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European Journal of Neurology|December 29, 2017
Severe 5,10-methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegiaA Perna, M Masciullo, A Modoni, et al.Acta Neurochirurgica. Supplement|December 28, 2023
Emergency Treatment of Cervical Vertebromedullary Trauma: 10 Years of Experience and Outcome EvaluationM C Meluzio, M I Borruto, A Perna, et al.European Review for Medical and Pharmacological Sciences|November 30, 2022
Subtrochanteric fractures in elderly people: functional and radiographic outcomes after intramedullary locked nail fixation with or without cerclageN Bonfiglio, A Smimmo, A Carosini, et al.Frontiers in Bioengineering and Biotechnology|August 7, 2023
Postural stability and plantar pressure parameters in healthy subjects: variability, correlation analysis and differences under open and closed eye conditionsP De Blasiis, P Caravaggi, A Fullin, et al.Kidney International|October 24, 2000
Pretreatment blood pressure reliably predicts progression of chronic nephropathies. GISEN GroupP Ruggenenti, A Perna, M Lesti, et al.Respiration; International Review of Thoracic Diseases|January 1, 1994
Protective effects of nedocromil sodium on cellular and biohumoral components present in the bronchial alveolar lavage fluid and in peripheral blood in atopic asthmaticsG Mazzarella, E Grella, L Romano, et al.Placenta|December 23, 2006
Expression and distribution of notch protein members in human placenta throughout pregnancyM De Falco, L Cobellis, D Giraldi, et al.European Review for Medical and Pharmacological Sciences|November 30, 2022
Megaprosthesis in articular fractures of the lower limbs in fragile patients: a proposal for the therapeutic algorithmR Vitiello, A Smimmo, A De Fazio, et al.Lancet (London, England)|August 7, 1999
Renoprotective properties of ACE-inhibition in non-diabetic nephropathies with non-nephrotic proteinuriaP Ruggenenti, A Perna, G Gherardi, et al.Journal of the American Society of Nephrology : JASN|April 24, 1999
Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic PurpuraM Noris, P Ruggenenti, A Perna, et al.Pageof 11