Damien Sternberg

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 5

Top Topics

Hypertrophic Cardiomyopathy

End Stage Renal Disease

Top Venues

Neurology. Clinical practice

Neurology. Genetics

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

Publications

Mohamed Islam Kediha, Meriem Tazir, Damien Sternberg, Bruno Eymard, Lamia Ali Pacha
Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes. Neurology. Clinical practice 14 (3) (2024)
Pierre-Louis Lanvin, Dong Li, Solène Conrad, Armelle Magot, Xavier Micaelli, Yann Péréon, Marie Vincent, Bertrand Isidor, Damien Sternberg, Elizabeth M McCormick, Hakon H Hakonarson, Sandra Mercier, Marni J Falk
Expanding the Spectrum of Congenital Myopathy Linked to Variants in the MYBPC1 Gene: A Clinical Report. Neurology. Clinical practice 14 (3) (2024)
Mohamed Islam Kediha, Meriem Tazir, Damien Sternberg, Bruno Eymard, Lamia Ali Pacha
Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes. Neurology. Clinical practice 14 (3) (2024)
Pierre-Louis Lanvin, Dong Li, Solène Conrad, Armelle Magot, Xavier Micaelli, Yann Péréon, Marie Vincent, Bertrand Isidor, Damien Sternberg, Elizabeth M McCormick, Hakon H Hakonarson, Sandra Mercier, Marni J Falk
Expanding the Spectrum of Congenital Myopathy Linked to Variants in the MYBPC1 Gene: A Clinical Report. Neurology. Clinical practice 14 (3) (2024)
Stéphanie Bauché, Alain Sureau, Damien Sternberg, John Rendu, Céline Buon, Julien Messéant, Myriam Boëx, Denis Furling, Julien Fauré, Xénia Latypova, Antoinette Bernabe Gelot, Michèle Mayer, Pierre Mary, Sandra Whalen, Emmanuel Fournier, Isabelle Cloix, Ganaelle Remerand, Fanny Laffargue, Marie-Christine Nougues, Bertrand Fontaine, Bruno Eymard, Arnaud Isapof, Laure Strochlic
New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes. Neurology. Genetics 6 (6) (2020)