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Research 391–420 of 567
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Atypical post-finasteride syndrome: A pharmacological riddle
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Acanthosis Nigricans during an HAIR-AN syndrome: "The Tree That Hides the Forest"
- Polycystic ovary syndrome
- Why waiting for Godot could not be an ideal technique to generate scientific data
- Systemic lupus erythematosus in a filly.
- Treatment of Satoyoshi syndrome: a systematic review
- Post COVID-19 Sequelae in Adults: A Review
- Myotonic dystrophy type 1
- Gastrointestinal Manifestation of Systemic Lupus Erythematosus - Lupus Enteritis
- Satoyoshi Syndrome: A Cause of Alopecia Universalis in Association with Neurologic and Bony Abnormalities
- Cutaneous Manifestations of Sarcoidosis : Reports of Two Cases
- Esssentials of Systemic Lupus Erythematosus
- Vogt-Koyanagi-Harada disease occurring during pegylated interferon-α2b and ribavirin combination therapy for chronic hepatitis C
- Alopecia areata. How not to miss Satoyoshi syndrome?
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions
- Extrapulmonary manifestations of coronavirus disease (COVID-19): current status (a literature review)
- The New Classification Criteria of Systemic Lupus Erythematosus
- Clinical Aspects and Spectrum of Illness of TSS: Overview
- Symptomatic hypercalcemia and scarring alopecia as presenting features of sarcoidosis
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- A novel finding of hair growth like vellus hairs on glabrous skin of distal phalanx of thumb in Vogt–Koyanagi–Harada disease: A case report
- 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증
- NEMO syndrome (incontinentia pigmenti) and systemic lupus erythematosus: A new disease association
- SAT-214 Satoyoshi Syndrome: A Rare Cause of Premature Ovarian Failure
- Pulmonary arterial aneurysm in Behçet's disease
- Characterisation of Myotonic Dystrophy type I cell models and drug evaluation by a cell- based quantification platform.
- Zinc: An overview and therapeutic uses in dermatology
- 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