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Research 121–150 of 1000+
- Acquired scalp alopecia. Part I: A review
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Evaluation of SALT score severity in correlation with trichoscopic findings in alopecia areata: a study of 303 patients
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- A unique presentation of trichofolliculoma in amniotic band syndrome
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Telogen Effluvium, Diagnosis and Management: A Narrative Review
- Inherited Epidermolysis Bullosa: A Clinical Case
- Mucocutaneous Manifestations of Endocrine Disorders
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Skin and hair: models for exploring organ regeneration
- Trichotillomania in Children
- Molecular Genetics of Alopecias
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- The human keratins: biology and pathology
- The Spectrum of Skin Disease Among Indian Children
- Morphological Approach to Hair Disorders
- Short anagen syndrome
- The Genetics of Human Skin Disease
- Alopecia Areata
- Skin signs of systemic diseases
- Gap junctions in Turing-type periodic feather pattern formation
- The clinical spectrum of parathyroid disease
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Trichodystrophies: A hair-raising differential diagnosis
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot