scholarly article | Q13442814 |
P50 | author | Franziska Flaig | Q92185454 |
Monika Führer | Q92185455 | ||
Kerstin Hein | Q92185460 | ||
P2093 | author name string | Gian Domenico Borasio | |
Kathrin Knochel | |||
Julia D Lotz | |||
P2860 | cites work | Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups | Q29618084 |
Neonatologist training to guide family decision making for critically ill infants | Q30227595 | ||
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When One Knows a Fetus Is Expected to Die: Palliative Care in the Context of Prenatal Diagnosis of Fetal Malformations | Q36264699 | ||
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Continuing with pregnancy after a diagnosis of lethal abnormality: experience of five couples and recommendations for management. | Q36599895 | ||
"Have no regrets:" Parents' experiences and developmental tasks in pregnancy with a lethal fetal diagnosis | Q36734157 | ||
Palliative care for the family carrying a fetus with a life-limiting diagnosis | Q36969593 | ||
Pregnancy continuation and organizational religious activity following prenatal diagnosis of a lethal fetal defect are associated with improved psychological outcome | Q37141479 | ||
Palliative care for prenatally diagnosed lethal fetal abnormality | Q37174618 | ||
Systematic review of the literature: parental outcomes after diagnosis of fetal anomaly | Q37897892 | ||
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Non-invasive prenatal testing for aneuploidy: current status and future prospects | Q38114375 | ||
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Late-term abortion for fetal anomaly: Vietnamese women's experiences | Q40047303 | ||
An alternative to termination of pregnancy | Q40969820 | ||
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Parental hopes, interventions, and survival of neonates with trisomy 13 and trisomy 18. | Q47608554 | ||
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Perinatal hospice. Comprehensive care for the family of the fetus with a lethal condition. | Q51023031 | ||
The decision to continue: the experiences and needs of parents who receive a prenatal diagnosis of holoprosencephaly. | Q52113842 | ||
Healing fictions': stories of choosing in the aftermath of the detection of fetal anomalies. | Q52202903 | ||
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Our children are not a diagnosis: the experience of parents who continue their pregnancy after a prenatal diagnosis of trisomy 13 or 18. | Q54482744 | ||
Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
"I Would Do It All Over Again": Cherishing Time and the Absence of Regret in Continuing a Pregnancy after a Life-Limiting Diagnosis | Q57141287 | ||
Prenatal diagnosis of fetal abnormality: psychological effects on women in low-risk pregnancies | Q57839624 | ||
Truth telling and severe fetal diagnosis: a virtue ethics perspective | Q58667184 | ||
Psychological Impact of the Announcement of a Fetal Abnormality on Pregnant Women and on Professionals | Q61901293 | ||
Perceptions of Lethal Fetal Abnormality among Perinatal Professionals and the Challenges of Neonatal Palliative Care | Q61943594 | ||
Prenatal diagnosis and caring | Q67572824 | ||
The health-care experiences of families given the prenatal diagnosis of trisomy 18 | Q80424382 | ||
Decision-making after ultrasound diagnosis of fetal abnormality | Q81931278 | ||
"Choosing the road less traveled" | Q83723197 | ||
Pregnant women's experiences, needs, and preferences regarding information about malformations detected by ultrasound scan | Q84113648 | ||
Personal growth after severe fetal diagnosis | Q84572278 | ||
He was my son, not a dying baby | Q85239227 | ||
P433 | issue | 6 | |
P304 | page(s) | 704-711 | |
P577 | publication date | 2019-03-07 | |
P1433 | published in | Palliative Medicine | Q7127852 |
P1476 | title | Perinatal Palliative Care: A qualitative study evaluating the perspectives of pregnancy counselors | |
P478 | volume | 33 |
Q89659928 | Objective Assessment of Counselling for Fetal Heart Defects: An Interdisciplinary Multicenter Study | cites work | P2860 |
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