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  1. Article ; Online: American Association for the Surgery of Trauma/American College of Surgeons-Committee on Trauma Clinical Consensus-Driven Protocol for glucose management in the post-resuscitation intensive care unit adult trauma patient.

    Jacovides, Christina L / Skeete, Dionne A / Werner, Nicole L / Toschlog, Eric A / Agarwal, Suresh / Coopwood, Ben / Crandall, Marie / Tominaga, Gail T

    The journal of trauma and acute care surgery

    2023  Volume 95, Issue 6, Page(s) 951–958

    MeSH term(s) Humans ; Adult ; United States ; Consensus ; Traumatology ; Trauma Centers ; Intensive Care Units ; Surgeons
    Language English
    Publishing date 2023-08-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2651070-4
    ISSN 2163-0763 ; 2163-0755
    ISSN (online) 2163-0763
    ISSN 2163-0755
    DOI 10.1097/TA.0000000000004124
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Colleges and Crime-Comparing Homicide and Suicide Rates Among College Towns and Their Counterparts.

    Prentice, Carter M / Song, Jamie / Degli Esposti, Michelle / Jay, Jonathan / Wiebe, Douglas J / Jacovides, Christina L / Seamon, Mark J / Kaufman, Elinore J

    The Journal of surgical research

    2023  Volume 293, Page(s) 490–496

    Abstract: Introduction: To investigate differences in homicide and suicide rates across college town status and determine whether college towns were predisposed to changes in rates over time.: Methods: We analyzed county-level homicide and suicide rates (total ...

    Abstract Introduction: To investigate differences in homicide and suicide rates across college town status and determine whether college towns were predisposed to changes in rates over time.
    Methods: We analyzed county-level homicide and suicide rates (total and by firearm) across college town status using 2015-2019 CDC death certificate data and data from the American Communities Project.
    Results: Population-level homicide rates were similar across college town status, but younger age groups were at increased risk for firearm homicide and total homicide in college towns. College town status was associated with lower population-level firearm suicide rates, but individuals aged less than 18 y were at increased risk for total and firearm suicide. Finally, college towns were not classified as outliers for changes in either firearm homicide or suicide rates over time.
    Conclusions: College towns had similar homicide rates and significantly lower firearm suicide rates than other counties; however, individuals aged less than 18 y were at increased risk for both outcomes. The distinctive demographic, social, economic, and cultural features of college towns may contribute to differing risk profiles among certain age groups, thus may also be amenable to focused prevention efforts.
    MeSH term(s) Humans ; United States/epidemiology ; Homicide ; Cities ; Suicide ; Firearms ; Population Surveillance ; Wounds, Gunshot/epidemiology
    Language English
    Publishing date 2023-10-10
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, P.H.S. ; Research Support, Non-U.S. Gov't
    ZDB-ID 80170-7
    ISSN 1095-8673 ; 0022-4804
    ISSN (online) 1095-8673
    ISSN 0022-4804
    DOI 10.1016/j.jss.2023.09.020
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Overcoming Barriers: Sex Disparity in Surgeon Ergonomics.

    Jacovides, Christina L / Guetter, Camila R / Crandall, Marie / McGuire, Kandace / Slama, Eliza M / Plotkin, Anastasia / Kashyap, Meghana V / Lal, Geeta / Henry, Marion C

    Journal of the American College of Surgeons

    2024  Volume 238, Issue 5, Page(s) 971–979

    Abstract: Background: Musculoskeletal discomfort is widely experienced by surgeons across multiple surgical specialties. Developing technologies and new minimally invasive techniques add further complexity and ergonomic stressors. These stressors differentially ... ...

    Abstract Background: Musculoskeletal discomfort is widely experienced by surgeons across multiple surgical specialties. Developing technologies and new minimally invasive techniques add further complexity and ergonomic stressors. These stressors differentially affect male and female surgeons, but little is known about the role these sex disparities play in surgical ergonomic stress. We reviewed existing literature to better understand how ergonomic stress varies between male and female surgeons.
    Study design: A literature search was performed via PubMed including but not limited to the following topics: ergonomics, surgeons, female surgeons, women surgeons, pregnancy, and operating room. A review of available quantitative data was performed.
    Results: Female surgeons endure more pronounced ergonomic discomfort than their male counterparts, with added ergonomic stress associated with pregnancy.
    Conclusions: A 4-fold method is proposed to overcome ergonomic barriers, including (1) improved education on prevention and treatment of ergonomic injury for active surgeons and trainees, (2) increased departmental and institutional support for ergonomic solutions for surgeons, (3) partnerships with industry to study innovative ergonomic solutions, and (4) additional research on the nature of surgical ergonomic challenges and the differential effects of surgical ergonomics on female surgeons.
    MeSH term(s) Humans ; Male ; Female ; Ergonomics/methods ; Surgeons ; Operating Rooms ; Specialties, Surgical ; Occupational Diseases ; Musculoskeletal Diseases
    Language English
    Publishing date 2024-04-17
    Publishing country United States
    Document type Review ; Journal Article
    ZDB-ID 1181115-8
    ISSN 1879-1190 ; 1072-7515
    ISSN (online) 1879-1190
    ISSN 1072-7515
    DOI 10.1097/XCS.0000000000001043
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Differentiating Primary Pancreatic Lymphoma Versus Primary Splenic Lymphoma: A Case Report.

    Ries, Robert A / Jacovides, Christina L / Rashti, Jennifer / Gong, Jerald Z / Yeo, Charles J

    Journal of pancreatic cancer

    2021  Volume 7, Issue 1, Page(s) 20–22

    Abstract: Background: ...

    Abstract Background:
    Language English
    Publishing date 2021-03-29
    Publishing country United States
    Document type Case Reports
    ISSN 2475-3246
    ISSN (online) 2475-3246
    DOI 10.1089/pancan.2020.0019
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Adolescent Gun Violence Shows an Age Group to Focus Trauma Prevention.

    Bailey, Joanelle A / Jacovides, Christina L / Butler, Dale / Bass, Gary A / Seamon, Mark J / Cannon, Jeremy / Martin, Niels D

    The Journal of surgical research

    2022  Volume 283, Page(s) 853–857

    Abstract: Introduction: Gun violence continues to escalate in America's urban areas. Peer groups of gun wound victims are potential targets for violence prevention initiatives; identification of this cohort is pivotal to efficient deployment strategies. We ... ...

    Abstract Introduction: Gun violence continues to escalate in America's urban areas. Peer groups of gun wound victims are potential targets for violence prevention initiatives; identification of this cohort is pivotal to efficient deployment strategies. We hypothesize a specific age at which the incidence of penetrating trauma increases significantly in adolescence, below which should be the focus on future trauma prevention.
    Methods: Adolescent trauma patients with gunshot wounds seen from July 2011 through June 2021 at a well-established, urban, academic level 1 trauma center were reviewed retrospectively and grouped by age. A linear regression and repeated measured analysis of variance evaluated the change in gunshot wound victims over this time, grouped by age. Demographics were extrapolated, and standard statistical analysis was performed.
    Results: A total of 1304 adolescent trauma patients were included. Those aged 15 y and under had an unchanged incidence of gunshot wounds. However, those aged 16 y and more experienced the majority of increased gun violence; 92% were Black and 90% were male with a mortality of 12%. Adolescents aged 15 y and below were 95% Black and 84% male, with a mortality of 18%.
    Conclusions: Primary prevention efforts to mitigate gun violence should be focused on adolescents below 16 y of age. Prevention of gun violence should include community outreach efforts directed toward middle school-aged children and younger, hoping to decrease the incidence of injury due to gun violence in older adolescents in the future.
    MeSH term(s) Child ; Humans ; Male ; Adolescent ; Female ; Wounds, Gunshot/epidemiology ; Wounds, Gunshot/prevention & control ; Gun Violence/prevention & control ; Retrospective Studies ; Violence/prevention & control ; Wounds, Penetrating/epidemiology
    Language English
    Publishing date 2022-12-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80170-7
    ISSN 1095-8673 ; 0022-4804
    ISSN (online) 1095-8673
    ISSN 0022-4804
    DOI 10.1016/j.jss.2022.10.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Daily quetiapine after severe TBI improves learning and memory.

    Bele, Priyanka / Thaploo, Advait / Coons, Michael / Culkin, Matthew C / Santos, Patricia / Martinez-Quinones, Patricia / Georges, Anastasia P / Anderson, Erin / Browne, Kevin D / Jacovides, Christina / Kaplan, Lewis J / Meaney, David F / Smith, Douglas H / Pascual, Jose L

    The journal of trauma and acute care surgery

    2024  

    Abstract: Background: Traumatic brain injury (TBI) induces cognitive deficits driven by neuroinflammation and cerebral edema. The commonly used atypical antipsychotic, quetiapine (QTP), has been recently shown to improve post-TBI outcomes. We hypothesized that ... ...

    Abstract Background: Traumatic brain injury (TBI) induces cognitive deficits driven by neuroinflammation and cerebral edema. The commonly used atypical antipsychotic, quetiapine (QTP), has been recently shown to improve post-TBI outcomes. We hypothesized that QTP would thereby improve animal learning and memory 2 weeks after severe TBI.
    Methods: CD1 male mice (n = 35) underwent severe TBI (controlled cortical impact, injury, I) or sham craniotomy (S), followed by BID saline (P, placebo) or QTP (10 or 20 mg/kg, IP) for 2 weeks. Animals underwent Morris Water Maze (MWM) exercises to gauge spatial learning and memory. The distance and time required for swimming animals to reach the platform area (Zone 5, Z5) located in quadrant 1 (Zone 1, Z1) was calculated from digital video recordings analyzed using Ethovision software. Animal bodyweights were recorded daily and on day 14, injured cerebral hemispheres were procured for edema determination (wet-to-dry ratio). Intergroup differences were evaluated with ANOVA/Bonferroni correction (p < 0.05).
    Results: On day 14, animal weight loss recovery was lowest in I + P compared to I + QTP20 and I + QTP10 (p ≤ 0.01 for either). Cerebral edema was greatest in I + P, and only significantly decreased in I + QTP20 (p < 0.05). Both QTP doses similarly improved spatial learning by significantly reducing latency time and travel distance to target zones (p < 0.05). In probe memory trials, only I + QTP20 and not I + QTP10 significantly favored animal reaching or crossing into target zones (p < 0.05).
    Conclusion: Post-TBI QTP reduces brain edema and improves spatial learning and memory with a potential dose dependence impact benefiting memory up to 14 days. These data suggest an unanticipated QTP benefit following brain injury that should be specifically explored.
    Language English
    Publishing date 2024-05-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2651070-4
    ISSN 2163-0763 ; 2163-0755
    ISSN (online) 2163-0763
    ISSN 2163-0755
    DOI 10.1097/TA.0000000000004400
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Delayed tranexamic acid after traumatic brain injury impedes learning and memory: Early tranexamic acid is favorable but not in sham animals.

    Culkin, Matthew C / Coons, Michael / Bele, Priyanka / Thaploo, Advait / Georges, Anastasia P / Anderson, Erin / Browne, Kevin D / Jacovides, Christina / Santos, Patricia / Kaplan, Lewis J / Meaney, David F / Smith, Douglas H / Pascual, Jose L

    The journal of trauma and acute care surgery

    2023  Volume 96, Issue 1, Page(s) 26–34

    Abstract: Background: Early but not late tranexamic acid (TXA) after TBI preserves blood-brain-barrier integrity, but it is unclear if and how dose timing affects cognitive recovery beyond hours postinjury. We hypothesized that early (1 hour post-TBI) but not ... ...

    Abstract Background: Early but not late tranexamic acid (TXA) after TBI preserves blood-brain-barrier integrity, but it is unclear if and how dose timing affects cognitive recovery beyond hours postinjury. We hypothesized that early (1 hour post-TBI) but not late (24 hours post-TBI) TXA administration improves cognitive recovery for 14 days.
    Methods: CD1 male mice (n = 25) were randomized to severe TBI (injury [I], by controlled cortical impact) or sham craniotomy (S) followed by intravenous saline at 1 hour (placebo [P1]) or 30 mg/kg TXA at 1 hour (TXA1) or 24 hours (TXA24). Daily body weights, Garcia Neurological Test scores, brain/lung water content, and Morris water maze exercises quantifying swimming traffic in the platform quadrant (zone [Z] 1) and platform area (Z5) were recorded for up to 14 days.
    Results: Among injured groups, I-TXA1 demonstrated fastest weight gain for 14 days and only I-TXA1 showed rapid (day 1) normalization of Garcia Neurological Test ( p = 0.01 vs. I-P1, I-TXA24). In cumulative spatial trials, compared with I-TXA1, I-TXA24 hindered learning (distance to Z5 and % time in Z1, p < 0.05). Compared with I-TXA1, I-TXA24 showed poorer memory with less Z5 time (0.51 vs. 0.16 seconds, p < 0.01) and Z5 crossing frequency. Unexpectedly, TXA in uninjured animals (S-TXA1) displayed faster weight gain but inferior learning and memory.
    Conclusion: Early TXA appears beneficial for cognitive and behavioral outcomes following TBI, although administration 24 hours postinjury consistently impairs cognitive recovery. Tranexamic acid in sham animals may lead to adverse effects on cognition.
    MeSH term(s) Animals ; Male ; Mice ; Brain ; Brain Injuries, Traumatic/complications ; Brain Injuries, Traumatic/drug therapy ; Maze Learning ; Tranexamic Acid/pharmacology ; Weight Gain
    Chemical Substances Tranexamic Acid (6T84R30KC1)
    Language English
    Publishing date 2023-10-19
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2651070-4
    ISSN 2163-0763 ; 2163-0755
    ISSN (online) 2163-0763
    ISSN 2163-0755
    DOI 10.1097/TA.0000000000004155
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Early posttraumatic brain injury tranexamic acid prevents blood-brain barrier hyperpermeability and improves surrogates of neuroclinical recovery.

    Culkin, Matthew C / Bele, Priyanka / Georges, Anastasia P / Lopez, Alfonso J / Niziolek, Grace / Jacovides, Christina L / Song, Hailong / Johnson, Victoria E / Kaplan, Lewis J / Smith, Douglas H / Pascual, Jose L

    The journal of trauma and acute care surgery

    2023  Volume 95, Issue 1, Page(s) 47–54

    Abstract: Background: Tranexamic acid (TXA) given early, but not late, after traumatic brain injury (TBI) appears to improve survival. This may be partly related to TXA-driven profibrinolysis and increased leukocyte (LEU)-mediated inflammation when administered ... ...

    Abstract Background: Tranexamic acid (TXA) given early, but not late, after traumatic brain injury (TBI) appears to improve survival. This may be partly related to TXA-driven profibrinolysis and increased leukocyte (LEU)-mediated inflammation when administered late post-injury. We hypothesized that early TXA (1 hour post-TBI), blunts penumbral, blood-brain barrier (BBB) leukocyte-endothelial cell (LEU-EC) interactions and microvascular permeability, in vivo when compared with late administration (24 hours post-TBI).
    Methods: CD1 male mice (n = 35) were randomized to severe TBI (injury by controlled cortical impact; injury: velocity, 6 m/s; depth, 1 mm; diameter, 3 mm) or sham craniotomy followed by intravenous saline (placebo) at 1 hour, or TXA (30 mg/kg) at 1 hour or 24 hours. At 48 hours, in vivo pial intravital microscopy visualized live penumbral LEU-EC interactions and BBB microvascular fluorescent albumin leakage. Neuroclinical recovery was assessed by the Garcia Neurological Test (motor, sensory, reflex, and balance assessments) and body weight loss recovery at 1 and 2 days after injury. Analysis of variance with Bonferroni correction assessed intergroup differences ( p < 0.05).
    Results: One-hour, but not 24-hour, TXA improved Garcia Neurological Test performance on day 1 post-TBI compared with placebo. Both 1 hour and 24 hours TXA similarly improved day 1 weight loss recovery, but only 1 hour TXA significantly improved weight loss recovery on day 2 compared with placebo ( p = 0.04). No intergroup differences were found in LEU rolling or adhesion between injured animal groups. Compared with untreated injured animals, only TXA at 1 hour reduced BBB permeability.
    Conclusion: Only early post-TBI TXA consistently improves murine neurological recovery. Tranexamic acid preserves BBB integrity but only when administered early. This effect appears independent of LEU-EC interactions and demonstrates a time-sensitive effect that supports only early TXA administration.
    MeSH term(s) Animals ; Male ; Mice ; Antifibrinolytic Agents/pharmacology ; Antifibrinolytic Agents/therapeutic use ; Blood-Brain Barrier ; Brain Edema/prevention & control ; Brain Injuries, Traumatic/drug therapy ; Tranexamic Acid/pharmacology ; Tranexamic Acid/therapeutic use ; Weight Loss
    Chemical Substances Antifibrinolytic Agents ; Tranexamic Acid (6T84R30KC1)
    Language English
    Publishing date 2023-04-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2651070-4
    ISSN 2163-0763 ; 2163-0755
    ISSN (online) 2163-0763
    ISSN 2163-0755
    DOI 10.1097/TA.0000000000003971
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Higher center volume is significantly associated with lower mortality in trauma patients with shock.

    Hornor, Melissa A / Blank, Jacqueline J / Hatchimonji, Justin S / Bailey, Joanelle A / Jacovides, Christina L / Reilly, Patrick M / Cannon, Jeremy W / Holena, Daniel N / Seamon, Mark J / Kaufman, Elinore J

    Injury

    2023  Volume 54, Issue 5, Page(s) 1400–1405

    Abstract: Introduction: Injured patients presenting in shock are at high risk of mortality despite numerous efforts to improve resuscitation. Identifying differences in outcomes among centers for this population could yield insights to improve performance. We ... ...

    Abstract Introduction: Injured patients presenting in shock are at high risk of mortality despite numerous efforts to improve resuscitation. Identifying differences in outcomes among centers for this population could yield insights to improve performance. We hypothesized that trauma centers treating higher volumes of patients in shock would have lower risk-adjusted mortality.
    Methods: We queried the Pennsylvania Trauma Outcomes Study from 2016 to 2018 for injured patients ≥16 years of age at Level I&II trauma centers who had an initial systolic blood pressure (SBP) of <90 mmHg. We excluded patients with critical head injury (abbreviated injury score [AIS] head ≥5) and patients coming from centers with a shock patient volume of ≤10 for the study period. The primary exposure was tertile of center-level shock patient volume (low, medium, or high volume). We compared risk-adjusted mortality by tertile of volume using multivariable Cox proportional hazards model incorporating age, injury severity, mechanism, and physiology.
    Results: Of 1,805 included patients at 29 centers, 915 (50.7%) died. The median annual shock trauma patient volume was 9 patients for low volume centers, medium 19.5, and high 37. Median ISS was higher at high volume compared to low volume centers (22 vs 18, p <0.001). Raw mortality was 54.9% at high volume centers, 46.7% for medium, and 42.9% for low. Time elapsed from arrival to emergency department (ED) to the operating room (OR) was lower at high volume than low volume centers (median 47 vs 78 min) p = 0.003. In adjusted analysis, hazard ratio for high volume centers (referenced to low volume) was 0.76 (95% CI 0.59-0.97, p = 0.030).
    Conclusion: After adjusting for patient physiology and injury characteristics, center-level volume is significantly associated with mortality. Future studies should seek to identify key practices associated with improved outcomes in high-volume centers. Furthermore, shock patient volume should be considered when new trauma centers are opened.
    MeSH term(s) Humans ; Trauma Centers ; Emergency Service, Hospital ; Shock ; Pennsylvania/epidemiology ; Outcome Assessment, Health Care ; Hospital Mortality ; Craniocerebral Trauma ; Injury Severity Score ; Retrospective Studies ; Wounds and Injuries/therapy
    Language English
    Publishing date 2023-03-21
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 218778-4
    ISSN 1879-0267 ; 0020-1383
    ISSN (online) 1879-0267
    ISSN 0020-1383
    DOI 10.1016/j.injury.2023.03.013
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  10. Article ; Online: Post-traumatic brain injury antithrombin III recovers Morris water maze cognitive performance, improving cued and spatial learning.

    ElSaadani, Mohamed / Ahmed, Syed M / Jacovides, Christina / Lopez, Alfonso / Johnson, Victoria E / Kaplan, Lewis J / Smith, Douglas H / Pascual, Jose L

    The journal of trauma and acute care surgery

    2021  Volume 91, Issue 1, Page(s) 108–113

    Abstract: Background: Neuroinflammation and cerebral edema development following severe traumatic brain injury (TBI) affect subsequent cognitive recovery. Independent of its anticoagulant effects, antithrombin III (AT-III) has been shown to block neurovascular ... ...

    Abstract Background: Neuroinflammation and cerebral edema development following severe traumatic brain injury (TBI) affect subsequent cognitive recovery. Independent of its anticoagulant effects, antithrombin III (AT-III) has been shown to block neurovascular inflammation after severe TBI, reduce cerebral endothelial-leukocyte interactions, and decrease blood-brain barrier permeability. We hypothesized that AT-III administration after TBI would improve post-TBI cognitive recovery, specifically enhancing learning, and memory.
    Methods: Fifteen CD1 male mice were randomized to undergo severe TBI (controlled cortical impact [CCI]: velocity, 6 m/s; depth, 1 mm; diameter, 3 mm) or sham craniotomy and received either intravenous AT-III (250 IU/kg) or vehicle (VEH/saline) 15 minutes and 24 hours post-TBI. Animals underwent Morris water maze testing from 6 to 14 days postinjury consisting of cued learning trials (platform visible), spatial learning trials (platform invisible, spatial cues present), and probe (memory) trials (platform removed, spatial cues present). Intergroup differences were assessed by the Kruskal-Wallis test (p < 0.05).
    Results: Morris water maze testing demonstrated that cumulative cued learning (overall mean time in seconds to reach the platform on days 6-8) was worst in CCI-VEH animals (26.1 ± 2.4 seconds) compared with CCI-AT-III counterparts (20.3 ± 2.1 seconds, p < 0.01). Cumulative noncued spatial learning was also worst in the CCI-VEH group (23.4 ± 1.8 seconds) but improved with AT-III (17.6 ± 1.5 seconds, p < 0.01). In probe trials, AT-III failed to significantly improve memory ability. Animals that underwent sham craniotomy demonstrated preserved learning and memory compared with all CCI counterparts (p < 0.05).
    Conclusion: Antithrombin III improves neurocognitive recovery weeks after TBI. This improvement is particularly related to improvement in learning but not memory function. Pharmacologic support of enhanced learning may support new skill acquisition or relearning to improve outcomes after TBI.
    Level of evidence: Therapeutic/care management, level II.
    MeSH term(s) Animals ; Antithrombin III/pharmacology ; Blood-Brain Barrier/drug effects ; Chronic Traumatic Encephalopathy/blood ; Chronic Traumatic Encephalopathy/drug therapy ; Cognition/drug effects ; Cues ; Disease Models, Animal ; Male ; Mice ; Morris Water Maze Test/drug effects ; Random Allocation
    Chemical Substances Antithrombin III (9000-94-6)
    Language English
    Publishing date 2021-03-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2651070-4
    ISSN 2163-0763 ; 2163-0755
    ISSN (online) 2163-0763
    ISSN 2163-0755
    DOI 10.1097/TA.0000000000003112
    Database MEDical Literature Analysis and Retrieval System OnLINE

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