Search or add a thesis

Advanced Search (Beta)
Home > Role of Burnout and Positive Work Environment in Patient Safety Practices Among Nurses

Role of Burnout and Positive Work Environment in Patient Safety Practices Among Nurses

Thesis Info

Author

Sana Ahmad

Supervisor

Aisha Zubair

Department

National Institute of Psychology, Centre of Excellence, QAU

Program

MSc

Institute

Quaid-i-Azam University

Institute Type

Public

City

Islamabad

Province

Islamabad

Country

Pakistan

Thesis Completing Year

2017

Thesis Completion Status

Completed

Page

v, 72+Aendices

Subject

Psychology

Language

English

Other

Call No: Diss / M.SC / PSY / 1007

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676718473492

Similar


Loading...
Loading...

Similar Books

Loading...

Similar Chapters

Loading...

Similar News

Loading...

Similar Articles

Loading...

Similar Article Headings

Loading...

شیخ بشارت علی فارانی

شیخ بشارت علی فارانی
شیخ بشارت علی فارانیؔ(۱۹۱۱ئ۔۱۹۸۰ئ) کا اصل نام بشارت علی اور فارانیؔ تخلص کرتے تھے۔ فارانیؔ ظفر وال پیدا ہوئے ۔ تقسیم ہند کے بعد آپ نے سیالکوٹ میں مستقل رہائش اختیار کی۔ (۵۶۲) آپ کا کلام روزنامہ ’’نظام‘‘ ،کراچی،ہفت روزہ،’’چاند‘‘ ،جموں اور ’’پریم‘‘ لاہور میں چھپتا رہا۔ آپ نے سیالکوٹ سے ایک ادبی رسالہ ماہنامہ ’’فردوس‘‘ بھی جاری کیا۔
فارانیؔ کی شاعری میں کوئی جدت نہیں۔ ان کی شاعری میں روایتی موضوعات کی جھلک دیکھی جا سکتی ہے۔ نمونہ کلام ملاحظہ ہو:
ہاتھ میں جب تک تیرا ہاتھ

دن ہی دن ہے کیسی رات

ہو جائے گی بات پرائی

لب پر آئی دل کی بات

عشق کے بندے سیدھے سادھے

یہ کیا جانیں پانچ اور سات

ایک نظر کی بات ہے ساری

عشق نہ پوچھے ذات اور پات

چھائے ہیں فرقت کے بادل

پھیکی پھیکی ہے برسات
(۵۶۳)

A Review of Opinions of Scholars on Contemporary Issues and Future Plans for Interfaith Harmony

Interfaith harmony refers to the peaceful coexistence and cooperation between people of different religious beliefs. This abstract focuses on the need for interfaith harmony, the challenges that hinder it, and the way forward towards achieving it. The need for interfaith harmony arises from the diversity of religious beliefs and practices around the world, which can lead to misunderstanding, conflict, and violence. Interfaith harmony promotes mutual respect, understanding, and cooperation among people of different faiths, which can lead to a more peaceful and just society. However, achieving interfaith harmony is not without challenges. These challenges include ignorance, prejudice, fear, and mistrust among people of different faiths. There are also social, economic, and political factors that can contribute to the breakdown of interfaith relations. To overcome these challenges, there are several ways forward towards achieving interfaith harmony. These include education and awareness-raising initiatives that promote interfaith understanding and dialogue. There are also interfaith organizations that bring people of different faiths together for mutual cooperation and support. Additionally, there are political and legal measures that can protect the rights of religious minorities and ensure their full participation in society. In conclusion, interfaith harmony is essential for building a peaceful and just society. While there are challenges to achieving it, there are also ways forward towards promoting interfaith understanding, cooperation, and respect.

Molecular Genetic Analysis of Selected Neurological Inherited Diseases

This study was conducted to identify the loci and genes responsible to cause congenital neurological inherited diseases in selective Pashtoon families of Khyber Pakhtunkhwa region of Pakistan. For this purpose, five consanguineous/tribal endogamy families (A-E) suffering from oculocutaneous albinism, usher syndrome, primary microcephaly, and isolated clinical anophthalmia were selected and pedigrees were drawn. Blood samples were collected with informed consent from affected, as well as normal members of these families, and screened for disease associated mutations. These families were analyzed for linkage to all the known loci of oculocutaneous albinism, usher syndrome, primary microcephaly, and isolated clinical anophthalmia, using microsatellite STR markers. Direct sequencing was performed to find out disease associated mutations in the candidate genes. Molecular genetic analysis of family A with oculocutaneous albinism and golden red hair at birth was mapped to MC1R locus on chromosome 16q24.1. A novel mutation c.917G>A of MC1R gene was found to be consisting with OCA2 phenotype in family A. The identification of c.917G>A mutation in Pakistani family and its direct association with OCA2 phenotype is the first demonstration of a mutation of MC1R gene responsible for causing OCA2 phenotype in humans. By genetic linkage analysis, family B with diseased phenotype of Usher syndrome was mapped to USH1F locus on chromosome 10q21.22 (USH1F), which harbors PCDH15 gene. On sequencing of the PCDH15 gene, a novel homozygous c.1304 A>C transversion mutation was identified to be associated with the usher phenotype in the USH1F mapped family. This c.1304 A>C mutation predicts an amino-acid substitution of aspartic acid with an alanine at codon 435 (p.D435A) of PCDH15 protein product.Two families C and D with primary microcephaly were mapped to ASPM gene locus. On mutation screening of ASPM gene by PCR amplification and direct DNA sequencing, a common c.3978G>A transition, was identified in exon 17 of ASPM gene to be responsible for diseased phenotype in both the families. The identified mutation results into the substitution of an amino acid residue at position 1326 from tryptophan to a stop codon (i.e., p.Trp1326Stop). The family E with isolated clinical anophthalmia was mapped to SOX2 gene, which is located at chromosome 3q26.3-q27. On exonic and regulatory regions mutation screening of SOX2 gene, no disease-associated mutation was identified. It shows that another gene responsible for the development of eye might be present at chromosome 3q26.3-q27 and need to be identified and screened for disease- associated mutation in this family. It was concluded that the disease phenotypes of families with oculocutaneous albinism, usher syndrome, primary microcephaly, and isolated clinical anophthalmia were mapped by genetic linkage analysis. The candidate genes (MC1R, PCDH15, ASPM and SOX2) in the mapped regions were screened for disease associated mutations by PCR amplification and direct DNA sequencing. The novel disease- associated mutations were identified in MC1R and PCDH15. The disease associated mutation identified in ASPM gene was also reported in several other families of Pakistani origin with primary microcephaly. However, no disease associated mutation was identified in SOX2 gene, which indicates that possibly another gene might be present in the mapped region for disease phenotype.