The PND Association maintains a current list of articles related to neurotransmitter diseases. Please contact us if you would like this information.
Tyrosine Hydroxylase Deficiency
For a complete list of articles on Tyrsosine Hydroxylase Deficiency, please refer to the
Online Mendelian Inheritance in Man (OMIM) which is linked below. Before clicking, you
will need to enter the following information at the OMIM site:
Key Words: 'Tyrosine Hydroxylase'
Access Listing: 191290
http://www.ncbi.nlm.nih.gov/omim
"Biochemical Hallmarks of Tyrosine Hydroxylase Deficiency".
Brautigam C., Wevers R., Jansen R., Smeitink J., De Rijk-Van Andel J., Gabreels F.,
Hoffmann G.,
Clinical Chemistry, 1998 44:9 1897-1904
Aromatic L-Amino Acid Decarboxylase Deficiency
For a complete list of articles on Aromatic L-Amino Acid Decarboxylase Deficiency, please
refer to the Online Mendelian Inheritance in Man (OMIM) which is linked below. Before
clicking, you will need to enter the following information at the OMIM site:
Key Words: 'Aromatic L-Amino Decarboxylase'
Access Listing: 107930
http://www.ncbi.nlm.nih.gov/omim
"Aromatic L-Amino Acid Decarboxylase
Deficiency: Clinical Features, Diagnosis, and Treatment of a New Inborn Error of
Neurotransmitter Amine Synthesis".
Hyland K., Surtees R., Rodeck C., Clayton P., Neurology, 1992:42:1980-1987.
"Clinical and Therapeutic
Observations in Aromatic L- Amino Acid Decarboxylase Deficiency".
Swoboda K.J., Hyland K., Godstein D., Kuban K.C.K., Arnold L.A., Holmes C.S., Levy H.L.,
Neurology, 1999: 53:1205-1211.
Cyclohydrolase I Deficiency (Dopa Responsive
Dystonia)
For a complete list of articles on Cyclohydrolase I Deficiency, please refer to the Online
Mendelian Inheritance in Man (OMIM) which is linked below. Before clicking, you will need
to enter the following information at the OMIM site:
Key Words: 'Cyclohydrolase I Deficiency'
Access Listing: 233910
http://www.ncbi.nlm.nih.gov/omim
Succinic Semialdehyde Dehydrogenase (SSADH)
Deficiency
For a complete list of articles on SSADH, please refer to the Online Mendelian Inheritance
in Man (OMIM) which is linked below. Before clicking, you will need to enter the following
information at the OMIM site:
Key Words: 'Succinic Semialdehyde
Dehydrogenase Deficiency'
Access Listing: 271980
http://www.ncbi.nlm.nih.gov/omim