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Human Molecular Genetics
|
March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity
O Bandmann, T G Nygaard, R Surtees, et al.
Annals of Neurology
|
November 1, 1992
Long-term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa-responsive dystonia
T G Nygaard, H Takahashi, G A Heiman, et al.
Annals of Neurology
|
March 1, 1995
The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q
H Tanaka, K Endo, S Tsuji, et al.
Journal of Inherited Metabolic Disease
|
June 29, 1999
Oral phenylalanine loading profiles in symptomatic and asymptomatic gene carriers with dopa-responsive dystonia due to dominantly inherited GTP cyclohydrolase deficiency
K Hyland, T G Nygaard, J M Trugman, et al.
Annals of Neurology
|
March 1, 1994
Biochemical and fluorodopa positron emission tomographic findings in an asymptomatic carrier of the gene for dopa-responsive dystonia
H Takahashi, R A Levine, M P Galloway, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1989
Tyrosine hydroxylase and levodopa responsive dystonia
N A Fletcher, I J Holt, A E Harding, et al.
Circulation
|
June 17, 1997
Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32
J H Morse, A C Jones, R J Barst, et al.
Chest
|
July 24, 1998
Familial primary pulmonary hypertension locus mapped to chromosome 2q31-q32
J H Morse, A C Jones, R J Barst, et al.
Nature Genetics
|
December 1, 1993
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q
T G Nygaard, K C Wilhelmsen, N J Risch, et al.
Neurology
|
August 1, 1993
Phenotypic expression of X-linked dystonia-parkinsonism (lubag) in two women
C H Waters, H Takahashi, K C Wilhelmsen, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 5
Human Molecular Genetics
|
March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity
O Bandmann, T G Nygaard, R Surtees, et al.
Annals of Neurology
|
November 1, 1992
Long-term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa-responsive dystonia
T G Nygaard, H Takahashi, G A Heiman, et al.
Annals of Neurology
|
March 1, 1995
The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q
H Tanaka, K Endo, S Tsuji, et al.
Journal of Inherited Metabolic Disease
|
June 29, 1999
Oral phenylalanine loading profiles in symptomatic and asymptomatic gene carriers with dopa-responsive dystonia due to dominantly inherited GTP cyclohydrolase deficiency
K Hyland, T G Nygaard, J M Trugman, et al.
Annals of Neurology
|
March 1, 1994
Biochemical and fluorodopa positron emission tomographic findings in an asymptomatic carrier of the gene for dopa-responsive dystonia
H Takahashi, R A Levine, M P Galloway, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1989
Tyrosine hydroxylase and levodopa responsive dystonia
N A Fletcher, I J Holt, A E Harding, et al.
Circulation
|
June 17, 1997
Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32
J H Morse, A C Jones, R J Barst, et al.
Chest
|
July 24, 1998
Familial primary pulmonary hypertension locus mapped to chromosome 2q31-q32
J H Morse, A C Jones, R J Barst, et al.
Nature Genetics
|
December 1, 1993
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q
T G Nygaard, K C Wilhelmsen, N J Risch, et al.
Neurology
|
August 1, 1993
Phenotypic expression of X-linked dystonia-parkinsonism (lubag) in two women
C H Waters, H Takahashi, K C Wilhelmsen, et al.
Page
of 5