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Research 451–480 of 1000+
- Ocular manifestations of Hutchinson-Gilford-Progeria syndrome: A rare presentation
- Areata-Like Lupus as a Clinical Manifestation of Cutaneous Lupus Erythematosus
- Black Dot Type Capitis Tinea Appreciates Bacterial Foliculitis
- Anti-DFS70 sebagai Penanda Kejadian Autoimun Nonsistemik (Primary Billiar Cholangitis) pada Systemic Lupus Erythematosus
- 034 Characterization of novel TMEM173 mutation causing a lupus- and SAVI-like phenotype, modified by polymorphisms in TMEM173 and IFIH1
- Frontal fibrosing alopecia: a pathology on the rise
- Erosive Lichen Planus of the Scalp and Hepatitis C Infection
- C003 Histopathology of the alopecias
- Segmental Vitiligo
- How We Do It
- Alopecia areata
- Late-Onset Systemic Lupus Erythematosus
- Androgen Receptor Antagonists (Antiandrogens) Structure-Activity Relationships
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Polycystic Ovary Syndrome
- Central centrifugal cicatricial alopecia
- Scalp Dermoscopy or Trichoscopy
- Clinical evaluation of alopecias using a handheld dermatoscope
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
- Trichoscopy
- Psoriatic alopecia
- Reflectance Confocal Microscopy of the Yellow Dot Pattern in Alopecia Areata
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- Clinical characteristics and outcomes of adult patients admitted with COVID-19 in East London: a retrospective cohort analysis
- Linear lupus panniculitis of the scalp presenting as alopecia along Blaschko’s lines: A distinct variant of lupus panniculitis in East Asians?
- Permanent alopecia in patients with breast cancer after taxane chemotherapy and adjuvant hormonal therapy: Clinicopathologic findings in a cohort of 10 patients
- Vitamin D‐dependent rickets Type II with alopecia: two case reports and review of the literature
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations