Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Faraz Farooq"'
Autor:
Nafisa Neault, Sean O'Reilly, Aiman Tariq Baig, Julio Plaza-Diaz, Mehrdad Azimi, Faraz Farooq, Stephen D Baird, Alex MacKenzie
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0256276 (2021)
Myotonic Dystrophy Type 1 (DM1) is the most common form of adult muscular dystrophy (~1:8000). In DM1, expansion of CTG trinucleotide repeats in the 3' untranslated region of the dystrophia myotonica protein kinase (DMPK) gene results in DMPK mRNA ha
Externí odkaz:
https://doaj.org/article/d2f4199a57cb4eb1b7f3e8037cd72e1a
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 16:705-708
Background: While the long-term cause of death in patients with STEMI is still undetermined, short-term mortality in patients experiencing PCI has been well-researched. Aims and Objectives: This study set out to investigate the connection among the t
Publikováno v:
Journal of Pharmaceutical Research International. :28-34
Introduction: Anemia is one of the potential comorbid condition in patients with acute decompensated heart failure (ADHF) which is linked to higher morbidity and mortality rates. Worldwide, its prevalence ranges from 4% to >70% in hospitalized patien
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 16:530-534
Introduction: Acute coronary syndrome(ACS) is associated with activation ofplateletsand thecoagulationsystem which could influence the incidence of early stentthrombosis(EST).Stent thrombosis is a relatively uncommon phenomenon, yet it is a serious c
Autor:
Nadeem Qamar, Tahir Saghir, Tariq Ashraf, Javed Akbar Sial, Atif Ahmed Khan, Ashok Kumar, Lajpat Rai, Syed Ahsan Raza, Iftikhar Ahmed, Faraz Farooq Memon, Altaf Hussain
Publikováno v:
Journal of Pharmaceutical Research International. :96-102
Objective: Mitral stenosis caused by rheumatic heart disease (RHD) is the most common cause of valvular lesion in adults and prevalent in developing countries like Pakistan. Higher natriuretic peptide (BNP) levels can be observed in patients with mod
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 16:1362-1364
Objective: To determine the frequency of contrast induced nephropathy in patients with acute coronary syndrome undergoing percutaneous coronary intervention. Material & Methods: This study was conducted on all patients underwent percutaneous coronary
Autor:
Irfan Ali Arbab, Faraz Farooq Memon, Muhammad Rafique, Sharwan Bhuro Mal, Ghulam Kubra, Shazia Rasheed
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 16:970-972
Background and Purpose: Left bundle branch block (LBBB) is a communal electrocardiographic (ECG) finding that may or may not be associated with overt heart disease at diagnosis. The current study was performed to determine the clinical picture and st
Autor:
Muhammad Tahseen Raza, Faraz Farooq Memon, Muhammad Kashif, Syed Ahsan Raza, Mehboob Ali, Feroz Memon, Zain Islam Arain
Publikováno v:
Journal of Pharmaceutical Research International. :79-85
Objective: Cardiovascular diseases are 1.7 times more prevalent in patients with diabetes mellitus. The aim behind this study was to examine the correlation of glycosylated hemoglobin and complexity of coronary artery disease among middle aged popula
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 12
International Journal of Molecular Sciences, Vol 22, Iss 6295, p 6295 (2021)
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Digibug: Repositorio Institucional de la Universidad de Granada
Universidad de Granada (UGR)
Volume 22
Issue 12
International Journal of Molecular Sciences, Vol 22, Iss 6295, p 6295 (2021)
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Digibug: Repositorio Institucional de la Universidad de Granada
Universidad de Granada (UGR)
The development of DNA microarray and RNA-sequencing technology has led to an explosion in the generation of transcriptomic differential expression data under a wide range of biologic systems including those recapitulating the monogenic muscular dyst
Autor:
Alex MacKenzie, Stephen Baird, Sean O'Reilly, Nafisa Neault, Julio Plaza-Díaz, Faraz Farooq, Aiman Tariq Baig, Mehrdad Azimi
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0256276 (2021)
PLoS ONE
PLoS ONE
Myotonic Dystrophy Type 1 (DM1) is the most common form of adult muscular dystrophy (~1:8000). In DM1, expansion of CTG trinucleotide repeats in the 3’ untranslated region of the dystrophia myotonica protein kinase (DMPK) gene results in DMPK mRNA