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Research 241–270 of 1000+
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Alopecia areta: a review
- 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
- Comparative Evaluation of Oral Baricitinib and Tofacitinib in Alopecia Areata: A Retrospective Cohort Study Based on SALT Scores
- Serum 25-Hydroxy Vitamin D Level in Patients with Alopecia Areata and Its Relationship with Severity of the Disease
- Scalp hair cortisol concentration in patients with alopecia areata and correlate its level with the disease variables
- Impacto del desequilibrio del microbioma del cuero cabelludo en la severidad de la alopecia areata, marcadores inflamatorios y cambios post-tratamiento
- Psychosocial Aspects of Skin Conditions and Diseases
- Correction of Diffuse Alopecia in Iron Deficiency Anemia
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- DERMOSCOPIC EVALUATION OF THERAPEUTIC RESPONSE IN ALOPECIA AREATA
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Hair Loss in Children
- Hair Changes due to Drugs
- Alopecia
- Cutaneous Lupus Erythematosus
- Non-Neoplastic Disorders of Hair
- Dermatological Issues in a Child with Diabetes Mellitus
- Cutaneous manifestations of systemic infection in children
- Cutaneous signals of immune system disease
- 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
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- LITERATURE REVIEW
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- Diseases of Hair and Nails
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix