Literature

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:

Tyrosine Hydroxylase Deficiency

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

2003 Pediatric Neurotransmitter Disease Association

www.pndassoc.org