1
40
7
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1017/s1478951512000417" target="_blank" rel="noreferrer">http://doi.org/10.1017/s1478951512000417</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Ethnicity, race, and advance directives in an inpatient palliative care consultation service.
Publisher
An entity responsible for making the resource available
Palliative & Supportive Care
Date
A point or period of time associated with an event in the lifecycle of the resource
2013
Subject
The topic of the resource
Female; Humans; Male; Adult; Aged; Middle Aged; Cross-Cultural Comparison; Program Evaluation; Spirituality; 80 and over; decision making; DNAR; Resuscitation Orders; Advance Directives/eh [Ethnology]; Attitude to Death/eh [Ethnology]; Palliative Care/og [Organization & Administration]; Referral and Consultation/og [Organization & Administration]; Terminal Care/og [Organization & Administration]; African Americans/statistics & numerical data; Asian Continental Ancestry Group/sn [Statistics & Numerical Data]; European Continental Ancestry Group/sn [Statistics & Numerical Data]; Hispanic Americans/sn [Statistics & Numerical Data]; New York/ep [Epidemiology]
Creator
An entity primarily responsible for making the resource
Zaide GB; Pekmezaris R; Nouryan CN; Mir Tanveer P; Sison CP; Liberman T; Lesser ML; Cooper LB; Wolf-Klein GP
Description
An account of the resource
OBJECTIVE: Although race and ethnic background are known to be important factors in the completion of advance directives, there is a dearth of literature specifically investigating the effect of race and ethnicity on advance directive completion rate after palliative care consultation (PCC)., METHOD: A chart review of all patients seen by the PCC service in an academic hospital over a 9-month period was performed. Data were compiled using gender, race, ethnicity, religion, and primary diagnosis. For this study, advance directives were defined as: "Do Not Resuscitate" (DNR) and/or "Do Not Intubate" (DNI)., RESULTS: Of the 400 medical records reviewed, 57% of patients were female and 71.3% documented their religion as Christian. The most common documented diagnosis was cancer (39.5%). Forty-seven percent reported their race as white. White patients completed more advance directives than did nonwhite patients both before (25.67% vs. 12.68%) and after (59.36% vs. 40.84%) PCC. There was a significantly higher proportion of whites who signed an advance directive after a PCC than of nonwhites (p = 0.021); of the 139 whites who did not have an advance directive at admission, 63 signed an advance directive after a PCC compared with 186/60 nonwhites (45% vs. 32%, respectively, p = 0.021). Further analysis revealed that African Americans differed from whites in the likelihood of advance directive execution rates pre-PCC, but not post-PCC., SIGNIFICANCE OF RESULTS: This study demonstrates the impact of a PCC on the completion of advance directives, on both whites and nonwhites. The PCC Intervention significantly reduced differences between whites and African Americans in completing advance directives, which have been consistently documented in the end-of-life literature.
2013
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1017/s1478951512000417" target="_blank" rel="noreferrer">10.1017/s1478951512000417</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2013
80 And Over
Adult
Advance Directives/eh [Ethnology]
African Americans/statistics & numerical data
Aged
Asian Continental Ancestry Group/sn [Statistics & Numerical Data]
Attitude to Death/eh [Ethnology]
Backlog
Cooper LB
Cross-cultural Comparison
Decision Making
DNAR
European Continental Ancestry Group/sn [Statistics & Numerical Data]
Female
Hispanic Americans/sn [Statistics & Numerical Data]
Humans
Journal Article
Lesser ML
Liberman T
Male
Middle Aged
Mir Tanveer P
New York/ep [Epidemiology]
Nouryan CN
Palliative & Supportive Care
Palliative Care/og [Organization & Administration]
Pekmezaris R
Program Evaluation
Referral and Consultation/og [Organization & Administration]
Resuscitation Orders
Sison CP
Spirituality
Terminal Care/og [organization & Administration]
Wolf-Klein GP
Zaide GB
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/j.jpeds.2009.07.019" target="_blank" rel="noreferrer">http://doi.org/10.1016/j.jpeds.2009.07.019</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Categorizing neonatal deaths: a cross-cultural study in the United States, Canada, and The Netherlands.
Publisher
An entity responsible for making the resource available
The Journal Of Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
2010
Subject
The topic of the resource
Female; Humans; infant; Male; United States; Intensive Care Units; Terminal Care; Canada; Netherlands; Cross-Cultural Comparison; Respiration; Neonatal; decision making; Newborn; gestational age; Artificial; Withholding Treatment/statistics & numerical data; Physician Assisted Dying PAD; decision making; Diseases/mortality; Diseases/mortality; Withholding Treatment/statistics & numerical data
Creator
An entity primarily responsible for making the resource
Verhagen AAE; Janvier A; Leuthner SR; Andrews B; Lagatta J; Bos AF; Meadow W
Description
An account of the resource
OBJECTIVE: To clarify the process of end-of-life decision-making in culturally different neonatal intensive care units (NICUs). STUDY DESIGN: Review of medical files of newborns >22 weeks gestation who died in the delivery room (DR) or the NICU during 12 months in 4 NICUs (Chicago, Milwaukee, Montreal, and Groningen). We categorized deaths using a 2-by-2 matrix and determined whether mechanical ventilation was withdrawn/withheld and whether the child was dying despite ventilation or physiologically stable but extubated for neurological prognosis. RESULTS: Most unstable patients in all units died in their parents' arms after mechanical ventilation was withdrawn. In Milwaukee, Montreal, and Groningen, 4% to 12% of patients died while receiving cardiopulmonary resuscitation. This proportion was higher in Chicago (31%). Elective extubation for quality-of-life reasons never occurred in Chicago and occurred in 19% to 35% of deaths in the other units. The proportion of DR deaths in Milwaukee, Montreal, and Groningen was 16% to 22%. No DR deaths occurred in Chicago. CONCLUSIONS: Death in the NICU occurred differently within and between countries. Distinctive end-of-life decisions can be categorized separately by using a model with uniform definitions of withholding/withdrawing mechanical ventilation correlated with the patient's physiological condition. Cross-cultural comparison of end-of-life practice is feasible and important when comparing NICU outcomes.
2010-01
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/j.jpeds.2009.07.019" target="_blank" rel="noreferrer">10.1016/j.jpeds.2009.07.019</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2010
Andrews B
Artificial
Backlog
Bos AF
Canada
Cross-cultural Comparison
Decision Making
Diseases/mortality
Female
Gestational Age
Humans
Infant
Intensive Care Units
Janvier A
Journal Article
Lagatta J
Leuthner SR
Male
Meadow W
Neonatal
Netherlands
Newborn
Physician Assisted Dying PAD
Respiration
Terminal Care
The Journal Of Pediatrics
United States
Verhagen AAE
Withholding Treatment/statistics & Numerical Data
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1017/S1478951509990289" target="_blank" rel="noreferrer">http://doi.org/10.1017/S1478951509990289</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
International comparison study on the primary concerns of terminally ill cancer patients in short-term life review interviews among Japanese, Koreans, and Americans
Publisher
An entity responsible for making the resource available
Palliative & Supportive Care
Date
A point or period of time associated with an event in the lifecycle of the resource
2009
Subject
The topic of the resource
Female; Humans; Male; United States; Aged; Middle Aged; Cross-Cultural Comparison; Life Change Events; Hospices; Spirituality; Religion and Psychology; Psychometrics; Japan; 80 and over; Psychological; Personality Inventory/statistics & numerical data; Republic of Korea; Interview; Terminal Care/psychology; Mental Recall; Neoplasms/ethnology/psychology; Social Values/ethnology
Creator
An entity primarily responsible for making the resource
Ando M; Morita T; Ahn SH; Marquez-Wong F; Ide S
Description
An account of the resource
OBJECTIVE: The aim of this study was to investigate the primary concerns of terminally ill cancer patients in a Short-Term Life Review among Japanese, Koreans, and Americans to develop intervention programs to be tailored to patients in other countries. METHOD: Twenty Japanese, 16 Korean, and 7 American terminally ill cancer patients who were in the hospice wards of general Christian hospitals in each country participated in this study. Medical staff members (nurses, social workers, clinical psychologists) performed Short-Term Life Review Interviews with each patient. Patients reviewed their lives in the first session, the interviewers made simple albums for each patient in the week following the first session, and patients and interviewers then confirmed the contents of the album. The treatment period was 1 week. Measurement instruments included the Functional Assessment Chronic Illness Therapy-Spiritual (FACIT-Sp) and the Hospital Anxiety and Depression Scale (HADS). The contents of each interview session were transcribed, and correspondence analysis and a significance test were conducted on these data to select characteristic words or phrases. RESULTS: Using the FACIT-Sp scores, the following concerns were chosen, in descending order of frequency. In Japan, primary concerns consisted of such ideas as "good human relationships and transcendence," "achievements and satisfaction," "good memories and important things," and "bitter memories." In Korea, "religious life," "right behavior for living," "strong consideration for children and will," and "life for living" were primary concerns. In the United States, "love, pride, will to children," "good, sweet memories," and "regret and a feeling of loss" were primary concerns. SIGNIFICANCE OF RESULTS: We clarify the differences among the primary concerns from the Short-Term Life Reviews, arguing that we can improve the spiritual well-being of terminally ill cancer patients by focusing on the primary concerns within each country.
2009
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1017/S1478951509990289" target="_blank" rel="noreferrer">10.1017/S1478951509990289</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2009
80 And Over
Aged
Ahn SH
Ando M
Backlog
Cross-cultural Comparison
Female
Hospices
Humans
Ide S
Interview
Japan
Journal Article
Life Change Events
Male
Marquez-Wong F
Mental Recall
Middle Aged
Morita T
Neoplasms/ethnology/psychology
Palliative & Supportive Care
Personality Inventory/statistics & numerical data
Psychological
Psychometrics
Religion and Psychology
Republic of Korea
Social Values/ethnology
Spirituality
Terminal Care/psychology
United States
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
PedPalASCNet Member Publications
Subject
The topic of the resource
A collection of relevant articles published by one or more of PedPalASCNet's members
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1097/00002820-199810000-00001" target="_blank" rel="noreferrer">http://doi.org/10.1097/00002820-199810000-00001</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Experiences of mothers in five countries whose child died of cancer
Publisher
An entity responsible for making the resource available
Cancer Nursing
Date
A point or period of time associated with an event in the lifecycle of the resource
1998
Subject
The topic of the resource
Child; Female; Humans; Male; United States; Palliative Care; Adult; Canada; Mother-Child Relations; Middle Aged; Attitude to Death; Cross-Cultural Comparison; adolescent; Preschool; bereavement; infant; Greece; Norway; Oncologic Nursing; Hong Kong; Neoplasms/nursing/psychology/therapy
Creator
An entity primarily responsible for making the resource
Davies B; Deveau E; deVeber B; Howell D; Martinson I; Papadatou D; Pask E; Stevens M
Description
An account of the resource
Although increasing attention is being focused on the emotional aspects of caring for dying children and their families, few research reports concentrate on the experiences of mothers, particularly in different countries. This article describes the findings of an exploratory, descriptive study that investigated the experiences of mothers from five different countries who each had a child die from cancer in the past 6 months. Principal investigators, members of the International Work Group on Death, Dying, and Bereavement, conducted semistructured interviews with 21 mothers in their own countries. No culturally related differences were noted among mothers, and the mothers' recall of their experiences are more similar than different. All mothers, irrespective of country, described similar reactions to the diagnosis, management of the end-stage illness, and challenge of coping with bereavement. Lessons learned from this project provide suggestions for future research across countries.
1998
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1097/00002820-199810000-00001" target="_blank" rel="noreferrer">10.1097/00002820-199810000-00001</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
1998
Adolescent
Adult
Attitude To Death
Backlog
Bereavement
Canada
Cancer Nursing
Child
Cross-cultural Comparison
Davies B
Deveau E
deVeber B
Female
Greece
Hong Kong
Howell D
Humans
Infant
Journal Article
Male
Martinson I
Middle Aged
Mother-child Relations
Neoplasms/nursing/psychology/therapy
Norway
Oncologic Nursing
Palliative Care
Papadatou D
Pask E
Preschool
Stevens M
United States
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1177/109019819402100204" target="_blank" rel="noreferrer">http://doi.org/10.1177/109019819402100204</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Empowerment through photo novella: portraits of participation
Publisher
An entity responsible for making the resource available
Health Education Quarterly
Date
A point or period of time associated with an event in the lifecycle of the resource
1994
Subject
The topic of the resource
Child; Female; Humans; Male; Adult; Communication; Socioeconomic Factors; Cross-Cultural Comparison; China; Health Education; Power (Psychology); Preschool; Non-U.S. Gov't; Research Support; infant; Comparative Study; Developing Countries; Health Policy/trends; Life Style; Demographic Factors; Population; Population Characteristics; Photography; Asia; Community Participation; Eastern Asia; Economic Factors; Films; Health Services Needs and Demand/trends; Mass Media; Organization And Administration; Rural Health/trends; Rural Population--women; Summary Report; Women's Health Services/trends; Women's Status
Creator
An entity primarily responsible for making the resource
Wang C; Burris MA
Description
An account of the resource
Photo novella does not entrust cameras to health specialists, policymakers, or professional photographers, but puts them in the hands of children, rural women, grassroots workers, and other constituents with little access to those who make decisions over their lives. Promoting what Brazilian educator Paulo Freire has termed "education for critical consciousness," photo novella allows people to document and discuss their life conditions as they see them. This process of empowerment education also enables community members with little money, power, or status to communicate to policymakers where change must occur. This paper describes photo novella's underpinnings: empowerment education, feminist theory, and documentary photography. It draws on our experience implementing the process among 62 rural Chinese women, and shows that two major implications of photo novella are its contributions to changes in consciousness and informing policy.; PIP: Contrary to the traditional approach of relying upon photographic images taken by health specialists, policymakers, and professional photographers to document what transpires in a particular community or subpopulation, photo novella encourages children, rural women, grassroots workers, and other constituents with little access to decision-makers to take their own photographs of life as they see it. This process of empowerment education enables community members with little money, power, or status to communicate to policymakers where change must occur. This paper describes photo novella's foundation in empowerment education, feminist theory, and documentary photography. It draws upon experience implementing the process among 62 rural Chinese women, highlighting the ability of photo novella to change consciousness and inform policy.
1994
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1177/109019819402100204" target="_blank" rel="noreferrer">10.1177/109019819402100204</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
1994
Adult
Asia
Backlog
Burris MA
Child
China
Communication
Community Participation
Comparative Study
Cross-cultural Comparison
Demographic Factors
Developing Countries
Eastern Asia
Economic Factors
Female
Films
Health Education
Health Education Quarterly
Health Policy/trends
Health Services Needs and Demand/trends
Humans
Infant
Journal Article
Life Style
Male
Mass Media
Non-U.S. Gov't
Organization And Administration
Photography
Population
Population Characteristics
Power (psychology)
Preschool
Research Support
Rural Health/trends
Rural Population--women
Socioeconomic Factors
Summary Report
Wang C
Women's Health Services/trends
Women's Status
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1191/026921600674582192" target="_blank" rel="noreferrer">http://doi.org/10.1191/026921600674582192</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Attitudes and beliefs of palliative care physicians regarding communication with terminally ill cancer patients.
Publisher
An entity responsible for making the resource available
Palliative Medicine
Date
A point or period of time associated with an event in the lifecycle of the resource
2000
Subject
The topic of the resource
Female; Humans; Male; Canada; Prognosis; Prospective Studies; Patient-Centered Care; Resuscitation Orders; Cross-Cultural Comparison; Europe; DNAR; Truth Disclosure; Palliative Care/px [Psychology]; Family/px [Psychology]; Physician-Patient Relations; Terminally Ill/px [Psychology]; Attitude of Health Personnel; Neoplasms/px [Psychology]; South America
Creator
An entity primarily responsible for making the resource
Bruera E; Neumann CM; Mazzocato C; Stiefel F; Sala R
Description
An account of the resource
The subject of communication between palliative care physicians and their patients regarding their diagnosis and prognosis has not been extensively researched. The purpose of this survey was to compare the attitudes and beliefs of palliative care specialists regarding communication with the terminally ill in Europe, South America, and Canada. A sample of palliative care physicians from South America (Argentina and Brazil), French-speaking Europe, and Canada were identified, and posted a questionnaire. Physicians who stated that they practised palliative care at least 30% of their time were considered evaluable as palliative care specialists. Of a total of 272 questionnaires, 228 were returned (84%); and 182/228 (81%) respondents were considered to be palliative care specialists. Palliative care physicians in all three regions believed that cancer patients should be informed of their diagnosis and the terminal nature of their illness. Physicians reported that at least 60% of their patients knew their diagnosis and the terminal stage of their illness in 52% and 24% of cases in South America, and 69% and 38% of cases in Europe, respectively. All physicians agreed that 'do not resuscitate' orders should be present, and should be discussed with the patient in all cases. While 93% of Canadian physicians stated that at least 60% of their patients wanted to know about the terminal stage of their illness, only 18% of South American, and 26% of European physicians said this (P < 0.001). Similar results were found when the physicians were asked the percentage of families who want patients to know the terminal stage of their illness. However, almost all of the physicians agreed that if they had terminal cancer they would like to know. There was a significant association between patient based decision-making and female sex (P = 0.007), older age (P = 0.04), and physicians from Canada and South America (P < 0.001). Finally, in their daily decision making, South American physicians were significantly more likely to support beneficence and justice as compared with autonomy. Canadian physicians were more likely to support autonomy as compared with beneficence. In summary, our findings suggest that there are major regional differences in the attitudes and beliefs of physicians regarding communication at the end of life. More research is badly needed on the attitudes and beliefs of patients, families, and health care professionals in different regions of the world.
2000
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1191/026921600674582192" target="_blank" rel="noreferrer">10.1191/026921600674582192</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2000
Attitude Of Health Personnel
Backlog
Bruera E
Canada
Cross-cultural Comparison
DNAR
Europe
Family/px [psychology]
Female
Humans
Journal Article
Male
Mazzocato C
Neoplasms/px [psychology]
Neumann CM
Palliative Care/px [psychology]
Palliative Medicine
Patient-centered Care
Physician-patient Relations
Prognosis
Prospective Studies
Resuscitation Orders
Sala R
South America
Stiefel F
Terminally Ill/px [Psychology]
Truth Disclosure
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
December 2017 List
URL Address
<a href="https://doi.org/10.1542/peds.2017-0690" target="_blank" rel="noreferrer">https://doi.org/10.1542/peds.2017-0690</a>
Notes
Copyright (c) 2017 by the American Academy of Pediatrics.
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Cross-Cultural Differences in Communication About a Dying Child.
Publisher
An entity responsible for making the resource available
Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
2017
Subject
The topic of the resource
Communication; Cross-cultural Comparison; Physician-patient Relations; Attitude To Death/ Ethnology; Child; Humans; Male; Pakistan/ethnology; Subacute Sclerosing Panencephalitis/ Diagnosis/ Ethnology; United States/ethnology
Creator
An entity primarily responsible for making the resource
Cochran D; Saleem S; Khowaja-Punjwani S; Lantos JD
Description
An account of the resource
There are more migrants, refugees, and immigrants adrift in the world today than at any time in the recent past. Doctors and hospitals must care for people from many different cultures, countries, and religious backgrounds. We sometimes find our own deeply held beliefs and values challenged. In this "Ethics Rounds," we present a case in which a Pakistani immigrant family faces a tragic medical situation and wants to deal with it in ways that might be normative in their own culture but are aberrant in ours. We asked the American doctors and 2 Pakistani health professionals to think through the issues. We also invited the father to talk about his own experience and preferences. We conclude that strict adherence to Western ethical norms may not always be the best choice. Instead, an approach based on cultural humility may often allow people on both sides of a cultural divide to learn from one another.
Identifier
An unambiguous reference to the resource within a given context
<a href="https://doi.org/10.1542/peds.2017-0690" target="_blank" rel="noreferrer">10.1542/peds.2017-0690</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2017
Attitude To Death/ Ethnology
Child
Cochran D
Communication
Cross-cultural Comparison
December 2017 List
Humans
Khowaja-Punjwani S
Lantos JD
Male
Pakistan/ethnology
Pediatrics
Physician-patient Relations
Saleem S
Subacute Sclerosing Panencephalitis/ Diagnosis/ Ethnology
United States/ethnology