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Research 181–210 of 1000+
- Blood zinc levels in nursing women from different regions of the West Bank of Palestine
- Developmental Toxicity of Levo-Alpha-Acetylmethadol (LAAM) in Tolerant Rats
- Studying the efficacy of a new radical treatment for acne vulgaris using a surgical technique
- Inconsolable Crying in Infants: Differential Diagnosis in the Pediatric Emergency Department
- Book Reviews
- Alopecia and Its homoeopathic treatment
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Program and Abstract of 16th APALMS 2018
- The skin findings of pregnant women and our treatment choices. A Turkish experience: a 5-year survey.
- Minoxidil
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- Clinical Management in Psychodermatology
- Syndromes of Severe Insulin Resistance (SSIRs)
- Atlas of Geriatric Dermatology
- A case report of a novel, integrative approach to Hashimoto’s thyroiditis with unexpected results
- The Case of the Elusive Androgen
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- Farmácia São Lázaro - Porto e nos Serviços Farmacêuticos do Hospital Privado de Vila Real (Grupo Trofa Saúde) - Vila Real
- TRICOSCOPIA – ESTRUTURAS TRICOSCÓPICAS E SUA APLICABILIDADE NAS PATOLOGIAS DO CABELO E DO COURO CABELUDO
- Particularidades dermatológicas, fisiológicas e as dermatoses na pele negra
- 9 Role of 5α-reductase in health and disease
- Quality of life in children with scalp hair loss: a Clinico-epidemiological study
- Hair in the Wrong Place
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Neurotrichosis: Hair‐shaft Abnormalities associated with Neurological Diseases
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Disorders of hair in infants and children other than alopecia
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review