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Research 61–90 of 213
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Autoimmune Diseases and Acquired Von Willebrand Disease in Two Cases of Progeria
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Disorders of pigmentation in infants and children
- Hair That Is Difficult to Manage in a Hispanic Girl
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- A Clinical Approach to Severe Insulin Resistance
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Pathology of Mouse Models of Accelerated Aging
- Diseases of Periocular Hair
- Quoi de neuf en recherche dermatologique ?
- Premature graying of hair
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Assessment of scalp hair survivin in patients with premature greying of hair
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- ST Premature Graying Hair in Seven Years Old Children
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Replicative stress, stem cells and aging
- Restoring neuropetide Y levels in the hypothalamus ameliorates premature aging phenotype in mice
- The Pattern of Hair Dyeing in Koreans with Gray Hair
- Hair loss
- Therapeutic approach and management of Marz-e-Shayb (Premature greying of hair) in the perspective of Unani medicine: A case study
- Hair Shaft Dysplasias
- Hair loss in elderly women
- Relationship between diet, atopy, family history, and premature hair graying
- The Microanatomy of Human Skin in Aging
- Aging Skin: A Window to the Body
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- Aging in hair follicle stem cells and niche microenvironment
- The urine as a diagnostic key for a homozygous EGFR mutation