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Research 121–150 of 1000+
- Congenital hair loss disorders: Rare, but not too rare
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Polarization Microscopy of Hair in Acrodermatitis Enteropathica
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- AN UPDATE OF HAIR SHAFT DISORDERS
- PA33 When bones speak through nails: insights from a paediatric case series
- Vulvovaginal involvement in Netherton syndrome: A case report
- Isotretinoin-unresponsive acne as a sign of a congenital disorder: a case of 21-hydroxylase deficiency
- Abordagens psicológicas e novas terapêuticas perante as escolhas do paciente portador da Síndrome de Morris
- Monilethrix with Acitretin
- Dermatologic Clinics: Hair Disorders
- From the Elephant Man to Barbie Girl: Dissecting the Freak from the Margins to the Mainstream
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- Correlation between MRI findings of pituitary gland and prolactin level among hyperprolactinemia adult female Saudi patients in rural areas: A retrospective multicentric study
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Hair Follicle Regeneration Using Grafted Rodent and Human Cells
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Atypical Protein Kinase C Isoform, aPKCλ, Is Essential for Maintaining Hair Follicle Stem Cell Quiescence
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Pathologic Quiz Case: An Anterior Neck Mass in a 5-Month-Old Female Infant
- Woodhouse-Sakati syndrome (WSS)
- NEW YORK ACADEMY OF MEDICINE, SECTION ON DERMATOLOGY AND SYPHILIS
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- [An infant with short stature and red cheeks (Rothmund-Thomson syndrome)].
- Safety assessment of <i>Linum usitatissimum</i> (Linn.) Ingestion in New Zealand rabbits
- HairSentinel: a time-aware anomaly detection framework for forecasting hairfall trends using temporal fusion transformers