Search
for
Sort by
Research 301–330 of 1000+
- ALOPESİ AREATA OLGULARINDA SANAT TERAPİSİNİN KULLANILMASI: BİR OLGU SUNUMU
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- Vitamin D-dependent Rickets Type II
- Clinical case of alopecia totalis in pediatric practice
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Clouston’s Syndrome-A Case Report
- Eruptive syringomas in Down’s syndrome
- 20th Annual Symposium of the British Society of Paediatric Dermatology, 11-12 November 2005, Newcastle upon Tyne, U.K.
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- Short anagen syndrome
- Minoxidil Topical Solution
- Childhood epidermolysis bullosa acquisita during squaric acid dibutyl ester immunotherapy for alopecia areata
- Alopecia Areata Universalis After Phenobarbital-Induced Anti-Convulsant Hypersensitivity Syndrome
- A sharply marginated erythematous dermatitis in a toddler
- KERION MICROSPORICUM WITH HEMATOGENOUS AND ECTOGENOUS MICROSPORIDS
- Cyclosporine-induced alopecia:a case report, FDA adverse event reporting system analysis and literature assessment
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- Botanical extracts in combination improve autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations
- Successful Treatment of Tinea Capitis Caused by Microsporum canis Using Griseofulvin
- Trachyonychia with juvenile pityriasis rubra pilaris
- Alopecia areata during the convalescent phase of kawasaki disease
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- A six-year old girl presenting with alopecia areata incognita: a case report
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- Hair as an Index of Protein Malnutrition
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- Chronic nonhealing ulcer in a finger of a toddler – a rare presentation of the hair thread tourniquet syndrome
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy