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American Journal of Medical Genetics
|
June 22, 2000
Heterogeneity in Paget disease of the bone
M A Nance, F Q Nuttall, M J Econs, et al.
Journal of Neurology
|
November 17, 2017
A new measure for end of life planning, preparation, and preferences in Huntington disease: HDQLIFE end of life planning
Noelle E Carlozzi, E A Hahn, S A Frank, et al.
American Journal of Medical Genetics
|
February 6, 1999
Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22
J L Anderson, M Khan, W S David, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
April 3, 2016
HDQLIFE: the development of two new computer adaptive tests for use in Huntington disease, Speech Difficulties, and Swallowing Difficulties
N E Carlozzi, S G Schilling, J-S Lai, et al.
American Journal of Human Genetics
|
April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia
I K Svenson, A E Ashley-Koch, P C Gaskell, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
July 10, 2016
New measures to capture end of life concerns in Huntington disease: Meaning and Purpose and Concern with Death and Dying from HDQLIFE (a patient-reported outcomes measurement system)
N E Carlozzi, N R Downing, M K McCormack, et al.
Neurology
|
June 9, 2004
Apolipoprotein E controls the risk and age at onset of Parkinson disease
Y J Li, M A Hauser, W K Scott, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
August 15, 2016
HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD)
N E Carlozzi, S G Schilling, J-S Lai, et al.
Neurology
|
April 12, 2003
Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease
J M van der Walt, E R Martin, W K Scott, et al.
JAMA
|
November 17, 2001
Complete genomic screen in Parkinson disease: evidence for multiple genes
W K Scott, M A Nance, R L Watts, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
American Journal of Medical Genetics
|
June 22, 2000
Heterogeneity in Paget disease of the bone
M A Nance, F Q Nuttall, M J Econs, et al.
Journal of Neurology
|
November 17, 2017
A new measure for end of life planning, preparation, and preferences in Huntington disease: HDQLIFE end of life planning
Noelle E Carlozzi, E A Hahn, S A Frank, et al.
American Journal of Medical Genetics
|
February 6, 1999
Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22
J L Anderson, M Khan, W S David, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
April 3, 2016
HDQLIFE: the development of two new computer adaptive tests for use in Huntington disease, Speech Difficulties, and Swallowing Difficulties
N E Carlozzi, S G Schilling, J-S Lai, et al.
American Journal of Human Genetics
|
April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia
I K Svenson, A E Ashley-Koch, P C Gaskell, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
July 10, 2016
New measures to capture end of life concerns in Huntington disease: Meaning and Purpose and Concern with Death and Dying from HDQLIFE (a patient-reported outcomes measurement system)
N E Carlozzi, N R Downing, M K McCormack, et al.
Neurology
|
June 9, 2004
Apolipoprotein E controls the risk and age at onset of Parkinson disease
Y J Li, M A Hauser, W K Scott, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
August 15, 2016
HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD)
N E Carlozzi, S G Schilling, J-S Lai, et al.
Neurology
|
April 12, 2003
Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease
J M van der Walt, E R Martin, W K Scott, et al.
JAMA
|
November 17, 2001
Complete genomic screen in Parkinson disease: evidence for multiple genes
W K Scott, M A Nance, R L Watts, et al.
Page
of 4