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Research 61–90 of 1000+
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Therapy of hypertrichosis
- Piggyback‐Acquired Hypertrichosis
- Local hypertrichosis: a rare complication of a temporary henna tattoo
- Hypertrichosis lanuginosa acquisita associated with autoimmune hepatitis
- ROLLED HAIRS AND HYPERTRICHOSIS
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- Postcast hypertrichosis in a patient with frontal fibrosing alopecia
- Momentary fluke of cyclosporine in incidental repigmentation and hypertrichosis of hair
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genital Rejuvenation: The Next Frontier in Medical and Cosmetic Dermatology
- Enhancing the Growth of Natural Eyelashes: The Mechanism of Bimatoprost-Induced Eyelash Growth
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Generalized hypertrichosis after 5% minoxidil solution in trichorhinophalangeal syndrome: A case report and review of the literatures
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- 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
- Botanical extracts in combination improve autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations
- 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