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Pediatric Radiology|August 21, 2007
Cranial ultrasound and chronological changes in molybdenum cofactor deficiencyMercedes Serrano, Isabel Lizarraga, Jochen Reiss, et al.Human Genetics|May 4, 2016
Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patientsJoanna Jakubiczka-Smorag, Jose Angel Santamaria-Araujo, Imke Metz, et al.Neuroscience Letters|October 7, 2004
Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer diseaseClaudia Günther, Kirsten von Hadeln, Tomas Müller-Thomsen, et al.Journal of Inherited Metabolic Disease|September 25, 2010
Chronological changes of the amplitude-integrated EEG in a neonate with molybdenum cofactor deficiencySintha D Sie, Rogier C J de Jonge, Henk J Blom, et al.Journal of Inherited Metabolic Disease|January 26, 2018
A mild case of molybdenum cofactor deficiency defines an alternative route of MOCS1 protein maturationSimon Julius Mayr, Jörn Oliver Sass, Julia Vry, et al.Pediatrics|April 14, 2010
Successful treatment of molybdenum cofactor deficiency type A with cPMPAlex Veldman, José Angel Santamaria-Araujo, Silvio Sollazzo, et al.Human Molecular Genetics|April 30, 2004
Rescue of lethal molybdenum cofactor deficiency by a biosynthetic precursor from Escherichia coliGünter Schwarz, José Angel Santamaria-Araujo, Stefan Wolf, et al.Brain & Development|October 2, 2009
Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalaciaJörn Oliver Sass, Aysegul Gunduz, Carolina Araujo Rodrigues Funayama, et al.Pageof 2