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Research 601–630 of 1000+
- How do You Treat Alopecia in Your Clinic?
- “Cloned” Hairlines
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- The Effect of Drugs on Hair
- Precocious Pubarche in a 7-Year-Old Patient. A Case Report
- Micro-segmental hair analysis: detailed procedures and applications in forensic toxicology
- Epithelial elements in superficial angiomyxomas: mimicry of adnexal development, and mesenchymal‐to‐epithelial transition
- Evolution of long scalp hair in humans
- Congenital hypotrichosis due to short anagen
- The Okuda Papers: an extraordinary - but unfortunately unrecognized - piece of work that could have changed the history of hair transplantation
- Biologic Rhythms Derived from Siberian Mammoths' Hairs
- Adams–Oliver syndrome: new evidence in variable expressivity?
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Family History and Risk of Hair Loss
- Concomitant presentation of alopecia areata in siblings: A rare occurrence
- Bald scalps and wrinkles
- An evidence based case report of alopecia areata treated with individualised homoeopathic medicine
- Psoriasis
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Favorable effect of herbal extract on androgenic alopecia: A case report
- Ambassadors in Dermatology and Venereology: An interview with Professor Fabio Ayala
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Bloom's syndrome–‐a first report from India
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Organizational principles of integumentary organs: Maximizing variations for effective adaptation
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- Genes for Hair and Avian Keratins
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Autoimmune Diseases and Acquired Von Willebrand Disease in Two Cases of Progeria