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Research 31–60 of 1000+
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Masquerading of trichotillomania in a family with monilethrix
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Monilethrix
- Trichoscopy in alopecias: Diagnosis simplified
- Treatment of monilethrix with oral minoxidil
- Monilethrix: an ultrastructural study
- Relação entre alopecia, estresse crônico e alterações no eixo hipotálamo-hipófise-adrenal: uma revisão integrativa de literatura
- [Studies on monilethrix].
- Discreet monilethrix: De novo mutation on the example of polish families
- Trichoscopy update 2011
- Monilethrix: A rare hereditary condition
- Hair loss and its management in children
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- Biology and Genetics of Hair
- Sparse hair in a female toddler
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Monitoring chemotherapy‐induced alopecia with trichoscopy
- SlPHL1, a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
- Intermittent and Persistent Type 2 lupus: patient perspectives on two distinct patterns of Type 2 SLE symptoms
- Farmácia Avenida - Guimarães e nos Serviços Farmacêuticos da Unidade Local de Saúde do Alto Ave, EPE - Guimarães
- AVALIAÇÃO DA CRIPTOSPORIDIOSE EM CÃES E SUAS IMPLICAÇÕES NA SAÚDE ÚNICA
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Current Genetics in Hair Diseases