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Research 151–180 of 1000+
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Beneficial effect of spironolactone on androgenic alopecia
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- <i>CCDC47</i> gene and trichohepatoneurodevelopmental syndrome: Report of the fifth and sixth cases from Saudi Arabia
- Skin signs in the diagnosis of thallium poisoning
- Management of diffuse alopecia
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- TELOGEN EFFLUVIUM: AN ETIOPATHOGENETIC THEORY
- Value of dermoscopy for the diagnosis of monilethrix
- Morphological changes in the skin in a rat model of stress-induced alopecia and their correction with nutrients
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Comparison of Alopecia areata in Human and Nonhuman Mammalian Species
- Anagen effluvium due to thallium poisoning derived from the intake of Chinese herbal medicine and rodenticide containing thallium salts
- Treatment and prevention of chemotherapy-induced alopecia with PTH-CBD, a collagen-targeted parathyroid hormone analog, in a non-depilated mouse model
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Selenium poisoning from consumption of contaminated wheat: a case series from rural Maharashtra, India
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Viral-Associated Trichodysplasia of Immunosuppression
- Obsessive-compulsive disorder in dermatology
- การศึกษาการเปลี่ยนแปลงของเส้นผมและหนังศีรษะในผู้ป่วย SLE
- Acquired Zinc Deficiency Dermatosis in Man
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- Pincer Nails – A Rare Manifestation of Systemic Lupus Erythematosus
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome