1. Bleeding and thrombotic risk in pregnant women with Fontan physiology. Issue 17 (24th November 2020) Authors: Girnius, Andrea; Zentner, Dominica; Valente, Anne Marie; Pieper, Petronella G; Economy, Katherine E; Ladouceur, Magalie; Roos-Hesselink, Jolien W; Warshak, Carri; Partington, Sara L; Gao, Zhiqian; Ollberding, Nicholas; Faust, Michelle; Girnius, Saulius; Kaemmerer, Harald; Nagdyman, Nicole; Cohen,... Journal: Heart Issue: Volume 107:Issue 17(2021) Page Start: 1390 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel. Issue 5 (9th February 2016) Authors: Al-Hamed, Mohamed H; Kurdi, Wesam; Alsahan, Nada; Alabdullah, Zainab; Abudraz, Rania; Tulbah, Maha; Alnemer, Maha; Khan, Rubina; Al-Jurayb, Haya; Alahmed, Ahmed; Tahir, Asma I; Khalil, Dania; Edwards, Noel; Al Abdulaziz, Basma; Binhumaid, Faisal S; Majid, Salma; Faquih, Tariq; El-Kalioby, Mohamed... Journal: Journal of medical genetics Issue: Volume 53:Issue 5(2016) Page Start: 338 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Identification of a novel MKS locus defined by TMEM107 mutation. (29th June 2015) Authors: Shaheen, Ranad; Almoisheer, Agaadir; Faqeih, Eissa; Babay, Zainab; Monies, Dorota; Tassan, Nada; Abouelhoda, Mohamed; Kurdi, Wesam; Al Mardawi, Elham; Khalil, Mohamed M.I.; Seidahmed, Mohammed Zain; Alnemer, Maha; Alsahan, Nada; Sogaty, Samira; Alhashem, Amal; Singh, Ankur; Goyal, Manisha; Kapoor... Journal: Human molecular genetics Issue: Volume 24:Number 18(2015:Sep. 15) Page Start: 5211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Knowledge and attitudes regarding non‐invasive prenatal testing among women in Saudi Arabia. (27th June 2021) Authors: Bawazeer, Shahad; AlSayed, Moeenaldeen; Kurdi, Wesam; Balobaid, Ameera Journal: Prenatal diagnosis Issue: Volume 41:Number 10(2021) Page Start: 1343 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mutation in MPDZ causes severe congenital hydrocephalus. Issue 1 (13th December 2012) Authors: Al-Dosari, Mohammed S; Al-Owain, Mohammed; Tulbah, Maha; Kurdi, Wesam; Adly, Nouran; Al-Hemidan, Amal; Masoodi, Tariq A; Albash, Buthainah; Alkuraya, Fowzan S Journal: Journal of medical genetics Issue: Volume 50:Issue 1(2013) Page Start: 54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Observational cohort study of perinatal outcomes of women with COVID-19. Issue 12 (December 2022) Authors: Al-Hajjar, Sami; Ibrahim, Lina; Kurdi, Wesam; Tulbah, Maha; Alnemer, Maha; Bin Jabr, Mohammed; Elsaidawi, Weam; Binmanee, Abdulaziz; Ali, Mohanned; Bukhari, Hanifa; Altuwaijri, Leena; Allaboon, Raneem; Alghamdi, Reem; Saeed, Bashayer; Adi, Yasser; Alhamlan, Fatima Journal: Journal of infection and public health Issue: Volume 15:Issue 12(2022) Page Start: 1503 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The effect of hyoscine-N-butylbromide on pain perception during and after hysterosalpingography in infertile women: a systematic review and meta-analysis of randomised controlled trials. (27th May 2022) Authors: Aboshama, Rehab Abdelhamid; Shareef, Mohammad Abrar; AlAmodi, Abdulhadi A.; Kurdi, Wesam; Al-Tuhaifi, Mohammed M.; Bintalib, Marwah Ghazi; Sileem, Sileem Ahmed; Abdelazem, Osama; Abdelhakim, Ahmed Mohamed; Sobh, Ahmed M. A.; Elbaradie, Sahar M. Y. Journal: Human fertility Issue: Volume 25:Number 3(2022) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The genetic landscape of familial congenital hydrocephalus. Issue 6 (June 2017) Authors: Shaheen, Ranad; Sebai, Mohammed Adeeb; Patel, Nisha; Ewida, Nour; Kurdi, Wesam; Altweijri, Ikhlass; Sogaty, Sameera; Almardawi, Elham; Seidahmed, Mohammed Zain; Alnemri, Abdulrahman; Madirevula, Sateesh; Ibrahim, Niema; Abdulwahab, Firdous; Hashem, Mais; Al‐Sheddi, Tarfa; Alomar, Rana; Alobeid, E... Journal: Annals of neurology Issue: Volume 81:Issue 6(2017) Page Start: 890 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The many faces of peroxisomal disorders: Lessons from a large Arab cohort. Issue 2 (18th December 2018) Authors: Alshenaifi, Jumanah; Ewida, Nour; Anazi, Shams; Shamseldin, Hanan E.; Patel, Nisha; Maddirevula, Sateesh; Al‐Sheddi, Tarfa; Alomar, Rana; Alobeid, Eman; Ibrahim, Niema; Hashem, Mais; Abdulwahab, Firdous; Jacob, Minnie; Alhashem, Amal; Alzaidan, Hamad I.; Seidahmed, Mohammed Z.; Alhashemi, Nadia; ... Journal: Clinical genetics Issue: Volume 95:Issue 2(2019) Page Start: 310 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗