Marie-Cécile Nassogne (Marie-Cecile Nassogne)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 14

Top Topics

Peritoneal Dialysis

Ejection Fraction

Top Venues

European journal of human genetics : EJHG

American journal of medical genetics. Part A

Acta neurologica Belgica

Acta neuropathologica communications

This page only lists publications with an associated author ORCID identifier.

Publications

Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A (2024)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Yeboah Kofi Gyening, Boris Keren, Mignot Cyril, Richard S Brush, Marie-Cécile Nassogne, Martin-Paul Agbaga
A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case report. Acta neuropathologica communications 11 (1) (2023)
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, Lisanne S Vijfhuizen, Sophie Nicole, Gaëtan Lesca, Emanuela Abiusi, Agnese Novelli, Lorena Di Pietro, null null, null null, Aster V E Harder, Nicole M Walley, Elisa De Grandis, Anne-Lise Poulat, Vincent Des Portes, Anne Lépine, Marie-Cécile Nassogne, Alexis A Arzimanoglou, Rosaria Vavassori, Jan Koenderink, Christopher H Thompson, Alfred L George, Fiorella Gurrieri, Arn M J M van den Maagdenberg, Erin L Heinzen
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. European journal of human genetics : EJHG 32 (2) (2023)
Charbel El Kosseifi, Karima Seddiki, Dana Dumitriu, Marie-Cécile Nassogne
Progressive hemiparesis reveals X-linked adrenoleukodystrophy in a 3.5-year-old boy. Acta neurologica Belgica 121 (1) (2020)
Océane Perdaens, Guus Koerts, Marie-Cécile Nassogne
Hydrocephalus in children under the age of five from diagnosis to short-/medium-/long-term progression: a retrospective review of 142 children. Acta neurologica Belgica 118 (1) (2018)