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  1. Article ; Online: Longitudinal assessment of Leydig cell function in male survivors of childhood cancer.

    Thrope, Alexandra / Gerber, Linda M / Thomas, Charlene / Antal, Zoltan

    Pediatric blood & cancer

    2023  Volume 71, Issue 3, Page(s) e30829

    Abstract: Background: As the number and longevity of childhood cancer survivors increases, assessing treatment-associated late effects remains crucial. We longitudinally examined the incidence of and associated risk factors for Leydig cell dysfunction (LCD) and ... ...

    Abstract Background: As the number and longevity of childhood cancer survivors increases, assessing treatment-associated late effects remains crucial. We longitudinally examined the incidence of and associated risk factors for Leydig cell dysfunction (LCD) and Leydig cell failure (LCF) in men treated for pediatric cancers at our institution.
    Procedure: We performed a retrospective longitudinal cohort study of adult male survivors treated for various childhood cancers who are at risk for LCD. The outcomes of interest were serum testosterone and luteinizing hormone (LH) levels during childhood and adulthood. Risk factors assessed included treatment with stem cell transplant, total body irradiation (TBI), and exposure to alkylating agents.
    Results: Out of 118 eligible subjects, 7.6% had LCF and 14.4% had LCD. Median age at last testosterone level was 20 years. Subjects with sufficient testosterone levels in adulthood (N = 105) remained sufficient for a mean of 11.1 years following completion of cancer treatment. We found significant associations between LCF and treatment with TBI (p < .003) and between LCF in adulthood and testosterone insufficiency in childhood (p < .001). No statistically significant association was found between LCF and cyclophosphamide equivalent dose greater than 20 g/m
    Conclusions: Incidence of LCF and LCD are low in male survivors of childhood cancer. Longitudinally, there is an association between childhood testosterone insufficiency and LCF in adulthood. Alkylating agents and stem cell transplant without TBI were not associated with LCF in our study.
    MeSH term(s) Adult ; Humans ; Male ; Child ; Young Adult ; Leydig Cells/physiology ; Neoplasms/drug therapy ; Cancer Survivors ; Retrospective Studies ; Longitudinal Studies ; Testosterone/pharmacology ; Testosterone/therapeutic use ; Survivors ; Alkylating Agents/pharmacology ; Alkylating Agents/therapeutic use
    Chemical Substances Testosterone (3XMK78S47O) ; Alkylating Agents
    Language English
    Publishing date 2023-12-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2131448-2
    ISSN 1545-5017 ; 1545-5009
    ISSN (online) 1545-5017
    ISSN 1545-5009
    DOI 10.1002/pbc.30829
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Establishing the minimum clinically important difference for the Genetic Counseling Outcome Scale (GCOS-24).

    Thomas, Charlene / McAllister, Marion

    Journal of genetic counseling

    2019  Volume 28, Issue 5, Page(s) 1003–1010

    Abstract: To establish the smallest change in genetic counseling outcome that is meaningful for patients, the aim of this study was to establish the Minimum Clinically Important Difference (MCID) for the Genetic Counseling Outcome Scale (GCOS-24). GCOS-24 is a ... ...

    Abstract To establish the smallest change in genetic counseling outcome that is meaningful for patients, the aim of this study was to establish the Minimum Clinically Important Difference (MCID) for the Genetic Counseling Outcome Scale (GCOS-24). GCOS-24 is a patient-reported outcome measure for clinical genetics services. Secondary aims included understanding what patients deem important for reaching this score. Participants were 74 new patients recruited from the All Wales Medical Genetics Service, between April 2016 and December 2016. An anchor-based, global transition question methodology was used to identify the MCID, by asking participants how much meaningful change they experienced following their genetics appointment, and comparing this with GCOS-24 change scores. This ensured that the established score was clinically meaningful to patients. Comments from a free text response box were analyzed using qualitative thematic analysis. The mean score of the group who felt "a little better" was determined to be the MCID. The MCID was established to be a GCOS-24 score increase of 10.3 points after a clinical genetics appointment. This score was significantly different from the group "neutral" (0.64 points), using an independent samples t test. Themes identified as important for reaching the MCID included "future and family". These findings contribute to interpretability of GCOS-24 and provide some useful insights for genetic counseling service development.
    MeSH term(s) Female ; Genetic Counseling/methods ; Humans ; Male ; Middle Aged ; Patient Reported Outcome Measures ; Wales
    Language English
    Publishing date 2019-07-30
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1117799-8
    ISSN 1573-3599 ; 1059-7700
    ISSN (online) 1573-3599
    ISSN 1059-7700
    DOI 10.1002/jgc4.1152
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  3. Article ; Online: Sim-Based Home Tracheostomy Care: A Mixed Methods Study on Outcomes and Parental Preparedness.

    Bergman, Charles M / Thomas, Charlene / Clapper, Timothy / Nellis, Marianne / Yuen, Anthony / Gerber, Linda / Ching, Kevin

    Hospital pediatrics

    2024  Volume 14, Issue 4, Page(s) 251–257

    Abstract: Objectives: To assess effects of a Simulation-Based Discharge Education Program (SDP) on long-term caregiver-reported satisfaction and to compare clinical outcomes for children with new tracheostomies whose caregivers completed SDP versus controls.: ... ...

    Abstract Objectives: To assess effects of a Simulation-Based Discharge Education Program (SDP) on long-term caregiver-reported satisfaction and to compare clinical outcomes for children with new tracheostomies whose caregivers completed SDP versus controls.
    Methods: The study employed a mixed methods approach: (1) a qualitative analysis of feedback from caregivers who previously completed SDP, and (2) a quantitative retrospective case-control study comparing outcomes between children with new tracheostomies whose caregivers completed SDP versus controls, matched on discharge disposition and age. The primary outcome was emergency department visits for tracheostomy-related issues within 1 year of discharge.
    Results: Feedback from 18 interviews was coded into 5 themes: knowledge acquisition, active learning, comfort and preparedness, home application of skills, and overall assessment. Caregivers of 27 children (median age 26 months [interquartile range (IQR) 5.5 months-11 years]) underwent SDP training. Clinical outcomes of these children were compared with 27 matched children in the non-SDP group (median age 16 months [IQR 3.5 months-10 years]). There was no significant difference in ED visits for tracheostomy-related complications within 1 year of discharge between the SDP group and non-SDP group (2 [IQR 0-2] vs 1 [IQR 0-2], P = .2).
    Conclusions: Caregivers reported overwhelmingly positive experiences with SDP that persisted even 4 years after training. Caregiver participation in SDP did not yield a significant difference in ED visits within 1 year of discharge for tracheostomy-related complications compared with control counterparts. Future steps will identify more effective methods for comparing and analyzing clinical outcomes to further validate impacts of simulation-based programs.
    MeSH term(s) Child ; Humans ; Infant ; Tracheostomy ; Retrospective Studies ; Case-Control Studies ; Home Care Services ; Caregivers/education ; Parents
    Language English
    Publishing date 2024-03-16
    Publishing country United States
    Document type Journal Article
    ISSN 2154-1671
    ISSN (online) 2154-1671
    DOI 10.1542/hpeds.2023-007539
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Screening for Anxiety and Depression in Children with Congenital Adrenal Hyperplasia

    Jacob, Marianne / Lin-Su, Karen / Catarozoli, Corinne / Thomas, Charlene / Poppas, Dix / Lekarev, Oksana

    Journal of clinical research in pediatric endocrinology

    2023  Volume 15, Issue 4, Page(s) 406–416

    Abstract: Objective: Congenital adrenal hyperplasia (CAH) is an inherited condition in which individuals require multiple daily doses of medication and are at risk for life-threatening adrenal crisis. The chronic nature and severity of CAH place children at risk ... ...

    Abstract Objective: Congenital adrenal hyperplasia (CAH) is an inherited condition in which individuals require multiple daily doses of medication and are at risk for life-threatening adrenal crisis. The chronic nature and severity of CAH place children at risk for psychiatric morbidity. The aim was to assess the degree of anxiety and depressive symptoms in children with CAH.
    Methods: A cross-sectional cohort study of children (7-17 years) with CAH and their caregivers were recruited between May and December 2021. Children with hypothyroidism (HT) and their caregivers served as unaffected controls. Validated mental health questionnaires [Children’s Depression Inventory 2 Self Report-Short (CDI-2), Screen for Child Anxiety Related Disorders (SCARED), Patient Health Questionnaire modified for Adolescents (PHQ-A); self and proxy] were completed by participants at one clinic visit. Higher scores indicated greater symptoms of anxiety and depression.
    Results: A total of 60 children and 56 parents participated. Among the children 34 had CAH (68% female, mean age 11.41±2.5, CAH duration 8.5±4.1) and 26 had HT (73% female, mean age 12.7±2.9 years, HT duration 6.0±4.2 years). There was no increase in anxiety and depression symptoms in children with CAH compared to controls. In sub-analyses, children with CAH and controls reported a greater number of anxiety and depression symptoms than their caregivers on the SCARED and CDI-2, respectively. There was no association between adrenal control and the degree of anxiety or depression symptoms.
    Conclusion: Children with CAH do not have more symptoms of anxiety or depression compared to controls. Child and caregiver-proxy responses lack agreement, suggesting that children with CAH may continue to benefit from routine mental health evaluation, regardless of voiced caregiver concern.
    MeSH term(s) Adolescent ; Child ; Humans ; Female ; Male ; Adrenal Hyperplasia, Congenital/complications ; Adrenal Hyperplasia, Congenital/diagnosis ; Adrenal Hyperplasia, Congenital/epidemiology ; Depression/diagnosis ; Depression/epidemiology ; Depression/etiology ; Cross-Sectional Studies ; Anxiety/diagnosis ; Anxiety/epidemiology ; Anxiety/etiology
    Language English
    Publishing date 2023-07-20
    Publishing country Turkey
    Document type Journal Article
    ZDB-ID 2641608-6
    ISSN 1308-5735 ; 1308-5727
    ISSN (online) 1308-5735
    ISSN 1308-5727
    DOI 10.4274/jcrpe.galenos.2023.2023-2-10
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Timing of Tracheostomy in Critically Ill Infants and Children With Respiratory Failure: A Pediatric Health Information System Study.

    Mehrotra, Priyanka / Thomas, Charlene / Gerber, Linda M / Maresh, Alison / Nellis, Marianne

    Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies

    2023  Volume 24, Issue 2, Page(s) e66–e75

    Abstract: Objectives: Tracheostomy placement in infants and children with respiratory failure has steadily increased over time, yet there is no consensus for optimal timing. We sought to: 1) describe tracheostomy timing and associated demographic and clinical ... ...

    Abstract Objectives: Tracheostomy placement in infants and children with respiratory failure has steadily increased over time, yet there is no consensus for optimal timing. We sought to: 1) describe tracheostomy timing and associated demographic and clinical characteristics in a large ICU cohort and 2) compare clinical outcomes between subgroups based on tracheostomy timing.
    Design: Retrospective observational study using the Pediatric Health Information System (PHIS).
    Setting: Neonatal ICUs and PICUs in the United States.
    Patients: PHIS was queried for patients less than 18 years who underwent tracheostomy from 2010 to 2020. Patients were included if admitted to an ICU with need for mechanical ventilation (MV) prior to tracheostomy in the same hospitalization. Patients were categorized as early tracheostomy (ET) (placement at MV day ≤ 14), late tracheostomy (LT) (MV days 15-60), and extended tracheostomy (ExT) (MV day > 60). Primary endpoints included demographic and clinical characteristics. Secondary endpoints included patient outcomes: in-hospital mortality, length of stay (LOS), hospital-acquired pneumonia (HAP), and hospital costs.
    Interventions: None.
    Measurements and main results: Sixteen thousand one hundred twenty-one patients underwent tracheostomy at 52 children's hospitals. Ten thousand two hundred ninety-five had complete data and were included in the analysis. Thirty-nine percent (4,006/10,295) underwent ET, 40% (4,159/10,295) underwent LT, and 21% (2,130/10,295) underwent ExT. Majority of patients in all subgroups had complex chronic conditions. Median age was significantly different between subgroups with ET being the oldest ( p < 0.001). A multivariable regression analysis showed that ET was associated with lower in-hospital mortality ( p < 0.001), shorter hospital LOS ( p < 0.001), shorter ICU LOS ( p < 0.001), shorter post-tracheostomy LOS ( p < 0.001), decreased HAP ( p < 0.001), and lower hospital costs ( p < 0.001) compared with those who underwent LT or ExT.
    Conclusions: In a large cohort of pediatric patients with respiratory failure, tracheostomy placement within 14 days of MV was associated with improved in-hospital outcomes. ET was independently associated with decreased mortality, LOS, HAP, and hospital costs.
    MeSH term(s) Infant, Newborn ; Humans ; Child ; Infant ; Tracheostomy ; Critical Illness/therapy ; Health Information Systems ; Respiration, Artificial ; Retrospective Studies ; Length of Stay ; Respiratory Insufficiency/therapy ; Intensive Care Units
    Language English
    Publishing date 2023-01-20
    Publishing country United States
    Document type Observational Study ; Journal Article
    ZDB-ID 2052349-X
    ISSN 1947-3893 ; 1529-7535
    ISSN (online) 1947-3893
    ISSN 1529-7535
    DOI 10.1097/PCC.0000000000003120
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  6. Article ; Online: Integration and usability of a digital cancer risk stratification tool to optimize identification of patients at risk for hereditary cancers: A pilot study.

    Webster, Emily M / Perez, Luiza / Ahsan, Muhammad Danyal / Levi, Sarah / Chandler, Isabelle / Thomas, Charlene / Babagbemi, Kemi / Sharaf, Ravi N / Frey, Melissa K

    Gynecologic oncology

    2024  Volume 183, Page(s) 1–6

    Abstract: Background: Patients with a personal or family history of cancer may have elevated risk of developing future cancers, which often remains unrecognized due to lapses in screening. This pilot study assessed the usability and clinical outcomes of a cancer ... ...

    Abstract Background: Patients with a personal or family history of cancer may have elevated risk of developing future cancers, which often remains unrecognized due to lapses in screening. This pilot study assessed the usability and clinical outcomes of a cancer risk stratification tool in a gynecologic oncology clinic.
    Methods: New gynecologic oncology patients were prompted to complete a commercially developed personal and family history-based risk stratification tool to assess eligibility for genetic testing using National Comprehensive Cancer Network criteria and estimated lifetime breast cancer risk using the Tyrer-Cuzick model. After use of the risk stratification tool, usability was assessed via completion rate and the System Usability Scale, and health literacy was assessed using the BRIEF Health Literacy Screening Tool.
    Results: 130 patients were prompted to complete the risk stratification tool; 93 (72%) completed the tool. Race and ethnicity and insurance type were not associated with tool completion. The median System Usability Scale score was 83 out of 100 (interquartile range, 60-95). Health literacy positively correlated with perceived usability. Public insurance and race or ethnicity other than non-Hispanic White was associated with lower perceived usability. Sixty (65%) patients met eligibility criteria for genetic testing, and 21 (38% of 56 eligible patients) were candidates for enhanced breast cancer screening based on an estimated lifetime breast cancer risk of ≥20%.
    Conclusions: A majority of patients completed the digital cancer risk stratification tool. Older age, lower health literacy, public insurance, and race or ethnicity other than non-Hispanic White were associated with lower perceived tool usability.
    Language English
    Publishing date 2024-03-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 801461-9
    ISSN 1095-6859 ; 0090-8258
    ISSN (online) 1095-6859
    ISSN 0090-8258
    DOI 10.1016/j.ygyno.2024.02.028
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  7. Article ; Online: Does the Use of Botulinum Toxin in Treatment of Myofascial Pain Disorder of the Masseters and Temporalis Muscles Reduce Pain, Improve Function, or Enhance Quality of Life?

    Reeve, Gwendolyn S / Insel, Owen / Thomas, Charlene / Houle, Ashley N / Miloro, Michael

    Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons

    2023  Volume 82, Issue 4, Page(s) 393–401

    Abstract: Background: The efficacy of botulinum toxin for management of myofascial pain disorder (MPD) remains controversial.: Purpose: The purpose was to determine if the use of onabotulinumtoxinA (onabotA) in patients with MPD reduces pain, improves function, ...

    Abstract Background: The efficacy of botulinum toxin for management of myofascial pain disorder (MPD) remains controversial.
    Purpose: The purpose was to determine if the use of onabotulinumtoxinA (onabotA) in patients with MPD reduces pain, improves function, or enhances quality of life (QoL).
    Study design, setting, and sample: This is a multicenter, prospective, randomized, double-blinded, placebo-controlled clinical trial. Subjects with orofacial pain were screened for MPD as defined by the Diagnostic Criteria for Temporomandibular Disorders.
    Predictor variable: The primary predictor variable was MPD treatment with random assignment to onabotA or placebo (saline).
    Main outcome variable: The primary outcome variable was pain before treatment (T0) and at 1 month (T1) using a visual analog scale. Secondary outcome variables included pain at 2 months (T2) and 3 months (T3), maximal incisal opening (MIO), jaw function (jaw functional limitation scale), and QoL (Short Form 36) measured at T0, T1, T2, and T3.
    Covariates: Covariates included subject demographics, prior treatments, and temporomandibular joint signs/symptoms.
    Analyses: Descriptive and bivariate statistics included χ
    Results: Seventy five subjects with a mean age of 37 (±11) and 35 (±12) years in the onabotA and placebo groups, respectively (P = .6). Females represented 32 (86%) and 29 (76%), respectively (P = .3). Mean visual analog scale pain score in the onabotA group was 58 (±15), 39 (±24), 38 (±23), and 38 (±20) at T0, T1, T2, and T3, respectively; and the placebo group was 54 (±14), 40 (±23), 34 (±20), and 36 (±22) at T0, T1, T2, and T3, respectively. There was no statistically significant difference in pain between groups at any time point (P = .36). There was no statistically significant difference between groups in MIO (P = .124), jaw function (P = .236), or QoL domains (P > .05) at any time point. Within-group improvement in pain was seen in both groups (P < .005). Within-group improvement in jaw function was seen in the onabotA (P = .007) and placebo (P = .005) groups. There was no within-group improvement in MIO or QoL with either group (P > .05).
    Conclusions: OnabotA and saline (placebo) injections both decrease pain and improve jaw function in subjects with MPD.
    MeSH term(s) Adult ; Female ; Humans ; Botulinum Toxins, Type A/therapeutic use ; Botulinum Toxins, Type A/adverse effects ; Facial Pain/drug therapy ; Muscles ; Pain Management ; Prospective Studies ; Quality of Life ; Somatoform Disorders/chemically induced ; Somatoform Disorders/drug therapy ; Treatment Outcome ; Male ; Young Adult ; Middle Aged
    Chemical Substances Botulinum Toxins, Type A (EC 3.4.24.69)
    Language English
    Publishing date 2023-12-28
    Publishing country United States
    Document type Randomized Controlled Trial ; Multicenter Study ; Journal Article
    ZDB-ID 392404-x
    ISSN 1531-5053 ; 0278-2391
    ISSN (online) 1531-5053
    ISSN 0278-2391
    DOI 10.1016/j.joms.2023.12.014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Dermatologist work practices and work-life balance during COVID-19: a cross-sectional survey.

    Waqas, Bukhtawar / Matushansky, Justin T / Thomas, Charlene / Lipner, Shari R

    International journal of dermatology

    2021  Volume 61, Issue 5, Page(s) e158–e162

    MeSH term(s) COVID-19 ; Cross-Sectional Studies ; Dermatologists ; Health Knowledge, Attitudes, Practice ; Humans ; Surveys and Questionnaires ; Work-Life Balance
    Language English
    Publishing date 2021-10-27
    Publishing country England
    Document type Letter
    ZDB-ID 412254-9
    ISSN 1365-4632 ; 0011-9059 ; 1461-1244
    ISSN (online) 1365-4632
    ISSN 0011-9059 ; 1461-1244
    DOI 10.1111/ijd.15955
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  9. Article ; Online: The Top 100 Most-Cited Articles on Nail Psoriasis: A Bibliometric Analysis.

    Malik, Shilpa / Matushansky, Justin T / Thomas, Charlene / Lipner, Shari R

    Cutis

    2021  Volume 108, Issue 2, Page(s) 76

    MeSH term(s) Bibliometrics ; Humans ; Nail Diseases ; Nails, Malformed ; Psoriasis
    Language English
    Publishing date 2021-11-04
    Publishing country United States
    Document type Letter
    ZDB-ID 391840-3
    ISSN 2326-6929 ; 0011-4162 ; 0151-9522
    ISSN (online) 2326-6929
    ISSN 0011-4162 ; 0151-9522
    DOI 10.12788/cutis.0311
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: A Urinary Drug-Disposing Approach as an Alternative to Intravesical Chemotherapy for Treating Nonmuscle Invasive Bladder Cancer.

    Bellat, Vanessa / Michel, Adam O / Thomas, Charlene / Stokol, Tracy / Choi, Benjamin B / Law, Benedict

    Cancer research

    2022  Volume 82, Issue 7, Page(s) 1409–1422

    Abstract: The standard treatment of nonmuscle invasive bladder cancer (NMIBC) is transurethral resection of the tumors, followed by intravesical therapy (IT), which comprises a direct instillation of a solution of Bacillus Calmette-Guérin vaccine or chemotherapy ... ...

    Abstract The standard treatment of nonmuscle invasive bladder cancer (NMIBC) is transurethral resection of the tumors, followed by intravesical therapy (IT), which comprises a direct instillation of a solution of Bacillus Calmette-Guérin vaccine or chemotherapy into the bladder. However, the recurrence rate in this disease remains unacceptably high. IT is a local treatment that fails to reach tumors developed in the upper urinary tract (ureter and renal pelvis). The catheterization procedure required for IT is invasive, painful, and poses an increased infection risk, resulting in poor patient quality of life and compliance. There is an unmet need for a potent, comprehensive, and noninvasive option. Without chemical modifications, peptides are rapidly removed by renal clearance. This "shortcoming" can be advantageous when used as a drug carrier for directing therapy to NMIBC. Here we develop a urinary drug-disposing (UDD) approach to improve NMIBC treatment. A 12-amino acid bio-inert peptide (Bdd) that can be exclusively eliminated via renal filtration was generated for delivering the microtubule inhibitor DM1 to NMIBC with minimal nonspecific accumulation in other organs. The UDD approach prolonged survival of mice bearing human bladder tumors. Unlike IT, the treatment was given noninvasively (intravenously). Furthermore, it was more effective at suppressing tumor growth than clinically used IT (mitomycin) and safer than free DM1. The application of this UDD approach to treat kidney tumors and deliver other drugs such as doxorubicin was also demonstrated. Overall, the rapid renal clearance of peptides can be exploited to direct cancer therapies to the urinary system.
    Significance: A noninvasive drug delivery approach that targets the urinary system overcomes the current barriers facing effective treatment of bladder cancer.
    MeSH term(s) Adjuvants, Immunologic ; Animals ; BCG Vaccine/therapeutic use ; Humans ; Mice ; Neoplasm Invasiveness/pathology ; Neoplasm Recurrence, Local/pathology ; Pharmaceutical Preparations ; Quality of Life ; Urinary Bladder/pathology ; Urinary Bladder Neoplasms/pathology
    Chemical Substances Adjuvants, Immunologic ; BCG Vaccine ; Pharmaceutical Preparations
    Language English
    Publishing date 2022-01-15
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1432-1
    ISSN 1538-7445 ; 0008-5472
    ISSN (online) 1538-7445
    ISSN 0008-5472
    DOI 10.1158/0008-5472.CAN-21-2897
    Database MEDical Literature Analysis and Retrieval System OnLINE

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