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Research 271–300 of 1000+
- Guadalupe fur seal alopecia: a metabolic syndrome associated to climatic anomalies?
- Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
- Generalized hypertrichosis after 5% minoxidil solution in trichorhinophalangeal syndrome: A case report and review of the literatures
- Iatrogenic Cushing Syndrome and Secondary Adrenal Insufficiency Due to an Interaction Between Fluticasone and Ritonavir
- Disorders of the Hair and Nails
- Hair loss evolving into a lifestyle and metabolic phenotype: A hypothesis exploring oxidative stress and acquired androgen sensitivity through reactive oxygen species
- Balding by 25: 5 Real Reasons Indian Men Are Losing Hair Decades Early (It's Not Just Genes)
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Clinical and Trichoscopy Features in Trichorhinophalangeal Syndrome: A Multicenter Retrospective Study
- Androgenetic alopecia and metabolic syndrome: from mechanisms to treatment strategies
- Netherton Syndrome – Responding to Oral Retinoids
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Skin as a mirror of metabolic syndrome: Do some dermatoses alarm internal metabolic sinister?
- Clinical case of Vogt–Koyanagi–Harada syndrome
- Two Incidental Sibling Diagnoses of Netherton Syndrome in Separate Visits: A Case Report
- Association of Obesity and Bariatric Surgery on Hair Health
- Vulvovaginal involvement in Netherton syndrome: A case report
- Alopecia Universalis with Frequently Relapsing Nephrotic Syndrome of Infantile Onset: A Rare Presentation
- SAT320 Cyclic Cushing Syndrome Caused By An ACTH-Producing Pheochromocytoma
- Gynecological and dermatological aspects of diagnostics of polycystic ovary syndrome from puberty to menopause
- Treatment of Alopecia Universalis in a Child with Down Syndrome
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- A rare clinical image of hypertrichosis (Werewolf syndrome)
- Data_Sheet_1_Disruption of Hars2 in Cochlear Hair Cells Causes Progressive Mitochondrial Dysfunction and Hearing Loss in Mice.docx
- Hair Shaft Disorders
- Síndrome de ovarios poliquísticos Polycystic ovary syndrome
- Sheehan Syndrome Leading to Acute Systolic and Diastolic Heart Failure: A Case Report
- Unusual Presentation of Rapunzel Syndrome in an 8-Year-Old Girl