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Research 91–120 of 1000+
- Dermatological diseases from a genetic perspective
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Hair Loss in Children, Etiologies, and Treatment
- Approach to Alopecia in Dogs in Clinical Practice
- The Roles of EDA2R in Ageing and Disease
- Edar Signaling in the Control of Hair Follicle Development
- Store-operated calcium channels in skin
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Acquired Uncombable Hair
- Genetic hair and nail disorders
- Connexin mutations in human disease
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Hair shaft disorders in children – An update
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Progeroide Syndrome
- Hair Shaft Dysplasias
- Cronkhite-Canada Syndrome: A Case Report
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Loose anagen hair syndrome
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Christmas article: Case of uncombable hair syndrome discovered after publication of article in Ugeskrift for Læger
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Morpho-Regulation of Ectodermal Organs
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia