Phenylketonuria (PKU)

Phenylketonuria (PKU) is an autosomal recessive disorder characterized by abnormalities in amino acid metabolism caused as a result of deficiency in phenylalanine hydroxylase, an enzyme that converts phenylalanine to tyrosine. Here is the latest research.

August 20, 2020

Inhibition of GSK-3β restores delayed gastric emptying in obesity-induced diabetic female mice

American Journal of Physiology. Gastrointestinal and Liver Physiology
Chethan SampathPandu R Gangula
September 16, 2020

Aging Dependent Morphological Crystallinity Determines Membrane Activity of L-Phenylalanine Self-Assembles

The Journal of Physical Chemistry Letters
Pavel BanerjeeNilmoni Sarkar
September 3, 2020
Open Access

Correction to: PKU dietary handbook to accompany PKU guidelines

Orphanet Journal of Rare Diseases
A MacDonaldF J van Spronsen
August 26, 2020
Open Access

InOperando X-ray Studies of High-Performance Lithium-Ion Storage in Keplerate-Type Polyoxometalate Anodes

ACS Applied Materials & Interfaces
Chia-Ching LinHan-Yi Chen
September 15, 2020

Neopterin derivatives - a novel therapeutic target rather than biomarker for atherosclerosis and related diseases

VASA. Zeitschrift für Gefässkrankheiten
Takuya Watanabe
August 28, 2020
Open Access

Persistent Pulmonary Hypertension of the Newborn: Pathophysiological Mechanisms and Novel Therapeutic Approaches

Frontiers in Pediatrics
Sofia MartinhoCarmen Brás-Silva
July 31, 2020

Novel immune biomarkers in complex regional pain syndrome

Journal of Neuroimmunology
Marc A RussoPaul J Austin
August 8, 2020
Open Access

Correction to: Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies

Orphanet Journal of Rare Diseases
Thomas OpladenInternational Working Group on Neurotransmitter related Disorders (iNTD)
August 26, 2020

The psychosocial burden of inflammatory bowel disease in adolescents and young adults

Internal Medicine Journal
Jessica HalloranSimon Denny
September 10, 2020

Treatment of classic phenylketonuria in Poland in the years 2009-2015 based on the database of the Polish National Health Fund

Pediatric endocrinology, diabetes, and metabolism
Agnieszka SzypowskaJoanna Taybert
September 5, 2020
Open Access

Dietary intake and nutritional status of patients with phenylketonuria in Taiwan

Scientific Reports
Hui-Ling WengYin-Hsiu Chien
July 24, 2020
Open Access

Bone Status in Patients with Phenylketonuria: A Systematic Review

María José de CastroMaría Luz Couce
August 22, 2020
Open Access

Phenylketonuria, from diet to gene therapy

Médecine sciences : M/S
Arnaud WiedemannFeillet François
July 25, 2020
Open Access

Phenylketonuria screening in Iranian newborns: a systematic review and meta-analysis

BMC Pediatrics
Mehdi ShokriMilad Azami
August 1, 2020
Open Access

Sepiapterin reductase: Characteristics and role in diseases

Journal of Cellular and Molecular Medicine
Yao WuMeixiao Zhan
August 4, 2020

Tetrahydrobioterin (BH4) pathway: from metabolism to neuropsychiatry

Current Neuropharmacology
Fanet H Vancassel S
September 4, 2020

Validation and utility study of the 10 item brief adult health capital scale (BACHS-10)

Journal of Health Psychology
Matthew Hanauer, Dubravka Svetina Valdivia

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