Loai A Eid - Dubai Kidney Center of Excellence, Dubai Hospital

基本信息

浏览量：0

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 10 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Treatment and long-term outcome in primary nephrogenic diabetes insipidus

Sergio C. Lopez-Garcia,Mallory L. Downie,Ji Soo Kim,Olivia Boyer,Stephen B. Walsh,Tom Nijenhuis,Svetlana Papizh,Pallavi Yadav,Ben C. Reynolds,Stephane Decramer,Martine Besouw,Manel Perello Carrascosa,Claudio La Scola,Francesco Trepiccione,Gema Ariceta,Aurelie Hummel,Claire Dossier,John A. Sayer,Martin Konrad,Mandy G. Keijzer-Veen,Atif Awan,Biswanath Basu,Dominique Chauveau,Leire Madariaga,Linda Koster-Kamphuis,Monica Furlano,Miriam Zacchia,Pierluigi Marzuillo,Yincent Tse,Ismail Dursun,Ayse Seda Pinarbasi,Despoina Tramma,Ewout J. Hoorn,Ibrahim Gokce,Kathleen Nicholls,Loai A. Eid,Lisa Sartz,Michael Riordan,Nakysa Hooman,Nikoleta Printza,Olivier Bonny,Pedro Arango Sancho,Raphael Schild, Rajiv Sinha,Stefano Guarino,Victo Martinez Jimenez,Lidia Rodriguez Pena,Hendrica Belge,Olivier Devuyst,Tanja Wlodkowski,Francesco Emma,Elena Levtchenko,Nine V. A. M. Knoers,Daniel G. Bichet,Franz Schaefer,Robert Kleta,Detlef Bockenhauer

NEPHROLOGY DIALYSIS TRANSPLANTATION（2023）

引用9浏览0WOS引用

A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome

Saeed AlZabali,Sawsan AlBatati,Khawla Rahim,Hassan Faqeehi, Abubaker Osman,Abdulaziz Bamhraz, Mohammed A. Saleh,Jameela A. Kari,Majed Aloufi,Loai Eid,Haydar Nasser, Abubakr Imam,Entesar AlHammadi,Omar Alkandari,Mohammed Al Riyami, Sidharth Sethi,Christoph Licht,Khalid A. Alhasan,Abdulkarim AlAnazi

Children（2022）

引用0浏览0WOS引用

Relapsing and refractory peritoneal dialysis peritonitis caused by Corynebacterium amycolatum

Shameer M. Habeeb, Haneen Yamin,Eva Simkova,Hazem S. Awad, Entesar A. Alhammadi,Loai A. Eid,Rubina Lone,Martin Bitzan

Pediatr Nephrol（2022）

引用1浏览0WOS引用

Reverse Phenotyping Facilitates Disease Allele Calling in Exome Sequencing of Patients with CAKUT

Genetics in Medicine（2022）

引用11浏览0WOS引用

Whole-Exome Sequencing Identifies Likely Deleterious Variants in 50 Families with Spina Bifida

Chunyan Wang,Steve Seltzsam,Bixia Zheng,Chen-Han W. Wu,Camille H. Nicolas Frank,Kirollos Yousef,Nina Mann,Sophia Schneider,Luca M. Schierbaum,Dalia Pantel,Jameela A. Kari,Sherif M. El desoky,Loai A. Eid,Velibor Tasic,Shirlee Shril,Michelle A. Baum,Carlos R. Estrada,Friedhelm Hildebrandt

Journal of the American Society of Nephrologyno. 10S (2021): 429-429

引用0浏览0引用

A Truncating NRIP1 Variant in an Arabic Family with Congenital Anomalies of the Kidneys and Urinary Tract

Bixia Zheng,Chunyan Wang,Steve Seltzsam,Sophia Schneider,Luca Schierbaum, Wilfred Wu,Rufeng Dai,Dervla M. Connaughton,Makiko Nakayama,Nina Mann,Stuart B. Bauer,Hazem S. Awad,Loai A. Eid,Velibor Tasic,Shirlee Shril,Friedhelm Hildebrandt

American journal of medical genetics Part A（2021）

引用2浏览0WOS引用

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

Dervla M. Connaughton,Rufeng Dai, Danielle J. Owen,Jonathan Marquez,Nina Mann, Adda L. Graham-Paquin,Makiko Nakayama,Etienne Coyaud,Estelle Mn Laurent,Jonathan R. St-Germain,Lot Snijders Blok,Arianna Vino,Verena Klambt,Konstantin Deutsch,Chen-Han Wilfred Wu,Caroline M. Kolvenbach,Franziska Kause,Isabel Ottlewski,Ronen Schneider,Thomas M. Kitzler,Amar J. Majmundar,Florian Buerger,Ana C. Onuchic-Whitford,Mao Youying,Amy Kolb,Daanya Salmanullah,Evan Chen,Amelie T. van der Ven,Jia Rao,Hadas Ityel,Steve Seltzsam, Johanna M. Rieke,Jing Chen,Asaf Vivante,Daw-Yang Hwang,Stefan Kohl,Gabriel C. Dworschak,Tobias Hermle,Marielle Alders,Tobias Bartolomaeus,Stuart B. Bauer,Michelle A. Baum,Eva H. Brilstra,Thomas D. Challman,Jacob Zyskind,Carrie E. Costin,Katrina M. Dipple,Floor A. Duijkers,Marcia Ferguson,David R. Fitzpatrick, Roger Fick,Ian A. Glass,Peter J. Hulick,Antonie D. Kline,Ilona Krey,Selvin Kumar,Weining Lu,Elysa J. Marco,Ingrid M. Wentzensen,Heather C. Mefford,Konrad Platzer,Inna S. Povolotskaya,Juliann M. Savatt,Natalia Shcherbakova,Prabha Senguttuvan,Audrey E. Squire,Deborah R. Stein,Isabelle Thiffault,Victoria Y. Voinova,Michael J. G. Somers,Michael A. Ferguson,Avram Z. Traum,Ghaleb H. Daouk,Ankana Daga,Nancy M. Rodig,Paulien A. Terhal,Ellen van Binsbergen,Loai A. Eid,Velibor Tasic,Hila Milo Rasouly,Tze Y. Lim,Dina F. Ahram, Ali G. Gharavi,Heiko M. Reutter,Heidi L. Rehm,Daniel G. MacArthur,Monkol Lek,Kristen M. Laricchia,Richard P. Lifton,Hong Xu,Shrikant M. Mane,Simone Sanna-Cherchi,Andrew D. Sharrocks,Brian Raught,Simon E. Fisher,Maxime Bouchard,Mustafa K. Khokha,Shirlee Shril,Friedhelm Hildebrandt

American journal of human genetics（2020）

引用20浏览0WOS引用

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract

Amelie T van der Ven,Dervla M Connaughton,Hadas Ityel,Nina Mann,Makiko Nakayama,Jing Chen,Asaf Vivante,Daw-Yang Hwang,Julian Schulz,Daniela A Braun,Johanna Magdalena Schmidt,David Schapiro,Ronen Schneider,Jillian K Warejko,Ankana Daga,Amar J Majmundar,Weizhen Tan,Tilman Jobst-Schwan,Tobias Hermle,Eugen Widmeier,Shazia Ashraf,Ali Amar,Charlotte A Hoogstraaten,Hannah Hugo,Thomas M Kitzler,Franziska Kause,Caroline M Kolvenbach,Rufeng Dai,Leslie Spaneas,Kassaundra Amann,Deborah R Stein,Michelle A Baum,Michael J G Somers,Nancy M Rodig,Michael A Ferguson,Avram Z Traum,Ghaleb H Daouk,Radovan Bogdanović,Natasa Stajić,Neveen A Soliman,Jameela A Kari,Sherif El Desoky,Hanan M Fathy,Danko Milosevic,Muna Al-Saffar,Hazem S Awad,Loai A Eid, Aravind Selvin,Prabha Senguttuvan,Simone Sanna-Cherchi,Heidi L Rehm,Daniel G MacArthur,Monkol Lek,Kristen M Laricchia,Michael W Wilson,Shrikant M Mane,Richard P Lifton,Richard S Lee,Stuart B Bauer,Weining Lu,Heiko M Reutter,Velibor Tasic,Shirlee Shril,Friedhelm Hildebrandt

Journal of the American Society of Nephrology JASNno. 9 (2018): 2348-2361

引用147浏览0WOS引用

147

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn