Search
for
Sort by
Research 31–60 of 1000+
- Zebrafish Model of Hereditary Pigmentary Disorders
- The Value of Genetic and Non-Genetic Factors in the Emergence and in the Development of Androgenetic Alopecia in Men: Multifactor Analysis
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Clinical characteristics and risk factors of female precocious puberty
- Topical Minoxidil Therapy in Hereditary Androgenetic Alopecia
- Current Genetics in Hair Diseases
- 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
- Consecuencias civiles en el impago de la primera prima o sucesivas de la póliza de seguro en los juicios penales por accidente de tráfico: ¿tiene cobertura por la aseguradora el conductor?
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Alopecia androgenética: aspectos etiopatogênicos, métodos diagnósticos e condutas terapêuticas
- Algorithm of Hair Restoration Surgery in Children
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals
- Various types of alopecia and options of the treatment
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- Assessing the Impact of Alopecia on Quality of Life, Depression, and Self-Esteem in Saudi Arabia
- A Precis of the alopecia (Hair loss) associated with therapies based on nanotechnology and its impact on quality of Life (QoL)
- Photobiomodulation therapy in ophthalmology
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- 66-Year-Old Woman With Painless Vesicular Lesions
- Androgenetic alopecia: Quality-of-life and associated lifestyle patterns
- Biology and Genetics of Hair
- Study of Postpartum Alopecia
- Androgenetic alopecia updates: Pathophysiology, diagnosis and treatment
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Hair loss in children.
- Molecular Genetics of Alopecias
- Molecular mechanisms of androgenetic alopecia
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Increasing of PCOs among Young Females