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Research 211–240 of 1000+
- Alopécie androgénogénétique chez la femme
- Male pattern hair loss
- Society's Knowledge About Physiological Causes of Hair Loss: A Cross-Sectional Study at The University of Basrah
- Clinical Snippets
- New Publications
- Advances in the treatment of androgenetic alopecia
- Relation between dermal papilla cells and androgenetic alopecia
- Associaton of Insulin Resistance Linked Diseases and Hair Loss in Elderly Men. Finnish Population-based Study
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Two females with hair loss
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Polarized microscopy in genetic hair disorders: case series
- Androgenic alopecia and differential diagnoses of alopecia
- Eziopatogenesi e terapia dell'acne:studio epidemiologico delle caratteristiche cliniche di una popolazione di pazienti affetti da acne e analisi dei polimorfismi del gene codificante per il recettore degli androgeni e del gene codificante per il citocromo P-450 1A1
- Androgenic alopecia
- TREATMENT OF HAIR LOSS
- Androgenetic alopecia: Quality-of-life and associated lifestyle patterns
- Vitamin D‐dependent rickets type I and type II
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Role of caffeine in the management of androgenetic alopecia
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Leukokoria sebagai Tanda Peringatan Penyakit Coats dan Gangguan Retina Lainnya
- Hair loss
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- Study of Postpartum Alopecia
- Molecular Genetics of Alopecias
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia