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Research 31–60 of 1000+
- Inherited ichthyosis: Syndromic forms
- Alopezien und Hypotrichosen im Kindesalter
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Sox9 expression in canine epithelial skin tumors
- Hair Loss Disorders in Domestic Animals
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Novel diagnostic tools and markers for inflammatory skin diseases
- Molecular Analysis of a Series of Israeli Families with Comèl-Netherton Syndrome
- Enhancing the diagnostic yield of monogenic diabetes in unresolved cases with early-onset hyperglycemia
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Plucked hair follicles from patients with chronic discoid lupus erythematosus show a disease-specific molecular signature
- Diagnostic Significance of MIG (Monokine Induced by Gamma Interferon) and IP-10 (Interferon gamma-induced protein 10) Chemokines in Alopecia Areata
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- THE ROLE OF EXOSOMES IN THE DIAGNOSIS AND TREATMENT OF IMMUNE MEDIATED DERMATOSIS, TREATMENT OF SKIN WOUNDS AND ALOPECIA
- Cell adhesion molecules in inflammatory and neoplastic skin diseases
- Transforming 300 billion points of data into diagnostics, therapeutics and new insights into disease
- Deep facial mycosis due to <i>Trichophyton verrucosum</i>—molecular genetic identification of the dermatophyte in paraffin‐embedded tissue—case report and review of the literature
- Signal Peptide-CUB-EGF-like Domain-Containing Protein 3 (SCUBE3): From Molecule to Therapy
- Ichthyosis with confetti: clinics, molecular genetics and management
- Transcriptional Profiling in Rat Hair Follicles following Simulated Blast Insult: A New Diagnostic Tool for Traumatic Brain Injury
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Rule-out test for autism using machine-learning analysis of molecular temporal dynamics in hair - a multicenter study
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Bioinformatics analysis and verification of m6A related genes based on the construction of keloid diagnostic model
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia