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Brain : a Journal of Neurology
|
June 1, 1994
Dysembryoplastic neuroepithelial tumor. Features in 16 patients
A A Raymond, S F Halpin, N Alsanjari, et al.
International Angiology : a Journal of the International Union of Angiology
|
November 13, 2003
The Asymptomatic Carotid Stenosis and Risk of Stroke (ACSRS) study. Aims and results of quality control
A Nicolaides, M Sabetai, S K Kakkos, et al.
Annals of Neurology
|
April 20, 2001
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease
D Chan, N C Fox, R I Scahill, et al.
Addiction (Abingdon, England)
|
October 4, 2021
Cross-national validation of the social media disorder scale: findings from adolescents from 44 countries
Maartje Boer, Regina J J M van den Eijnden, Catrin Finkenauer, et al.
International Journal of Methods in Psychiatric Research
|
July 28, 2012
A brief observational instrument for the assessment of infant home environment: development and psychometric testing
Jolien Rijlaarsdam, Gonneke W J M Stevens, Jan van der Ende, et al.
Clinical Radiology
|
July 1, 1989
Clinical diagnosis from digital displays: preliminary findings of the St Mary's Evaluation Project
R M Dawood, J O Craig, J H Highman, et al.
Child Maltreatment
|
March 20, 2014
Maternal Childhood Maltreatment and Offspring Emotional and Behavioral Problems: Maternal and Paternal Mechanisms of Risk Transmission
Jolien Rijlaarsdam, Gonneke W J M Stevens, Pauline W Jansen, et al.
Brain : a Journal of Neurology
|
April 25, 2000
Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study
J C Janssen, M Hall, N C Fox, et al.
Brain : a Journal of Neurology
|
March 1, 1997
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor
N C Fox, A M Kennedy, R J Harvey, et al.
Archives of Neurology
|
June 19, 2001
Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutation
J C Janssen, P L Lantos, N C Fox, et al.
Page
of 28
Search research articles
Search
Showing results (251-260 of 272) with videos related to
Sort By:
Page
of 28
Brain : a Journal of Neurology
|
June 1, 1994
Dysembryoplastic neuroepithelial tumor. Features in 16 patients
A A Raymond, S F Halpin, N Alsanjari, et al.
International Angiology : a Journal of the International Union of Angiology
|
November 13, 2003
The Asymptomatic Carotid Stenosis and Risk of Stroke (ACSRS) study. Aims and results of quality control
A Nicolaides, M Sabetai, S K Kakkos, et al.
Annals of Neurology
|
April 20, 2001
Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease
D Chan, N C Fox, R I Scahill, et al.
Addiction (Abingdon, England)
|
October 4, 2021
Cross-national validation of the social media disorder scale: findings from adolescents from 44 countries
Maartje Boer, Regina J J M van den Eijnden, Catrin Finkenauer, et al.
International Journal of Methods in Psychiatric Research
|
July 28, 2012
A brief observational instrument for the assessment of infant home environment: development and psychometric testing
Jolien Rijlaarsdam, Gonneke W J M Stevens, Jan van der Ende, et al.
Clinical Radiology
|
July 1, 1989
Clinical diagnosis from digital displays: preliminary findings of the St Mary's Evaluation Project
R M Dawood, J O Craig, J H Highman, et al.
Child Maltreatment
|
March 20, 2014
Maternal Childhood Maltreatment and Offspring Emotional and Behavioral Problems: Maternal and Paternal Mechanisms of Risk Transmission
Jolien Rijlaarsdam, Gonneke W J M Stevens, Pauline W Jansen, et al.
Brain : a Journal of Neurology
|
April 25, 2000
Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study
J C Janssen, M Hall, N C Fox, et al.
Brain : a Journal of Neurology
|
March 1, 1997
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor
N C Fox, A M Kennedy, R J Harvey, et al.
Archives of Neurology
|
June 19, 2001
Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutation
J C Janssen, P L Lantos, N C Fox, et al.
Page
of 28