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Research 91–120 of 106
- Clinical Management in Psychodermatology
- An Evaluation System to Enhance Patient Selection for Alopecia-Reducing Surgery
- Cutaneous manifestations of systemic infection in children
- P448: Identification of a novel RPS6KA3 variant in a female child with features of Coffin-Lowry syndrome: A case study
- Ceramide Synthase 4 Regulates Stem Cell Homeostasis and Hair Follicle Cycling
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- The sternum reconstruction: Present and future perspectives
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Chemical Scalp Burn after Hair Coloring—Case Report with Literature Review
- TONGUE, RED
- Inhibition of neurosteroid synthesis increases asphyxia-induced brain injury in the late gestation fetal sheep
- Allopregnanolone Alters the Gene Expression Profile of Human Glioblastoma Cells
- Simultaneous Determination of Selected Steroids with Neuroactive Effects in Human Serum by Ultrahigh-Performance Liquid Chromatography–Tandem Mass Spectrometry
- Recent Progress in Health Benefits of Hederagenin and Its Glycosides
- Causes and therapeutic limitations of clinical alopecia and the advent of human pluripotent stem cell follicular transplantation
- Becker's Nevus Syndrome
- Síndrome do nevo de Becker
- Cantú syndrome with coexisting familial pituitary adenoma
- Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature
- Uncombable hair syndrome and beyond
- Oral Manifestations of Hematologic and Nutritional Diseases
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Ptosis in childhood
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- E-Poster
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Autologous platelet-rich plasma (PRP) to treat androgenetic alopecia: evidence synthesis, analysis of technological standards, and pros- pects for a personalized approach (a literature review)
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- Rare clinical features of the Ellis van Creveld syndrome: A case report and literature review