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Research 151–180 of 1000+
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Hypotrichosis and Hair Loss on the Occipital Scalp
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Case of autosomal recessive woolly hair/hypotrichosis with compound heterozygous mutations in the <i>LIPH</i> gene at c.742C > A and c.614A > G: The first Japanese case
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Botanical extracts in combination improve autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Hypotrichosis and Alopecia
- Hypotrichosis in a child with olmsted syndrome
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Clinicopathological insights into the phenotypic variation of autosomal recessive hypotrichosis/wooly hair by c.736T>A LIPH mutation
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Hypertrichose
- Hypotrichosis congenita of Marie Unna
- Bimatoprost in the treatment of eyelash hypotrichosis
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- Acquired Hypertrichosis Lanuginosa: A Rare Cutaneous Paraneoplastic Syndrome
- Generalized hypertrichosis after treatment with topical minoxidil
- What are the Factors That Induce Paradoxical Hypertrichosis After Laser Hair Removal?
- Traumatic panniculitis with localized hypertrichosis: Two new cases and considerations