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Research 961–990 of 1000+
- 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 Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- Hair That Is Difficult to Manage in a Hispanic Girl
- 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
- A Unique Case of Pili Multigemini Complicated by Folliculitis: Unveiling the Intricacies of a Rare Hair-Follicle Disorder
- Long-Term Effects of Sirolimus on Human Skin TSC2-Null Fibroblast‒Like Cells
- Alopecia management from a comparative perspective: pharmacological and pharmaceutical insights in humans, dogs, and cats
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- 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
- Animals in Dermatology
- 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
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- 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
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1