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Research 421–450 of 1000+
- Structures of three polycystic kidney disease-like domains from<i>Clostridium histolyticum</i>collagenases ColG and ColH
- Successful Treatment of Temporal Triangular Alopecia by Hair Restoration Surgery Using Follicular Unit Transplantation
- Possible Carbamazepine-Induced Reversible Onychomadesis
- Kerion
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- Imipramine-lnduced Alopecia Areata-like Lesions
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Rhomboid Minigrafts in Hair Restoration Surgery
- Keratosis Follicularis Spinulosa Decalvans: Diagnosis and Therapeutic Evaluation.
- Trichoscopic changes in tinea capitis before and after treatment
- Two Cases of Danon Disease – A ‘Cousin’ of Pompe Disease
- The structure of people’s hair
- Keratosis Follicularis Spinulosa Decalvans Associated with Acne Keloidalis Nuchae and Tufted Hair Folliculitis
- Performance scanning electron microscopic investigations and elemental analysis of hair of the different animal species for forensic identification
- Scanning electron microscopy and morphometric analysis of the hair in dromedaries with SEM-EDX in relation to age
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Ichthyosis follicularis with alopecia and photophobia syndrome with coexisting palmoplantar keratoderma treated with acitretin
- P448: Identification of a novel RPS6KA3 variant in a female child with features of Coffin-Lowry syndrome: A case study
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Perspectives of Kennedy's disease
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Change in Hair Color in Mice Induced by Injection of α-MSH
- Efficacy of platelet-rich plasma in the treatment of androgenetic (male-patterned) alopecia: A pilot randomized controlled trial
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Structural and dynamic insights into substrate binding and catalysis of human lipocalin prostaglandin D synthase
- Folliculosebaceous cystic hamartoma with hair shaft fragments.
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum