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Nessrine Mezzi, Olfa Messaoud, Rahma Mkaouar, Nadia Zitouna, Safa Romdhane, Ghaith Abdessalem, Cherine Charfeddine, Faouzi Maazoul, Ines Ouerteni, Yosr Hamdi, Anissa Zaouak, Ridha Mrad, Sonia Abdelhak & Lilia Romdhane. (2021) Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved. Genes 12:11, pages 1820.
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Tracy B. Lowe, Jane DeLuca & Georgianne Arnold. (2020) Neurocognitive, neuropsychiatric, and neurological outcomes associated with phenylalanine hydroxylase deficiency: Assessment considerations for nurse practitioners. Journal for Specialists in Pediatric Nursing 26:1.
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Tracy Brock Lowe, Jane DeLuca & Georgianne L. Arnold. (2020) Similarities and differences in key diagnosis, treatment, and management approaches for PAH deficiency in the United States and Europe. Orphanet Journal of Rare Diseases 15:1.
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Kazanasmaz Halil & Karaca Meryem. (2020) Plasma amino acid levels in a cohort of patients in Turkey with classical phenylketonuria. Asian Biomedicine 14:2, pages 59-65.
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