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Research 151–180 of 1000+
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Localized Telogen Effluvium after Face Lift Surgery
- Discreet monilethrix: De novo mutation on the example of polish families
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Trichorrhexis Nodosa Secondary to Argininosuccinicaciduria
- Morphological analyses in fragility of pili torti with Björnstad syndrome
- Acute telogen effluvium associated with SARS-CoV-2 infection
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Loose anchoring of anagen hairs and pili torti due to erlotinib
- Hair shaft miRNA‐221 levels as a new tumor marker of malignant melanoma
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Cysteine and Glutamine level in hair shaft fractures patients
- 1376 Dermal white adipose tissue enhances proliferation, pigmentation and hair shaft elongation in human hair follicles ex vivo
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Hair growth promoting effects of adipose tissue-derived stem cells
- Hair shaft disorders in children – An update
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Dermatoscopy of hair shaft disorders
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- Woolly Hair in Two Siblings
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity