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Research 61–90 of 1000+
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- A Mutation of the Androgen Receptor Associated with Partial Androgen Resistance, Familial Gynecomastia, and Fertility*
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Case Series of Frontal Fibrosing Alopecia and Fibrosing Alopecia in a Pattern Distribution: Is There a Familial Correlation?
- Polycystic ovary syndrome
- Genetics of polycystic ovary syndrome: searching for the way out of the labyrinth
- Vitiligo and alopecia areata: apples and oranges?
- Cylindroma as Tumor of Hair Follicle Origin
- Canine Zinc-Responsive Dermatosis
- Eyebrow Loss
- REVIEW OF SO-CALLED ASEPTIC NEUTROPHILIC DERMATOSES
- Women’s Health Considerations for Lipid Management
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Early onset androgenetic alopecia in men and associated risk factors: a hospital based study
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Fibrosing alopecia in a pattern distribution in two brothers with pili multigemini
- Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families
- The Skin and Subcutaneous Tissues
- Hair loss and cardiovascular health
- Adrenal causes of endocrine hypertension in childhood or adolescence
- 42761 The elusive BAP1 mutation in pediatric melanocytic tumors
- Spiny Keratoderma
- “Be Enthusiastic – Be Curious”
- Inflammatory and non-melanocytic tumoral pathology of the nail
- A University Center for the Performing Arts