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Research 91–120 of 382
- The Rotterdam Study: 2016 objectives and design update
- Posters Presented at the 19th Joint Meeting of the International Society of Dermatopathology, March 2–3, 2016, Hilton Crystal City at Washington Reagan National Airport, Arlington, Virginia, USA
- Mesenchymal Stem Cells for Regenerative Medicine
- Pathology of Mouse Models of Accelerated Aging
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
- Coffea arabica: An Emerging Active Ingredient in Dermato-Cosmetic Applications
- Frontal fibrosing alopecia in males: A systematic review
- Hydrogel-mediated extracellular vesicles for enhanced wound healing: the latest progress, and their prospects for 3D bioprinting
- Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects
- Role of Dermal Factors Involved in Regulating the Melanin and Melanogenesis of Mammalian Melanocytes in Normal and Abnormal Skin
- Premature gray hair development in the interbrow region owing to the loss of maxillary first molars in young mice
- TONGUE, RED
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Unraveling Translational Insights into Systemic Multi-Organ Toxicity of Cytosine Arabinoside (Ara-C): A Systematic Review of Preclinical Animal Evidence
- The Rotterdam Study: objectives and design update
- Ultra‐structural hair alterations in Friedreich's ataxia: A scanning electron microscopic investigation
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Abnormal Saccadic Oscillations Associated with Severe Acute Respiratory Syndrome Coronavirus 2 Encephalopathy and Ataxia
- Phenotypic variation in biotinidase deficiency
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Sjogren-Larsson Syndrome
- Copper deficiency in dairy goats and kids
- Biotinidase deficiency: a survey of 10 cases.
- Late presentation of biotinidase deficiency with acute visual loss and gait disturbance
- <i>De novo</i> mutation in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene (A3243G) with rapid segregation resulting in MELAS in the offspring
- Diagnosis of Trichothiodystrophy in 2 Siblings
- Arginosuccinicaciduria
- Balint’s syndrome—missed or mistaken?
- From the Hair Follicle to the Spinal Cord: Scurvy as a Clue to Nutritional Myelopathy
- Biotinidase Enzyme Deficiency ( Case Report )