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Research 181–210 of 362
- Contents Vol. 4, 2018
- Trichoscopy and Trichogram
- A Look Back at Hair Restoration through History
- Dermatopathology Workshop Summary, Berlin 2004
- Hair Today
- Analysis of Female Pattern Hair loss
- Frequency of the Types of Alopecia at Twenty-Two Specialist Hair Clinics: A Multicenter Study
- Primary Scarring Alopecia: Clinical-Pathological Review of 72 Cases and Review of the Literature
- Exfoliative cutaneous lupus erythematosus in German shorthaired pointer dogs: disease development, progression and evaluation of three immunomodulatory drugs (ciclosporin, hydroxychloroquine, and adalimumab) in a controlled environment
- Clinical Approach to the Patient With Alopecia
- Vertical vs. transverse sections of scalp biopsy specimens: a pilot study on the comparison of the diagnostic value of two techniques in alopecia
- Dilation of Multiple Eccrine Ducts as a Highly Specific Marker for Cicatricial Alopecia
- Social Status May Interfere in the Prognosis of Frontal Fibrosing Alopecia in Female Patients: An Observational Study
- Dermatology and Pregnancy
- Line-Field Optical Coherence Tomography: Usefulness in the Non-Invasive Differential Diagnosis of Congenital Alopecia of Infancy
- Retrospektive Analyse von Wirksamkeit, Sicherheit, prognostischen Parametern und Faktoren der Lebensqualität bei der topischen Immuntherapie der Alopecia areata mit Diphenylcyclopropenon
- 4 Platelet-Rich Plasma for Alopecia and Hair Restoration
- Therapeutic Updates on Lichen planopilaris and Frontal Fibrosing Alopecia: A Systematic Review
- Subject Index
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- The role of vitamin D receptor mutations in the development of alopecia
- Ichthyosis Follicularis With Alopecia and Photophobia
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Expert consensus on the management of telogen effluvium in India
- Telogen Effluvium
- Nonshaven Follicular Unit Extraction
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis