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Research 871–900 of 1000+
- Premature aging syndromes: From patients to mechanism
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Eyelash Transplantation Using Leg Hair by Follicular Unit Extraction
- Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects
- Clinical study on the effect of biotin on skin conditions in dogs
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Use of fluorescent light energy for the management of bacterial skin infection associated with canine calcinosis cutis lesions
- GRowing an Epidermal Tumor
- Congenital atrichia associated with situs inversus and mesocardia
- Congenital atrichia with papular lesions
- Hypotrichosis with juvenile macular dystrophy
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Connexin mutations in human disease
- Value of dermoscopy for the diagnosis of monilethrix
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Refractory/relapse thrombocytopenia in a patient with Evans' syndrome successfully treated with zanubrutinib
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms
- Steroid Responsive Mononeuritis Multiplex in the Cronkhite–Canada Syndrome
- Introduction to JID Symposium Proceedings 52nd Annual Montagna Symposium on the Biology of Skin “Stem Cells in Skin” Held at Snowmass, Colorado, USA, June 13–17, 2003
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Poster presentationsDP11 Bright, eosinophilic intracytoplasmic inclusion bodies: a rare presentation of acquired epidermodysplasia verruciformis with widespread human papillomavirus infection in a transplant recipient
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- A case of chronic kidney disease patient with rapid deterioration of renal function, hair loss, and spontaneous resolution of facial warts after COVID‐19 infection
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Characterization of Rickets Type II Model Rats to Reveal Functions of Vitamin D and Vitamin D Receptor
- S2608 A Rare Case of Iron Deficiency Anemia: Cronkhite-Canada Syndrome