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U Ramaswami

Showing results (1-10 of 20) with videos related to

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Journal of Inherited Metabolic Disease|October 31, 2009
Ear symptoms in children with Fabry disease: data from the Fabry Outcome SurveyA Keilmann, D Hajioff, U Ramaswami, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 2010
Safety of agalsidase alfa in patients with Fabry disease under 7 yearsU Ramaswami, R Parini, C Kampmann, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 2, 1999
Growth hormone therapy in hypochondroplasiaU Ramaswami, P C Hindmarsh, C G Brook
The Journal of Pediatrics|July 22, 1998
Genotype and phenotype in hypochondroplasiaU Ramaswami, G Rumsby, P C Hindmarsh, et al.
Molecular Genetics and Metabolism|August 10, 2010
Age adjusting severity scores for Anderson-Fabry diseaseD A Hughes, U Ramaswami, M-Á Barba Romero, et al.
The British Journal of Ophthalmology|June 26, 2010
Fabry disease in children: correlation between ocular manifestations, genotype and systemic clinical severityL E Allen, E M Cosgrave, J P Kersey, et al.
Clinical Genetics|April 5, 2011
Fabry disease in children and response to enzyme replacement therapy: results from the Fabry Outcome SurveyU Ramaswami, R Parini, G Pintos-Morell, et al.
Pediatric Research|October 6, 1999
Treatment of achondroplasia with growth hormone: six years of experienceU Ramaswami, G Rumsby, H A Spoudeas, et al.
Journal of Inherited Metabolic Disease|September 17, 2010
Dietary modifications in patients receiving miglustatH Champion, U Ramaswami, J Imrie, et al.
Archives of Disease in Childhood|February 1, 1997
Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centresA Vellodi, E P Young, A Cooper, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|October 31, 2009
Ear symptoms in children with Fabry disease: data from the Fabry Outcome SurveyA Keilmann, D Hajioff, U Ramaswami, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 2010
Safety of agalsidase alfa in patients with Fabry disease under 7 yearsU Ramaswami, R Parini, C Kampmann, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 2, 1999
Growth hormone therapy in hypochondroplasiaU Ramaswami, P C Hindmarsh, C G Brook
The Journal of Pediatrics|July 22, 1998
Genotype and phenotype in hypochondroplasiaU Ramaswami, G Rumsby, P C Hindmarsh, et al.
Molecular Genetics and Metabolism|August 10, 2010
Age adjusting severity scores for Anderson-Fabry diseaseD A Hughes, U Ramaswami, M-Á Barba Romero, et al.
The British Journal of Ophthalmology|June 26, 2010
Fabry disease in children: correlation between ocular manifestations, genotype and systemic clinical severityL E Allen, E M Cosgrave, J P Kersey, et al.
Clinical Genetics|April 5, 2011
Fabry disease in children and response to enzyme replacement therapy: results from the Fabry Outcome SurveyU Ramaswami, R Parini, G Pintos-Morell, et al.
Pediatric Research|October 6, 1999
Treatment of achondroplasia with growth hormone: six years of experienceU Ramaswami, G Rumsby, H A Spoudeas, et al.
Journal of Inherited Metabolic Disease|September 17, 2010
Dietary modifications in patients receiving miglustatH Champion, U Ramaswami, J Imrie, et al.
Archives of Disease in Childhood|February 1, 1997
Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centresA Vellodi, E P Young, A Cooper, et al.
Pageof 2