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FEBS Letters|February 19, 1998
High structural side chain specificity required at the second position of immunogenic peptides to obtain stable MHC/peptide complexesR Gavioli, R Guerrini, M G Masucci, et al.Journal of Inherited Metabolic Disease|May 7, 2005
Increased NO production in lysinuric protein intoleranceL Mannucci, F Emma, M Markert, et al.American Journal of Medical Genetics|November 1, 1991
Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiencyA Ballabio, M Zollo, R Carrozzo, et al.Muscle & Nerve|September 1, 1997
Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitineG Brevetti, M Fanin, V De Amicis, et al.The Journal of Clinical Investigation|October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiencyA Martinuzzi, L Vergani, R Carrozzo, et al.British Journal of Pharmacology|March 7, 1998
A new selective antagonist of the nociceptin receptorR Guerrini, G Calo, A Rizzi, et al.Brain & Development|September 16, 1999
Are there generalised spike waves and typical absences in benign rolandic epilepsy?P Gelisse, P Genton, M Bureau, et al.Epilepsia|October 1, 1996
Early clinical and EEG features of infantile spasms in Down syndromeM L Silva, C Cieuta, R Guerrini, et al.Pediatric Neurology|November 27, 1998
Seizures in Klinefelter's syndromeW O Tatum, E A Passaro, M Elia, et al.Human Molecular Genetics|February 1, 1997
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.Pageof 33