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Research 451–480 of 1000+
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- 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
- 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
- Familial Sexual Precocity
- 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 Dyskeratotic Comedones: A Case Report and Literature Review
- Familial congenital generalized hypertrichosis
- Familial coexistence of vitiligo and alopecia areata: successful treatment with intralesional corticosteroids
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- A clinical case of familial alopecia areata in combination with immune pathology
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- How safe and effective is minoxidil for familial baldness in women?
- Familial association of polycystic ovary syndrome (PCOS) in women attending the gynaecological endocrinology clinic at Groote Schuur Hospital
- Analysis of familial history in Chinese patients with androgenetic alopecia