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Research 331–360 of 1000+
- Mimicking Senescence Factors to Characterize the Mechanisms Responsible for Hair Regression and Hair Loss: An In Vitro Study
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Current Genetics in Hair Diseases
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Frontal Fibrosing Alopecia: Update and Review of Challenges and Successes
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Nutrition and hair
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- 'Atrophic telogen effluvium' from cytotoxic drugs and a randomized controlled trial to investigate the possible protective effect of pretreatment with a topical vitamin D3 analogue in humans
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- 2018 ISPAN Meeting Abstracts
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- The hair shaft: normality, abnormality, and genetics
- Familial frontal fibrosing alopecia: A cross‐sectional study of 20 cases from nine families
- POSTĘP W DIAGNOZIE I LECZENIU STWARDNIENIA ROZSIANEGO
- PŁYNY- NIE ZA DUŻO, NIE ZA MAŁO, LECZ W SAM RAZ
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Low concentration zinc sulphate solution in the management of recurrent herpes simplex infection
- Avoiding pitfalls in planning a hair transplant
- Cutaneous Drug Reaction Case Reports
- Correlation of symptoms to serum vitamin D levels?
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function
- Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report