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J Swoboda

Showing results (31-40 of 174) with videos related to

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The Journal of Pediatrics|October 12, 2015
Responses to Fasting and Glucose Loading in a Cohort of Well Children with Spinal Muscular Atrophy Type IIRebecca Hurst Davis, Elizabeth A Miller, Ren Zhe Zhang, et al.
Journal of Molecular Neuroscience : MN|July 20, 2010
Alpha-synuclein loss in spinal muscular atrophyGyula Acsadi, Xingli Li, Kelley J Murphy, et al.
American Journal of Medical Genetics. Part A|February 28, 2013
Public attitudes regarding a pilot study of newborn screening for spinal muscular atrophyErin Rothwell, Rebecca A Anderson, Kathryn J Swoboda, et al.
The New England Journal of Medicine|December 14, 2017
Case 38-2017. A 20-Year-Old Woman with Seizures and Progressive DystoniaFlorian S Eichler, Kathryn J Swoboda, Ann L Hunt, et al.
Pediatrics|September 2, 2003
An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosisJoshua L Bonkowsky, Justine Johnson, John C Carey, et al.
Neuromuscular Disorders : NMD|June 6, 2006
A modified Hammersmith functional motor scale for use in multi-center research on spinal muscular atrophyKristin J Krosschell, Jo Anne Maczulski, Thomas O Crawford, et al.
Clinical Genetics|May 26, 2010
Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes diseaseV Desai, A Donsante, K J Swoboda, et al.
Journal of Child Neurology|January 22, 2013
Vitamin D intake is inadequate in spinal muscular atrophy type I cohort: correlations with bone healthJennifer Aton, Rebecca Hurst Davis, Kristine C Jordan, et al.
Annals of Neurology|August 2, 2003
Aromatic L-amino acid decarboxylase deficiency: overview of clinical features and outcomesKathryn J Swoboda, J Philip Saul, Catherine E McKenna, et al.
Muscle & Nerve|January 14, 1998
Mutilating hand syndrome in an infant with familial carpal tunnel syndromeK J Swoboda, E C Engle, B Scheindlin, et al.
Pageof 18

Showing results (31-40 of 174) with videos related to

Sort By:
Pageof 18
The Journal of Pediatrics|October 12, 2015
Responses to Fasting and Glucose Loading in a Cohort of Well Children with Spinal Muscular Atrophy Type IIRebecca Hurst Davis, Elizabeth A Miller, Ren Zhe Zhang, et al.
Journal of Molecular Neuroscience : MN|July 20, 2010
Alpha-synuclein loss in spinal muscular atrophyGyula Acsadi, Xingli Li, Kelley J Murphy, et al.
American Journal of Medical Genetics. Part A|February 28, 2013
Public attitudes regarding a pilot study of newborn screening for spinal muscular atrophyErin Rothwell, Rebecca A Anderson, Kathryn J Swoboda, et al.
The New England Journal of Medicine|December 14, 2017
Case 38-2017. A 20-Year-Old Woman with Seizures and Progressive DystoniaFlorian S Eichler, Kathryn J Swoboda, Ann L Hunt, et al.
Pediatrics|September 2, 2003
An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosisJoshua L Bonkowsky, Justine Johnson, John C Carey, et al.
Neuromuscular Disorders : NMD|June 6, 2006
A modified Hammersmith functional motor scale for use in multi-center research on spinal muscular atrophyKristin J Krosschell, Jo Anne Maczulski, Thomas O Crawford, et al.
Clinical Genetics|May 26, 2010
Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes diseaseV Desai, A Donsante, K J Swoboda, et al.
Journal of Child Neurology|January 22, 2013
Vitamin D intake is inadequate in spinal muscular atrophy type I cohort: correlations with bone healthJennifer Aton, Rebecca Hurst Davis, Kristine C Jordan, et al.
Annals of Neurology|August 2, 2003
Aromatic L-amino acid decarboxylase deficiency: overview of clinical features and outcomesKathryn J Swoboda, J Philip Saul, Catherine E McKenna, et al.
Muscle & Nerve|January 14, 1998
Mutilating hand syndrome in an infant with familial carpal tunnel syndromeK J Swoboda, E C Engle, B Scheindlin, et al.
Pageof 18