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Research 901–930 of 1000+
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Dysplastic nevi, cutaneous melanoma, and other skin neoplasms in patients with myotonic dystrophy type 1: A cross-sectional study
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Frequency of body dysmorphic disorder among patients with complaints of hair loss
- The self in the obsessive–compulsive-related disorders: hoarding disorder, body dysmorphic disorder, and trichotillomania
- Three cases of androgen‐dependent disease associated with myotonic dystrophy
- Follicular dystrophy of immunosuppression
- Late presentation of myotonic dystrophy
- Body Dysmorphic Disorder, Psychiatric Symptoms, and Quality of Life in Female Dermatological Patients
- 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
- Body Modifications in Patients with Chronic Dermatoses: Associations with Body Dysmorphic Disorder and Illness Acceptance
- Perfectionism and Body Dysmorphic Disorder Symptoms among Men Seeking and Not Seeking Hair Transplant
- Hair-Related Dysmorphic Disorder in a Patient with Bipolar Disorder
- 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
- 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
- Corticosteroids for the treatment of Duchenne muscular dystrophy
- Existence of Neural Crest–Derived Progenitor Cells in Normal and Fuchs Endothelial Dystrophy Corneal Endothelium
- 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
- 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
- Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular Dystrophy
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl