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K Hyland

Showing results (91-100 of 95) with videos related to

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Journal of Inherited Metabolic Disease|February 7, 2014
Decreased cerebral spinal fluid neurotransmitter levels in Smith-Lemli-Opitz syndromeS E Sparks, C A Wassif, H Goodwin, et al.
Neurology|May 26, 2004
Infantile Parkinsonism-dystonia and elevated dopamine metabolites in CSFB E Assmann, R O Robinson, R A H Surtees, et al.
Human Genetics|August 14, 1998
A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch populationL P van den Heuvel, B Luiten, J A Smeitink, et al.
Molecular Genetics and Metabolism|November 16, 2004
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the testR Saunders-Pullman, N Blau, K Hyland, et al.
Neurology|March 23, 2005
Cerebral folate deficiency with developmental delay, autism, and response to folinic acidP Moretti, T Sahoo, K Hyland, et al.
Pageof 10

Showing results (91-100 of 95) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 95 results.
Journal of Inherited Metabolic Disease|February 7, 2014
Decreased cerebral spinal fluid neurotransmitter levels in Smith-Lemli-Opitz syndromeS E Sparks, C A Wassif, H Goodwin, et al.
Neurology|May 26, 2004
Infantile Parkinsonism-dystonia and elevated dopamine metabolites in CSFB E Assmann, R O Robinson, R A H Surtees, et al.
Human Genetics|August 14, 1998
A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch populationL P van den Heuvel, B Luiten, J A Smeitink, et al.
Molecular Genetics and Metabolism|November 16, 2004
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the testR Saunders-Pullman, N Blau, K Hyland, et al.
Neurology|March 23, 2005
Cerebral folate deficiency with developmental delay, autism, and response to folinic acidP Moretti, T Sahoo, K Hyland, et al.
Pageof 10