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Research 331–360 of 1000+
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Skin manifestations among<i>GATA2</i>-deficient patients
- Clinical Approach to the Patient With Alopecia
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Skin manifestations of chronic kidney disease
- Hair Shaft Dysplasias
- Unruly hair
- Short anagen hair with persistent synchronized pattern of scalp hair growth
- The Effect of Parathyroid Hormones on Hair Follicle Physiology: Implications for Treatment of Chemotherapy-Induced Alopecia
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Diagnosis and management of hair loss in children
- Melanocytes and Vitiligo (and Hair Graying)
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Racial and Gender Influences on Skin Disease
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Friends Turned Foes: Angiogenic Growth Factors beyond Angiogenesis
- Evolving approaches to profiling the microbiome in skin disease
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Skin Conditions in Figure Skaters, Ice-Hockey Players and Speed Skaters
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- National scientific medical meeting 1996 abstracts
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Keratins: the hair shaft's backbone revealed