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Progress in Brain Research|May 1, 2016
New horizons in neurometabolic and neurovascular coupling from calibrated fMRIC Y Shu, B G Sanganahalli, D Coman, et al.JIMD Reports|February 11, 2015
Hepatic Copper Accumulation: A Novel Feature in Transient Infantile Liver Failure Due to TRMU Mutations?Z Grover, P Lewindon, A Clousten, et al.JIMD Reports|August 3, 2016
DMP1-CDG (CDG1e) with Significant Gastrointestinal Manifestations; Phenotype and Genotype ExpansionC Bursle, D Brown, J Cardinal, et al.Healthcare (Basel, Switzerland)|January 28, 2021
Let's Not Joke about It Too Much! Exposure to COVID-19 Messaging, Attitudes and Protective Behavioral IntentionsPetru L Curșeu, Andra D Coman, Oana C Fodor, et al.The British Journal of Dermatology|November 12, 2009
Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlationS E Clements, T Techanukul, D Coman, et al.Pediatric Nephrology (Berlin, Germany)|October 26, 2005
Renal transplantation in a 14-year-old girl with vitamin B12-responsive cblA-type methylmalonic acidaemiaD Coman, J Huang, S McTaggart, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 25, 2007
Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotypeD Coman, J McGill, R MacDonald, et al.JIMD Reports|November 6, 2016
COXPD9 an Evolving Multisystem Disease; Congenital Lactic Acidosis, Sensorineural Hearing Loss, Hypertrophic Cardiomyopathy, Cirrhosis and Interstitial NephritisC Bursle, A Narendra, R Chuk, et al.JIMD Reports|August 26, 2015
Normal Neurodevelopmental Outcomes in PNPO Deficiency: A Case Series and Literature ReviewJ Hatch, D Coman, P Clayton, et al.JIMD Reports|December 18, 2017
Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse MyelitisC Bursle, K Riney, J Stringer, et al.Pageof 3