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J Burn

Showing results (141-150 of 561) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2006
Clinical phenotype of subjects with Parkinson's disease and orthostatic hypotension: autonomic symptom and demographic comparisonLiesl M Allcock, Rose Anne Kenny, David J Burn
Clinical Genetics|December 1, 1996
Further evidence of genetic heterogeneity in hereditary hydronephrosisD McHale, M E Porteous, J Wentzel, et al.
Journal of Medical Genetics|October 1, 1990
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult maleF Martin, J Platt, E J Tawn, et al.
Clinical Dysmorphology|April 1, 1993
Agnathia-holoprosencephaly: a new recessive syndrome?M E Porteous, C Wright, D Smith, et al.
Postgraduate Medical Journal|January 5, 2000
Extrinsic cerebral venous sinus obstruction resulting in intracranial hypertensionP Goldsmith, D J Burn, A Coulthard, et al.
BMJ (Clinical Research Ed.)|February 11, 1989
Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposisP D Chapman, W Church, J Burn, et al.
JAMA Neurology|August 2, 2016
Spectrum of Movement Disorders in Mitochondrial Disorders-ReplyMika H Martikainen, David J Burn, Doug M Turnbull
Movement Disorders : Official Journal of the Movement Disorder Society|February 6, 1998
Tardive diaphragmatic flutterD J Burn, A Coulthard, S Connolly, et al.
Pediatric Cardiology|March 1, 1993
Congenital heart disease in CHARGE associationR K Wyse, S al-Mahdawi, J Burn, et al.
The British Journal of Surgery|January 1, 1997
Endoscopic screening and surgery for familial adenomatous polyposis: dangerous delaysS J Mills, P D Chapman, J Burn, et al.
Pageof 57

Showing results (141-150 of 561) with videos related to

Sort By:
Pageof 57
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2006
Clinical phenotype of subjects with Parkinson's disease and orthostatic hypotension: autonomic symptom and demographic comparisonLiesl M Allcock, Rose Anne Kenny, David J Burn
Clinical Genetics|December 1, 1996
Further evidence of genetic heterogeneity in hereditary hydronephrosisD McHale, M E Porteous, J Wentzel, et al.
Journal of Medical Genetics|October 1, 1990
A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult maleF Martin, J Platt, E J Tawn, et al.
Clinical Dysmorphology|April 1, 1993
Agnathia-holoprosencephaly: a new recessive syndrome?M E Porteous, C Wright, D Smith, et al.
Postgraduate Medical Journal|January 5, 2000
Extrinsic cerebral venous sinus obstruction resulting in intracranial hypertensionP Goldsmith, D J Burn, A Coulthard, et al.
BMJ (Clinical Research Ed.)|February 11, 1989
Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposisP D Chapman, W Church, J Burn, et al.
JAMA Neurology|August 2, 2016
Spectrum of Movement Disorders in Mitochondrial Disorders-ReplyMika H Martikainen, David J Burn, Doug M Turnbull
Movement Disorders : Official Journal of the Movement Disorder Society|February 6, 1998
Tardive diaphragmatic flutterD J Burn, A Coulthard, S Connolly, et al.
Pediatric Cardiology|March 1, 1993
Congenital heart disease in CHARGE associationR K Wyse, S al-Mahdawi, J Burn, et al.
The British Journal of Surgery|January 1, 1997
Endoscopic screening and surgery for familial adenomatous polyposis: dangerous delaysS J Mills, P D Chapman, J Burn, et al.
Pageof 57