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Research 151–180 of 1000+
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Marie-unna hereditary hypotrichosis
- Obesity in Adults: Position Statement of Polish Association for the Study on Obesity, Polish Association of Endocrinology, Polish Association of Cardiodiabetology, Polish Psychiatric Association, Section of Metabolic and Bariatric Surgery of the Association of Polish Surgeons, and the College of Family Physicians in Poland
- Androgenetic Alopecia in Polycystic Ovary Syndrome: A Cutaneous Marker of Systemic Metabo-inflammatory and Endocrine Dysfunction: A Narrative Review
- Immortality Reconsidered: Clinical Challenges at the Frontier of Plastic Surgery
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Causal Link of Distinct Mental Disorders with Androgenetic Alopecia and Alopecia Areata: A Bidirectional Two-Sample Mendelian Randomization Study
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Review on Alopecia Areata in the Middle East and Africa: Landscape and Unmet Needs
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- An unusual presentation of X-linked adrenoleukodystrophy
- Polycystic ovary syndrome
- Female pattern hair loss
- Androgenetic Alopecia: A Review
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Biotinidase deficiency characterized by skin and hair findings
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Successful Management of Trichotillomania with an Integrated Approach: A Case Study
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies
- Erythromelanosis Follicularis Faciei et Colli: A Case Report
- Drug-induced male infertility: a real-world study using FAERS and EudraVigilance databases
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Fertility and Sterility Vol 101 No 4, April 2014
- Review of Pippalyadi Agad in Cumulative Toxicity of Cosmetics w.s.r. to Dushivisha
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin