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Showing results (61-70 of 83) with videos related to

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Journal of Inherited Metabolic Disease|April 8, 2006
Refining the diagnosis of mitochondrial HMG-CoA synthase deficiencyR Aledo, C Mir, R N Dalton, et al.
Pediatric Neurology|October 12, 2010
Adenylosuccinate lyase deficiency in the United Kingdom pediatric population: first three casesClaire T Lundy, Heinz Jungbluth, Keith R E Pohl, et al.
Journal of the American Veterinary Medical Association|January 14, 2026
Respiratory distress in a sheepChia-Lin Hsiou, Amy D Bartholomew, Brittany D Cronk, et al.
Case Reports in Nephrology|May 8, 2024
The Challenges of Distinguishing Different Causes of TMA in a Pregnant Kidney Transplant RecipientA Krelle, S Price, M M Law, et al.
Annals of Human Genetics|January 11, 2008
The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East EnglandP Hardelid, M Cortina-Borja, A Munro, et al.
Neuromuscular Disorders : NMD|April 25, 2008
Muscle MRI findings in siblings with juvenile-onset acid maltase deficiency (Pompe disease)Nomazulu Dlamini, Wajanat Jan, Fiona Norwood, et al.
Orphanet Journal of Rare Diseases|December 3, 2010
The diagnosis of inherited metabolic diseases by microarray gene expression profilingMonica Arenas Hernandez, Reiner Schulz, Tracy Chaplin, et al.
Journal of Inherited Metabolic Disease|May 22, 2007
A novel starch for the treatment of glycogen storage diseasesK Bhattacharya, R C Orton, X Qi, et al.
Lasers in Surgery and Medicine|January 1, 1987
Laser treatment of obstructive endobronchial tumors: factors which determine responseS Lam, N L Muller, R R Miller, et al.
Journal of Inherited Metabolic Disease|August 21, 2007
High frequency of missense mutations in glycogen storage disease type VIN J Beauchamp, J Taybert, M P Champion, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Journal of Inherited Metabolic Disease|April 8, 2006
Refining the diagnosis of mitochondrial HMG-CoA synthase deficiencyR Aledo, C Mir, R N Dalton, et al.
Pediatric Neurology|October 12, 2010
Adenylosuccinate lyase deficiency in the United Kingdom pediatric population: first three casesClaire T Lundy, Heinz Jungbluth, Keith R E Pohl, et al.
Journal of the American Veterinary Medical Association|January 14, 2026
Respiratory distress in a sheepChia-Lin Hsiou, Amy D Bartholomew, Brittany D Cronk, et al.
Case Reports in Nephrology|May 8, 2024
The Challenges of Distinguishing Different Causes of TMA in a Pregnant Kidney Transplant RecipientA Krelle, S Price, M M Law, et al.
Annals of Human Genetics|January 11, 2008
The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East EnglandP Hardelid, M Cortina-Borja, A Munro, et al.
Neuromuscular Disorders : NMD|April 25, 2008
Muscle MRI findings in siblings with juvenile-onset acid maltase deficiency (Pompe disease)Nomazulu Dlamini, Wajanat Jan, Fiona Norwood, et al.
Orphanet Journal of Rare Diseases|December 3, 2010
The diagnosis of inherited metabolic diseases by microarray gene expression profilingMonica Arenas Hernandez, Reiner Schulz, Tracy Chaplin, et al.
Journal of Inherited Metabolic Disease|May 22, 2007
A novel starch for the treatment of glycogen storage diseasesK Bhattacharya, R C Orton, X Qi, et al.
Lasers in Surgery and Medicine|January 1, 1987
Laser treatment of obstructive endobronchial tumors: factors which determine responseS Lam, N L Muller, R R Miller, et al.
Journal of Inherited Metabolic Disease|August 21, 2007
High frequency of missense mutations in glycogen storage disease type VIN J Beauchamp, J Taybert, M P Champion, et al.
Pageof 9