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IEEE Transactions on Image Processing : a Publication of the IEEE Signal Processing Society
|
January 7, 2010
Multistatic synthetic aperture radar image formation
V Krishnan, J Swoboda, C E Yarman, et al.
Methods of Information in Medicine
|
August 15, 2001
Putting the pieces together: using "off-the-shelf" software to safely transfer medical data
W J Swoboda, M Göttler, K Zinnhobler, et al.
Medical Care
|
October 1, 1978
Changes in utilization patterns in a National Health Service Corps community
R Kane, D Olsen, D Wright, et al.
Pediatric Physical Therapy : the Official Publication of the Section on Pediatrics of the American Physical Therapy Association
|
March 29, 2014
Perceptions of equine-assisted activities and therapies by parents and children with spinal muscular atrophy
Danielle Lemke, Erin Rothwell, Tara M Newcomb, et al.
The Journal of Pediatrics
|
July 22, 2009
Vascular perfusion abnormalities in infants with spinal muscular atrophy
Alexandra prufer de Queiroz Campos Araujo, Mario Araujo, Kathryn J Swoboda
Child Development
|
June 1, 1978
Memory factors in vowel discrimination of normal and at-risk infants
P J Swoboda, J Kass, P A Morse, et al.
American Journal of Medical Genetics. Part A
|
November 15, 2006
A new distal arthrogryposis syndrome characterized by plantar flexion contractures
D A Stevenson, K J Swoboda, R K Sanders, et al.
Journal of Clinical Pharmacology
|
December 15, 2011
Population pharmacokinetics of valproic acid in pediatric patients with epilepsy: considerations for dosing spinal muscular atrophy patients
Jason H Williams, Bhuvaneswari Jayaraman, Kathryn J Swoboda, et al.
Molecular Genetics and Metabolism
|
April 1, 2006
Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12
Sharon E Smith, Hannah C Kinney, Kathryn J Swoboda, et al.
American Journal of Medical Genetics. Part A
|
September 21, 2004
Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2
Thomas W Prior, Kathryn J Swoboda, H Denman Scott, et al.
Page
of 18
Search research articles
Search
Showing results (21-30 of 174) with videos related to
Sort By:
Page
of 18
IEEE Transactions on Image Processing : a Publication of the IEEE Signal Processing Society
|
January 7, 2010
Multistatic synthetic aperture radar image formation
V Krishnan, J Swoboda, C E Yarman, et al.
Methods of Information in Medicine
|
August 15, 2001
Putting the pieces together: using "off-the-shelf" software to safely transfer medical data
W J Swoboda, M Göttler, K Zinnhobler, et al.
Medical Care
|
October 1, 1978
Changes in utilization patterns in a National Health Service Corps community
R Kane, D Olsen, D Wright, et al.
Pediatric Physical Therapy : the Official Publication of the Section on Pediatrics of the American Physical Therapy Association
|
March 29, 2014
Perceptions of equine-assisted activities and therapies by parents and children with spinal muscular atrophy
Danielle Lemke, Erin Rothwell, Tara M Newcomb, et al.
The Journal of Pediatrics
|
July 22, 2009
Vascular perfusion abnormalities in infants with spinal muscular atrophy
Alexandra prufer de Queiroz Campos Araujo, Mario Araujo, Kathryn J Swoboda
Child Development
|
June 1, 1978
Memory factors in vowel discrimination of normal and at-risk infants
P J Swoboda, J Kass, P A Morse, et al.
American Journal of Medical Genetics. Part A
|
November 15, 2006
A new distal arthrogryposis syndrome characterized by plantar flexion contractures
D A Stevenson, K J Swoboda, R K Sanders, et al.
Journal of Clinical Pharmacology
|
December 15, 2011
Population pharmacokinetics of valproic acid in pediatric patients with epilepsy: considerations for dosing spinal muscular atrophy patients
Jason H Williams, Bhuvaneswari Jayaraman, Kathryn J Swoboda, et al.
Molecular Genetics and Metabolism
|
April 1, 2006
Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12
Sharon E Smith, Hannah C Kinney, Kathryn J Swoboda, et al.
American Journal of Medical Genetics. Part A
|
September 21, 2004
Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2
Thomas W Prior, Kathryn J Swoboda, H Denman Scott, et al.
Page
of 18