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Research 871–900 of 1000+
- Berardinelli–Seip syndrome
- A Silvery Hair Revolution: Case Report of Marie Antoinette Syndrome in a Child
- Clinical Presentation of Polycystic Ovary Syndrome
- A 7‐Year‐Old Male With a Linear Band‐Like Hair Patch
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- PA33 When bones speak through nails: insights from a paediatric case series
- Premature isolated adrenarche in a six-year-old girl
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Supplementary Material for: A Silvery Hair Revolution: Case Report of Marie Antoinette syndrome in a child
- Supplementary Material for: A Silvery Hair Revolution: Case Report of Marie Antoinette syndrome in a child
- Glucocorticoids and mineralocorticoids in hair: facilitating accurate diagnosis of adrenal-related endocrine disorders
- 7745 Hirsutism in young girls: Beyond PCOS
- 7696 Ovarian Steroid Cell Tumor Presenting As Non-classical Adrenal Hyperplasia
- Diagnosis and Management of Hair Loss in Pediatric
- Hair loss and its Unani concept and management
- Nonfebrile Seizures in Pediatrics: Key Points to Remember
- Targeting Pharmacological and Nanotechnology Based Therapeutics for Management of Hirsutism: A Comprehensive State-of-the-Art
- Severe Hypernatremia as Presentation of Netherton Syndrome
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- A Review on-Types and Treatment of Alopecia
- A solitary triangular alopecia
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Chemical Danger in Hair Keratin Care
- Hirsutism and Hypertrichosis
- Alternative androgen pathways
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review