A rare case of giant multiseptated thoracic myelomeningocele with segmental placode: Commentary

Por Beuriat, Pierre-Aurelien, Szathmari, Alexandru, Di Rocco, Federico, Mottolese, Carmine
Publicado no Surg Neurol Int (2016)

Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations

Por di Rocco, Federico, Baujat, Geneviève, Arnaud, Eric, Rénier, Dominique, Laplanche, Jean-Louis, Daire, Valérie Cormier, Collet, Corinne
Publicado no Eur J Hum Genet (2014)

Posterior Cranial Fossa Gangliogliomas

Por Safavi-Abbasi, Sam, Di Rocco, Federico, Chantra, Kraisri, Feigl, Guenther C., El-Shawarby, Amr, Samii, Amir, Samii, Madjid
Publicado em 2007

Thrombophilia Due to Factor V and Factor II Mutations and Formation of a Dural Arteriovenous Fistula: Case Report and Review of a Rare Entity

Por Safavi-Abbasi, Sam, Di Rocco, Federico, Nakaji, Peter, Feigl, Guenther C., Gharabaghi, Alireza, Samii, Madjid, Valavanis, Anton, Samii, Amir
Publicado em 2008

Has Management of Epidermoid Tumors of the Cerebellopontine Angle Improved? A Surgical Synopsis of the Past and Present

Por Safavi-Abbasi, Sam, Di Rocco, Federico, Bambakidis, Nicholas, Talley, Melani C., Gharabaghi, Alireza, Luedemann, Wolf, Samii, Madjid, Samii, Amir
Publicado em 2008

Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease

Por Armanet, Narjes, Metay, Corinne, Brisset, Sophie, Deschenes, Georges, Pineau, Dominique, Petit, François M, Di Rocco, Federico, Goossens, Michel, Tachdjian, Gérard, Labrune, Philippe, Tosca, Lucie
Publicado no Mol Cytogenet (2015)

Quantification of Facial Skeletal Shape Variation in Fibroblast Growth Factor Receptor-Related Craniosynostosis Syndromes

Por Heuzé, Yann, Martínez-Abadías, Neus, Stella, Jennifer M., Arnaud, Eric, Collet, Corinne, Fructuoso, Gemma García, Alamar, Mariana, Lo, Lun-Jou, Boyadjiev, Simeon A., Di Rocco, Federico, Richtsmeier, Joan T.
Publicado em 2014

Meckel’s and condylar cartilages anomalies in achondroplasia result in defective development and growth of the mandible

Por Biosse Duplan, Martin, Komla-Ebri, Davide, Heuzé, Yann, Estibals, Valentin, Gaudas, Emilie, Kaci, Nabil, Benoist-Lasselin, Catherine, Zerah, Michel, Kramer, Ina, Kneissel, Michaela, Porta, Diana Grauss, Di Rocco, Federico, Legeai-Mallet, Laurence
Publicado no Hum Mol Genet (2016)

Multimodal optical analysis discriminates freshly extracted human sample of gliomas, metastases and meningiomas from their appropriate controls

Por Zanello, Marc, Poulon, Fanny, Pallud, Johan, Varlet, Pascale, Hamzeh, H., Abi Lahoud, Georges, Andreiuolo, Felipe, Ibrahim, Ali, Pages, Mélanie, Chretien, Fabrice, Di Rocco, Federico, Dezamis, Edouard, Nataf, François, Turak, Baris, Devaux, Bertrand, Abi Haidar, Darine
Publicado no Sci Rep (2017)

Evaluation of the Therapeutic Potential of a CNP Analog in a Fgfr3 Mouse Model Recapitulating Achondroplasia

Por Lorget, Florence, Kaci, Nabil, Peng, Jeff, Benoist-Lasselin, Catherine, Mugniery, Emilie, Oppeneer, Todd, Wendt, Dan J., Bell, Sean M., Bullens, Sherry, Bunting, Stuart, Tsuruda, Laurie S., O'Neill, Charles A., Di Rocco, Federico, Munnich, Arnold, Legeai-Mallet, Laurence
Publicado em 2012

Tyrosine kinase inhibitor NVP-BGJ398 functionally improves FGFR3-related dwarfism in mouse model

Por Komla-Ebri, Davide, Dambroise, Emilie, Kramer, Ina, Benoist-Lasselin, Catherine, Kaci, Nabil, Le Gall, Cindy, Martin, Ludovic, Busca, Patricia, Barbault, Florent, Graus-Porta, Diana, Munnich, Arnold, Kneissel, Michaela, Di Rocco, Federico, Biosse-Duplan, Martin, Legeai-Mallet, Laurence
Publicado no J Clin Invest (2016)