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Neuromuscular Disorders : NMD
|
June 12, 2003
Reduction in excess daytime sleepiness by modafinil in patients with myotonic dystrophy
K Talbot, J Stradling, J Crosby, et al.
Journal of Medical Genetics
|
December 1, 1996
Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophy
K Talbot, N Rodrigues, G Bernert, et al.
Neuromuscular Disorders : NMD
|
April 9, 2008
Candidate screening of the bovine and feline spinal muscular atrophy genes reveals no evidence for involvement in human motor neuron disorders
N J Parkinson, D Baumer, A Rose-Morris, et al.
Journal of Molecular Biology
|
March 5, 1987
Characterization of a cDNA defining a gene family encoding TM30p1, a human fibroblast tropomyosin
A R MacLeod, K Talbot, L B Smillie, et al.
Antimicrobial Agents and Chemotherapy
|
December 1, 1989
Reactivation of peptidoglycan synthesis in ether-permeabilized Escherichia coli after inhibition by beta-lactam antibiotics
M K Talbot, F Schaefer, V Brocks, et al.
QJM : Monthly Journal of the Association of Physicians
|
December 26, 2006
Treatment of vasculitic peripheral neuropathy: a retrospective analysis of outcome
L Mathew, K Talbot, S Love, et al.
Nucleic Acids Research
|
November 11, 1986
The mRNA and RNA-copy pseudogenes encoding TM30nm, a human cytoskeletal tropomyosin
A R MacLeod, C Houlker, F C Reinach, et al.
British Journal of Anaesthesia
|
May 5, 2019
The sensory and affective components of pain: are they differentially modifiable dimensions or inseparable aspects of a unitary experience? A systematic review
K Talbot, V J Madden, S L Jones, et al.
Clinical Medicine (London, England)
|
September 10, 2011
Catastrophic hyperkalaemia following administration of suxamethonium chloride to a patient with undiagnosed amyotrophic lateral sclerosis
M R Turner, H Lawrence, I Arnold, et al.
Journal of Clinical Microbiology
|
November 1, 1977
Two outbreaks of Flavobacterium meningosepticum type E in a neonatal intensive care unit
B T Hazuka, A S Dajani, K Talbot, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 87) with videos related to
Sort By:
Page
of 9
Neuromuscular Disorders : NMD
|
June 12, 2003
Reduction in excess daytime sleepiness by modafinil in patients with myotonic dystrophy
K Talbot, J Stradling, J Crosby, et al.
Journal of Medical Genetics
|
December 1, 1996
Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophy
K Talbot, N Rodrigues, G Bernert, et al.
Neuromuscular Disorders : NMD
|
April 9, 2008
Candidate screening of the bovine and feline spinal muscular atrophy genes reveals no evidence for involvement in human motor neuron disorders
N J Parkinson, D Baumer, A Rose-Morris, et al.
Journal of Molecular Biology
|
March 5, 1987
Characterization of a cDNA defining a gene family encoding TM30p1, a human fibroblast tropomyosin
A R MacLeod, K Talbot, L B Smillie, et al.
Antimicrobial Agents and Chemotherapy
|
December 1, 1989
Reactivation of peptidoglycan synthesis in ether-permeabilized Escherichia coli after inhibition by beta-lactam antibiotics
M K Talbot, F Schaefer, V Brocks, et al.
QJM : Monthly Journal of the Association of Physicians
|
December 26, 2006
Treatment of vasculitic peripheral neuropathy: a retrospective analysis of outcome
L Mathew, K Talbot, S Love, et al.
Nucleic Acids Research
|
November 11, 1986
The mRNA and RNA-copy pseudogenes encoding TM30nm, a human cytoskeletal tropomyosin
A R MacLeod, C Houlker, F C Reinach, et al.
British Journal of Anaesthesia
|
May 5, 2019
The sensory and affective components of pain: are they differentially modifiable dimensions or inseparable aspects of a unitary experience? A systematic review
K Talbot, V J Madden, S L Jones, et al.
Clinical Medicine (London, England)
|
September 10, 2011
Catastrophic hyperkalaemia following administration of suxamethonium chloride to a patient with undiagnosed amyotrophic lateral sclerosis
M R Turner, H Lawrence, I Arnold, et al.
Journal of Clinical Microbiology
|
November 1, 1977
Two outbreaks of Flavobacterium meningosepticum type E in a neonatal intensive care unit
B T Hazuka, A S Dajani, K Talbot, et al.
Page
of 9