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ISA Transactions|November 17, 2019
A novel feature extraction method for bearing fault classification with one dimensional ternary patternsMelih Kuncan, Kaplan Kaplan, Mehmet Recep Mi Naz, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|July 16, 2021
Impact of patient and family engagement in improving continuous positive airway pressure adherence in patients with obstructive sleep apnea: a randomized controlled trialNazia Naz S Khan, David Todem, Shireesha Bottu, et al.
RSC Advances|May 6, 2022
Development and application of novel bio-magnetic membrane capsules for the removal of the cationic dye malachite green in wastewater treatmentImran Ali, Changsheng Peng, Iffat Naz, et al.
Regional Anesthesia and Pain Medicine|April 6, 2013
Ultrasound-guided popliteal block through a common paraneural sheath versus conventional injection: a prospective, randomized, double-blind studyAnahi Perlas, Patrick Wong, Faraj Abdallah, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 10, 2013
Estimation of toxic elements in the samples of different cigarettes and their impact on human health of Irish hypertensive consumersHassan Imran Afridi, Tasneem Gul Kazi, Farah Naz Talpur, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|December 7, 2013
Protection from cyclophosphamide-induced ovarian damage with bone marrow-derived mesenchymal stem cells during pubertySevtap Kilic, Ferda Pinarli, Candan Ozogul, et al.
Clinical Genetics|February 27, 2010
Epidemiology of Van der Woude syndrome from mutational analyses in affected patients from PakistanS Malik, N Kakar, S Hasnain, et al.
Human Genetics|January 8, 2010
Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3Gul Naz, Ghazanfar Ali, Syed Kamran-ul-Hassan Naqvi, et al.
Clinical Case Reports|April 12, 2018
Angioimmunoblastic T-cell lymphoma: a rare subtype of peripheral T-cell lymphomaManoj Ponadka Rai, Prabhjot Singh Bedi, Edwin B Marinas, et al.
Gene|April 28, 2019
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing lossMemoona Ramzan, Hafiza Idrees, Ghulam Mujtaba, et al.
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