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Research 211–240 of 1000+
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Micrografting and Hair Transplantation Surgery
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Atlas of Geriatric Dermatology
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Trichotillomania associated with a 25-hydroxy vitamin D deficiency: A case report
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Dermatosis associated with menopause
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Low‐Dose Oral Minoxidil in Lichen Planopilaris: Efficacy and Safety
- A hair loss pandemic: 19 cases of COVID-19 induced telogen effluvium
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Infections, Infestations and Neoplasms of the Scalp
- Hair shaft disorders in children – An update
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- TONGUE, RED
- Off-label uses of retinoids in dermatology
- Hirsutism: diagnosis and treatment
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Subject Index
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Dilated tonic pupils with tabes dorsalis in neurosyphilis as first manifestation of HIV/AIDS: a video report
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report