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Research 631–660 of 1000+
- Delayed Diagnosis of Familial Adenomatous Polyposis-related Colon Cancer in an Adolescent with Coexisting Eating Disorder: A Case Report
- O cuidado à família de portadores de transtorno mental: visão dos trabalhadores
- Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
- Dominant dystrophic epidermolysis bullosa: Seven familial cases
- Effectiveness of Anastrozole and Cyproterone Acetate in Two Brothers with Familial Male Precocious Puberty
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- An alternative diagnostic method of eruptive vellus hair cysts: Report of a familial case with pruritus
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- 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
- 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
- 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
- 42761 The elusive BAP1 mutation in pediatric melanocytic tumors
- Spiny Keratoderma
- “Be Enthusiastic – Be Curious”
- Inflammatory and non-melanocytic tumoral pathology of the nail