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Research 61–90 of 1000+
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Molecular Genetics of Alopecias
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Woolly Hair in Two Siblings
- Approach to the adult female patient with diffuse nonscarring alopecia
- Review of quality of life studies in women with alopecia
- Providing mesotherapy to prevent and treat hair loss in aesthetic practice
- Biology and Genetics of Hair
- Congenital Atrichia: A Case Report
- Androgenetic Alopecia
- Distancia promedio de la línea de implantación pilosa frontal y sus estructuras en una población de mujeres colombianas
- Follicular Transplantation
- Acquired scalp alopecia. Part I: A review
- Review of Human Hair Follicle Biology: Dynamics of Niches and Stem Cell Regulation for Possible Therapeutic Hair Stimulation for Plastic Surgeons
- The Contribution of Endogenous and Exogenous Factors to Female Alopecia
- The genetically programmed hair growth cycle and alopecia: what is there to know?
- Fibrosing Frontal Alopecia: A comprehensive study to understand its etiology
- Correlation between sebum level and severity of male androgenetic alopecia
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population