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1. Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency). Issue 7 (2nd July 2004)

7. Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype. Issue 6 (June 1996)

8. Identification of Pseudomonas aeruginosa and Aspergillus fumigatus mono- and co-cultures based on volatile biomarker combinations. (29th January 2016)

10. New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype. Issue 9 (26th August 2010)