Diagnosis of tetrahydrobiopterin deficiency using filter paper blood spots: further development of the method and 5 years experience

By Opladen Thomas   Abu Seda Bettina   Rassi Anahita   Thöny Beat   Hoffmann Georg   Blau Nenad  

Journal of Inherited Metabolic Disease, Vol. 34, Iss. 3, 2011-06 ,pp. : 819-826

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Erratum to: Diagnosis of tetrahydrobiopterin deficiency using filter paper blood spots: further development of the method and 5 years experience

By Opladen Thomas   Abu Seda Bettina   Rassi Anahita   Thöny Beat   Hoffmann Georg   Blau Nenad  

Journal of Inherited Metabolic Disease, Vol. 34, Iss. 3, 2011-06 ,pp. : 843-843

Springer Publishing Company

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Newborn urine screening programme in the province of Quebec: An update of 30 years' experience

By Auray-Blais C.   Giguére R.   Lemieux B.  

Journal of Inherited Metabolic Disease, Vol. 26, Iss. 4, 2003-06 ,pp. : 393-402

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Succinic semialdehyde dehydrogenase deficiency: Lessons from mice and men

By Pearl P.   Gibson K.   Cortez M.   Wu Y.   Carter Snead O.   Knerr I.   Forester K.   Pettiford J.   Jakobs C.   Theodore W.  

Journal of Inherited Metabolic Disease, Vol. 32, Iss. 3, 2009-06 ,pp. : 343-352

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Pharmacokinetics of orally administered tetrahydrobiopterin in patients with phenylalanine hydroxylase deficiency

By Zurflüh M.   Fiori L.   Fiege B.   Ozen I.   Demirkol M.   Gärtner K.   Thöny B.   Giovannini M.   Blau N.  

Journal of Inherited Metabolic Disease, Vol. 29, Iss. 6, 2006-12 ,pp. : 725-731

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