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Research 301–330 of 1000+
- Androgen Replacement in Women: A Commentary
- Androgens and Female Sexual Function and Dysfunction—Findings From the Fourth International Consultation of Sexual Medicine
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- The role of macrophages in skin homeostasis
- Polycystic Ovaries Are Inherited as an Autosomal Dominant Trait: Analysis of 29 Polycystic Ovary Syndrome and 10 Control Families
- Telogen effluvium: a comprehensive review
- Nonclassic adrenal hyperplasia
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Pediatric Systemic Lupus Erythematosus: More Than a Positive Antinuclear Antibody
- The therapeutic use of androgens in women
- Do Changes in Chromosomes Cause Aging?
- Long-Term Bezafibrate Treatment Improves Skin and Spleen Phenotypes of the mtDNA Mutator Mouse
- Scalp condition impacts hair growth and retention via oxidative stress
- ‘A detective look’ at hair biopsies from African-American patients
- What may be the markers of the male equivalent of polycystic ovary syndrome?
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- CLINICAL AND LABORATORY EVALUATION OF AIDS TRICHOPATHY
- The rationale for physiological testosterone replacement in women
- LACK OF EFFECT OF OESTROGENS ON ADRENAL ANDROGEN SECRETION IN CHILDREN AND ADOLESCENTS WITH A COMMENT ON OESTROGENS AND PUBIC HAIR GROWTH
- Use of Hair Products Containing Hormone or Placenta by US Military Personnel
- Prevalence of metabolic syndrome in the family members of women with polycystic ovary syndrome from North India
- A descriptive study of alopecia patterns and their relation to thyroid dysfunction
- Proposing a Simpler Classification of Telogen Effluvium
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Expression patterns of the glial cell line–derived neurotrophic factor, neurturin, their cognate receptors GFRα-1, GFRα-2, and a common signal transduction element c-Ret in the human skin hair follicles
- Epidermal Deletion of Rac1 Causes Stem Cell Depletion, Irrespective of whether Deletion Occurs during Embryogenesis or Adulthood
- The Influence of Age-Related Cues on Health and Longevity
- Congenital adrenal hyperplasia
- Prematurity: is it a risk factor for striae distensae?