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Author/Creator Hamed, Sherifa A.

6. Genetic and phenotypic characterization of complex hereditary spastic paraplegia. (23rd May 2016)

Authors:
Kara, Eleanna; Tucci, Arianna; Manzoni, Claudia; Lynch, David S.; Elpidorou, Marilena; Bettencourt, Conceicao; Chelban, Viorica; Manole, Andreea; Hamed, Sherifa A.; Haridy, Nourelhoda A.; Federoff, Monica; Preza, Elisavet; Hughes, Deborah; Pittman, Alan; Jaunmuktane, Zane; Brandner, Sebastian; Xi...
Journal:
Brain
Issue:
Volume 139:Part 7(2016:Jul.)
Page Start:
1904
Record Type:
Journal Article
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7. Homozygous nonsense mutation in SGCA is a common cause of limb‐girdle muscular dystrophy in Assiut, Egypt. Issue 4 (24th August 2016)

Authors:
Reddy, Hemakumar M.; Hamed, Sherifa A.; Lek, Monkol; Mitsuhashi, Satomi; Estrella, Elicia; Jones, Michael D.; Mahoney, Lane J.; Duncan, Anna R.; Cho, Kyung‐ah; Macarthur, Daniel G.; Kunkel, Louis M.; Kang, Peter B.
Journal:
Muscle & nerve
Issue:
Volume 54:Issue 4(2016)
Page Start:
690
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗