Treating bipolar depression with esketamine: Safety and effectiveness data from a naturalistic multicentric study on esketamine in bipolar versus unipolar treatment-resistant depression

Autor: Martinotti, G., Dell'Osso, B., Dilorenzo, G., Maina, G., Bertolino, A., Clerici, M., Barlati, S., Rosso, G., Dinicola, M., Marcatili, M., D'Andrea, G., Cavallotto, C., Chiappini, S., Defilippis, S., Nicolo, G., Defazio, P., Andriola, I., Zanardi, R., Nucifora, D., Dimauro, S., Bassetti, R., Pettorruso, M., Mcintyre, R. S., Sensi, S. L., di Giannantonio, M., Vita, A., Baldacci, G., Belletti, S., Bellomo, A., Benatti, B., Carminati, M., Carullo, R., de Berardis, D., de Filippis, R., Chiaie, R. D., di Carlo, F., Di Petta, G., Galluzzo, A., Giorgelli, V., Lombardozzi, G., Martiadis, V., Mattei, C., Mosca, A., Niolu, C., Olivola, M., Percudani, M., Pepe, M., Rossi, E., Scardigli, M. I., Tati, F., Valchera, A., Vismara, M.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e0aa8df26d21c279e4af5a48ee0031b
https://hdl.handle.net/2318/1891433

Placental Involvement in Glycogen Storage Disease Type IV

Autor: Konstantinidou, A.E., Anninos, H., Dertinger, S., Nonni, A., Petersen, M., Karadimas, C., Havaki, S., Marinos, E., Akman, H.O., DiMauro, S., Patsouris, E.

Publikováno v: In Placenta 2008 29(4):378-381

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Risk of developing a mitochondrial DNA deletion disorder.

Autor: Chinnery PF (AUTHOR), DiMauro S (AUTHOR), Shanske S (AUTHOR), Schon EA (AUTHOR), Zeviani M (AUTHOR), Mariotti C (AUTHOR), Carrara F (AUTHOR), Lombes A (AUTHOR), Laforet P (AUTHOR), Ogier H (AUTHOR), Jaksch M (AUTHOR), Lochmüller H (AUTHOR), Horvath R (AUTHOR), Deschauer M (AUTHOR), Thorburn DR (AUTHOR), Bindoff LA (AUTHOR), Poulton J (AUTHOR), Taylor RW (AUTHOR), Matthews JNS (AUTHOR), Turnbull DM (AUTHOR)

Publikováno v: Lancet. 8/14/2004, Vol. 364 Issue 9434, p592-596. 5p.

CEREBELLAR ATAXIA AND SEVERE MUSCLE CoQ10 DEFICIENCY IN A PATIENT WITH A NOVEL MUTATION IN ADCK3

Autor: Barca, E., Musumeci, O., Montagnese, F., Marino, S., Granata, F., Nunnari, D., Peverelli, L., DiMauro, S., Quinzii, C.M., Toscano, A.

Inherited ataxias are a group of heterogeneous disorders in children or adults but their genetic definition remains still undetermined in almost half of the patients. However, CoQ10 deficiency is a rare cause of cerebellar ataxia and ADCK3 is the mos

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e8b8a0067e2315b18c6e88d3266fc6d5
http://hdl.handle.net/11570/3091791