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Research 91–120 of 1000+
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Disease causing homozygous variants in the human hairless gene
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- A study on histopathological and dermoscopic correlations in pityriasis versicolor
- Specific dermatologic features of the polycystic ovary syndrome and its association with biochemical markers of the metabolic syndrome and hyperandrogenism
- The tumescent technique facilitates hair micrografting
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation
- The urine as a diagnostic key for a homozygous EGFR mutation
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Biotinidase deficiency – clinching the diagnosis rapidly can make all the difference!
- The Tumescent Technique Facilitates Hair Micrografting
- 원저 : Mohs 미세도식 수술을 이용한 안검부 기저세포암의 준임상적 침윤 유형에 관한 연구
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Issues About Axial Diffusion During Segmental Hair Analysis
- Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
- Interest of High-Dose Pulse Corticosteroid Therapy Combined with Methotrexate for Severe Alopecia Areata: A Retrospective Case Series
- Pulse Corticosteroid Therapy for Alopecia Areata in Children: A Retrospective Study
- Ultrasound Detection of Retained Hair Tracts in Hidradenitis Suppurativa
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Prognostic factors in methylprednisolone pulse therapy for alopecia areata
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Medium-dose prednisolone pulse therapy in alopecia areata
- Intravenous methylprednisolone pulse therapy in severe alopecia areata
- The effect of night shift work on the expression of clock genes in beard hair follicle cells
- Low-dose spironolactone in the treatment of female hirsutism.