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Research 151–180 of 1000+
- Subject Index
- 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
- LITERATURE REVIEW
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Cicatricial alopecia
- Clinicoepidemiological Observational Study of Acquired Alopecias in Females Correlating with Anemia and Thyroid Function
- Evaluation of Hair Loss
- Atlas of Geriatric Dermatology
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- Current standards in the diagnostics and therapy of hair diseases - hair consultation
- Dermoscopy: distinguishing malignant tumors from benign
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- Impacto del desequilibrio del microbioma del cuero cabelludo en la severidad de la alopecia areata, marcadores inflamatorios y cambios post-tratamiento
- Cutaneous Manifestations of Lupus Erythematosus
- British Society for Dermatopathology: Summaries of Papers
- National scientific medical meeting 1996 abstracts
- Cutaneous signals of immune system disease
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Keratins: the hair shaft's backbone revealed
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Molecular Genetics of Human Hair Diseases
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness