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Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11.
Published in:
PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013750
By:
- Roll, Patrice;
- Sanlaville, Damien;
- Cillario, Jennifer;
- Labalme, Audrey;
- Bruneau, Nadine;
- Massacrier, Annick;
- Délepine, Marc;
- Dessen, Philippe;
- Lazar, Vladimir;
- Robaglia-Schlupp, Andrée;
- Lesca, Gaëtan;
- Jouve, Elisabeth;
- Rudolf, Gabrielle;
- Rochette, Jacques;
- Lathrop, G. Mark;
- Szepetowski, Pierre
Publication type:
Article
Functional Variant in Complement C3 Gene Promoter and Genetic Susceptibility to Temporal Lobe Epilepsy and Febrile Seizures.
Published in:
PLoS ONE, 2010, v. 5, n. 9, p. 1, doi. 10.1371/journal.pone.0012740
By:
- Jamali, Sarah;
- Salzmann, Annick;
- Perroud, Nader;
- Ponsole-Lenfant, Magali;
- Cillario, Jennifer;
- Roll, Patrice;
- Roeckel-Trevisiol, Nathalie;
- Crespel, Ariel;
- Balzar, Jorg;
- Schlachter, Kurt;
- Gruber-Sedlmayr, Ursula;
- Pataraia, Ekaterina;
- Baumgartner, Christoph;
- Zimprich, Alexander;
- Zimprich, Fritz;
- Malafosse, Alain;
- Szepetowski, Pierre
Publication type:
Article
Blinded Independent Central Review (BICR) in New Therapeutic Lung Cancer Trials.
Published in:
Cancers, 2021, v. 13, n. 18, p. 4533, doi. 10.3390/cancers13184533
By:
- Beaumont, Hubert;
- Iannessi, Antoine;
- Wang, Yi;
- Voyton, Charles M.;
- Cillario, Jennifer;
- Liu, Yan
Publication type:
Article
Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero.
Published in:
Brain: A Journal of Neurology, 2013, v. 136, n. 8, p. 2457, doi. 10.1093/brain/awt161
By:
- Salmi, Manal;
- Bruneau, Nadine;
- Cillario, Jennifer;
- Lozovaya, Natalia;
- Massacrier, Annick;
- Buhler, Emmanuelle;
- Cloarec, Robin;
- Tsintsadze, Timur;
- Watrin, Françoise;
- Tsintsadze, Vera;
- Zimmer, Céline;
- Villard, Claude;
- Lafitte, Daniel;
- Cardoso, Carlos;
- Bao, Lan;
- Lesca, Gaetan;
- Rudolf, Gabrielle;
- Muscatelli, Françoise;
- Pauly, Vanessa;
- Khalilov, Ilgam
Publication type:
Article
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 24, p. 4848, doi. 10.1093/hmg/ddq415
By:
- Roll, Patrice;
- Vernes, Sonja C.;
- Bruneau, Nadine;
- Cillario, Jennifer;
- Ponsole-Lenfant, Magali;
- Massacrier, Annick;
- Rudolf, Gabrielle;
- Khalife, Manal;
- Hirsch, Edouard;
- Fisher, Simon E.;
- Szepetowski, Pierre
Publication type:
Article
Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 23, p. 3617, doi. 10.1093/hmg/ddn256
By:
- Royer-Zemmour, Barbara;
- Ponsole-Lenfant, Magali;
- Gara, Hyam;
- Roll, Patrice;
- Lévêque, Christian;
- Massacrier, Annick;
- Ferracci, Géraldine;
- Cillario, Jennifer;
- Robaglia-Schlupp, Andrée;
- Vincentelli, Renaud;
- Cau, Pierre;
- Szepetowski, Pierre
Publication type:
Article

Found: 6

Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11.

Functional Variant in Complement C3 Gene Promoter and Genetic Susceptibility to Temporal Lobe Epilepsy and Febrile Seizures.

Blinded Independent Central Review (BICR) in New Therapeutic Lung Cancer Trials.

Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero.

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR.