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Movement Disorders : Official Journal of the Movement Disorder Society
|
April 11, 2012
To sleep, perchance to dement: RBD and cognitive decline in Parkinson's disease
David J Burn, Kirstie Anderson
Practical Neurology
|
January 20, 2017
ABN News
Joanne Lawrence, David J Burn
Practical Neurology
|
January 26, 2017
ABN News
David J Burn, Joanne Lawrence
British Medical Journal
|
November 3, 1979
"Pseudonormonatraemia"
J Burn, G V Gill
Journal of Medical Genetics
|
May 1, 1990
Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitalia
M E Porteous, J Burn
Molecular Medicine Today
|
January 27, 2000
UFD1L is not the monogenic basis for heart defects associated with the CATCH phenotype
J A Goodship, J Burn
Biology of the Neonate
|
January 1, 1976
Isoelectric focusing of non-specific esterases of developing human brain in thin-layer polyacrylamide gels
S S Papiha, J Burn
Journal of Medical Genetics
|
October 1, 1982
Fraser syndrome presenting as bilateral renal agenesis in three sibs
J Burn, R P Marwood
Molecular Pathology : MP
|
November 29, 2001
Multiple system atrophy: cellular and molecular pathology
D J Burn, E Jaros
Lancet (London, England)
|
November 15, 2000
Effect of anti-epileptic drugs on intrauterine growth
R H Finnell, J Burn
Page
of 57
Search research articles
Search
Showing results (51-60 of 561) with videos related to
Sort By:
Page
of 57
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 11, 2012
To sleep, perchance to dement: RBD and cognitive decline in Parkinson's disease
David J Burn, Kirstie Anderson
Practical Neurology
|
January 20, 2017
ABN News
Joanne Lawrence, David J Burn
Practical Neurology
|
January 26, 2017
ABN News
David J Burn, Joanne Lawrence
British Medical Journal
|
November 3, 1979
"Pseudonormonatraemia"
J Burn, G V Gill
Journal of Medical Genetics
|
May 1, 1990
Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitalia
M E Porteous, J Burn
Molecular Medicine Today
|
January 27, 2000
UFD1L is not the monogenic basis for heart defects associated with the CATCH phenotype
J A Goodship, J Burn
Biology of the Neonate
|
January 1, 1976
Isoelectric focusing of non-specific esterases of developing human brain in thin-layer polyacrylamide gels
S S Papiha, J Burn
Journal of Medical Genetics
|
October 1, 1982
Fraser syndrome presenting as bilateral renal agenesis in three sibs
J Burn, R P Marwood
Molecular Pathology : MP
|
November 29, 2001
Multiple system atrophy: cellular and molecular pathology
D J Burn, E Jaros
Lancet (London, England)
|
November 15, 2000
Effect of anti-epileptic drugs on intrauterine growth
R H Finnell, J Burn
Page
of 57