SilviaRussoMD(She/Her)

PubMed

• 2 citations
  Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome.
  Roberto Angelini, Silvia Russo, Angela Corcelli, Simona Lobasso> ;Journal of Visualized Experiments. 2022 Mar 23
• 1 citations
  Clinical Reasoning: A 35-year-old woman with hyperstartling, stiffness, and accidental falls: A startling diagnosis.
  Silvia Russo, Barbara Fossati, Mauro Toffetti, Jacopo Lanzone, Rosanna Cardani, Giovanni Meola> ;Neurology. 2017 Jan 31
• 25 citations
  Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia.
  Ethan G. Geier, Mathieu Bourdenx, Nadia J. Storm, J. Nicholas Cochran, Daniel W. Sirkis, Ji Hye Hwang, Luke W. Bonham, Eliana Marisa Ramos, Antonio Diaz, Victoria Van ...> ;Acta Neuropathologica. 2019 Jan 1
• 42 citations
  Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers
  Lieke H.H. Meeter, Tania F. Gendron, Ana C. Sias, Lize C. Jiskoot, Silvia P. Russo, Laura Donker Kaat, Janne M. Papma, Jessica L. Panman, Emma L. van der Ende, Elise G...> ;Annals of Clinical and Translational Neurology. 2018 May 1
• The Drop That Spilled the Cup: Acute Myocardial Infarction in a Young Woman with Underlying Thrombophilic Polymorphisms and Oral Contraceptive Use
  Nunzio Russo, Enrico Franzì, Gianfranco Capilli, Anella Antonietta Patané, Silvia Paola Russo, Rosario Evola> ;Case Reports in Cardiology. 2014 Dec 23
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Journal Articles

• Rare Variants in the Neuronal Ceroid Lipofuscinosis Gene MFSD8 Are Candidate Risk Factors for Frontotemporal Dementia  
  William W Seeley, Suzee E Lee, Salvatore Spina, Silvia P Russo, Acta Neuropathologica
• Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers  
  Meeter, Lieke H.H. Gendron, Tania F. Sias, Ana C. Jiskoot, Lize C. Russo, Silvia P. Donker Kaat, Laura Papma, Janne M. Panman, Jessica L. van der Ende, Emma L. Dopper,..., Annals of Clinical and Translational Neurology, 2018