| Rapid progression and mortality of lysosomal acid lipase deficiency presenting in infants SA Jones, V Valayannopoulos, E Schneider, S Eckert, M Banikazemi, ... Genetics in Medicine 18 (5), 452-458, 2016 | 105 | 2016 |
| Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation study SA Jones, S Rojas-Caro, AG Quinn, M Friedman, S Marulkar, F Ezgu, ... Orphanet journal of rare diseases 12, 1-11, 2017 | 92 | 2017 |
| l-Carnitine supplementation improves the behavioral symptoms in autistic children SF Fahmy, MH El-Hamamsy, OK Zaki, OA Badary Research in Autism Spectrum Disorders 7 (1), 159-166, 2013 | 69 | 2013 |
| Cytogenetic study in cases with recurrent abortion in Saudi Arabia M Al Hussain, L Al-Nuaim, ZA Talib, OK Zaki Annals of Saudi Medicine 20 (3-4), 233-236, 2000 | 53 | 2000 |
| Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I A Mosaeilhy, MM Mohamed, HSA El Abd, R Gamal, OK Zaki, H Zayed Metabolic brain disease 32, 1417-1426, 2017 | 50 | 2017 |
| Glutaric aciduria type 1: neuroimaging features with clinical correlation SA Mohammad, HS Abdelkhalek, KA Ahmed, OK Zaki Pediatric radiology 45, 1696-1705, 2015 | 49 | 2015 |
| Structural chromosomal abnormalities in couples with recurrent abortion in Egypt NEA Gaboon, AR Mohamed, SM Elsayed, OK Zaki, MA Elsayed Turkish journal of medical sciences 45 (1), 208-213, 2015 | 40 | 2015 |
| Genotype–phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants OK Zaki, G Priya Doss C, SA Ali, GG Murad, SA Elashi, MSA Ebnou, ... Human Molecular Genetics 26 (16), 3105-3115, 2017 | 37 | 2017 |
| Two patients with Canavan disease and structural modeling of a novel mutation OK Zaki, N Krishnamoorthy, HS El Abd, SA Harche, RA Mattar, RS Al Disi, ... Metabolic brain disease 32, 171-177, 2017 | 37 | 2017 |
| The use of glycomacropeptide in dietary management of phenylketonuria OK Zaki, L El-Wakeel, Y Ebeid, HS Ez Elarab, A Moustafa, N Abdulazim, ... Journal of Nutrition and Metabolism 2016, 2016 | 32 | 2016 |
| A survey of 1,000 cases referred for cytogenetic study to King Khalid University Hospital, Saudi Arabia M Al Husain, OK Zaki Human heredity 49 (4), 208-214, 1999 | 30 | 1999 |
| Severe and rapid disease course in the natural history of infants with lysosomal acid lipase deficiency SA Jones, D Bernstein, M Bialer, A Dhawan, C Hendriksz, CB Whitley, ... Molecular Genetics and Metabolism 2 (111), S57-S58, 2014 | 26 | 2014 |
| Vitamin D intake and sun exposure in autistic children SF Fahmy, NA Sabri, MH El Hamamsy, M El Sawi, OK Zaki International Journal of Pharmaceutical Sciences and Research 7 (3), 1043, 2016 | 19 | 2016 |
| Increased seroprevalence of chronic toxoplasmosis in autistic children: Special reference to the pathophysiology of IFN-g and NO overproduction J Prandota, NAF Elleboudy, KA Ismail, OK Zaki, HH Shehata International Journal of Neurology Research 1 (3), 102-122, 2015 | 16 | 2015 |
| Clinical, biochemical, neuroradiological and molecular characterization of Egyptian patients with glutaric acidemia type 1 H Zayed, H El Khayat, H Tomoum, O Khalifa, E Siddiq, SA Mohammad, ... Metabolic brain disease 34, 1231-1241, 2019 | 15 | 2019 |
| Tryptophane as a tuberculostatic agent MM Abdel Kader, O Zaki Experientia 14, 455-456, 1958 | 13 | 1958 |
| Mutation analysis of methylmalonyl CoA mutase gene exon 2 in Egyptian families: identification of 25 novel allelic variants DA Ghoraba, MM Mohammed, OK Zaki Meta gene 3, 71-88, 2015 | 11 | 2015 |
| Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene A Moseilhy, MM Hassan, HSA El Abd, SA Mohammad, R El Bekay, ... Metabolic brain disease 32, 35-40, 2017 | 10 | 2017 |
| Novel mutation in an Egyptian patient with infantile Canavan disease OK Zaki, HS El Abd, SA Mohamed, H Zayed Metabolic brain disease 31, 573-577, 2016 | 9 | 2016 |
| Screening of diseases associated with abnormal metabolites for evaluation of HPLC in organic aciduria profiling DA Ghoraba, MM Mohamed, OK Zaki Egyptian Journal of Medical Human Genetics 15 (1), 69-78, 2014 | 8 | 2014 |
Vassili ValayannopoulosCentre de Référence Maladies Métaboliques- Hôpital Necker-Enfants MaladesVerified email at nck.aphp.fr
