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Research 961–990 of 1000+
- A Mutation of the Androgen Receptor Associated with Partial Androgen Resistance, Familial Gynecomastia, and Fertility*
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Economic disparities in parental hair cortisol are associated with externalizing behavior in children
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Alopecia: Association with Resistance to Thyroid Hormones
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- [Monilethrix--rare syndrome of structural hair abnormalities].
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Association of Frailty Index with Clinical BPH Progression and Serious Adverse Events: the MTOPS Trial
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Prodrugs of butyric acid from bench to bedside: Synthetic design, mechanisms of action, and clinical applications
- Familial scarring alopecia associated with scalp psoriasis
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Cantú syndrome with coexisting familial pituitary adenoma
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- A Clinical Study of Androgenetic Alopecia (III)
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Coordinated inhibition of SOX9 and cell cycle progression by microRNA-200 restricts sebaceous gland fate specification
- Pancytopenia in epidemic dropsy: a case report
- Association of Baldness with Coronary Artery Disease and Its Severity
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- Trichoscopic Features, Clinical Correlates, and Risk Prediction in Female Pattern Hair Loss: A Retrospective Case-Control Study
- Trichoscopic Features, Clinical Correlates, and Risk Prediction in Female Pattern Hair Loss: A Retrospective Case-Control Study
- Biotinidase Enzyme Deficiency ( Case Report )
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization