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The Journal of Clinical Investigation|January 22, 2000
Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)S Kim, V Westphal, G Srikrishna, et al.The Journal of Clinical Investigation|November 24, 1999
Mutation causing congenital myasthenia reveals acetylcholine receptor beta/delta subunit interaction essential for assemblyP A Quiram, K Ohno, M Milone, et al.Journal of Physics. Conference Series|May 3, 2016
High-throughput Toroidal Grating Beamline for Photoelectron Spectroscopy at CAMDO Kizilkaya, R W Jiles, M C Patterson, et al.Journal of Neurosurgery|December 1, 1981
Pineal tumors in children and adolescents. Treatment by CSF shunting and radiotherapyE O Abay, E R Laws, G L Grado, et al.Neurology|April 21, 2012
Development of a suspicion index to aid diagnosis of Niemann-Pick disease type CF A Wijburg, F Sedel, M Pineda, et al.The Journal of Pediatrics|December 10, 1999
Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndromeD Babovic-Vuksanovic, M C Patterson, W F Schwenk, et al.American Journal of Veterinary Research|April 1, 1997
Use of Rhodococcus equi virulence-associated protein for immunization of foals against R equi pneumoniaJ F Prescott, V M Nicholson, M C Patterson, et al.Neurology|December 1, 1992
A clinical staging classification for type C Niemann-Pick diseaseJ J Higgins, M C Patterson, J M Dambrosia, et al.The American Journal of Cardiology|September 1, 1986
Spectrum of cardiac involvement in Friedreich's ataxia: clinical, electrocardiographic and echocardiographic observationsE T Alboliras, C Shub, M R Gomez, et al.The American Journal of Cardiology|August 15, 1995
Tuberous sclerosis and cardiac rhabdomyomaA Nir, A J Tajik, W K Freeman, et al.Pageof 13