Showing results (31-40 of 57) with videos related to
Sort By:
Pageof 6
Minerva Chirurgica|March 1, 1997
[Diagnosis and treatment of gastrointestinal carcinoid. Report of a clinical case with duodenal site]C Pastore, A D'Annibale, A Piazza, et al.Neuromolecular Medicine|June 19, 2012
Assessing pathogenicity for novel mutation/sequence variants: the value of healthy older individualsMayana Zatz, Rita de Cassia M Pavanello, Naila Cristina V Lourenço, et al.AJNR. American Journal of Neuroradiology|April 21, 2018
Noninvasive Assessment of Hemodynamic Stress Distribution after Indirect Revascularization for Pediatric Moyamoya VasculopathyD Tortora, M Severino, M Pacetti, et al.Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|August 24, 2004
Protein and DNA analysis for the prenatal diagnosis of alpha2-laminin-deficient congenital muscular dystrophyLydia U Yamamoto, Thomas R Gollop, Nadyr F Naccache, et al.Chirurgia Italiana|July 17, 2001
[Multidisciplinary approach to the patient with oropharyngeal dysphagia]M Pavanello, F Benvegnù, F Collatuzzo, et al.Minerva Pediatrica|October 2, 2009
[Neurologic emergency in children's hospital. Stroke]A Palmieri, A C Molinari, A Rossi, et al.Neuromuscular Disorders : NMD|July 23, 2014
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophinM Zatz, R C M Pavanello, M Lazar, et al.Minerva Pediatrica|November 13, 2013
Glioneuronal tumors and epilepsy in children: seizure outcome related to lesionectomyA Consales, P Striano, P Nozza, et al.Journal of Neuromuscular Diseases|November 19, 2016
Reviewing Large LAMA2 Deletions and Duplications in Congenital Muscular Dystrophy PatientsJorge Oliveira, Ana Gonçalves, Márcia E Oliveira, et al.Muscle & Nerve|January 18, 2007
Central core disease due to recessive mutations in RYR1 gene: is it more common than described?Patrícia M Kossugue, Júlia F Paim, Monica M Navarro, et al.Pageof 6