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Human Molecular Genetics|September 22, 2017
Abnormal polyamine metabolism is unique to the neuropathic forms of MPS: potential for biomarker development and insight into pathogenesisChristian Hinderer, Nathan Katz, Jean-Pierre Louboutin, et al.
Intensive Care Medicine|September 27, 2012
Predictive value of bronchoscopy after infant cardiac surgery: a prospective studyP P Nayak, J Sheth, P N Cox, et al.
The Journal of Trauma|December 17, 2009
Risk factors for compartment syndrome in traumatic brachial artery injuries: an institutional experience in 139 patientsJohn Y S Kim, Donald W Buck, Antonio J V Forte, et al.
Journal of Paediatrics and Child Health|December 30, 2020
Revealing the clinical phenotype of atypical neuronal ceroid lipofuscinosis type 2 disease: Insights from the largest cohort in the worldCharles M Lourenço, Andre Pessoa, Carmen C Mendes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2018
Long-term outcomes of systemic therapies for Hurler syndrome: an international multicenter comparisonJulie B Eisengart, Kyle D Rudser, Yong Xue, et al.
BMC Medical Genetics|September 2, 2014
Biotinidase deficiency: clinical and genetic studies of 38 Brazilian patientsTaciane Borsatto, Fernanda Sperb-Ludwig, Louise L C Pinto, et al.
Journal of Ultrasound|November 1, 2018
Multiparametric ultrasound evaluation with CEUS and shear wave elastography for carotid plaque risk stratificationN Di Leo, L Venturini, V de Soccio, et al.
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