Noonan syndrome,PTPN11mutations, and brain tumors. A clinical report and review of the literature

Author:

Siegfried Aurore12,Cances Claude3,Denuelle Marie4,Loukh Najat2,Tauber Maïté5,Cavé Hélène67,Delisle Marie-Bernadette28

Affiliation:

1. Department of Pathology; Institut Universitaire du Cancer; Oncopole; Toulouse France

2. Neuropathology; University Laboratory of Pathology; CHU Toulouse; Université Toulouse III-Paul Sabatier; Toulouse France

3. Pediatric Neurology; Hôpital des Enfants; CHU Toulouse; Toulouse France

4. Neurophysiological Investigation Department; Hôpital Pierre-Paul Riquet; CHU Toulouse; Toulouse France

5. Endocrinology; Obesity; Bone Disease; Genetics and Medical Gynecology; Hôpital des Enfants; INSERM UMR1043; Université Toulouse III-Paul Sabatier; Toulouse France

6. INSERM UMR-S1131; University Institute of Hematology; Université Paris Diderot; Sorbonne-Paris-Cité; Paris France

7. Genetics Department; Assistance Publique des Hôpitaux de Paris (AP-HP); Hôpital Robert Debré; Paris France

8. INSERM UMR 1214 ToNIC; Université Toulouse III-Paul Sabatier; Toulouse France

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference40 articles.

1. Epilepsy surgery in neurofibromatosis type 1;Barba;Epilepsy Res,2013

2. Dysembryoplastic neuroepithelial tumor in two relatives with Noonan syndrome and a PTPN11 mutation;Bendel;Neuro Oncol,2012

3. Bendel A Pond D. 2014

4. Acute lymphoblastic leukemia in the context of RASopathies;Cavé;Eur J Med Genet,2016

5. Dysembryoplastic neuroepithelial tumors share with pleomorphic xanthoastrocytomas and gangliogliomas BRAF(V600E) mutation and expression;Chappé;Brain Pathol,2013

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