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- Man made disease: Clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse study
- Phénylcétonurie de l’adulte : manifestations neurologiques et modalités évolutives
- Widespread erythematous scaly eruption in an infant with phenylketonuria
- Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics
- Neonatal screening in Sweden and disease-causing variants in phenylketonuria, galactosaemia and biotinidase deficiency
- Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuria
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Role of Phenylalanine and Its Metabolites in Health and Neurological Disorders
- Hair Amino Acids: Normal Values and Results in Metabolic Errors
- Hair loss
- Premature graying of hair
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Role of Trichoscopy in Children's Scalp and Hair Disorders
- Scleroderma and L-tryptophan: A possible explanation of the eosinophilia-myalgia syndrome
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Diseases of Periocular Hair
- Assessment of scalp hair survivin in patients with premature greying of hair
- Nutraceutical : An emerging Pharmaceutical Towards Prevention Of Diseases
- Hair Disorders
- Methylmalonic Acidemia: Can Treatment be Improved?
- Westwood Carolina Conference on Clinical Dermatology
- HAIR AND SYSTEMATIC DISEASE
- Diet in dermatology: Revisited
- Nonclassic 21-hydroxylase deficiency
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- Inborn Errors of Metabolism
- P78 Acrodermatitis enteropathica in children: clinical cases
- Dermatoscopy of hair shaft disorders
- The Role of Nutrition on Thyroid Function
- Cutaneous gene therapy