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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 comparison
Liesl M Allcock, Rose Anne Kenny, David J Burn
Clinical Genetics
|
December 1, 1996
Further evidence of genetic heterogeneity in hereditary hydronephrosis
D 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 male
F 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 hypertension
P 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 polyposis
P D Chapman, W Church, J Burn, et al.
JAMA Neurology
|
August 2, 2016
Spectrum of Movement Disorders in Mitochondrial Disorders-Reply
Mika H Martikainen, David J Burn, Doug M Turnbull
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 6, 1998
Tardive diaphragmatic flutter
D J Burn, A Coulthard, S Connolly, et al.
Pediatric Cardiology
|
March 1, 1993
Congenital heart disease in CHARGE association
R 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 delays
S J Mills, P D Chapman, J Burn, et al.
Page
of 57
Search research articles
Search
Showing results (141-150 of 561) with videos related to
Sort By:
Page
of 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 comparison
Liesl M Allcock, Rose Anne Kenny, David J Burn
Clinical Genetics
|
December 1, 1996
Further evidence of genetic heterogeneity in hereditary hydronephrosis
D 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 male
F 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 hypertension
P 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 polyposis
P D Chapman, W Church, J Burn, et al.
JAMA Neurology
|
August 2, 2016
Spectrum of Movement Disorders in Mitochondrial Disorders-Reply
Mika H Martikainen, David J Burn, Doug M Turnbull
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 6, 1998
Tardive diaphragmatic flutter
D J Burn, A Coulthard, S Connolly, et al.
Pediatric Cardiology
|
March 1, 1993
Congenital heart disease in CHARGE association
R 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 delays
S J Mills, P D Chapman, J Burn, et al.
Page
of 57