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Research 271–300 of 1000+
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Clinical Hair Loss: Diagnosis and Treatment
- Interleukins gene polymorphism in alopecia areata patients: a systematic review
- Acne as a chronic systemic disease
- Biotin and Acetazolamide for Treatment of an Unusual Child With Autism Plus Lack of Nail and Hair Growth
- The Review on Alopecia Areata : A Comprehensive Review of Pathogenesis, Diagnosis, Clinical Pattern and Remedies
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Hormonal regulation of hair follicles exhibits a biological paradox
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Generation of a Novel Inducible and Dermal Papilla‐Specific <i>Wif1‐CreER</i> Knock‐In Mouse Line for Hair Follicle Research
- Premature graying of hair: Risk factors, co‐morbid conditions, pharmacotherapy and reversal—A systematic review and meta‐analysis
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Trichothiodystrophy in a child with occult learning disorder
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Hormonal and Genetic Controls of Hirsutism: Link Between hyperprolactinemia, Polycystic ovary syndrome and Hirsutism
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Primary scarring alopecias. A literature review
- <i>De novo</i> mutations in monilethrix
- Androgеnеtic Alopеcia Pathogеnеsis, Diagnosis, and Trеatmеnt
- Androgenetic alopecia updates: Pathophysiology, diagnosis and treatment