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- Horn With Miliary Calcification in Squamous Cell Carcinoma
- 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
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- Trichilemmal cyst of the eyelid: An unusual presentation in paediatric age group
- Calcified Epidermal Cyst on the Neck
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Polyglandular Syndrome Type 1 Complicated with Dilated Cardiomyopathy: A Case Report
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Soft-tissue calcification in systemic lupus erythematosus
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- The self in the obsessive–compulsive-related disorders: hoarding disorder, body dysmorphic disorder, and trichotillomania
- Clinical Case Notes. Optical coherence tomography of adult-onset foveomacular vitelliform dystrophy
- Idiopathic hypoparathyroidism with extensive intracranial calcification in children
- Pilomatrixoma of the Forearm in an Elderly Male
- Inherited Epidermolysis Bullosa: A Clinical Case
- Practice and Educational Gaps in Dermatology
- Dermatological drugs, topical agents, and cosmetics
- Porphyria Cutanea Tarda in a Patient With Agnogenic Myeloid Metaplasia
- Pilomatricoma in the neck of an adult male
- 1400 Low-intensity ultrasound protects human scalp hair follicles from taxane-induced toxicity
- Clinical Case Notes. Tamoxifen optic neuropathy
- Clinical Case Notes. Intraorbital ophthalmic artery aneurysms
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Uncombable hair syndrome and beyond
- POSTĘP W DIAGNOZIE I LECZENIU STWARDNIENIA ROZSIANEGO
- PŁYNY- NIE ZA DUŻO, NIE ZA MAŁO, LECZ W SAM RAZ