Journal of Genetic Disorders & Genetic ReportsISSN: 2327-5790

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WB Hanley Author

whanley@pathcom.com

Subjects of specialization
Phenylketonuria

Affiliation
Division of Clinical & Metabolic Genetics, The Hospital for Sick Children at the University of Toronto, Canada

Biography

WB Hanley belongs to Division of Clinical & Metabolic Genetics intrested in the field PKU: Phenylketonuria; BH4: Tetrahydrobiopterin; NBS: Newborn Screening; PAH: Phenylalanine Hydroxylase; MS/MS: Tandem Mass Spectrometry; Phe: Phenylalanine; MRS: Magnetic Resonance Spectroscopy; MPKUS: Maternal PKU Syndrome; MRI: Magnetic Resonance Imaging; LNAA: Large Neutral Amino Acids
from The Hospital for Sick Children at the University of Toronto, Canada

Publications

Review Article Open Access

Phenylketonuria (PKU) - What Next? Mini-Review

Author(s):

WB Hanley

Phenylketonuria (PKU) - What Next? Mini-Review

treatment of PKU is presented. This includes: 1. Worldwide expansion of newborn screening. 2. Uniform classification of the phenotypes. 3. Exploring the frequency of normal intellectual function in untreated patients. 4. Defining the reasons for suboptimal intellectual function in early treated PKU. 5. Developing centers of excellence for the treatment of adults with PKU. 6. Exploring new adjunct/alternative treatments/cures.

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DOI: 10.4172/2327-5790.1000108

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