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Research 421–450 of 1000+
- Approach to Alopecia in Dogs in Clinical Practice
- Expression and Analysis of TBX3 Gene in the Skin from Three Locations on Dun Mongolian Bider Horse
- Cutaneous signals of immune system disease
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Associaton of Insulin Resistance Linked Diseases and Hair Loss in Elderly Men. Finnish Population-based Study
- Morphological Approach to Hair Disorders
- Acquired scalp alopecia. Part II: A review
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Síndrome do nevo de Becker
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Hair Shaft Dysplasias
- Dermatologic manifestations of endocrine disorders
- Common Baldness in Women
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- The genetically programmed hair growth cycle and alopecia: what is there to know?
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Disorders of ovulation
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Syndromes of Severe Insulin Resistance (SSIRs)
- Subject Index
- <i>Hedychium spicatum</i>: a systematic review on traditional uses, phytochemistry, pharmacology and future prospectus
- Transforming growth factor-β in stem cells and tissue homeostasis
- Morpho‐regulation in diverse chicken feather formation: Integrating branching modules and sex hormone‐dependent morpho‐regulatory modules
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- Hair and scalp disorders
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis