Search
for
Sort by
Research 31–60 of 928
- Sarcoidosis: Are there differences in your skin of color patients?
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Pancytopenia in epidemic dropsy: a case report
- Treatment of Pseudofolliculitis With a Pulsed Infrared Laser
- Unmasking Melasma: Confronting the Treatment Challenges
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- Mucocutaneous Manifestations of Endocrine Disorders
- Persistent Papular Eruption in a Young Adult: Importance of Histopathology in Diagnosing Eruptive Vellus Hair Cysts
- Woolly Antics between the Sheaths
- Pathophysiology of the burn scar
- Skin aging: mechanisms, evaluation, and rejuvenation
- Skin as a Window to Endocrine Dysfunction: Dermatological and Metabolic Interactions in Polycystic Ovary Syndrome
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Making the head: Caspases in life and death
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Myotonic Dystrophy—A Progeroid Disease?
- Epidermal Nevi
- Malicious Mites—Sarcoptes scabiei in Raccoon Dogs (Nyctereutes procyonoides) in Schleswig-Holstein, Germany
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Inherited Disorders of the Hair
- Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children
- Beneath the surface: dermatology and psychiatry
- Cutaneous Lupus Erythematosus
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- [4-t-Butylphenyl]-N-(4-imidazol-1-yl phenyl)sulfonamide (ISCK03) inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin production in mice and brownish guinea pigs
- Síndrome do nevo de Becker