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Quality of Life of Individuals With Intellectual Disability a Cross Sectional Survey

Thesis Info

Author

Abida Hussan

Supervisor

Nayab Iftikhar

Program

MS

Institute

Riphah International University

Institute Type

Private

City

Islamabad

Country

Pakistan

Thesis Completing Year

2015

Thesis Completion Status

Completed

Page

xi, 49 . : ill. ; 29 cm. +CD

Subject

Social Sciences

Language

English

Other

In partial fulfillment of requirements for the award of degree of MS-SLP; Includes references.; Thesis (MS-SLP) Riphah College of Rehabilitation Sciences; Call No: 362.3 ABI

Added

2021-02-17 19:49:13

Modified

2023-01-07 07:10:22

ARI ID

1676711734293

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مولوی عبدالباری

مولوی عبدالباری
افسوس ہے کہ دارالمصفین کے قدیم اور مخلص خدمت گذار مولوی عبدالباری صاحب ۳۰؍ جون کو وفات پاگئے، ان کی عمر ۹۰ سال سے متجاوز تھی، دارالمصنفین کے ابتدائی دور میں حضرت مولانا سید سلیمان ندویؒ نے انہیں تصحیح اور کتب خانہ کی نگرانی کے کام پر مامور کیا تھا جس کو دو برس پہلے تک وہ انجام دیتے رہے، دارالمصنفین کے عروج کا دور دیکھنے والے اب تنہا وہی رہ گئے تھے، ان کی تعلیم مدرسۃ الاصلاح سرائمیر میں ہوئی تھی اور وہ مولانا امین اصلاحی مدظلہ، کے ہم سبق تھے، دارالمصنفین سے وابستگی کی وجہ سے انہیں مضمون نگاری کا چسکہ لگ گیا تھا، ابو علی اثری اور ابو علی اعظمی کے نام سے مدۃالعمر اخباروں اور رسالوں میں مضامین لکھتے رہے، علامہ شبلیؒ کے بڑے مداح اور سیدصاحب کے نہایت عقیدت مند تھے، ان کا ذکر برابر لطف ولذت سے کرتے تھے ان پر اور مولانا ابو الکلام آزاد پر بے شمار مضامین لکھے، دونوں بزرگوں پر ان کے مضامین کے ایک ایک مجموعے ضیاء اﷲ کھوکھر صاحب (گوجرانوالہ، پاکستان) نے شایع کیا تھا، اپنی خودداری کی وجہ سے کسی کا منت کش ہونا گوارا نہیں کیا اور قناعت پسندی کی بنا پر ایک قلیل مشاہرہ پر پوری زندگی گذار دی، اﷲ تعالیٰ ان کی بشری لغزشوں کو معاف فرمائے اور جنت نعیم میں جگہ دے، آمین۔ (ضیاء الدین اصلاحی، جولائی ۱۹۹۳ء)

Comparative Analysis of Islamic Banking Products in Pakistan and Malaysia

A comparison of the Islamic Banking products offered in the two countries of Pakistan and Malaysia has been discussed in this paper. The research paper uses document analysis to identify different products offered by five full-fledged Islamic banks in Malaysia and Pakistan. It is evident from the research that Islamic banking sector in Pakistan is not tapping its full growth potential as in case of Malaysia. It is also concluded that the trade financing and asset financing products offered by Islamic banks in Malaysia are more diverse than the products offered by its counterparts in Pakistan. The paper gives insight to the Shariah complaint board to introduce new products while learning from the experience of other countries. This research does not focus on investigating the reasons behind these differences; however, it initiates a discourse in this direction.

A Study of Molecular and Genetic Determinants of Primary Congenital Glaucoma

The study reported in this thesis document was undertaken to characterize molecular and genetic basis of primary congenital glaucoma (PCG) in Pakistani population. For this purpose, traditional strategy of homozygosity mapping was used to identify disease causing mutations and to map novel loci/genes responsible for autosomal recessive primary congenital glaucoma (arPCG). Thirty consanguineous families with arPCG were enrolled from different parts of Pakistan. Genomic DNAs from these families were subjected to linkage analysis for the exclusion of previously reported genes/loci for autosomal recessive primary congenital glaucoma. The phenotypes of 17 PCG families (PKGL028, 032, 040, 047, 050, 051, 058, 060, 065, 066, 067, 068, 069, 070, 071, 072 & 073) were found linked to GLC3A locus harboring Cytochrome P450 Family 1 Subfamily B Member 1 (CYP1B1) gene. Sanger sequencing of CYP1B1 identified five missense mutations; p.Y81N, p.E229K, p.R368H, p.R444Q and p.R469W in families PKGL051, PKGL047, PKGL058, PKGL050 and PKGL028 respectively. Another homozygous missense mutation; p.R390H was identified in nine PCG families designated as; PKGL040, PKGL060, PKGL065, PKGL066, PKGL067, PKGL069, PKGL070, PKGL071 and PKGL073. In PKGL032, a 10bp homozygous duplication; c.1200_1209dupTCATGCCACC (p.T404Sfs*30) was identified. Two novel frameshift mutations; p.W246Lfs*81 and p.P442Qfs*15 were identified in PKGL047 and PKGL068 respectively. Furthermore, mutational analysis identified a known homozygous nonsense mutation; p.Q37X in family PKGL072. Three consanguineous families; PKGL042 PKGL015 and PKGL076 were found linked to another known PCG locus; GLC3D harboring Latent Transforming Growth Factor Beta Binding Protein 2 (LTBP2) gene. Sanger sequencing of LTBP2 identified two missense and a frameshift mutation; p.D1010N, p.Q1143Rfs*35 and p.C1757Y in PKGL076, PKGL015 and PKGL042 respectively, all of these were novel. These results show that pathogenic mutations in CYP1B1 and LTBP2 gene are responsible for PCG phenotype in these nineteen families. Three large consanguineous PCG families which remained unlinked in linkage studies were selected for genome wide scan. A novel locus for autosomal recessive primary congenital glaucoma was mapped to chromosome 1p33-32.3 in one family; PKGL061 with a maximum two point LOD score of 5.33 obtained with marker D1S386 at recombination fraction zero. This study reports identification of five novel and eight known pathogenic mutations in already reported genes; CYP1B1 and LTBP2. Furthermore, a novel disease locus at chromosome 1p33-32.3 in a large consanguineous PCG family was identified. These findings provide insight into genetic and molecular determinants responsible for autosomal recessive primary congenital glaucoma, thus providing a better understanding of mechanisms underlying the disease.