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  1. Article ; Online: Mentorship in the Field of Aging

    Patricia W. Slattum / Tiffany R. Washington / Sarah Dys / Patricia M. D’Antonio / Tonya J. Roberts / Matthew Lee Smith

    Health Behavior Research, Vol 5, Iss

    Purposes, Pivots, and Priorities

    2022  Volume 3

    Abstract: The Gerontological Society of America (GSA) is a multi-disciplinary organization dedicated to advancing the field of aging and improving the lives of older adults. With a long-standing commitment to mentorship and career development, this article focuses ...

    Abstract The Gerontological Society of America (GSA) is a multi-disciplinary organization dedicated to advancing the field of aging and improving the lives of older adults. With a long-standing commitment to mentorship and career development, this article focuses on GSA’s Mentoring Consultancies and Career Conversations events and their pivot to meet the needs and demands of current and future gerontologists amid the COVID-19 pandemic. This article provides a description of these events in the context of planning, content, and member engagement. Recommendations are provided to other organizations seeking to enrich their membership through mentorship and career development activities.
    Keywords gerontology ; professional society ; mentoring ; career development ; Special aspects of education ; LC8-6691 ; Public aspects of medicine ; RA1-1270
    Language English
    Publishing date 2022-08-01T00:00:00Z
    Publisher New Prairie Press
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: The Effect of the APOE4 Gene on Accumulation of Aβ40 After Brain Injury Cannot Be Reversed by Increasing apoE4 Protein.

    Washington, Patricia M / Burns, Mark P

    Journal of neuropathology and experimental neurology

    2016  Volume 75, Issue 8, Page(s) 770–778

    Abstract: The apolipoprotein E (apoE) protein is involved in clearance of β-amyloid (Aβ) from the brain; and the APOE4 gene is associated with Aβ plaque formation in humans following traumatic brain injury (TBI). Here, we examined the association between apoE and ... ...

    Abstract The apolipoprotein E (apoE) protein is involved in clearance of β-amyloid (Aβ) from the brain; and the APOE4 gene is associated with Aβ plaque formation in humans following traumatic brain injury (TBI). Here, we examined the association between apoE and Aβ
    Language English
    Publishing date 2016-06-12
    Publishing country England
    Document type Journal Article
    ZDB-ID 3088-0
    ISSN 1554-6578 ; 0022-3069
    ISSN (online) 1554-6578
    ISSN 0022-3069
    DOI 10.1093/jnen/nlw049
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: The Nephrology Nursing Shortage: Insights From a Pandemic.

    Boyle, Suzanne M / Washington, Rhonda / McCann, Patricia / Koul, Sheetal / McLarney, Brett / Gadegbeku, Crystal A

    American journal of kidney diseases : the official journal of the National Kidney Foundation

    2021  Volume 79, Issue 1, Page(s) 113–116

    MeSH term(s) Humans ; Nephrology ; Nephrology Nursing ; Pandemics
    Language English
    Publishing date 2021-08-16
    Publishing country United States
    Document type Editorial
    ZDB-ID 604539-x
    ISSN 1523-6838 ; 0272-6386
    ISSN (online) 1523-6838
    ISSN 0272-6386
    DOI 10.1053/j.ajkd.2021.07.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Polypathology and dementia after brain trauma: Does brain injury trigger distinct neurodegenerative diseases, or should they be classified together as traumatic encephalopathy?

    Washington, Patricia M / Villapol, Sonia / Burns, Mark P

    Experimental neurology

    2016  Volume 275 Pt 3, Page(s) 381–388

    Abstract: Neuropathological studies of human traumatic brain injury (TBI) cases have described amyloid plaques acutely after a single severe TBI, and tau pathology after repeat mild TBI (mTBI). This has helped drive the hypothesis that a single moderate to severe ... ...

    Abstract Neuropathological studies of human traumatic brain injury (TBI) cases have described amyloid plaques acutely after a single severe TBI, and tau pathology after repeat mild TBI (mTBI). This has helped drive the hypothesis that a single moderate to severe TBI increases the risk of developing late-onset Alzheimer's disease (AD), while repeat mTBI increases the risk of developing chronic traumatic encephalopathy (CTE). In this review we critically assess this position-examining epidemiological and case control human studies, neuropathological evidence, and preclinical data. Epidemiological studies emphasize that TBI is associated with the increased risk of developing multiple types of dementia, not just AD-type dementia, and that TBI can also trigger other neurodegenerative conditions such as Parkinson's disease. Further, human post-mortem studies on both single TBI and repeat mTBI can show combinations of amyloid, tau, TDP-43, and Lewy body pathology indicating that the neuropathology of TBI is best described as a 'polypathology'. Preclinical studies confirm that multiple proteins associated with the development of neurodegenerative disease accumulate in the brain after TBI. The chronic sequelae of both single TBI and repeat mTBI share common neuropathological features and clinical symptoms of classically defined neurodegenerative disorders. However, while the spectrum of chronic cognitive and neurobehavioral disorders that occur following repeat mTBI is viewed as the symptoms of CTE, the spectrum of chronic cognitive and neurobehavioral symptoms that occur after a single TBI is considered to represent distinct neurodegenerative diseases such as AD. These data support the suggestion that the multiple manifestations of TBI-induced neurodegenerative disorders be classified together as traumatic encephalopathy or trauma-induced neurodegeneration, regardless of the nature or frequency of the precipitating TBI.
    MeSH term(s) Alzheimer Disease/classification ; Alzheimer Disease/diagnosis ; Alzheimer Disease/etiology ; Animals ; Brain/pathology ; Brain Injuries/complications ; Brain Injuries/diagnosis ; Brain Injury, Chronic/classification ; Brain Injury, Chronic/diagnosis ; Brain Injury, Chronic/etiology ; Dementia/classification ; Dementia/diagnosis ; Dementia/etiology ; Humans ; Neurodegenerative Diseases/classification ; Neurodegenerative Diseases/diagnosis ; Neurodegenerative Diseases/etiology ; Plaque, Amyloid/pathology
    Language English
    Publishing date 2016-01
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 207148-4
    ISSN 1090-2430 ; 0014-4886
    ISSN (online) 1090-2430
    ISSN 0014-4886
    DOI 10.1016/j.expneurol.2015.06.015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Injury-Induced Neurogenesis: Mechanisms and Relevance.

    Yu, Tzong-Shiue / Washington, Patricia M / Kernie, Steven G

    The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry

    2014  Volume 22, Issue 1, Page(s) 61–71

    Abstract: Partial recovery from brain injury due to trauma, hypoxia, or stroke, is ubiquitous and occurs largely through unknown mechanisms. It is now well accepted that injury enhances proliferation of quiescent stem and progenitor cells in specialized niches ... ...

    Abstract Partial recovery from brain injury due to trauma, hypoxia, or stroke, is ubiquitous and occurs largely through unknown mechanisms. It is now well accepted that injury enhances proliferation of quiescent stem and progenitor cells in specialized niches within the brain. However, whether this injury-induced neurogenesis contributes to recovery after brain injury remains controversial. Recent evidence suggests that hippocampal neural stem/precursor cell activation and subsequent neurogenesis are responsible for at least some aspects of spontaneous recovery following brain injury from a variety of causes. However, other aspects of injury-induced neurogenesis, including its contribution to adverse sequelae such as seizures, are still being investigated. The purpose of this review is to provide an overview of adult hippocampal neurogenesis and how it relates to injury and explain how current mouse technology is allowing for better understanding of whether manipulating this natural process might eventually help inform therapy following brain injury.
    MeSH term(s) Animals ; Brain/physiopathology ; Brain Injuries/physiopathology ; Humans ; Neurogenesis/physiology
    Language English
    Publishing date 2014-12-17
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 1233753-5
    ISSN 1089-4098 ; 1073-8584
    ISSN (online) 1089-4098
    ISSN 1073-8584
    DOI 10.1177/1073858414563616
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Hyaluronidase reduced edema after experimental traumatic brain injury.

    Washington, Patricia M / Lee, Changhee / Dwyer, Mary Kate R / Konofagou, Elisa E / Kernie, Steven G / Morrison, Barclay

    Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism

    2019  Volume 40, Issue 10, Page(s) 2026–2037

    Abstract: Cerebral edema and the subsequent increased intracranial pressure are associated with mortality and poor outcome following traumatic brain injury. Previous in vitro studies have shown that the Gibbs-Donnan effect, which describes the tendency of a porous, ...

    Abstract Cerebral edema and the subsequent increased intracranial pressure are associated with mortality and poor outcome following traumatic brain injury. Previous in vitro studies have shown that the Gibbs-Donnan effect, which describes the tendency of a porous, negatively charged matrix to attract positive ions and water, applies to brain tissue and that enzymatic reduction of the fixed charge density can prevent tissue swelling. We tested whether hyaluronidase, an enzyme that degrades the large, negatively charged glycosaminoglycan hyaluronan, could reduce brain edema after traumatic brain injury. In vivo, intracerebroventricular injection of hyaluronidase after controlled cortical impact in mice reduced edema in the ipsilateral hippocampus at 24 h by both the wet-weight/dry-weight method (78.15 ± 0.65% vs. 80.4 ± 0.46%; p < 0.01) and T
    MeSH term(s) Animals ; Behavior, Animal/drug effects ; Blood-Brain Barrier/diagnostic imaging ; Body Water/metabolism ; Brain Edema/diagnostic imaging ; Brain Edema/drug therapy ; Brain Edema/etiology ; Brain Injuries, Traumatic/complications ; Brain Injuries, Traumatic/diagnostic imaging ; Brain Injuries, Traumatic/drug therapy ; Hippocampus/diagnostic imaging ; Hyaluronoglucosaminidase/administration & dosage ; Hyaluronoglucosaminidase/therapeutic use ; Injections, Intraventricular ; Magnetic Resonance Imaging ; Male ; Maze Learning/drug effects ; Mice ; Mice, Inbred C57BL ; Psychomotor Performance/drug effects ; Recovery of Function
    Chemical Substances Hyaluronoglucosaminidase (EC 3.2.1.35)
    Language English
    Publishing date 2019-10-24
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 604628-9
    ISSN 1559-7016 ; 0271-678X
    ISSN (online) 1559-7016
    ISSN 0271-678X
    DOI 10.1177/0271678X19882780
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Identifying labile DOM components in a coastal ocean through depleted bacterial transcripts and chemical signals.

    Vorobev, Alexey / Sharma, Shalabh / Yu, Mengyun / Lee, Juhyung / Washington, Benjamin J / Whitman, William B / Ballantyne, Ford / Medeiros, Patricia M / Moran, Mary Ann

    Environmental microbiology

    2018  Volume 20, Issue 8, Page(s) 3012–3030

    Abstract: Understanding which compounds comprising the complex and dynamic marine dissolved organic matter (DOM) pool are important in supporting heterotrophic bacterial production remains a major challenge. We eliminated sources of labile phytoplankton products, ... ...

    Abstract Understanding which compounds comprising the complex and dynamic marine dissolved organic matter (DOM) pool are important in supporting heterotrophic bacterial production remains a major challenge. We eliminated sources of labile phytoplankton products, advected terrestrial material and photodegradation products to coastal microbial communities by enclosing water samples in situ for 24 h in the dark. Bacterial genes for which expression decreased between the beginning and end of the incubation and chemical formulae that were depleted over this same time frame were used as indicators of bioavailable compounds, an approach that avoids augmenting or modifying the natural DOM pool. Transport- and metabolism-related genes whose relative expression decreased implicated osmolytes, carboxylic acids, fatty acids, sugars and organic sulfur compounds as candidate bioreactive molecules. FT-ICR MS analysis of depleted molecular formulae implicated functional groups ~ 30-40 Da in size cleaved from semi-polar components of DOM as bioreactive components. Both gene expression and FT-ICR MS analyses indicated higher lability of compounds with sulfur and nitrogen heteroatoms. Untargeted methodologies able to integrate biological and chemical perspectives can be effective strategies for characterizing the labile microbial metabolites participating in carbon flux.
    MeSH term(s) Bacteria/chemistry ; Bacteria/genetics ; Bacteria/metabolism ; Bacterial Proteins/chemistry ; Bacterial Proteins/genetics ; Bacterial Proteins/metabolism ; Carbon Cycle ; Microbiota ; Nitrogen/metabolism ; Oceans and Seas ; Organic Chemicals/chemistry ; Phytoplankton ; Seawater/chemistry ; Seawater/microbiology ; Sulfur/analysis
    Chemical Substances Bacterial Proteins ; Organic Chemicals ; Sulfur (70FD1KFU70) ; Nitrogen (N762921K75)
    Language English
    Publishing date 2018-07-30
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2020213-1
    ISSN 1462-2920 ; 1462-2912
    ISSN (online) 1462-2920
    ISSN 1462-2912
    DOI 10.1111/1462-2920.14344
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: It's money! Real-world grant experience through a student-run, peer-reviewed program.

    Dumanis, Sonya B / Ullrich, Lauren / Washington, Patricia M / Forcelli, Patrick A

    CBE life sciences education

    2013  Volume 12, Issue 3, Page(s) 419–428

    Abstract: Grantsmanship is an integral component of surviving and thriving in academic science, especially in the current funding climate. Therefore, any additional opportunities to write, read, and review grants during graduate school may have lasting benefits on ...

    Abstract Grantsmanship is an integral component of surviving and thriving in academic science, especially in the current funding climate. Therefore, any additional opportunities to write, read, and review grants during graduate school may have lasting benefits on one's career. We present here our experience with a small, student-run grant program at Georgetown University Medical Center. Founded in 2010, this program has several goals: 1) to give graduate students an opportunity to conduct small, independent research projects; 2) to encourage graduate students to write grants early and often; and 3) to give graduate students an opportunity to review grants. In the 3 yr since the program's start, 28 applications have been submitted, 13 of which were funded for a total of $40,000. From funded grants, students have produced abstracts and manuscripts, generated data to support subsequent grant proposals, and made new professional contacts with collaborators. Above and beyond financial support, this program provided both applicants and reviewers an opportunity to improve their writing skills, professional development, and understanding of the grants process, as reflected in the outcome measures presented. With a small commitment of time and funding, other institutions could implement a program like this to the benefit of their graduate students.
    MeSH term(s) Education, Graduate/methods ; Financing, Organized/economics ; Financing, Organized/organization & administration ; Peer Review, Research ; Program Evaluation ; Research Personnel/education ; Research Support as Topic/economics ; Research Support as Topic/organization & administration ; Students
    Language English
    Publishing date 2013-09-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2465176-X
    ISSN 1931-7913 ; 1931-7913
    ISSN (online) 1931-7913
    ISSN 1931-7913
    DOI 10.1187/cbe.12-05-0058
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Apolipoprotein E Regulates Injury-Induced Activation of Hippocampal Neural Stem and Progenitor Cells.

    Hong, Sue / Washington, Patricia M / Kim, Ahleum / Yang, Cui-Ping / Yu, Tzong-Shiue / Kernie, Steven G

    Journal of neurotrauma

    2015  Volume 33, Issue 4, Page(s) 362–374

    Abstract: Partial recovery from even severe traumatic brain injury (TBI) is ubiquitous and occurs largely through unknown mechanisms. Recent evidence suggests that hippocampal neural stem/progenitor cell (NSPC) activation and subsequent neurogenesis are ... ...

    Abstract Partial recovery from even severe traumatic brain injury (TBI) is ubiquitous and occurs largely through unknown mechanisms. Recent evidence suggests that hippocampal neural stem/progenitor cell (NSPC) activation and subsequent neurogenesis are responsible for at least some aspects of spontaneous recovery following TBI. Apolipoprotein E (ApoE) regulates postnatal neurogenesis in the hippocampus and is therefore a putative mediator of injury-induced neurogenesis. Further, ApoE isoforms in humans are associated with different cognitive outcomes following TBI. To investigate the role of ApoE in injury-induced neurogenesis, we exposed wild-type, ApoE-deficient, and human ApoE isoform-specific (ApoE3 and ApoE4) transgenic mice crossed with nestin-green fluorescent protein (GFP) reporter mice to controlled cortical impact (CCI) and assessed progenitor activation at 2 d post-injury using unbiased stereology. GFP+ progenitor cells were increased by approximately 120% in the ipsilateral hippocampus in injured wild-type mice, compared with sham mice (p<0.01). Co-localization of GFP+ cells with bromodeoxyrudine (BrdU) to label dividing cells indicated increased proliferation of progenitors in the injured hippocampus (p<0.001). This proliferative injury response was absent in ApoE-deficient mice, as no increase in GFP+ cells was observed in the injured hippocampus, compared with sham mice, despite an overall increase in proliferation indicated by increased BrdU+ cells (86%; p<0.05). CCI-induced proliferation of GFP+ cells in both ApoE3 and ApoE4 mice but the overall response was attenuated in ApoE4 mice due to fewer GFP+ cells at baseline. We demonstrate that ApoE is required for injury-induced proliferation of NSPCs after experimental TBI, and that this response is influenced by human APOE genotype.
    MeSH term(s) Animals ; Apolipoproteins E/physiology ; Brain Injuries/metabolism ; Brain Injuries/pathology ; Female ; Hippocampus/metabolism ; Hippocampus/pathology ; Humans ; Male ; Mice ; Mice, Knockout ; Mice, Transgenic ; Neural Stem Cells/metabolism ; Neural Stem Cells/pathology ; Neurogenesis/physiology ; Stem Cells/metabolism ; Stem Cells/pathology
    Chemical Substances Apolipoproteins E
    Language English
    Publishing date 2015-06-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 645092-1
    ISSN 1557-9042 ; 0897-7151
    ISSN (online) 1557-9042
    ISSN 0897-7151
    DOI 10.1089/neu.2014.3860
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Early Identification of Autism Spectrum Disorder Among Children Aged 4 Years - Early Autism and Developmental Disabilities Monitoring Network, Six Sites, United States, 2016.

    Shaw, Kelly A / Maenner, Matthew J / Baio, Jon / Washington, Anita / Christensen, Deborah L / Wiggins, Lisa D / Pettygrove, Sydney / Andrews, Jennifer G / White, Tiffany / Rosenberg, Cordelia Robinson / Constantino, John N / Fitzgerald, Robert T / Zahorodny, Walter / Shenouda, Josephine / Daniels, Julie L / Salinas, Angelica / Durkin, Maureen S / Dietz, Patricia M

    Morbidity and mortality weekly report. Surveillance summaries (Washington, D.C. : 2002)

    2020  Volume 69, Issue 3, Page(s) 1–11

    Abstract: Problem/condition: Autism spectrum disorder (ASD).: Period covered: 2016.: Description of system: The Early Autism and Developmental Disabilities Monitoring (Early ADDM) Network, a subset of the overall ADDM Network, is an active surveillance ... ...

    Abstract Problem/condition: Autism spectrum disorder (ASD).
    Period covered: 2016.
    Description of system: The Early Autism and Developmental Disabilities Monitoring (Early ADDM) Network, a subset of the overall ADDM Network, is an active surveillance program that estimates ASD prevalence and monitors early identification of ASD among children aged 4 years. Children included in surveillance year 2016 were born in 2012 and had a parent or guardian who lived in the surveillance area in Arizona, Colorado, Missouri, New Jersey, North Carolina, or Wisconsin, at any time during 2016. Children were identified from records of community sources including general pediatric health clinics, special education programs, and early intervention programs. Data from comprehensive evaluations performed by community professionals were abstracted and reviewed by trained clinicians using a standardized ASD surveillance case definition with criteria from the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5).
    Results: In 2016, the overall ASD prevalence was 15.6 per 1,000 (one in 64) children aged 4 years for Early ADDM Network sites. Prevalence varied from 8.8 per 1,000 in Missouri to 25.3 per 1,000 in New Jersey. At every site, prevalence was higher among boys than among girls, with an overall male-to-female prevalence ratio of 3.5 (95% confidence interval [CI] = 3.1-4.1). Prevalence of ASD between non-Hispanic white (white) and non-Hispanic black (black) children was similar at each site (overall prevalence ratio: 0.9; 95% CI = 0.8-1.1). The prevalence of ASD using DSM-5 criteria was lower than the prevalence using Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) criteria at one of four sites that used criteria from both editions. Among sites where ≥60% of children aged 4 years had information about intellectual disability (intelligence quotient ≤70 or examiner's statement of intellectual disability documented in an evaluation), 53% of children with ASD had co-occurring intellectual disability. Of all children aged 4 years with ASD, 84% had a first evaluation at age ≤36 months and 71% of children who met the surveillance case definition had a previous ASD diagnosis from a community provider. Median age at first evaluation and diagnosis for this age group was 26 months and 33 months, respectively. Cumulative incidence of autism diagnoses received by age 48 months was higher for children aged 4 years than for those aged 8 years identified in Early ADDM Network surveillance areas in 2016.
    Interpretation: In 2016, the overall prevalence of ASD in the Early ADDM Network using DSM-5 criteria (15.6 per 1,000 children aged 4 years) was higher than the 2014 estimate using DSM-5 criteria (14.1 per 1,000). Children born in 2012 had a higher cumulative incidence of ASD diagnoses by age 48 months compared with children born in 2008, which indicates more early identification of ASD in the younger group. The disparity in ASD prevalence has decreased between white and black children. Prevalence of co-occurring intellectual disability was higher than in 2014, suggesting children with intellectual disability continue to be identified at younger ages. More children received evaluations by age 36 months in 2016 than in 2014, which is consistent with Healthy People 2020 goals. Median age at earliest ASD diagnosis has not changed considerably since 2014.
    Public health action: More children aged 4 years with ASD are being evaluated by age 36 months and diagnosed by age 48 months, but there is still room for improvement in early identification. Timely evaluation of children by community providers as soon as developmental concerns have been identified might result in earlier ASD diagnoses, earlier receipt of evidence-based interventions, and improved developmental outcomes.
    MeSH term(s) Autism Spectrum Disorder/diagnosis ; Autism Spectrum Disorder/epidemiology ; Child, Preschool ; Diagnostic and Statistical Manual of Mental Disorders ; Early Diagnosis ; Female ; Humans ; Male ; Population Surveillance ; Prevalence ; United States/epidemiology
    Language English
    Publishing date 2020-03-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605652-0
    ISSN 1545-8636 ; 0892-3787
    ISSN (online) 1545-8636
    ISSN 0892-3787
    DOI 10.15585/mmwr.ss6903a1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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