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Research 31–60 of 50
- Treatment of Cystathionine β-Synthase Deficiency in Mice Using a Minicircle-Based Naked DNA Vector
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- Nutritional Disorders of the Hair and Their Management
- Study of the international epidemiology of androgenetic alopecia in young caucasian men using photographs from the internet
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- The Physiological Impact of Melatonin, Its Effect on the Course of Diseases and Their Therapy and the Effect of Magnetic Fields on Melatonin Secretion—Potential Common Pathways of Influence
- Premature Graying of Hair: A Comprehensive Review and Recent Insights
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Biochemistry of Vitamin B: Metabolic Regulations, Deficiency Disorders and Emerging Therapeutic Strategies
- PCR108 QUALITATIVE AND PSYCHOMETRIC EVALUATION OF THE CLINRO MEASURE FOR EYEBROW HAIR LOSS AND CLINRO MEASURE FOR EYELASH HAIR LOSS IN ADULTS AND ADOLESCENTS WITH SEVERE ALOPECIA AREATA
- Chirality Effect on Physical and Biological Properties of Peptide-Based Hydrogels
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Sulforaphane-Rich Broccoli Sprout Extract Promotes Hair Regrowth in an Androgenetic Alopecia Mouse Model via Enhanced Dihydrotestosterone Metabolism
- Gray Hair: From Preventive to Treatment
- Ernährungsstörungen des Haares und deren Management
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- A Profuse Pipeline of Promising Options
- Diversifying the case study: How far has physiology education come in integrating equality, diversity and inclusion into the curricula?
- TONGUE, RED
- 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