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The American Journal of Pathology|January 10, 2006
Caveolin-1 deficiency (-/-) conveys premalignant alterations in mammary epithelia, with abnormal lumen formation, growth factor independence, and cell invasivenessFederica Sotgia, Terence M Williams, William Schubert, et al.Seizure|January 20, 2010
Galloway-Mowat syndrome: an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literatureMarianna Pezzella, Nune S Yeghiazaryan, Pierangelo Veggiotti, et al.Seizure|March 24, 2018
De novo 12q22.q23.3 duplication associated with temporal lobe epilepsyMaria Stella Vari, Monica Traverso, Tommaso Bellini, et al.Journal of Child Neurology|September 19, 2003
Role of gabapentin in spinal muscular atrophy: results of a multicenter, randomized Italian studyLuciano Merlini, Alessandra Solari, Giuseppe Vita, et al.Biochemical and Biophysical Research Communications|June 14, 2005
Chemokine receptor CCR7 is expressed in muscle fibers in juvenile dermatomyositisCarlo Minetti, Marco Gattorno, Silvia Repetto, et al.Biochemical and Biophysical Research Communications|November 22, 2005
Multiplex real-time PCR for detection of deletions and duplications in dystrophin geneMonica Traverso, Mauro Malnati, Carlo Minetti, et al.Journal of Child Neurology|May 23, 2003
Mitochondrial myopathy and respiratory failure associated with a new mutation in the mitochondrial transfer ribonucleic acid glutamic acid geneClaudio Bruno, Oliviero Sacco, Filippo M Santorelli, et al.The Journal of International Medical Research|December 7, 2017
Detection of early nocturnal hypoventilation in neuromuscular disordersFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.Clinical Endocrinology|December 18, 2003
A reappraisal of the Rb1 gene abnormalities in the diagnosis of parathyroid cancerFilomena Cetani, Elena Pardi, Paolo Viacava, et al.Biochemical and Biophysical Research Communications|July 12, 2011
Mitochondrial myopathy in a child with a muscle-restricted mutation in the mitochondrial transfer RNAAsn geneClaudio Bruno, Denise Cassandrini, Fabiana Fattori, et al.Pageof 20