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Research 931–960 of 1000+
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Hypotrichosis with juvenile macular dystrophy
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Hair Loss Dysmorphic Disorder – a Frequently Encountered and Often Neglected Disorder
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with <i>AIRE</i> gene mutation (autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy, APECED syndrome) treated with ruxolitinib
- Characterisation of Myotonic Dystrophy type I cell models and drug evaluation by a cell- based quantification platform.
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Glucocorticoid corticosteroids for Duchenne muscular dystrophy
- Complex Regional Pain Syndrome I (Reflex Sympathetic Dystrophy)
- Efficacy and safety of glucocorticoids in the treatment of progressive muscular dystrophy in children: a systematic review and meta-analysis
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Annurca Apple Polyphenols Protect Murine Hair Follicles from Taxane Induced Dystrophy and Hijacks Polyunsaturated Fatty Acid Metabolism toward β-Oxidation
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- Botulinum toxin A in the treatment of facial reflex sympathetic dystrophy: A case report
- Topical Estrogen Accelerates Hair Regrowth in Mice After Chemotherapy-Induced Alopecia by Favoring the Dystrophic Catagen Response Pathway to Damage
- Exploring lncRNA-Mediated Mechanisms in Muscle Regulation and Their Implications for Duchenne Muscular Dystrophy
- 441 Anti-melanoma gene signature in dermal sheath fibroblasts from scalp hair follicles in Recessive Dystrophic Epidermolysis Bullosa (RDEB)
- Clinical Case Notes. Optical coherence tomography of adult-onset foveomacular vitelliform dystrophy
- Relation of Selenium, Vitamin E and Other Factors to Muscular Dystrophy in the Rabbit
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- 051 γδ T cells as novel players in alopecia areata pathobiology: Vδ1 + T lymphocytes may recognize “stressed” hair follicle keratinocytes, leading to IFNγ-dependent hair follicle dystrophy and immune privilege collapse
- Corkscrew Hair: A New Dermoscopic Sign for Diagnosis of Tinea Capitis in Black Children
- A Guide to Assessing Damage Response Pathways of the Hair Follicle: Lessons From Cyclophosphamide-Induced Alopecia in Mice
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Comparison of Alopecia areata in Human and Nonhuman Mammalian Species
- Skin signs in the diagnosis of thallium poisoning
- Chemotherapy Targets the Hair-Follicle Vascular Network but Not the Stem Cells