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Multiple Sclerosis (Houndmills, Basingstoke, England)|January 23, 2024
The absence of antibodies in longitudinally extensive transverse myelitis may predict a more favourable prognosisChiara Rocchi, Mirasol Forcadela, Patricia Kelly, et al.
Frontiers in Endocrinology|March 26, 2016
Dissecting the Genetic Susceptibility to Graves' Disease in a Cohort of Patients of Italian OriginAngela Lombardi, Francesca Menconi, David Greenberg, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|November 5, 2025
Endovascular Management of Acute Lower Limb Ischaemia in Adult Patients: A Systematic Review and Meta-analysisStefan Acosta, Vincent Jongkind, Konstantinos Stavroulakis, et al.
Multiple Sclerosis and Related Disorders|October 21, 2023
Do we still need OCBs in MS diagnosis and how many?Mirasol Forcadela, Katherine Birch, Chiara Rocchi, et al.
American Journal of Physical Medicine & Rehabilitation|January 16, 2022
A Countermovement Jump for the Midterm Assessment of Force and Power Exertion After Anterior Cruciate Ligament ReconstructionLuciana Labanca, Francesco Budini, Ludovica Cardinali, et al.
Journal of Neurosurgery|January 28, 2004
Inflammation markers and risk factors for recurrence in 35 patients with a posttraumatic chronic subdural hematoma: a prospective studyAlessandro Frati, Maurizio Salvati, Fabrizio Mainiero, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Potential involvement of ubiquinone in myotonic dystrophy pathophysiology: new diagnostic approaches for new rationale therapeuticsD Tedeschi, V Lombardi, M Mancuso, et al.
Gene|October 31, 2000
Analysis of the murine phosphoinositide 3-kinase gamma geneE Hirsch, M P Wymann, E Patrucco, et al.
Nature|October 5, 2001
Positive selection of a gene family during the emergence of humans and African apesM E Johnson, L Viggiano, J A Bailey, et al.
Muscle & Nerve|October 19, 2011
Subclinical autonomic dysfunction in spinobulbar muscular atrophy (Kennedy disease)Camilla Rocchi, Viviana Greco, Andrea Urbani, et al.
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