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Level of Awairness of Learning Disabilities Among Junior

Thesis Info

Author

Yasmin Naqvi

Supervisor

Irum Nawaz

Program

MS

Institute

Riphah International University

Institute Type

Private

City

Islamabad

Country

Pakistan

Thesis Completing Year

2014

Thesis Completion Status

Completed

Page

53 . : ill. (col.) 29 cm. +CD

Subject

Education

Language

English

Other

Submitted in fulfillment of the requirement for the degree of Speech Language Pathology; Includes bibliographical references; Thesis (MS)--Riphah International University, 2014; English; Call No: 371.9 YAS

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676711669043

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ڈاکٹر ذاکر حسین خان

آہ ذاکر صاحب !
ڈاکٹر ذاکر حسین صاحب کی ناگہانی وفات ہندوستان کا بہت بڑا قومی حادثہ ہے، وہ اسکا گوہر بے بہا تھے، ان کی موت سے وہ ایسی دولت سے محروم ہوگیا جس کی تلافی نہیں ہوسکتی، کم سے کم مسلمانوں میں ان کا بدل پیدا ہونا بہت دشوار ہے اور اب وہ اس نقصان کو محسوس کریں گے، وہ اپنے علمی کمالات ، فہم و فراست، قومی و تعلیمی خدمات، ایثار و قربانی اور اخلاق و سیرت کے لحاظ سے بہت بڑے انسان تھے، انھوں نے سیاست کے میدان میں کبھی قدم نہیں رکھا، لیکن اپنی بصیرت سے بڑی بڑی سیاسی گتھیوں کو آسانی سے سلجھا دیتے تھے، پنڈت جواہرلال نہرو کے بعد بین الاقوامی دنیا میں ہندستان کا وقار اُن ہی نے قائم رکھا۔
ان میں ابتدا سے غیر معمولی صلاحیتیں تھیں، ان کا آغاز ہی ان کے روشن مستقبل کا پتہ دیتا تھا طالب علمی ہی کے زمانہ سے ان کا قومی خدمت کا ولولہ اور ایثار و قربانی کا جذبہ تعلیم یافتہ نوجوانوں اور قومی کارکنوں کے لیے نمونہ تھا، اس زمانہ اور اس عمر میں جب ہونہار نوجوانوں کا منتہائے نظر اور ترقی کی سب سے بڑی معراج سرکاری عہدے اور تعیش کی زندگی تھی، انھوں نے ان کی طرف آنکھ اٹھا کر بھی نہ دیکھا، اور ان کے مقابلہ میں قومی خدمت اور غربت کی زندگی کو ترجیح دی اور اس راہ میں عمر کا بہترین حصہ صرف کردیا، ان کا زندہ کارنامہ ہندوستان کی پہلی آزاد قومی درسگاہ جامعہ ملیہ ہے، گو اس کے بانی حضرت شیخ الہند حکیم اجمل خاں اور مولانا محمد علی وغیرہ تھے۔ لیکن اس کے اصلی معمار وہی تھے، اور ان ہی نے جامعہ کو جامعہ بنایا اور اپنی زندگی میں اپنے لگائے ہوئے پودے کو ایک تناور درخت بنا گئے، اور آج...

The Universality and Scope of Justice in Islam

Definition of justice and its scope is something about what legal and political philosophers could never reach a unified position throughout a history. In these days, many in the West are trying to present Islam and its law and justice as something utterly uncivilized, unjust, cruel, and outdated and of no use in modern world. Positivist's concept of justice that prevails in the world today, mostly based on temporary secular-materialistic values, is in most of the cases opposed to the eternal principles and rules laid down by God Almighty. Justice according to the early proponents of Natural law, if not based on the universal values in itself is not justice, and as such is doomed to failure. Today we are witnessing the kind of global justice that threatens even to destroy humanity.  The present article is an effort to find out the most suitable definition of justice according to the Islamic law, and present the concept of universality and scope of justice in Islam in a way to show the absolute God's principles and values are unchangeable and everlasting, and only rightful solution to be followed today.

Molecular Profiling of Bioactive Constituents from Zizyphus Oxyphylla Edgew.

This PhD thesis envisages the phytochemical and pharmacological studies of an important member of Rhamnaceae family, Zizyphus oxyphylla Edgew. The main objective behind this investigation was to authenticate the folkloric history of this plant. Some of the folkloric uses of genus Zizyphus from the available literature include antidiabetic, hepatic protective, antioxidant, and antiulcerinic, antibacterial and anticancer while specifically Zizyphus oxyphylla is famous for its analgesic, antipyretic and hepatic protective uses. Fractions of stem, leaves and roots of Z. oxyphylla were screened for phytochemical constituents while fractions of stem and leaves were screened for pharmacological activities. This scientific pursuit resulted in some significant findings. The phytochemical studies on Z. oxyphylla resulted in isolation and structural elucidation of three new compounds. Two of the new compounds were cyclopeptide alkaloids named Oxyphylline B (1) and Oxyphylline C (2) while the third new compound was a flavone i.e. (+)-R, S Maackiain (3). Apart from these new compounds four other compounds Oxyphylline D (4), Nummularine-C (5), Nummularine-R (6), b-Sitosterol (7) and Stigmasterol 3- O- b-glucosides (8) were also isolated. Amongst these known compounds only Nummularine-R (6) was previously isolated from Z. oxyphylla while other known compounds were isolated for the first time from this plant and thus new source. Oxyphylline B (1), Oxyphylline C (2) and Nummularine-R (6) were isolated from the chloroform fraction of stem of Z. oxyphylla. From the dichloromethane fraction of roots Oxyphylline D (4) and Nummularine-C (5) were isolated while (+)-R, S Maackiain (3), b-Sitosterol (7) and Stigmasterol 3- O- b-glucoside (8) were isolated from the ethyl acetate fraction of leaves of Z. oxyphylla. Stem and leaves oils sub fractions, when analyzed by GC-MS, yielded fatty acids, lipids, long chain hydrocarbons and long chain ketones. Some major compounds which were yielded in high percentage were Heptacosane (10.0782 % in sample WO3), Tetracosane acid, methyl ester (9.2234 % in sample WO2), Dotriacontane, 1-Hexacosene and 1-Eicosene (6.4403, 6.6830 and 6.1095 respectively in sample WO5), 11decyl Tetracosane, (4.2749 % in sample WO1), Azafirin (4.4609 % in sample WO1) and 9-octyl Hexacosane, (3.7489 % in sample WO1). While other known compounds below were 3 % concentrations. Few of the peaks in gas chromatogram and their respective mass spectral data remained unidentified. As regards to pharmacological studies, some interesting and significant findings were obtained. Crude extracts, fraction and some of the isolated compounds were investigated for antibacterial, antifungal, toxicity tests (Brine shrimp bioassay, lemna bioassay, insecticidal), in vitro anti-inflammatory activity and enzyme inhibition bioassays including urease and carbonic anhydrase inhibition bioassays. Only ethyl acetate fraction of leaves showed moderate antibacterial activity. Crude extract and n-hexane fraction of leaves and only n- hexane fraction of stem exhibited 35 % inhibition of fungal growth. Maximum phytotoxic activity was revealed by both stem and leaves at the highest concentration used. Crude extract of leaves gave the highest inhibition (90 %) while chloroform was the most active fraction of stem of Z. oxyphylla. Neither of the extracts and subsequent fractions from stem or leaves were able to produce an impression as active cytotoxic agent. n-hexane and ethyl acetate fraction of leaves exhibited 40 % mortality against Callosobruchus analis. Two fractions of leaves (chloroform and n-hexane) gave excellent anti inflammatory activity when screened for in vitro anti- inflammatory activity. Polar fractions of stem showed the maximum urease inhibitory activity. Ethyl acetate fraction of the stem gave maximum reading of 86.7 % ± 0.03, while leaves showed low urease inhibitory activity. Stem and leaves of Z. oxyphylla exhibited low to moderate carbonic anhydrase activity. Oxyphylline B (1) showed comparatively better antibacterial activities against Escherichia coli and Pseudomonas aeruginosa (MIC: 0.1 mg/mL). Oxyphylline C (2) showed a lower antibacterial activity as compared to Oxyphylline B. Oxyphylline D (3) showed its highest antibacterial activity against E. coli and it lowest antibacterial activity against Shigella flexenari. Nummularine-C (5) and Nummularine-R (6) when compared we found that Nummularine-C was more active than Nummularine-R in many cases. Oxyphylline B (1) showed low activity against Candida albicans. While in the case of Oxyphylline C (2) it was found that it was moderately active against three fungal strains i.e. C. albicans, Micropspoum canis and Fusarium solani. Nummularine-R (6) and Oxyphylline B (1) showed low inhibition of Jake bean urease. Both of them gave readings of 35.73 and 34.24 % inhibition. Maximum urease inhibitory activity was shown by Oxyphylline D (3). It inhibited the urease enzyme by 58.21 %. When IC50 ± SEM value was calculated it came out to be 420.11 ± 1.22 μM. New compounds