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Research 91–120 of 1000+
- Genetics of Structural Hair Disorders
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Disorders of hair in children
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Successful induction of oral tolerance in Netherton syndrome
- Medications
- The Genetics of Human Skin Disease
- Keratin disorders: from gene to therapy
- Trichoscopy in Hair Shaft Disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Secondary cicatricial and other permanent alopecias
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Histologic morphology and involucrin, filaggrin, and keratin expression in normal canine skin from dogs of different breeds and coat types
- Acne
- Hair loss in infancy and childhood
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Congenital Atrichia: A Case Report
- Abnormal fingerprints and immigration delay disease
- 9. Immunology and Genetics
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Molecular Genetics of Alopecias
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Three-Dimensional Analysis of Cell Division Orientation in Epidermal Basal Layer Using Intravital Two-Photon Microscopy
- Immunological control of skin development: from homeostasis to developmental pathologies
- Group IID, IIE, IIF and III secreted phospholipase A2s
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Evolving approaches to profiling the microbiome in skin disease