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The Impact of Metro Bus Project on Socio-Economic Aspects of Lives of People

Thesis Info

Author

Umair Abdullah

Department

Department of Sociology, QAU

Program

MSc

Institute

Quaid-i-Azam University

Institute Type

Public

City

Islamabad

Province

Islamabad

Country

Pakistan

Thesis Completing Year

2015

Thesis Completion Status

Completed

Page

viii,92

Subject

Sociology

Language

English

Other

Call No: Diss / M .Sc / SOC / 152

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676719181294

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تندرستی ہزار نعمت ہے

تندرستی ہزار نعمت ہے
اللہ تعالیٰ نے بنی نوع انسان کی تخلیق فرمائی تو اس کو بے شمار نعمتوں سے سرفراز فرمایا۔ دیکھنے کے لیے آنکھیں، سننے کے لیے کان، بولنے کے لیے زبان، چکھنے کے لیے قوت ذائقہ، سونگھنے کے لیے قوت، چلنے کے لیے قوت، سوچنے کے لیے قوت، غور وفکر کے لیے قوت یعنی انسان کوقوائے جسمانی کی صورت میں انعاماتِ ربانی وافر مقدار میں میسر آئے۔
قرآنِ پاک میں ارشادِ باری تعالیٰ ہے کہ اگر اللہ تعالیٰ کی نعمتوں کا شمار کرنا چاہو تو تم ان کو گنتی میں نہیں لا سکتے ہو، ان بے شمار نعمتوں کا درود بنی نوع انسان کے لیے ہوا ہے اور انسان وہ ہے جو جسم اور روح کا مرکب ہے اگر انسان صحت مند ہے تو یہ جملہ انعامات ِربانی اس کے لیے نعمت غیر مترقبہ ہیں اور اگر مرد بیمار ہے تو وہ ہر نعمت سے بیگانہ ہے، ہر نعمت اس کے لیے غیر مفید ہے، ہر نعمت اس کے لیے نعمت نہیں بلکہ زحمت ہے، ہر نعمت کا وجود اس کے لیے غیرمحمود ہے۔
انسان گلستانِ سرسبز میں گلہائے رنگارنگ کے حسین و جمیل مناظر سے متمتع ہوسکتا ہے لیکن چشمائے انسانی میں بینائی شرط ہے، انسان کوئل کی مسحور کن آواز سے، قاری قرآن کی تلاوت سے، خطیب ممبر رسول صلی اللہ علیہ و آلہٖ وسلم کی خوش الحانی سے، واعظ شیر یںلسان کی شعلہ بیانی سے کما حقہٗ فائدہ اٹھا سکتا ہے بشرطیکہ قوت سماعت جوبن پر ہو، اعضائے جسمانی کی سا لمیت تکمیل انسانیت کے لیے اہم کردار ادا کرتی ہے۔
صحت مند انسان معاشرے کا اہم رکن ہوتا ہے۔ گھر کے لیے ، خاندان کے لیے اس کا وجودکسی نعمت سے کم نہیں ہوتا، اس کی نشست و برخاست معیاری ہوتی ہے، وہ حسن وزیبائش کا مرقع ہوتا ہے، وہ...

الامام ضیاء المقدسی و منھجہ فی کتابہ الاحادیث المختارۃ

Different scholars have compiled the books which contain a large numbers of authentic Ahadith (Ahadith Sahiha), to achieve this purpose, they introduced different hadith sciences to distinguish between the true and the fabricated hadith. The authentic Sunnah is contained within the vast body of Hadith literature. One of them is Imam Zia ul Maqdasi. Imam Zia Uddin Muhammad bin Abdul Wahid Maqdasi’s book “Al Ahadith al Makhtara” is one of the best books of its kind. Many Islamic scholars have declared it better than Imam Hakim’s book Al Mustadrak. Allama Iraqi, one of his contemporaries said that the Ahadith given in his book Al Ahadith al Makhtara were not ascertained to be authentic before. Only those Ahadith have been given in this book whose asaneed are correct but they have not been reported by Imam Bukhari and Imam Muslim. Also, one of the strengths of this book is that it reflects the glimpses of Muajam. Imam Maqdasi wrote this book in the manner of Masaneed that is to say that he mentioned the name of the companion of the Holy Prophet (SAW) and then reported his traditions. Sometimes he also indicates the factors responsible for the interruption in the authenticity of Ahadith. But, sadly, Imam Maqdasi passed away and could not complete this great book. In this article I will discuss the Imam Zia ul Maqdasi approach towards “Ahadith Sahiha” in his book Al Ahadith ul Mukhtara.

Study of Synergistic Anticonvulsant Effects of Pregabalin/Nimodipine and Pregabalin/Amlodipine on Acute and Chronic Seizure Models in Mice

After stroke epilepsy is the second most common neurological disorder. It occurs due to abnormal neuronal discharge. It is characterized by unprovoked and recurrent seizures which are known as epileptic seizures. Clinically it is manifested in variety of ways from minor physical convulsions to severe tonic-clonic seizures with or without loss of consciousness. Status epilepticus is an acute exacerbation of common epilepsies and life threatening medical emergency, it must be treated or else it may cause serious damage to the brain and even death in many cases. For the management of epilepsy, the antiepileptic drugs, including second and third generations have extensively widened the choice of the drugs for the physicians; however, the efficacy and the antiseizure effects of these drugs are not satisfactory. There is limited choice of drugs for the management of status epilepticus. Keeping these challenges in mind the present study was carried out to investigate the synergistic anti-seizure/antiepileptic effects of combined regimens of Pregabalin with Amlodipine (PGB/AML) and Pregabalin with Nimodipine (PGB/NMD )on acute and kindled models of epilepsy in mice. Current research suggests that calcium influx in neurons plays important role in the genesis of seizures, therefore, the calcium antagonists have potential to be used as anticonvulsants. Anti-seizure actions of PGB can be augmented/potentiated or modified if given in combination with calcium channel inhibitors AML and NMD.The rationale for selecting this combination was based on facts thatAML and NMDhave synergisticanti seizure effects s on PGB and calcium channel blockers have inhibitory effects on voltage-gated calcium channel blockers. we designed the working hypothesis for the present study stating that the in combination-therapies AML and NMD would potentiate and enhance the anti-seizure effects of PGBby theirinhibitory and modulating effects on the calcium channels of the CNS.We examined and analyzed the combination therapy from multiple dimensions both in acute model of seizures as well as in kindled model of epileptogenesis.Our proposed hypothesis that anti-seizure actions of PGB can be augmented or modified if given in combination with AML and NMD had been substantiated by our results. The Combination regimens we employed in the instant experimental animal study were novel and demonstrated significant seizure protection. Our study has established that in both in-vivo models of seizures the combined regimens have demonstrated synergism between PGB and both calcium channel blockers (AML and NMD) incrasing the latent periods,reducing the duration of seizuresand increasing the mortality protection in mice.. We are inclined to hold that PGB:AML and PGB:NMD provided synergistic antiseizure effects in both seizure models. PGB:AMLin acute as well as inkindled modelsprovidedupto 100 percent seizure protection and complelety abolished the generation of seizures at the doses of 5055mg/kg of PGB with 12.5-15 mg/kg of AML(fifth and sixth doses)comparable to reference drugsVPT, PHTand DZ. PGB:NMDprovided 100 percent seizure protectionat the dose of 55mg/kg of PGB with 15 mg/kg (sixth dose) onlyin Kindled model of seizure. PGP:AML demonstratedmore efficacious and potent anti seizure effects as compared to PGB:NMD. We presume that both the calcium channel blockersexhibited their anti seizure effects by potentiating the antiseizure effects of PGB in both combined regimens.In the light of present study the major advantage of combination therpy would be that low doses of PGB could be employed that would be atleast six times in potency to itsindividual effects, thus reducing the doses of the PGB.The combination regimens broader spectrum of antiepileptic usage as compared to ther AEDs is another advantage.This study has provided some basic ground-work guidelines for the future clinical use of combination therapies of PGB with AML and NMD in various forms of epilepsies both for the short term management in conditions like status epilepticus and non epilepticus seizures as well as for the long term management of epilepsy. AML and NMDdeserves attention from a clinical point of view, as a potentially favorable drugs that could be applied in epileptic patients treated with PGB, who additionally requires calcium channel antagonist for reasons other than epilepsy such as hypertensive patients. Though, presently intravenous/ parenteral preparations of PGB is not available, however, it can be hoped that in near future the the availability of PGB parenteral formulations would provide alternate treatment options as combination therapies with calcium antagonist for the management of acute seizures