Search
for
Sort by
Research 511–540 of 1000+
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Fundamentals
- Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions
- Male androgenetic alopecia
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- FGF5 is a crucial regulator of hair length in humans
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Female Pattern Hair Loss: a clinical and pathophysiological review
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Evaluation of noninvasive biospecimens for transcriptome studies
- Monilethrix in three generations
- RETRACTED: Serum lipids may causally affect the occurrence of alopecia areata: A Mendelian randomization study
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Diagnostic imaging in congenital adrenal hyperplasia – how does it help?
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Familial Frontal Fibrosing Alopecia
- Pili trianguli et canaliculi as a phenotypic subtype in patients with central centrifugal cicatricial alopecia: A scanning electron microscopy study
- Understanding sex and gender disparities in COVID-19 mortality: a narrative review beyond biology
- The first 20 years of skin of color dermatology: An era of advancements in skin, hair, and nail disorders
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality