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- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- HAIR AND SYSTEMATIC DISEASE
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Genetic Hair Disorders: A Review
- Learning from nudity: lessons from the nude phenotype
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Oral Presentations
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Immunological and Metabolic Causes of Infertility in Polycystic Ovary Syndrome
- Genetic Variants and Protective Immunity against SARS-CoV-2
- The eosinophilia-myalgia syndrome
- Antioxidants in dermatology
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Scleroderma and L-tryptophan: A possible explanation of the eosinophilia-myalgia syndrome
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Graft-versus-host disease
- Perspectives on Dermatopathology
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Satoyoshi Syndrome: Difficult to find or treat?
- A comparative analysis of three explanatory models of mental disorder and a preferred focus of explanation
- Regulatory T cells in dominant immunologic tolerance
- Genetic Disorders and Defects in Vitamin D Action
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Testosterone Reduces Knee Passive Range of Motion and Expression of Relaxin Receptor Isoforms via 5α-Dihydrotestosterone and Androgen Receptor Binding