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Research 481–510 of 1000+
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome with Concomitant Lymphopenia: A Novel TP63 Mutation
- Abstract 1835: Development of mammary hyperplasia, dysplasia, and invasive ductal carcinoma in transgenic mice expressing the 8p11 amplicon oncogene NSD3 (WHSC1L1)
- Epidermal hyperplasia and oral carcinoma in mice overexpressing the transcription factor ATF3 in basal epithelial cells
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Lentiginous melanoma. A clinically malignant entity that histopathologically seems benign. Case study harbouring BRAF V 600R mutation
- Topikal Retinoidler
- Abstract LB-039: Chronic inflammation-mediated contribution of bone marrow-derived epithelial cells and hair follicle stem cells to development of cutaneous neoplasms
- Abstract LB-039: Chronic inflammation-mediated contribution of bone marrow-derived epithelial cells and hair follicle stem cells to development of cutaneous neoplasms
- GENOTYPE ? PHENOTYPE CORRELATIONS IN CUTANEOUS MELANOMA PATIENTS CARRIER OF THE MITF p.E318K PATHOGENIC VARIANT
- Lymphoproliferative Disorders: Hot Topics in Dermatology 2019
- Age-associated inflammation connects RAS-induced senescence to stem cell dysfunction and epidermal malignancy
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Iperplasia Collaterale Nella Oncogenesi Sperimentale Del Ratto: Rilievi in corso di trattamento con Vitamina A
- Trichothiodystrophy
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Atrichia With Papular Lesions
- Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association.
- [Trichothiodystrophy: a morphological and biochemical study].
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations