An atypical case of trigeminal trophic syndrome: A legal medicine perspective in medical responsibility

Por di Luca, Alessandro, Ralli, Massimo, Hemied, Sara, de Vincentiis, Marco, di Luca, Natale Mario
Publicado no SAGE Open Med Case Rep (2017)

Sudden hearing loss in sarcoidosis: otoneurological study and neuroradiological correlates

Por CAMA, E., SANTARELLI, R., MUZZI, E., INCHES, I., CURTOLO, S., DI PAOLA, F., ARSLAN, E., FACCINI, E.
Publicado em 2011

Mediterranean spotted fever and hearing impairment: a rare complication

Por Raffaella Rossio, Valeria Conalbi, Valentina Castagna, Sebastiano Recalcati, Adriana Torri, Massimo Coen, Lucia Restano Cassulini, Flora Peyvandi
Publicado em 2015-06-01

A Case of Hypokalemic Paralysis in a Patient With Neurogenic Diabetes Insipidus

Por Nguyen, Frederic N., Kar, Jitesh K., Verduzco-Gutierrez, Monica, Zakaria, Asma
Publicado em 2014

Pontine extension of a tentorial schwannoma without cranial nerve involvement: a case report

Por D'Urso, Pietro Ivo, Marino, Michele, Di Blasi, Arturo, Muccio, Carmine Franco, De Cillis, Pompilio, Catapano, Giuseppe
Publicado em 2011

Mercaptopurine Treatment in an Adult Man with Orbital and Intracranial Rosai-Dorfman Disease

Por Valentina Arnao, Marianna Riolo, Giovanni Savettieri, Paolo Aridon
Publicado em 2016-01-01

CMT2A Harboring Mitofusin 2 Mutation with Optic Nerve Atrophy and Normal Visual Acuity

Por Guerriero S, D'Oria F, Rossetti G, Favale RA, Zoccolella S, Alessio G, Petruzzella V
Publicado em 2020-02-01

Total thyroidectomy and central lymph node dissection. Experience of a referral centre for endocrine surgery

Por MONACELLI, M., LUCCHINI, R., POLISTENA, A., TRIOLA, R., CONTI, C., AVENIA, S., DI PATRIZI, M.S., BARILLARO, I., BOCCOLINI, A., SANGUINETTI, A., AVENIA, N.
Publicado no G Chir (2014)

Neuropathic pain

Por Giuseppe Re, Virgilio Ricci, Fabrizio Rasi
Publicado em 2009-02-01

Water as an Independent Taste Modality

Por Rosen, Andrew M., Roussin, Andre T., Di Lorenzo, Patricia M.
Publicado em 2010

2 Novel deletions of the sterol 27-hydroxylase gene in a Chinese Family with Cerebrotendinous Xanthomatosis

Por Tian, Di, Zhang, Zai-qiang
Publicado em 2011

von Hippel-Lindau Syndrome: Genetic Study of Case With a Rare Pathogenic Variant With Optic Nerve Hemangioblastoma, a Rare Phenotypic Expression

Por Sandra Di Felice Boratto, Pedro Augusto Soffner Cardoso, Pedro Augusto Soffner Cardoso, Denise Gonçalves Priolli, Ricardo Vieira Botelho, Alberto Goldenberg, Bianca Bianco, Jaques Waisberg, Jaques Waisberg
Publicado em 2020-02-01

Validation of the peroneal nerve test to diagnose critical illness polyneuropathy and myopathy...

Por Nicola Latronico, Giovanni Nattino, Bruno Guarneri, Nazzareno Fagoni, Aldo Amantini, Guido Bertolini, and GiVITI Study Investigators
Publicado em 2014-07-01

Hyperventilation-induced nystagmus in a large series of vestibular patients

Por CALIFANO, L., MELILLO, M.G., VASSALLO, A., MAZZONE, S.
Publicado em 2011

Video-assisted thyroidectomy: lessons learned after more than one decade

Por Lombardi, CP, Raffaelli, M, De Crea, C, D’amore, A, Bellantone, R
Publicado em 2009

Intracranial lesion as onset symptom in a patient with early undifferentiated connective tissue disease: a case report

Por Du, Ying, Li, Chuan, Zhao, Dai-di, Lu, Jia-rui, Zhang, Wei, Li, Zhu-yi
Publicado no BMC Neurol (2017)

Ultrasound-guided Central Venous Catheterization for Home Parenteral Nutrition and Hydratation...

Por Cavanna, Luigi, Cordani, Maria Rosa, Biasini, Claudia, Di Nunzio, Camilla, Monfredo, Michela, Stroppa, Elisa, Muroni, Monica, Ambroggi, Massimo, Muroni, Lara, Di Cicilia, Roberto, Cremona, Gabriele, Nobili, Elisabetta, Zaffignani, Elena, Civardi, Giuseppe
Publicado no World J Oncol (2011)

Intracranial aneurysms and optic glioma – an unusual combination: a case report

Por De Paulis, Danilo, Nicosia, Giancarlo, Taddei, Graziano, Di Vitantonio, Hambra, Gallieni, Massimo, Del Maestro, Mattia, Raysi Dechordi, Soheila, Galzio, Renato Juan
Publicado no J Med Case Rep (2016)

Cataract and optic disk drusen in a patient with glycogenosis and di George syndrome: clinical and molecular report

Por Allegrini, D., Penco, S., Pece, A., Autelitano, A., Montesano, G., Paci, S., Montanari, C., Maver, A., Peterlin, B., Damante, G., Rossetti, L.
Publicado no BMC Ophthalmol (2017)

A rare 3q13.31 microdeletion including GAP43 and LSAMP genes

Por Gimelli, Stefania, Leoni, Massimiliano, Di Rocco, Maja, Caridi, Gianluca, Porta, Simona, Cuoco, Cristina, Gimelli, Giorgio, Tassano, Elisa
Publicado em 2013