E-LIB Suche - Ergebnisse für: Zaki, Osama K.

1

Inherited metabolic disorders in a cohort of Egyptian child..:

Abdelsattar, Shimaa ; Obada, Manar ; El-Hawy, Mahmoud A....
Egyptian Liver Journal. 12 (2022) 1 - p. , 2022

2

CYP1B1 Gene Mutation Impact on Prognosis of Primary Congeni..:

Mohammad, Noha S ; Rashad, Saad M ; el Maamoun, Tarek A...
QJM: An International Journal of Medicine. 114 (2021) Supplement_1 - p. , 2021

Link: https://doi.org/10.1093/..

3

Investigating the structural impacts of a novel missense va..:

Ibrahim, Ali Zaki ; Thirumal Kumar, D. ; Abunada, Taghreed...
Molecular Genetics and Metabolism Reports. 25 (2020) - p. 100645 , 2020

Link: https://doi.org/10.1016/..

4

Clinical, biochemical, neuroradiological and molecular char..:

Zayed, Hatem ; El Khayat, Hamed ; Tomoum, Hoda...
Metabolic Brain Disease. 34 (2019) 4 - p. 1231-1241 , 2019

Link: https://doi.org/10.1007/..

5

Prevalence of congenital heart defects among 54 Egyptian ch..:

Kotby, Alyaa A. ; Al-Fahham, Marwa M. ; Elabd, Heba Salah A..
Egyptian Journal of Medical Human Genetics. 19 (2018) 1 - p. 37-41 , 2018

Link: https://doi.org/10.1016/..

6

Genotype–phenotype correlation in patients with isovaleric ..:

Zaki, Osama K. ; Priya Doss C, George ; Ali, Salsabil A....
Human Molecular Genetics. , 2017

Link: https://doi.org/10.1093/..

7

Corrigendum to "Mutation Analysis of Methylmalonyl COA Muta..:

Ghoraba, Dina A. ; Mohammed, Magdy M. ; Zaki, Osama K.
Meta Gene. 11 (2017) - p. 136 , 2017

Link: https://doi.org/10.1016/..

8

Genotype-phenotype correlation in 18 Egyptian patients with..:

Mosaeilhy, Ahmed ; Mohamed, Magdy M. ; C, George Priya Doss...
Metabolic Brain Disease. 32 (2017) 5 - p. 1417-1426 , 2017

Link: https://doi.org/10.1007/..

9

Severe neurological manifestations in an Egyptian patient w..:

Moseilhy, Ahmed ; Hassan, Magdy M. ; El Abd, Heba S. A....
Metabolic Brain Disease. 32 (2016) 1 - p. 35-40 , 2016

Link: https://doi.org/10.1007/..

10

Two patients with Canavan disease and structural modeling o..:

Zaki, Osama K ; Krishnamoorthy, Navaneethakrishnan ; El Abd, Heba S...
Metabolic Brain Disease. 32 (2016) 1 - p. 171-177 , 2016

Link: https://doi.org/10.1007/..

11

Challenges in diagnosis and counseling of a family with two..:

Abd-Elkhalek, Heba S. ; Gamal, Radwa ; Zaki, Osama K..
Egyptian Journal of Medical Human Genetics. 17 (2016) 3 - p. 247-250 , 2016

Link: https://doi.org/10.1016/..

12

The Use of Glycomacropeptide in Dietary Management of Pheny..:

Zaki, Osama K. ; El-Wakeel, Lamia ; Ebeid, Yasmin...
Journal of Nutrition and Metabolism. 2016 (2016) - p. 1-5 , 2016

Link: https://doi.org/10.1155/..

13

Glutaric aciduria type 1: neuroimaging features with clinic..:

Mohammad, Shaimaa Abdelsattar ; Abdelkhalek, Heba Salah ; Ahmed, Khaled A..
Pediatric Radiology. 45 (2015) 11 - p. 1696-1705 , 2015

Link: https://doi.org/10.1007/..

14

Novel mutation in an Egyptian patient with infantile Canava..:

Zaki, Osama K. ; El Abd, Heba S. ; Mohamed, Shaimaa A..
Metabolic Brain Disease. 31 (2015) 3 - p. 573-577 , 2015

Link: https://doi.org/10.1007/..

15

Mutation analysis of methylmalonyl CoA mutase gene exon 2 i..:

Ghoraba, Dina A. ; Mohammed, Magdy M. ; Zaki, Osama K.
Meta Gene. 3 (2015) - p. 71-88 , 2015

Link: https://doi.org/10.1016/..