Home › Researcher directory › Philippe Ryvlin

Philippe Ryvlin

Affiliation : Lyon 1 Université · Hospices Civils de Lyon

3Publications (affiliation in France)
635Total publications
25875Citations
83h-index

Research profile

Philippe Ryvlin has 3 indexed publications (2010–2019). Their work appears mainly in “Seizure”, “Human Molecular Genetics” and “Epilepsia”. Their most cited article, “Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease” (2010), has been cited 45 times. Their work is co-authored with at least 12 researchers, including institutions in Mauritania, Tunisia.

Is this you? Get your research seen

Create your free DzCademia profile and add your articles: they will show up more easily on Google and in AI assistants like ChatGPT, so more people can read and cite your work.

Create my free profile Add my publications

Research areas

Epilepsy research and treatment
Neurological disorders and treatments
Pharmacological Effects and Toxicity Studies
EEG and Brain-Computer Interfaces
Diet and metabolism studies

Publications (3)

Disappearance of symptomatic generalized 3-Hz discharges after focal surgery in a patient with tuberous sclerosis
2019 · Seizure
Galanin pathogenic mutations in temporal lobe epilepsy
2015 · Human Molecular Genetics · cited 28 times
Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease
2010 · Epilepsia · cited 45 times

Publication venues

Seizure × 1
Human Molecular Genetics × 1
Epilepsia × 1

Publications per year

20191
20151
20101

Collaborations

Partner institutions : Université de Nouakchott · Inserm · Centre Hospitalier Régional et Universitaire de Nancy · CHU Dijon Bourgogne · Hôpitaux Universitaires de Strasbourg

Co-authors’ countries : Mauritania · Tunisia

Co-authors

Bibliographic data from OpenAlex (open database).