Imtenan Sharif
Overview
Explore the profile of Imtenan Sharif including associated specialties, affiliations and a list of published articles.
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6
Citations
21
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0
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Recent Articles
1.
Khokale R, S Mathew G, Ahmed S, Maheen S, Fawad M, Bandaru P, et al.
Cureus
. 2023 May;
15(4):e37559.
PMID: 37193429
Virtual reality (VR) and augmented reality (AR) are noble adjunctive technologies currently being studied for the neuro-rehabilitation of post-stroke patients, potentially enhancing conventional therapy. We explored the literature to find...
2.
Mallick N, Hassan A, Sultan Bhatti R, Rafique D, Jaffery A, Sharif I, et al.
Cureus
. 2023 Feb;
14(12):e33083.
PMID: 36721569
Objectives The objective is to assess the overall quality of life (QoL) in patients who had undergone renal transplant within the last three years and correlate this index with various...
3.
Rashid Z, Sharif I, Khushk I, Raja A
Pak J Med Sci
. 2021 Jun;
37(3):663-667.
PMID: 34104144
Background And Objectives: Clinicians need to build an astute doctor-patient relationship. The term clinical empathy is the ability of doctor to cognitively appreciate a patient's perspective, experiences, and deliver such...
4.
Ghafoor T, Sharif I, Bashir F, Ahmed S, Ashraf T, Khalil S, et al.
J Pak Med Assoc
. 2021 Jan;
70(12(B)):2316-2322.
PMID: 33475535
Objective: To analyse the common causes of death in paediatric acute myeloid leukaemia cases at a tertiary care facility. Methodology: The retrospective study was conducted at the Paediatric Oncology Department...
5.
Ghafoor T, Khalil S, Farah T, Ahmed S, Sharif I
Cancer Rep (Hoboken)
. 2020 Oct;
3(5):e1259.
PMID: 33085844
Background: In the developed world, 5-years survival of childhood acute myeloid leukaemia (AML) has improved to 70%. However, the survival rates in the developing world are below 40%. The main...
6.
Shahid M, Firasat S, Satti H, Satti T, Ghafoor T, Sharif I, et al.
Congenit Anom (Kyoto)
. 2019 Feb;
60(1):32-39.
PMID: 30809872
Fanconi anemia (FA) is a recessive disorder that predispose to bone marrow failure and multiple congenital anomalies in affected individuals worldwide. To date, 22 FA genes are known to harbor...