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Neurology|August 1, 1988
Glucose metabolism alterations in Friedreich's ataxiaG Finocchiaro, G Baio, P Micossi, et al.Journal of Physics. Condensed Matter : an Institute of Physics Journal|February 4, 2017
Electron transport in ultra-thin films and ballistic electron emission microscopyY Claveau, S Di Matteo, P L de Andres, et al.La Clinica Terapeutica|October 22, 1998
Effect of L-carnitine on plasma lipoprotein fatty acids pattern in patients with primary hyperlipoproteinemiaC Stefanutti, A Vivenzio, G Lucani, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|May 1, 1996
Can adrenarche influence the degree of osteopenia in thalassemic children?A Filosa, S Di Maio, A Saviano, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 9, 1982
Pyruvate kinase deficiency: characterization of two new genetic variantsL Dente, M D'Urso, S Di Maio, et al.Kidney International|July 2, 1998
On-line assessment of delivered dialysis doseS Di Filippo, S Andrulli, C Manzoni, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|May 20, 1998
[Role of echocardiography in the diagnosis of congenital abnormalities of the thoracic aorta]A Bozio, F Sassolas, S Di Filippo, et al.Minerva Chirurgica|April 1, 1997
[Abdominal abscesses: their treatment and the study of prognostic factors]L Giangreco, S Di Palo, M Castrucci, et al.Journal of Thermal Biology|April 17, 2021
Clock gene per 2 daily rhythm: Correlation with the serum level of uncoupling protein 1 (UCP1) in goat and horseC Giannetto, F Arfuso, E Giudice, et al.Neurology|July 1, 1988
Multisystem triglyceride storage disease is due to a specific defect in the degradation of endocellularly synthesized triglyceridesS Di Donato, B Garavaglia, P Strisciuglio, et al.Pageof 283