1. A novel POU1F1 pathogenic variant: Two familial case reports with phenotype expansion. Issue 5 (11th August 2021) Authors: Musa, Noha; Elmonem, Mohamed A.; Beetz, Christian; Hafez, Mona; Hassan, Mona; Rolfs, Arndt; Selim, Laila; Elkhateeb, Nour Journal: Clinical genetics Issue: Volume 100:Issue 5(2021) Page Start: 641 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Assessment of urinary podocalyxin as a marker of glomerular injury in obesity‐related kidney disease in children and adolescents with obesity compared to urinary albumin creatinine ratio. Issue 4 (2nd April 2021) Authors: Musa, Noha; Ramzy, Tarek; Hamdy, Ahmed; Arafa, Noha; Hassan, Mona Journal: Clinical obesity Issue: Volume 11:Issue 4(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. CYP21A2 genetic profile in 14 Egyptian children with suspected congenital adrenal hyperplasia: a diagnostic challenge. Issue 1 (21st December 2017) Authors: Elmougy, Fatma; Sharaf, Sahar; Hafez, Mona; Khattab, Ahmed; Abou‐Yousef, Hazem; Elsharkawy, Marwa; Baz, Heba; Ekladious, Sherif; Sherif, Balsam; Musa, Noha; Elshiwy, Yasmin; Afif, Alaa; Abdullatif, Mona; Thabet, Ghada; Rady, Normeen; Ibrahim, Amany; Soliman, Hend Other Names: Zaidi Mone guestEditor. Journal: Annals of the New York Academy of Sciences Issue: Volume 1415:Issue 1(2018) Page Start: 11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗