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Gerald F Cox

Showing results (41-50 of 75) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2003
Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND geneTaosheng Huang, Angela E Lin, Gerald F Cox, et al.
Molecular Genetics and Metabolism|January 2, 2017
Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher RegistryAmal El-Beshlawy, Anna Tylki-Szymanska, Ashok Vellodi, et al.
Circulation|January 31, 2007
Epidemiology and cause-specific outcome of hypertrophic cardiomyopathy in children: findings from the Pediatric Cardiomyopathy RegistrySteven D Colan, Steven E Lipshultz, April M Lowe, et al.
Molecular Genetics and Metabolism|November 14, 2017
Corrigendum to "Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases" [Mol. Genet. Metab. 118 (2016) 206-213]David Cassiman, Seymour Packman, Bruno Bembi, et al.
Molecular Genetics and Metabolism|May 21, 2016
Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new casesDavid Cassiman, Seymour Packman, Bruno Bembi, et al.
The Journal of Pediatrics|March 18, 2003
Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edemaJonathan D Picker, Ana C Puga, Harvey L Levy, et al.
Molecular Genetics and Metabolism|June 8, 2015
Successful within-patient dose escalation of olipudase alfa in acid sphingomyelinase deficiencyMelissa P Wasserstein, Simon A Jones, Handrean Soran, et al.
Radiology|November 24, 2005
Type B Niemann-Pick disease: findings at chest radiography, thin-section CT, and pulmonary function testingDavid S Mendelson, Melissa P Wasserstein, Robert J Desnick, et al.
American Heart Journal|September 18, 2012
Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: a study from the Pediatric Cardiomyopathy RegistryJames D Wilkinson, April M Lowe, Bonnie A Salbert, et al.
Pediatrics|January 2, 2009
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis ILorne A Clarke, J Edmond Wraith, Michael Beck, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2003
Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND geneTaosheng Huang, Angela E Lin, Gerald F Cox, et al.
Molecular Genetics and Metabolism|January 2, 2017
Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher RegistryAmal El-Beshlawy, Anna Tylki-Szymanska, Ashok Vellodi, et al.
Circulation|January 31, 2007
Epidemiology and cause-specific outcome of hypertrophic cardiomyopathy in children: findings from the Pediatric Cardiomyopathy RegistrySteven D Colan, Steven E Lipshultz, April M Lowe, et al.
Molecular Genetics and Metabolism|November 14, 2017
Corrigendum to "Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases" [Mol. Genet. Metab. 118 (2016) 206-213]David Cassiman, Seymour Packman, Bruno Bembi, et al.
Molecular Genetics and Metabolism|May 21, 2016
Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new casesDavid Cassiman, Seymour Packman, Bruno Bembi, et al.
The Journal of Pediatrics|March 18, 2003
Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edemaJonathan D Picker, Ana C Puga, Harvey L Levy, et al.
Molecular Genetics and Metabolism|June 8, 2015
Successful within-patient dose escalation of olipudase alfa in acid sphingomyelinase deficiencyMelissa P Wasserstein, Simon A Jones, Handrean Soran, et al.
Radiology|November 24, 2005
Type B Niemann-Pick disease: findings at chest radiography, thin-section CT, and pulmonary function testingDavid S Mendelson, Melissa P Wasserstein, Robert J Desnick, et al.
American Heart Journal|September 18, 2012
Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: a study from the Pediatric Cardiomyopathy RegistryJames D Wilkinson, April M Lowe, Bonnie A Salbert, et al.
Pediatrics|January 2, 2009
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis ILorne A Clarke, J Edmond Wraith, Michael Beck, et al.
Pageof 8