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Journal of the Neurological Sciences|August 1, 1990
Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case reportR J Wanders, E Boltshauser, B Steinmann, et al.
European Journal of Pediatrics|March 1, 1997
Heterogeneity in Schwartz-Jampel chondrodystrophic myotoniaA Giedion, E Boltshauser, J Briner, et al.
Indian Journal of Gastroenterology : Official Journal of the Indian Society of Gastroenterology|October 16, 2019
Efficacy of enteral glutamine supplementation in patients with severe and predicted severe acute pancreatitis- A randomized controlled trialMadhulika Arutla, M Raghunath, G Deepika, et al.
Nature Genetics|October 1, 1993
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2M R Pollak, Y H Chou, J J Cerda, et al.
Pediatric Research|April 1, 1985
Prenatal diagnosis of hereditary tyrosinemia by determination of fumarylacetoacetase in cultured amniotic fluid cellsE A Kvittingen, B Steinmann, R Gitzelmann, et al.
Brain Research. Molecular Brain Research|June 6, 2000
A novel kinase, AATYK induces and promotes neuronal differentiation in a human neuroblastoma (SH-SY5Y) cell lineM Raghunath, R Patti, P Bannerman, et al.
The European Respiratory Journal|February 20, 2009
Suberoylanilide hydroxamic acid: a potential epigenetic therapeutic agent for lung fibrosis?Z Wang, C Chen, S N Finger, et al.
Seminars in Thoracic and Cardiovascular Surgery|August 29, 2016
Computer-Aided Nodule Assessment and Risk Yield Risk Management of Adenocarcinoma: The Future of Imaging?Finbar Foley, Srinivasan Rajagopalan, Sushravya M Raghunath, et al.
The Indian Journal of Medical Research|January 22, 2010
Modulation of macronutrient metabolism in the offspring by maternal micronutrient deficiency in experimental animalsM Raghunath, L Venu, I Padmavathi, et al.
Schweizer Archiv Fur Tierheilkunde|April 3, 2010
[Swiss warmblood horse with symptoms of hereditary equine regional dermal asthenia without mutation in the cyclophylin B gene (PPIB)]S Rüfenacht, R Straub, B Steinmann, et al.
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