Search
for
Sort by
Research 211–240 of 1000+
- Syndromes of Severe Insulin Resistance (SSIRs)
- The hair in childhood and old age
- The Pilocutaneous Syndrome of Menopause
- Polarized microscopy in genetic hair disorders: case series
- Mitochondrial dysfunction in metabolic syndrome and inflammatory skin disease
- Comment on Current Investigations into the Postfinasteride Syndrome
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Hypotrichosis in a child with olmsted syndrome
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Hair Loss: A Harbinger of the Morbidities to Come!
- Tourniquet syndrome in children (literature review and own observation)
- Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
- Clinico-Epidemiological, Trichoscopic, and Light Microscopic Evaluation of Pediatric Hair and Scalp Disorders: A Cross-Sectional Study from a Tertiary Care Hospital
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- Hair cortisol analysis: An update on methodological considerations and clinical applications
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Polycystic Ovary Syndrome
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Sjögren's Syndrome in Scurvy
- Metabolic syndrome and the skin: a more than superficial association. Reviewing the association between skin diseases and metabolic syndrome and a clinical decision algorithm for high risk patients
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Basaloid follicular hamartoma, total body hair loss and SLE
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Alopecia and the metabolic syndrome
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Polycystic ovary syndrome (PCOS)
- State-dependent signaling by Ca<sub>v</sub>1.2 regulates hair follicle stem cell function
- Long‐Term Management with Adipose Tissue‐Derived Mesenchymal Stem Cells and Conventional Treatment in a Dog with Hepatocutaneous Syndrome
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population