Muhammad Tariq

ORCID: 0000-0003-0345-2144
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Research Areas
  • Forensic and Genetic Research
  • Forensic Anthropology and Bioarchaeology Studies
  • Genetic Neurodegenerative Diseases
  • SARS-CoV-2 and COVID-19 Research
  • Liver Disease Diagnosis and Treatment
  • Pediatric Urology and Nephrology Studies
  • Genetic diversity and population structure
  • Neurogenetic and Muscular Disorders Research
  • Muscle Physiology and Disorders
  • Kidney Stones and Urolithiasis Treatments
  • Yersinia bacterium, plague, ectoparasites research
  • Electricity Theft Detection Techniques
  • Facial Nerve Paralysis Treatment and Research
  • Peripheral Nerve Disorders
  • Vascular Procedures and Complications
  • Congenital gastrointestinal and neural anomalies
  • Hereditary Neurological Disorders
  • Race, Genetics, and Society
  • Therapeutic Uses of Natural Elements
  • Prion Diseases and Protein Misfolding
  • Lipid metabolism and disorders
  • Smart Grid Security and Resilience
  • Influenza Virus Research Studies
  • South Asian Studies and Conflicts
  • Diabetes, Cardiovascular Risks, and Lipoproteins

Nanjing Agricultural University
2025

Islamia College University
2017-2025

Mary Washington Hospital
2025

Bahawal Victoria Hospital
2013-2024

Jinnah Medical & Dental College
2024

Pakistan Institute of Medical Sciences
2024

Hazara University
2019-2021

Riphah International University
2020

Vanderbilt University
2019

To compare the complications rate of percutaneous nephrostomy and double J ureteral stenting in management obstructive uropathy.Total number 300 patients age 20-80 years who underwent JJ or for uropathy were included this study. Patients divided two groups i.e. A & B. In group A, 100 while B, 200 tube insertion included. The stent was inserted retrograde by using cystoscope, under mild sedation local anesthesia. While done ultrasound guidance anesthetic agent. Complications noted immediate...

10.12669/pjms.293.3563 article EN cc-by Pakistan Journal of Medical Sciences 2013-04-30

Charcot–Marie–Tooth disease (CMT) and autosomal recessive spastic ataxia of Charlevoix–Saguenay type (ARSACS) are large heterogeneous groups sensory, neurological genetic disorders characterized by sensory neuropathies, muscular atrophies, abnormal conduction velocities, ataxia. CMT2EE (OMIM: 618400) is caused mutations in MPV17 137960), CMT4F 614895) PRX 605725), CMTX1 302800) GJB1 304040), ARSACS 270550) SACS 604490). In this study, we enrolled four families: DG-01, BD-06, MR-01, ICP-RD11,...

10.3390/genes14020328 article EN Genes 2023-01-27

Background: Bell’s palsy is an acute unilateral facial nerve disorder resulting in partial to complete muscle paralysis, significantly affecting communication and social interactions. The condition associated with viral infections, immune responses, vascular ischemia. Its prevalence increases age observed more frequently rural populations. Recovery depends on the severity of timely intervention. Recent cases have been linked COVID-19 its vaccines. Physiotherapy plays a crucial role improving...

10.71000/7bm79g43 article EN cc-by-nc-nd 2025-02-28

Phytoestrogens are secondary plant metabolites that structurally analogous to endogenous oestrogens and bind Bovine G Protein-Coupled Receptors (GPCRs) in animals. Their interaction with GPCRs activates intracellular signalling cascades, such as the cAMP/PKA pathway, which plays a crucial role ovarian follicle development luteinisation. These interactions may enhance reproductive performance by improving fertility, synchronising estrous cycles, promoting ovulation. also influence regularity...

10.1111/rda.70033 article EN Reproduction in Domestic Animals 2025-03-01

Abstract Objectives From a genetic perspective, relatively little is known about how mass emigrations of African, European, and Asian peoples beginning in the 16th century affected Indigenous Caribbean populations. Therefore, we explored impact serial colonization on variation first islanders. Materials methods Sixty‐four members St. Vincent's Garifuna Community 36 Trinidad's Santa Rosa First People's (FPC) Arima were characterized for mitochondrial DNA Y‐chromosome diversity via direct...

10.1002/ajpa.23859 article EN American Journal of Physical Anthropology 2019-05-24

Smart grid (SG) will transform contemporary businesses by offering efficient solutions to improve existing power systems' efficiency, stability, and resilience. SG provides long-term supply interconnecting electrical grids communications infrastructures. However, SGs are plagued with problems complexities, particularly regarding capacity, reliability, security. The main concerning issues for consumers data breaches malicious hacking of personal equipment. In addition, the growing integration...

10.1109/icept58859.2023.10152331 article EN 2023-05-06

Vein of Galen malformation (VOGM) is a rare congenital arteriovenous affecting the pediatric population, characterized by fistula between diencephalon and dilated vein Galen. The present study reports case 6-month-old male infant referred for developmental delays abnormal head circumference. A clinical examination revealed macrocephaly, scalp veins neurological abnormalities. Neuroimaging confirmed large VOGM with associated hydrocephalus. multidisciplinary team devised treatment plan...

10.3892/mi.2024.187 article EN Medicine International 2024-08-05

To determine the frequency of metabolic abnormalities in serum and urine patients with urinary stones disease.Two hundred either multiple or recurrent urolithiasis diagnosed on ultrasonography intravenous urography were included this study. 24 hour sample collected from each patient sent for PH, specific gravity, Creatinine, uric acid, calcium, phosphate, oxalate, citrate magnesium. In addition, blood was also levels urea, creatinine, phosphate calcium.Mean age 38 ± 7.75 years male to female...

10.12669/pjms.296.4007 article EN cc-by Pakistan Journal of Medical Sciences 2013-09-07

Background: The radial artery is the smaller terminal branch of brachial artery. It one most commonly used arteries for various interventions. Anatomical variations exist and can predispose patients to iatrogenic injury if operator unaware normal morphology. present study focuses on giving detailed information about measurements in our local population. Methods: This was a cross-sectional observational study, conducted anatomy department Jinnah Medical College Peshawar from 2017 2018. 42...

10.37978/pjsm.v1i1.98 article EN Pakistan Journal of Surgery and Medicine 2024-07-26

Cardiovascular Diseases (CVD) have been the main cause of mortality in non-communicable diseases. Managing hypertriglyceridemia is crucial for lowering risk cardiovascular disease. Objective: To find out frequency increased triglycerides local population patients with ischemic heart Methods: A descriptive study design was conducted from October 16, 2020, to April 15, 2021, at Lady Reading Hospital Department Medicine Peshawar. total 182 were enrolled using non-probability consecutive...

10.54393/pjhs.v5i07.1733 article EN cc-by Pakistan Journal of Health Sciences 2024-07-31

Hemodialysis (HD) patients often face hyperkalemia due to various reasons. Level of and ECG changes may be discordant among HD in a significant number patients. This study was conducted investigate whether or not there is unique characteristic that predicts individuals with chronic kidney disease (CKD). OBJECTIVE: To determine an association between (raised serum potassium) T- (atypical T-wave) on CKD versus METHODOLOGY 200 4 & 5 HD, fulfiling the inclusion criteria were enrolled study....

10.53778/pjkd83275 article EN Pakistan Journal of Kidney Diseases 2024-09-29

OBJECTIVE To assess the level of knowledge, attitude and practice basic life support among physical therapy practitioners. METHODS The descriptive cross-sectional study was conducted at Riphah International University, Islamabad, Pakistan, from February to July 2018, comprised data collected practitioners working four public-sector hospitals in Rawalpindi Islamabad. A 30-item structured questionnaire adapted American Heart Association used. Data analysed using SPSS 21. RESULTS Of 100...

10.5455/jpma.19087 article EN cc-by Journal of the Pakistan Medical Association 2020-01-01

Abstract Northwest Pakistan has served as a point of entry to South Asia for different populations since ancient times. However, relatively little is known about the population genetic history people residing within this region. To better understand human dispersal in region broader subcontinent, we analyzed mtDNA diversity 659 and Y-chromosome 678 individuals, respectively, from five ethnic groups (Gujars, Jadoons, Syeds, Tanolis Yousafzais), Swabi Buner Districts, Khyber Pakhtunkhwa...

10.1038/s41598-022-05076-3 article EN cc-by Scientific Reports 2022-01-19
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