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Research 601–630 of 1000+
- Hair Disorders
- Committee on database of hair restoration results on patients with cicatricial alopecia and hair diseases other than androgenetic alopecia
- Dermatologic Disorders
- Corticotropin releasing factor-1 receptor antagonism associated with favorable outcomes of male reproductive health biochemical parameters
- Clinical and trichoscopic characteristics of temporal triangular alopecia: A multicenter study
- Adult Patients with Aphallia: Were they Fertile?
- CECHY ZASTOSOWANIA FIZJOTERAPII WRODZONEGO KRĘCZU SZYI
- Hair Shaft Disorders
- Alopecia Triangular Temporal. Revisión de las manifestaciones clínicas y Dermatoscópicas.
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Persistent Hypoglycemia and Macrosomia in a Newborn
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"
- Follicular ichthyosis
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Pathologic Quiz Case: An Anterior Neck Mass in a 5-Month-Old Female Infant
- A Case of Hair Transplantation in a Nevus Sebaceus Followed by Secondary Tumors, Maintaining the Hair Cycle for Approximately 40 years
- 236 Wnt/planar cell polarity impairment and the genetics of yellow nail syndrome
- Clinical report of a Holstein's calf with ichthyosis.
- From the Elephant Man to Barbie Girl: Dissecting the Freak from the Margins to the Mainstream
- Cell Polarization Defects in Early Heart Development
- Association between digit ratio (2D:4D) and palmaris longus muscle agenesis according to gender: a radiological study
- A clinical case of familial alopecia areata in combination with immune pathology
- Fetal Arrhythmia with a Myriad of Complications
- Trichorrhexis Nodosa Secondary to Argininosuccinicaciduria
- Trichorhinophalangeal Syndrome
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14