June 2011

Recent insights into cerebral cavernous malformations: the molecular genetics of CCM.

FEBS J 2010 Mar 22;277(5):1070-5. Epub 2010 Jan 22.

AP-HP, Hôpital Lariboisière, Laboratoire de Génétique, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1742-4658.2009.07535.xDOI Listing
March 2010

Genetics of cavernous angiomas.

Lancet Neurol 2007 Mar;6(3):237-44

INSERM, U740, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S1474-4422(07)70053-4DOI Listing
March 2007

Genotype-phenotype correlations in cerebral cavernous malformations patients.

Ann Neurol 2006 Nov;60(5):550-6

Institut National de la Sante et de la Recherche Médicale U740, Faculté de Médecine Lariboisière, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ana.20947DOI Listing
November 2006

Turnover of hepatitis B virus X protein is regulated by damaged DNA-binding complex.

J Virol 2002 Jul;76(13):6495-501

Unité de Recombinaison et Expression Génétique (INSERM U163), Institut Pasteur, 28 rue du Dr Roux, 75724 Paris Cedex 15, France.

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC136256PMC
http://dx.doi.org/10.1128/jvi.76.13.6495-6501.2002DOI Listing
July 2002