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- Familial aggregation of alopecia areata
- Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Family History and Risk of Hair Loss
- Association of premature hair graying with family history, smoking, and obesity: A cross-sectional study
- Familial and Sporadic Porphyria Cutanea Tarda
- Case series of familial frontal fibrosing alopecia and a review of the literature
- Familial Nonmembranous Aplasia Cutis of the Scalp
- Familial Occurrence of Eruptive Vellus Hair Cysts
- Familial scarring alopecia associated with scalp psoriasis
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Analysis of familial factors using the basic and specific (BASP) classification in Korean patients with androgenetic alopecia
- Familial frontal fibrosing alopecia treated with dutasteride, minoxidil and artificial hair transplantation
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Central centrifugal cicatricial alopecia: possible familial aetiology in two African families from South Africa
- Family planning 2011: better use of existing methods, new strategies and more informed choices for female contraception
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Familial Sexual Precocity
- Familial frontal fibrosing alopecia: A cross‐sectional study of 20 cases from nine families
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Familial frontal fibrosing alopecia in two male families
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Familial hypertriglyceridemia in pregnancy
- Familial Androgenetic Alopecia in Siblings with Normal Endocrinological Status
- Familial patterns of alopecia areata: A systematic review and meta-analysis
- Familial Background in Aberrant Mammary Tissue Is a ‘Protective’ Factor against the Development of Nephrourinary Anomalies
- Familial Frontal Fibrosing Alopecia
- Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families
- FAMILY ACTIONS TO OVERCOME THE SIDE EFFECTS OF CHEMOTHERAPY IN PATIENTS AT HOME