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Research 571–600 of 1000+
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- A Case Report of Kaphaja Granthi w.s.r. to Trichilemmal Cyst
- Sparse Brittle Hair and Bilateral Temporal Alopecia in a Child
- ST Premature Graying Hair in Seven Years Old Children
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- Dermoscopic Features of Pili Annulati: Features of PA
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- The Role of rs6152 Allele and Non-Genetic Factors in Androgenetic Alopecia: A Pilot Study in the Indonesian Local Population
- Reviewer #3 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Pearly Pinna Papules in a Young Female
- Hypotrichosis and Hair Loss on the Occipital Scalp
- Molecular Basis of Hereditary Hair Diseases
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Evaluation of hair structural abnormalities in children with different neurological diseases
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Clinical and molecular genetic studies in hereditary hair loss
- Clinical report of a Holstein's calf with ichthyosis.
- Hair Shaft Defect in a Teenage Girl: Trichoscopy Saves the Day!
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Two females with hair loss
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Monilethrix – Case report of a rare disease
- Disorders of Keratinization