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Research 931–960 of 1000+
- Cutaneous lupus erythematosus
- Ovarian Hypertension: Polycystic Ovary Syndrome
- Epoxy Fatty Acids and Inhibition of the Soluble Epoxide Hydrolase Selectively Modulate GABA Mediated Neurotransmission to Delay Onset of Seizures
- Targeted delivery of extracellular vesicles: the mechanisms, techniques and therapeutic applications
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- The Evaluation and Management of Hirsutism
- <i>Hoxc13</i> and the development of hair follicle
- Hair loss
- 66-Year-Old Woman With Painless Vesicular Lesions
- Discreet monilethrix: De novo mutation on the example of polish families
- Alopecia and cardiovascular events
- P-19 A case of Birt Hogg Dube syndrome presented with parathyroid carcinoma
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Management of Polycystic Ovary Syndrome in Women by Implementing a Healthy Lifestyle and Effective Diet: A Review
- Case 3: The Hypothermic Newborn
- POLYCYSTIC OVARY SYNDROME (PCOS)–AN OVERVIEW
- An Infant with Worsening Rash
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- Hair Loss Effects and Surgical/Drug Treatments for the Alopecias
- Efficacy, Safety, and Real-World Aspects of Janus Kinase Inhibitors to Treat Patients With Alopecia Areata
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- New Pharmaceutical Concepts for Sebaceous Gland Diseases: Implementing Today’s Pre-Clinical Data into Tomorrow’s Daily Clinical Practice
- Double Dosing
- Oral Retinoids in Dermatology
- Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome