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  1. Effects of Sex Steroids on Innate and Adaptive Immunity

    Estrogens and androgens are classically recognized as reproductive sex steroid hormones because of their well-documented effects on reproductive...
    S. Ansar Ahmed, Ebru Karpuzoglu, Deena Khan in Sex Hormones and Immunity to Infection
    Chapter
  2. Fatal Hemorrhage Complicating Intracranial Stenting After Failed Thrombectomy for Intracranial Atherosclerotic Stenosis in a Patient with Moderate Stroke: Risk Factors for Hemorrhagic Transformation, Red Flags, and Lessons Learned

    Most large vessel occlusions (LVOs) are secondary to emboli of cardiac or cervical artery origin. Current stent retrieval and aspiration thrombectomy...
    José E. Cohen, Hans Henkes in The Ischemic Stroke Casebook
    Living reference work entry 2024
  3. Post-traumatic Epilepsy and Neuropsychiatric Comorbidities

    Post-traumatic epilepsy (PTE) is a form of acquired epilepsy that arises from traumatic brain injury (TBI). It presents a complex relationship with...
    Nurul Atiqah Zulazmi, Irma Wati Ngadimon, ... Mohd. Farooq Shaikh in Handbook of Neurodegenerative Disorders
    Living reference work entry 2024
  4. The Genetics of Cerebral Microbleeds

    Cerebral microbleeds are a radiological marker of small areas of haemorrhage in the brain, seen on magnetic resonance imaging sequences sensitive to...
    Gargi Banerjee, David S. Lynch, David J. Werring in Stroke Genetics
    Chapter 2024
  5. Intracerebral Hemorrhage and Cerebral Amyloid Angiopathy

    Intracerebral hemorrhage (ICH) is the acute manifestation of chronic cerebral small vessel disease. ICH is classified according to the affected brain...
    Ernst Mayerhofer, Alessandro Biffi, Jonathan Rosand in Stroke Genetics
    Chapter 2024
  6. Genetics of Small Vessel Disease

    Cerebral small vessel disease (CSVD) is highly prevalent in the general population and is overall a leading cause of disability. CSVD manifestations...
    Sandro Marini, Livia Parodi, ... Christopher D. Anderson in Stroke Genetics
    Chapter 2024
  7. Diagnosis, Investigation, Treatment and Management of Young Stroke in Clinic

    It has been estimated that approximately 10% of all strokes occur in young adults. Stroke in young people has a significant long-term socioeconomic...
    Gabriela Trifan, Fernando Daniel Testai, José Biller in Stroke Genetics
    Chapter 2024
  8. Multi-Omics Approaches to Discovering Acute Stroke Injury and Recovery Mechanisms

    Millions of people suffer an acute stroke each year, resulting in an enormous global burden of residual disability and mortality. Despite decades of...
    James A. Giles, **-Moo Lee, Rajat Dhar in Stroke Genetics
    Chapter 2024
  9. Smith-Kingsmore Syndrome (SKS)

    Gene defect: mTOR gene
    Cena Aram in Genetic Syndromes
    Living reference work entry 2024
  10. Popliteal Pterygium Syndrome

    The first scientific reports of this syndrome date back to the latter part of the nineteenth century in cases described by Trelat (1869) and Wolff...
    Navid Jabalameli in Genetic Syndromes
    Living reference work entry 2024
  11. Berlin Ectodermal Dysplasia Syndrome

    Ectodermal dysplasia, Berlin type, is a rare congenital disorder consisting of generalized melanoleukoderma, hypodontia, hypotrichosis, infantilism,...
    Sara Sadeghi, Yasamin Kalantari in Genetic Syndromes
    Living reference work entry 2024
  12. Potocki-Lupski Syndrome

    Potocki-Lupski syndrome (PTLS) is a rare neurodevelopmental disorder that occurs by heterozygous de novo microduplication in the short arm of...
    Anisha David, Akash Gautam in Genetic Syndromes
    Living reference work entry 2024
  13. Mitochondrial Complex IV Deficiency, Nuclear (MC4DN) Types 1–24

    Mitochondrial illnesses are a broad, diverse group of molecular disorders affecting the mitochondrial electron transport chain. Mitochondrial complex...
    Sumit Jamwal, Akash Gautam in Genetic Syndromes
    Living reference work entry 2024
  14. Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa (ILNEB)

    ILNEB is an extremely rare disease caused by mutations in the ITGA3 gene, which encodes the integrin α3 subunit of the major adhesion...
    Raha Zamani, Sara Hanaei in Genetic Syndromes
    Living reference work entry 2024
  15. Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy, and Myopathy (GDRM)

    Myo-Ectoderma-Gonadal Dysgenesis (MEGD) Syndrome.
    Tulay Guran in Genetic Syndromes
    Living reference work entry 2024
  16. Paradigm Change–A Comment from Philosophy of Science

    The necessity of various paradigm changes for progress in medicine described here was motivated by a barely comprehensive delay in scientific...
    Chapter 2024
  17. Diagnosis of the Chronic Disease as an Emergent Whole

    With the understanding of chronic disease as a stable, self-organizing complex system, new challenges arise for adequate diagnostics.
    Chapter 2024
  18. Knowledge Base: Complex Systems

    Elementary concepts of complexity science and their applications are conveyed using examples from disease research. The consequences of nonlinear...
    Chapter 2024
  19. The Cerebrospinal Fluid—Liquor Cerebrospinalis

    Elementary properties, biological function, and dynamics of this fluid in the brain are presented as an overview with the aim of explaining the role...
    Chapter 2024
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