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John Walter

Showing results (11-20 of 33) with videos related to

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Nucleic Acids Symposium Series (2004)|November 22, 2007
Studies on DNA dynamics using 2-N-tert-butylaminoxylpurinesMariko Aso, John Walter Mirc, Manami Kurita, et al.
Nucleic Acids Symposium Series (2004)|December 8, 2006
Properties and EPR studies of oligodeoxynucleotides containing 2-N-tert-butylaminoxylpurinesMariko Aso, Toshiyuki Kaneko, John Walter Mirc, et al.
Clinical Rehabilitation|February 7, 2012
A prospective, multicentre, randomized, double-blind, placebo-controlled trial of onabotulinumtoxinA to treat plantarflexor/invertor overactivity after strokeJohn Walter Dunne, Jean-Michel Gracies, Michael Hayes, et al.
Augmentative and Alternative Communication (Baltimore, Md. : 1985)|December 28, 2020
Effect of online instruction on volunteers who support people with complex communication needs in active recreationDavid J Hajjar, John Walter McCarthy, Joann Paula Benigno, et al.
JIMD Reports|September 13, 2014
Treatment Adherence in Type 1 Hereditary Tyrosinaemia (HT1): A Mixed-Method Investigation into the Beliefs, Attitudes and Behaviour of Adolescent Patients, Their Families and Their Health-Care TeamSumaira Malik, Sinead NiMhurchadha, Christina Jackson, et al.
Nucleic Acids Symposium Series (2004)|September 9, 2008
Dynamics of 2-N-tert-butylaminoxyladenosine incorporated into oligodeoxynucleotidesMariko Aso, Manami Kurita, John Walter Mirc, et al.
Neuromuscular Disorders : NMD|May 30, 2008
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathyEmma Blakely, Langping He, Julie L Gardner, et al.
Chemical Research in Toxicology|August 20, 2003
Three novel hydroxybenzoate saxitoxin analogues isolated from the dinoflagellate Gymnodinium catenatumAndrew Negri, David Stirling, Michael Quilliam, et al.
American Journal of Medical Genetics. Part A|January 25, 2014
An unusual phenotype of X-linked developmental delay and extreme behavioral difficulties associated with a mutation in the EBP geneVerity L Hartill, Carolyn Tysoe, Nigel Manning, et al.
Molecular Genetics and Metabolism|August 11, 2007
Glycogen storage disease type IX: High variability in clinical phenotypeNicholas James Beauchamp, Ann Dalton, Uma Ramaswami, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Nucleic Acids Symposium Series (2004)|November 22, 2007
Studies on DNA dynamics using 2-N-tert-butylaminoxylpurinesMariko Aso, John Walter Mirc, Manami Kurita, et al.
Nucleic Acids Symposium Series (2004)|December 8, 2006
Properties and EPR studies of oligodeoxynucleotides containing 2-N-tert-butylaminoxylpurinesMariko Aso, Toshiyuki Kaneko, John Walter Mirc, et al.
Clinical Rehabilitation|February 7, 2012
A prospective, multicentre, randomized, double-blind, placebo-controlled trial of onabotulinumtoxinA to treat plantarflexor/invertor overactivity after strokeJohn Walter Dunne, Jean-Michel Gracies, Michael Hayes, et al.
Augmentative and Alternative Communication (Baltimore, Md. : 1985)|December 28, 2020
Effect of online instruction on volunteers who support people with complex communication needs in active recreationDavid J Hajjar, John Walter McCarthy, Joann Paula Benigno, et al.
JIMD Reports|September 13, 2014
Treatment Adherence in Type 1 Hereditary Tyrosinaemia (HT1): A Mixed-Method Investigation into the Beliefs, Attitudes and Behaviour of Adolescent Patients, Their Families and Their Health-Care TeamSumaira Malik, Sinead NiMhurchadha, Christina Jackson, et al.
Nucleic Acids Symposium Series (2004)|September 9, 2008
Dynamics of 2-N-tert-butylaminoxyladenosine incorporated into oligodeoxynucleotidesMariko Aso, Manami Kurita, John Walter Mirc, et al.
Neuromuscular Disorders : NMD|May 30, 2008
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathyEmma Blakely, Langping He, Julie L Gardner, et al.
Chemical Research in Toxicology|August 20, 2003
Three novel hydroxybenzoate saxitoxin analogues isolated from the dinoflagellate Gymnodinium catenatumAndrew Negri, David Stirling, Michael Quilliam, et al.
American Journal of Medical Genetics. Part A|January 25, 2014
An unusual phenotype of X-linked developmental delay and extreme behavioral difficulties associated with a mutation in the EBP geneVerity L Hartill, Carolyn Tysoe, Nigel Manning, et al.
Molecular Genetics and Metabolism|August 11, 2007
Glycogen storage disease type IX: High variability in clinical phenotypeNicholas James Beauchamp, Ann Dalton, Uma Ramaswami, et al.
Pageof 4