Muhammad Waqar Arshad
Overview
Explore the profile of Muhammad Waqar Arshad including associated specialties, affiliations and a list of published articles.
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5
Citations
8
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0
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Recent Articles
1.
Khan J, Asif S, Ghani S, Khan H, Arshad M, Khan S, et al.
BMC Ophthalmol
. 2024 Aug;
24(1):345.
PMID: 39143519
Background: Oculocutaneous albinism (OCA) is a genetically heterogeneous condition that is associated with reduced or absent melanin pigment in the skin, hair, and eyes, resulting in reduced vision, high sensitivity...
2.
Qureshi H, Basheer A, Faheem M, Arshad M, Rai S, Jamal S
Front Genet
. 2024 Jun;
15:1361610.
PMID: 38826807
has been recognized as the second most prevalent pathogen associated with diarrhea that contains blood, contributing to 12.9% of reported cases, and it is additionally responsible for approximately 200,000 deaths...
3.
Arshad M, Shabbir M, Asif S, Shahzad M, Leydier L, Rai S
Genes (Basel)
. 2023 Feb;
14(2).
PMID: 36833273
Congenital idiopathic nystagmus (CIN) is an oculomotor disorder characterized by repetitive and rapid involuntary movement of the eye that usually develops in the first six months after birth. Unlike other...
4.
Arshad M, Lee Y, Malik M, Khan J, Khan A, Kareem A, et al.
J Pak Med Assoc
. 2019 Feb;
69(2):183-189.
PMID: 30804581
Objective: To identify the underlying genetic anomalies in two consanguineous Pakistani families with autosomal recessive achromatopsia. Methods: The exploratory study was conducted under the patronage of International Islamic University, Islamabad,...
5.
Bhinder M, Arshad M, Zahoor M, Shehzad W, Tariq M, Shabbir M
J Coll Physicians Surg Pak
. 2017 Jun;
27(5):308-310.
PMID: 28599695
Junctional epidermolysis bullosa (JEB) is a recessively inherited skin blistering disease and is caused due to abnormalities in proteins that hold layers of the skin. Herlitz JEB is the severe...