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Research 91–120 of 183
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- Congenital Atrichia: A Case Report
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Subject Index
- Immunopathogenesis of Primary Cicatricial Alopecia
- Was the epidemic skin disease of 1891 due to acute arsenic poisoning?
- Non-Neoplastic Disorders of Hair
- Dermatological drugs, topical agents, and cosmetics
- Cutaneous signals of immune system disease
- Cicatricial alopecia
- Cytokines
- Progeroide Syndrome
- Farmácia Militar do Laboratório Nacional do Medicamento, Porto e Serviços Farmacêuticos do Centro Hospitalar Universitário do Porto (Hospital de Santo António), EPE, Porto
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- Clinical Management in Psychodermatology
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Evaluating the Prevalence of Migraine Headache among Patients with Female-Pattern Baldness
- Dilated tonic pupils with tabes dorsalis in neurosyphilis as first manifestation of HIV/AIDS: a video report
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Ulerythema ophryogenes with multiple congenital anomalies
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Alopecia following oral acyclovir for the treatment of herpes simplex keratitis