Search Results - "Farooq, Ahsen"

Effects of high-intensity multi-modal exercise training (HIT-MMEX) on bone mineral density and muscle performance in postmenopausal women. A Pilot randomized controlled trial by Riaz, Huma, Babur, Muhammad Naveed, Farooq, Ahsen

“…To determine the effects of high-intensity multimodal exercise training on bone mineral density and muscle performance in postmenopausal women. The two-armed,…”
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EFFECTS OF ELECTROMYOGRAPHIC BIOFEEDBACK ON THE PERFORMANCE OF VASTUS MEDIALIS OBLIQUE MUSCLE IN KNEE OSTEOARTHRITIS: A RANDOMIZED CONTROLLED TRIAL by Khan, Huma, Riaz, Huma, Farooq, Ahsen, Farid, Fazeela

“…Background: Knee osteoarthritis is a common musculoskeletal disorder, enhancing performance of Vastus Medialis Oblique (VMO) can reduce the symptoms…”
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Association of Portal Vein Doppler Parameters with Chronic Liver Disease Child Pugh Classes: A Single Center Experience at Rawalpindi, Pakistan by Abdul Ahad Farooq , Ahsen Farooq , Muhammad Rashid , Junaid Haris Farooq , Salma Umbreen , Rabia Waseem

“…Objective: To determine the association between Doppler Parameters of average peak portal vein velocity and flow direction and Child Pugh classes of patients…”
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Frequency of Primary Headache Syndromes in Patients with a Major Depressive Disorder by Muneer, Ather, Farooq, Ahsen, Farooq, Junaid H, Qurashi, Muhammad Siddique, Kiani, Immad A, Farooq, Javeria S

“…Purpose The primary objective of this study was to assess the overall frequency of primary headaches in subjects with a moderate to severe major depressive…”
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Response on Huma Riaz, et al. (J Pak Med Assoc. 72: 1904-1908, 2022) Effects of high-intensity multi-modal exercise training (HIT-MMEX) on bone mineral density and muscle performance in postmenopausal women. A Pilot randomized controlled trial by Riaz, Huma, Babur, Muhammad Naveed, Farooq, Ahsen

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AFGHAN MUTATION OF CA-II GENE: OSTEOPETROSIS AND CARBONIC ANHYDRASE II DEFICIENCY WITH CRANIOFACIAL DISPROPORTION IN AN AFGHAN CHILD by Faisal, Anila, Kiani, Amarah, Farooq, Ahsen

“…Carbonic anhydrase-II deficiency is an autosomal recessive disorder groundedon a triad of cerebral calcification, osteopetrosis and renal tubular acidosis away…”
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AFGHAN MUTATION OF CA-II GENE; OSTEOPETROSIS AND CARBONIC ANHYDRASE II DEFICIENCY WITH CRANIOFACIAL DISPROPORTION IN AN AFGHAN CHILD by Faisal, Dr Anila, Kiani, Dr Amarah, Farooq, Dr Ahsen

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