Results 291 to 300 of about 101,529 (354)
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2011
Clinical characteristics and pahophysiologies of dopa-responsive dystonia are discussed by reviewing autosomal-dominant GTP cyclohydrolase-I deficiency (AD GCHI D), recessive deficiencies of enzymes of pteridine metabolism, and recessive tyrosine hydroxylase (TH).
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Clinical characteristics and pahophysiologies of dopa-responsive dystonia are discussed by reviewing autosomal-dominant GTP cyclohydrolase-I deficiency (AD GCHI D), recessive deficiencies of enzymes of pteridine metabolism, and recessive tyrosine hydroxylase (TH).
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Archives of Dermatology, 1972
To the Editor.— We are grateful to Dr. Okun for his detailed consideration of dopa and tyrosine oxidases. In our study of lichen planus we observed a striking reduction of dopa-positive melanocytes in the basal region of the epidermis where the lichen planus was active. In the dermal infiltrate we observed a few weekly dopa-positive cells, but we were
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To the Editor.— We are grateful to Dr. Okun for his detailed consideration of dopa and tyrosine oxidases. In our study of lichen planus we observed a striking reduction of dopa-positive melanocytes in the basal region of the epidermis where the lichen planus was active. In the dermal infiltrate we observed a few weekly dopa-positive cells, but we were
openaire +1 more source
Animal models of l‐dopa‐induced dyskinesia in Parkinson's disease
Movement Disorders, 2018M. A. Cenci, Alan R. Crossman
semanticscholar +1 more source
Sydney multicenter study of Parkinson's disease: Non‐L‐dopa–responsive problems dominate at 15 years
Movement Disorders, 2005Mariese A. Hely +3 more
semanticscholar +1 more source