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- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Uncombable hair (pili trianguli et Canaliculi): Evidence for dominant inheritance with complete penetrance based on scanning electron microscopy
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Congenital hypotrichosis due to short anagen
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- The role of microneedling in treatment of melasma
- Diagnostic approach to low‐renin hypertension
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Primary cicatricial alopecias
- Premature graying of hair
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- The clinical spectrum of parathyroid disease
- Molecular Genetics of Alopecias
- Secondary cicatricial and other permanent alopecias
- Review of Human Hair Follicle Biology: Dynamics of Niches and Stem Cell Regulation for Possible Therapeutic Hair Stimulation for Plastic Surgeons
- Clinical manifestations of polycystic ovary syndrome
- Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability