Search
for
Sort by
Research 181–210 of 200
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Calcium regulation of stem cells
- Skin manifestations associated with COVID-19
- Sorafenib-Associated Facial Acneiform Eruption
- Anti-programmed cell death protein 1-induced lichenoid changes of the nail unit: Histopathologic description
- Highlighting nuances of blue light phototherapy: Mechanisms and safety considerations
- Human iPS Cell-Derived Cell Aggregates Exhibited Dermal Papilla Cell Properties in in vitro Three-Dimensional Assemblage Mimicking Hair Follicle Structures
- Pathologic Quiz Case: A Nodule on the Back
- Skin Diseases Associated With COVID-19: A Narrative Review
- Medical Dermatology
- Atypical bilateral hyperpigmented macules on the lower legs possibly due to cyclophosphamide.
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report
- Pilomatricoma in the Infraorbital Region
- Dermatological Manifestations of COVID-19: A Comprehensive Review
- Extensive Spiculated Follicular Porokeratosis With Alopecia: A Case Report
- Pilomatricoma in the infraorbital region
- Keratosis Pilaris-like Eruption during Treatment of Chronic Myeloid Leukemia with Tyrosine Kinase Inhibitors: Literature Review and Report of a Case Related to Imatinib
- Author Index
- Congenital dyserythropoietic anaemia and dyskeratosis in Australian Poll Hereford calves
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Glabellar pomade crust mimicking dyskeratosis follicularis
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Papular Acantholytic Dyskeratosis of the Vulva: A Case Report and Literature Review
- Severe Variant of X‐linked Dyskeratosis Congenita (Hoyeraal‐Hreidarsson Syndrome) Causes Significant Enterocolitis in Early Infancy
- Clinical cases of Darier-White follicular dyskeratosis
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Shared Phenotypes Among Segmental Progeroid Syndromes Suggest Underlying Pathways of Aging
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter