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Research 211–240 of 1000+
- Body dysmorphic concerns, social adaptation, and motivation for psychotherapeutic support in dermatological outpatients
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Selenium in the supplement as the probable cause of hair loss and nail dystrophy
- Body Modifications in Patients with Chronic Dermatoses: Associations with Body Dysmorphic Disorder and Illness Acceptance
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Perfectionism and Body Dysmorphic Disorder Symptoms among Men Seeking and Not Seeking Hair Transplant
- Hair-Related Dysmorphic Disorder in a Patient with Bipolar Disorder
- MULTIPLE HEMANGIOMAS OF THE TONGUE AND ORAL CAVITY IN A MYOTONIC DYSTROPHY TYPE 1 PATIENT: A CASE REPORT
- Dengue-Associated Telogen Effluvium Causing Body Dysmorphic Disorder
- Myotonic dystrophy type 1
- 307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis
- 494 Epidermolysis bullosa pruriginosa, muscular dystrophy, and immune-mediated myasthenia gravis in a patient with homozygous nonsense PLEC mutation
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- SAT-510 Association of Myotonic Dystrophy with Autoimmune Endocrinopathies and Thyroid Carcinoma
- Evaluation of body dysmorphic disorder in hair loss patients and benefit after hair restoration
- Clinical study on 88 cases of Korean 20-nail dystrophy
- Corticosteroids for the treatment of Duchenne muscular dystrophy
- Existence of Neural Crest–Derived Progenitor Cells in Normal and Fuchs Endothelial Dystrophy Corneal Endothelium
- Therapeutic Efficacy of Combination Therapy Using Oral Cyclosporine with a Dietary Supplement (Pantogar®) in Twenty-Nail Dystrophy
- A Case of Idiopathic Twenty-Nail Dystrophy
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Cutaneous Neoplasms in Myotonic Dystrophy Type 1
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Twenty-Nail Dystrophy of Alopecia Areata
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- Characterization of<i>CDH3</i>-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy
- Histopathology of Hypotrichosis with Juvenile Macular Dystrophy
- Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome