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Research 31–60 of 882
- Neonatal lupus syndrome in a Nigerian child
- Frontal Fibrosing Alopecia
- Unmasking Melasma: Confronting the Treatment Challenges
- VISIA Skin Analysis System as a Tool to Evaluate the Reduction of Pigmented Skin and Vascular Lesions Using the 532 Nm Laser
- Acquired Hyperpigmentation and Cicatricial Alopecia
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Lichen Planus Pigmentosus as a Cutaneous Extrahepatic Manifestation of Chronic Hepatitis C Virus Infection: A Case Report
- Disorders of pigmentation in infants and children
- Epidermal Nevi
- The Skin and Subcutaneous Tissues
- Clinical and Dermoscopic Evaluation of the Efficacy Melasma Treatment with Oral Tranexamic Acid
- LP-161 Tjalma syndrome (Pseudo-Pseudo Meigs Syndrome): polyserositis with increased CA-125 in patients with systemic lupus erythematosus
- PHYSIOLOGIC SKIN CHANGES ASSOCIATED WITH PREGNANCY
- Role of Dermal Melanocytes in Cutaneous Pigmentation of Stasis Dermatitis
- Atypical clinical presentation of primary and secondary cutaneous follicle center lymphoma (FCL) on the head characterized by macular lesions
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Central Centrifugal Cicatricial Alopecia
- Central centrifugal cicatricial alopecia
- Treatment of frontal fibrosing alopecia and lichen planopilaris
- Primary Care of Adult Women
- Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome
- Bilateral Eyelash Poliosis with Raccoon Erythema and Hypopigmentation-Contact Follicular Leukoderma
- A Case Series on a Rare Clinical Presentation of Lichen Planopilaris Restricted to the Face
- Folliculotropic mycosis fungoides of the scalp: A case report
- Cutaneous Reactions to Drugs
- Dermoscopy in General Dermatology: A Practical Overview
- Alopecia Areata Update
- Dermoscopy: distinguishing malignant tumors from benign
- Atlas of Geriatric Dermatology
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn