Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Sarwar Noori Mahmood"'
Publikováno v:
European Urology Open Science, Vol 37, Iss , Pp 45-49 (2022)
Background: Mini percutaneous nephrolithotomy (MPCNL) is a newer surgical procedure that has changed the management of paediatric renal stones. Objective: To evaluate MPCNL morbidity and success rates for renal stones as a function of patient age in
Externí odkaz:
https://doaj.org/article/bebf64453078430a9ee81b9e5917bbc0
Autor:
Sarwar Noori Mahmood, Mohammed Hussein Babarasul, Saman Salih Fakhralddin, Hewa Mahmood Tawfeeq
Publikováno v:
African Journal of Urology, Vol 27, Iss 1, Pp 1-6 (2021)
Abstract Background Treating renal stones in patients with a solitary functioning kidney is challenging. The present study was aimed to assess the competence and safety of retrograde intrarenal surgery (RIRS) for the treatment of renal stones in a so
Externí odkaz:
https://doaj.org/article/22ba1a8c66a04a0ea53ea270cdaf7f5d
Publikováno v:
Asian Journal of Urology, Vol 7, Iss 3, Pp 309-317 (2020)
Objective: To evaluate the efficacy and safety of sheathless and fluoroscopy-free flexible ureterorenoscopic laser lithotripsy (FURSL) for treating renal stones. Methods: Between May 2015 and May 2017, 135 patients with renal stones treated with shea
Externí odkaz:
https://doaj.org/article/f3c78b9d2dc540e0b0af5e8fef9ac860
Autor:
Ali Ibrahim Mohammed MD, FICMS, Aveen M. Raouf Abdulqader MD, PhD, Sana Dlawar Jalal MD, FICMS, Sarwar Noori Mahmood MD, FICMS, FEBU
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 26 (2020)
Thromboembolism (TE) is a complex disease caused by various acquired and inherited factors. The common mutations; factor V Leiden G1691A (FVL G1691A), prothrombin G20210A (PTG20210A), and methylene tetrahydrofolate reductase C677T (MTHFR C677T) are i
Externí odkaz:
https://doaj.org/article/a6cec175c64541a1ac9874548a6cb317
Autor:
Aveen M. Raouf Abdulqader MD, PhD, Ali Ibrahim Mohammed MD, FICMS, Shwan Rachid PhD, Peyman Ghoraishizadeh PhD, Sarwar Noori Mahmood MD, FICMS, FEBU
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 26 (2020)
Hemophilia A (HA) is a severe coagulation disorder affecting 1 in 5000 to 10 000 male births. In severe cases, the most deleterious large DNA rearrangements are inversions of intron 22 (Inv22) and intron 1 (Inv1) of the factor VIII (FVIII) gene. Thes
Externí odkaz:
https://doaj.org/article/035e50602d3b41168e3dd724bfb30061
Autor:
Aveen M. Raouf Abdulqader MD, MSc, Shwan Rachid PhD, Ali Ibrahim Mohammed MD, PhD, Sarwar Noori Mahmood MD, PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)
Hemophilia A (HA) is the most common congenital X-linked coagulopathy caused by mutations in the factor VIII gene. One in 5000 to 10 000 male persons worldwide suffer from HA. It is the archetype of high-cost, low-volume disease. Therefore, identific
Externí odkaz:
https://doaj.org/article/94ab17c133bc44a193dd239b4f0ea9ae
Autor:
Sarwar Noori, Mahmood, Choman J, Ahmed, Hewa, Tawfeeq, Rawa, Bapir, Saman Salih, Fakhralddin, Berwn A, Abdulla, Renato N, Pedro, Noor, Buchholz
Publikováno v:
Annals of Medicine & Surgery. 81
Retrograde intrarenal surgery (RIRS) and mini-percutaneous nephrolithotomy (mPCNL) are viable options for the treatment of renal calculi 1-2 cm. Both have their pros and cons, but also vary in costs. We aimed to evaluate them in an economically chall
Publikováno v:
Journal of Sulaimani Medical College. 9:255-263
Autor:
Alaa Abbas Ali, Fahmi H. Kakamad, Sarwar Noori Mahmood, Abdulwahid M. Salih, Deedar Kamaran Qader, Saman Salih Fakhralddin, Hiwa O. Abdullah
Publikováno v:
International Journal of Surgery Case Reports
Introduction Mullerianosis is a sporadic condition of the urinary bladder. The study aims to present a case of mullerianosis with a brief literature review. Case presentation A 52-year-old lady presented with hematuria for one-year duration. A genera
Publikováno v:
Journal of Sulaimani Medical College. 9:77-85