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Research 181–210 of 1000+
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Focal and Generalized Alopecia
- Management of congenital ichthyoses: European guidelines of care, part two
- METHOTREXATE FOR GENERALIZED PUSTULAR PSORIASIS IN A 2-YEAR-OLD CHILD
- Treatment of monilethrix with oral minoxidil
- Secondary cicatricial and other permanent alopecias
- The eye and the skin in endocrine metabolic diseases
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Ingestion of topical steroid triggering pustular psoriasis?
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Acne in Dark Skin
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- Minoxidil-induced hypertrichosis in a child with alopecia areata
- Causes and Management of Hypertrichosis
- Multiple congenital smooth muscle hamartoma: A case report
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Generalized trichoepitheliomas with alopecia and myasthenia gravis: Clinicopathologic and immunohistochemical study and comparison with classic and desmoplastic trichoepithelioma
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Hair and Nail Relationship
- Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation