Wali Y - Search Results

1

Omani experience with the use of factor IX Fc fusion protein.

Alzadjali SI, Wali Y. Alzadjali SI, et al. Among authors: wali y. BMJ Case Rep. 2021 Jul 21;14(7):e241154. doi: 10.1136/bcr-2020-241154. BMJ Case Rep. 2021. PMID: 34290003 Free PMC article.

2

Home treatment of haemarthrosis with recombinant activated factor VII in patients with haemophilia A or B and inhibitors: experience from developing countries.

Bensadok M, Almomen A, Alzoebie A, Benchikh El Fegoun S, Wali Y, Hamzy F, Mehalhal NG, Grifi F, Hamdi S, Mesli N, Owaidah T, Saad HA, Mansour NS, Touhami H. Bensadok M, et al. Among authors: wali y. Blood Coagul Fibrinolysis. 2017 Mar;28(2):145-151. doi: 10.1097/MBC.0000000000000564. Blood Coagul Fibrinolysis. 2017. PMID: 27100303 Free PMC article.

3

Extensive porto-splenic venous thrombosis postsplenectomy in a sickle cell disease: a rare complication.

Al Barhi T, Wali Y, Al Sibai S, Al Balushi Z. Al Barhi T, et al. Among authors: wali y. BMJ Case Rep. 2022 Jan 17;15(1):e245085. doi: 10.1136/bcr-2021-245085. BMJ Case Rep. 2022. PMID: 35039344 Free PMC article.

4

Cystic biliary atresia in a neonate with antenatally detected abdominal cyst.

Rahamtalla D, Al Rawahi Y, Jawa ZM, Wali Y. Rahamtalla D, et al. Among authors: wali y. BMJ Case Rep. 2022 Feb 28;15(2):e246081. doi: 10.1136/bcr-2021-246081. BMJ Case Rep. 2022. PMID: 35228221 Free PMC article.

5

Intramural duodenal haematoma in a child post-endoscopic biopsy.

Rahamtalla D, Al Rawahi Y, Al Abri H, Wali Y. Rahamtalla D, et al. Among authors: wali y. BMJ Case Rep. 2022 Dec 30;15(12):e250884. doi: 10.1136/bcr-2022-250884. BMJ Case Rep. 2022. PMID: 36585043

6

Homozygous mild beta-thalassaemia promoter transversion -71 C>T HBB:c.-121 C>T.

Hassan SM, Alrawas A, Al Khanbashi L, Wali Y. Hassan SM, et al. Among authors: wali y. BMJ Case Rep. 2023 Apr 4;16(4):e254416. doi: 10.1136/bcr-2022-254416. BMJ Case Rep. 2023. PMID: 37015769

7

Delayed myelopathy in a child following organic phosphate poisoning.

Al Amrani F, Wali Y, Mittal A, Al Futaisi A. Al Amrani F, et al. Among authors: wali y. BMJ Case Rep. 2023 Oct 24;16(10):e253456. doi: 10.1136/bcr-2022-253456. BMJ Case Rep. 2023. PMID: 37879708

8

Mitochondrial 3-hydroxymethylglutaryl-CoA synthase-2 (HMGCS2) deficiency: a rare case with bicytopenia and coagulopathy.

El-Sayed D, El-Karaksy H, Wali Y, Youssry I. El-Sayed D, et al. Among authors: wali y. BMJ Case Rep. 2023 Nov 6;16(11):e257011. doi: 10.1136/bcr-2023-257011. BMJ Case Rep. 2023. PMID: 37931961

9

ZAP-70 mutation: a case with familial autoimmune haemolytic anaemia and immune deficiency.

Abd Elhamed MM, Wali Y, Youssry I. Abd Elhamed MM, et al. Among authors: wali y. BMJ Case Rep. 2024 Mar 18;17(3):e258835. doi: 10.1136/bcr-2023-258835. BMJ Case Rep. 2024. PMID: 38499350

10

Lumbar puncture in haemophilia A: controversy in the management.

Beshlawi I, Al Lamki Z, Rawas A, Abdel-Baki MS, Wali Y. Beshlawi I, et al. Among authors: wali y. Haemophilia. 2014 Mar;20(2):e175-7. doi: 10.1111/hae.12343. Epub 2013 Dec 30. Haemophilia. 2014. PMID: 24372668 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

141 results

Search Page