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Author/Creator Sunbul, Rawda

1. Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group. Issue 1 (December 2015)

Authors:
Al Jasmi, Fatma; Al Jumah, Mohammed; Alqarni, Fatimah; Al-Sanna'a, Nouriya; Al-Sharif, Fawziah; Bohlega, Saeed; Cupler, Edward; Fathalla, Waseem; Hamdan, Mohamed; Makhseed, Nawal; Nafissi, Shahriar; Nilipour, Yalda; Selim, Laila; Shembesh, Nuri; Sunbul, Rawda; Tonekaboni, Seyed
Journal:
BMC neurology
Issue:
Volume 15:Issue 1(2015)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Infantile Serine Biosynthesis Defect Due to Phosphoglycerate Dehydrogenase Deficiency: Variability in Phenotype and Treatment Response, Novel Mutations, and Diagnostic Challenges. (May 2017)

Authors:
Benke, Paul J.; Hidalgo, Ryan J.; Braffman, Bruce H.; Jans, Judith; Gassen, Koen L.I. van; Sunbul, Rawda; El-Hattab, Ayman W.
Journal:
Journal of child neurology
Issue:
Volume 32:Number 6(2017:Jun.)
Page Start:
543
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. 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) ↗