Results 171 to 180 of about 2,204 (208)

Characterization of Sapropterin Dihydrochloride Tablet

Tapan Kumar Jena, Rakesh Kumar Jat
openalex   +2 more sources

A reply to ‘Metabolic effects of sapropterin treatment in autism spectrum disorder: a preliminary study’

, 2016
Keith Fluegge
openalex   +1 more source

Extended Experience of Lower Dose Sapropterin in Irish Adults with Mild Phenylketonuria

, 2017
Samantha Doyle, M O'Regan, C. Stenson, Jean Bracken, Una Hendroff, Asta Agasarova, Deirdre Deverell, Eileen P. Treacy   +7 more
openalex   +2 more sources

Our lives with PKU: German patient voices - "Nothing about us without us". [PDF]

Mol Genet Metab Rep
Lange K, Böhmer J, Deich Y, Dickneite D, Fuchs P, Naunheim V, Scholz A, Heimbold C.   +7 more
europepmc   +1 more source

First successful outcomes of pegvaliase (PALYNZIQ) in children. [PDF]

BMC Med Genomics
Alfadhel M, Albarakati R.
europepmc   +1 more source

Phenylketonuria from the perspectives of patients in Türkiye. [PDF]

Orphanet J Rare Dis
Esgi M, Ergun H, Kaya NY, Atakay DY, Erucar E, Celik F.   +5 more
europepmc   +1 more source

Navigating phenylketonuria management to improve it in Latin America: a systematic literature review and applicability analysis. [PDF]

Front Nutr
Aguirre AS, Haro E, Campodónico A, Mendoza A, Bahamonde B, Romero VI.   +5 more
europepmc   +1 more source

Dietary intervention in the management of phenylketonuria: current perspectives [PDF]

core   +2 more sources

A Case of <i>DNAJC12</i>-Deficient Hyperphenylalaninemia Detected on Newborn Screening: Clinical Outcomes from Early Detection. [PDF]

Int J Neonatal Screen
Donnelly C, Estrella L, Ginevic I, Ganesh J.   +3 more
europepmc   +1 more source

Treating the whole patient: Facilitating health care for patients facing health inequity. [PDF]

Mol Genet Metab Rep
Sanchez-Valle A, Hicks C.
europepmc   +1 more source