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M Luquette

Showing results (1-10 of 10) with videos related to

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Pediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|January 1, 1995
Hypothesis: pathogenesis of skip areas in long-segment Hirschsprung's diseaseR P Kapur, D J deSa, M Luquette, et al.
Journal of Child Neurology|July 11, 1998
Congenital muscular dystrophy with complete laminin-alpha2-deficiency, cortical dysplasia, and cerebral white-matter changes in childrenC Y Tsao, J R Mendell, J Rusin, et al.
Brain & Development|September 1, 1994
Partial NADH dehydrogenase defect presenting as spastic cerebral palsyC Y Tsao, F S Wright, C P Boesel, et al.
Journal of Child Neurology|February 24, 2001
Mitochondrial DNA depletion in childrenC Y Tsao, J R Mendell, M Luquette, et al.
Journal of Child Neurology|August 2, 2000
Mitochondrial respiratory-chain defects presenting as nonspecific features in childrenC Y Tsao, J R Mendell, W D Lo, et al.
Journal of Child Neurology|December 7, 2000
Myasthenia gravis and associated autoimmune diseases in childrenC Y Tsao, J R Mendell, W D Lo, et al.
Pediatric Pulmonology|July 1, 1997
Massive hemoptysis as the presenting manifestation in a child with histoplasmosisJ P Shaffer, W Barson, M Luquette, et al.
Clinical EEG (Electroencephalography)|October 31, 1997
Leigh syndrome, cytochrome C oxidase deficiency and hypsarrhythmia with infantile spasmsC Y Tsao, M Luquette, J A Rusin, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 28, 2009
Morphological changes of the enteric nervous system, interstitial cells of cajal, and smooth muscle in children with colonic motility disordersM M van den Berg, C Di Lorenzo, H M Mousa, et al.
The Journal of Pediatrics|June 4, 1999
Infantile encephalopathy associated with the MELAS A3243G mutationC M Sue, C Bruno, A L Andreu, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Pediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|January 1, 1995
Hypothesis: pathogenesis of skip areas in long-segment Hirschsprung's diseaseR P Kapur, D J deSa, M Luquette, et al.
Journal of Child Neurology|July 11, 1998
Congenital muscular dystrophy with complete laminin-alpha2-deficiency, cortical dysplasia, and cerebral white-matter changes in childrenC Y Tsao, J R Mendell, J Rusin, et al.
Brain & Development|September 1, 1994
Partial NADH dehydrogenase defect presenting as spastic cerebral palsyC Y Tsao, F S Wright, C P Boesel, et al.
Journal of Child Neurology|February 24, 2001
Mitochondrial DNA depletion in childrenC Y Tsao, J R Mendell, M Luquette, et al.
Journal of Child Neurology|August 2, 2000
Mitochondrial respiratory-chain defects presenting as nonspecific features in childrenC Y Tsao, J R Mendell, W D Lo, et al.
Journal of Child Neurology|December 7, 2000
Myasthenia gravis and associated autoimmune diseases in childrenC Y Tsao, J R Mendell, W D Lo, et al.
Pediatric Pulmonology|July 1, 1997
Massive hemoptysis as the presenting manifestation in a child with histoplasmosisJ P Shaffer, W Barson, M Luquette, et al.
Clinical EEG (Electroencephalography)|October 31, 1997
Leigh syndrome, cytochrome C oxidase deficiency and hypsarrhythmia with infantile spasmsC Y Tsao, M Luquette, J A Rusin, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 28, 2009
Morphological changes of the enteric nervous system, interstitial cells of cajal, and smooth muscle in children with colonic motility disordersM M van den Berg, C Di Lorenzo, H M Mousa, et al.
The Journal of Pediatrics|June 4, 1999
Infantile encephalopathy associated with the MELAS A3243G mutationC M Sue, C Bruno, A L Andreu, et al.
Pageof 1