I agree that this site is using cookies. You can find further informations here.
X
Ismail, Samira
208  results:
Search for persons X
?
1

PCSK9 Involvement in Autism Etiology: Sequence Variations, ..:

Salem, Sohair ; Mosaad, Rehab ; Lotfy, Randa..
Archives of Medical Research.  54 (2023)  6 - p. 102860 , 2023
Link: https://doi.org/10.1016/..
 
?
2

Expansion of the phenotypic and mutational spectrum of Carp..:

Khairat, Rabab ; Elhossini, Rasha ; Sobreira, Nara...
European Journal of Medical Genetics.  65 (2022)  1 - p. 104377 , 2022
Link: https://doi.org/10.1016/..
 
?
3

The potential impact of COMT gene variants on dopamine regu..:

Esmaiel, Nora N. ; Ashaat, Engy A. ; Mosaad, Rehab...
Behavioural Brain Research.  378 (2020)  - p. 112272 , 2020
Link: https://doi.org/10.1016/..
 
?
4

Clinical and genetic characterization of ten Egyptian patie..:

Mekkawy, Mona K. ; Kamel, Alaa K. ; Thomas, Manal M....
Molecular Genetics & Genomic Medicine.  9 (2020)  2 - p. , 2020
Link: https://doi.org/10.1002/..
 
?
5

A novel homozygous variant in the TRAPPC9 gene causing inte..:

Ashaat, Engy A. ; El Ruby, Mona O. ; Westenberger, Ana...
Meta Gene.  26 (2020)  - p. 100783 , 2020
Link: https://doi.org/10.1016/..
 
?
6

A founder mutation in PEX12 among Egyptian patients in pero..:

Zaki, Maha S. ; Issa, Mahmoud Y. ; Thomas, Manal M....
Neurological Sciences.  42 (2020)  7 - p. 2737-2745 , 2020
Link: https://doi.org/10.1007/..
 
?
7

Exploiting the Autozygome to Support Previously Published M..:

Maddirevula, Sateesh ; Shamseldin, Hanan E. ; Sirr, Amy...
Frontiers in Genetics.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
?
8

Blepharophimosis‐ptosis‐intellectual disability syndrome: A..:

Zaki, Maha S. ; Otaify, Ghada A. ; Ismail, Samira...
American Journal of Medical Genetics Part A.  182 (2020)  12 - p. 2857-2866 , 2020
Link: https://doi.org/10.1002/..
 
?
9

Investigation of POU5F1 gene in sample of Egyptian patients..:

Ramadan, Abeer ; Alnaggar, Alshaimaa Rezk L.R. ; Ashaat, Engy.
Meta Gene.  22 (2019)  - p. 100604 , 2019
Link: https://doi.org/10.1016/..
 
?
10

Genetic assessment of ten Egyptian patients with Sjögren–La..:

Amr, Khalda ; El-Bassyouni, Hala T. ; Ismail, Samira...
Archives of Dermatological Research.  311 (2019)  9 - p. 721-730 , 2019
Link: https://doi.org/10.1007/..
 
?
11

Study of C677T variant of methylene tetrahydrofolate reduct..:

Ismail, Samira ; Senna, Azza Abo ; Behiry, Eman G....
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  180 (2019)  5 - p. 305-309 , 2019
Link: https://doi.org/10.1002/..
 
?
12

Genetic variants in components of the NALCN–UNC80–UNC79 ion..:

Bramswig, Nuria C. ; Bertoli-Avella, Aida M. ; Albrecht, Beate...
Human Genetics.  137 (2018)  9 - p. 753-768 , 2018
Link: https://doi.org/10.1007/..
 
?
13

GAPO syndrome in seven new patients: Identification of five..:

Abdel‐Hamid, Mohamed S. ; Ismail, Samira ; Zaki, Maha S....
American Journal of Medical Genetics Part A.  179 (2018)  2 - p. 237-242 , 2018
Link: https://doi.org/10.1002/..
 
?
14

Molybdenum cofactor and isolated sulphite oxidase deficienc..:

Zaki, Maha S. ; Selim, Laila ; EL-Bassyouni, Hala T....
European Journal of Paediatric Neurology.  20 (2016)  5 - p. 714-722 , 2016
Link: https://doi.org/10.1016/..
 
?
15

Clinical and molecular characterization of seven Egyptian f..:

Aglan, Mona ; Amr, Khalda ; Ismail, Samira...
American Journal of Medical Genetics Part A.  167 (2015)  12 - p. 3054-3061 , 2015
Link: https://doi.org/10.1002/..
 
1-15