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Research 271–300 of 1000+
- 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
- Autosomal Dominant Obstructive Sleep Apnea Syndrome Due to the New Variant c.980_984dup in COL1A2: A Case Report
- Serum markers thrombophilia in pregnant women with Systemic Lupus Erythematosus
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Pathology in Practice
- Serine palmitoyltransferase and peripheral neuropathy: studies on neuropathy-causing mutations and their biochemical hallmarks
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Female Androgenetic (?) Alopecia
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Alopecia X em cães: revisão