E-LIB Suche - Ergebnisse für: Sahly, Nora N.

1

Cisplatinum and docetaxel for ovarian cancer in pregnancy:

Rouzi, Abdulrahim A. ; Sahly, Nora N. ; Sahly, Naif F..
Archives of Gynecology and Obstetrics. 280 (2009) 5 - p. 823-825 , 2009

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

2

Molecular differential analysis of uterine leiomyomas and l..:

Nora Naif Sahly (6086105) ; Babajan Banaganapalli (704628) ; Ahmed N. Sahly (4025636)...
https://figshare.com/articles/dataset/Molecular_differential_analysis_of_uterine_leiomyomas_and_leiomyosarcomas_through_weighted_gene_network_and_pathway_tracing_approaches/14184579. , 2021

Link: https://doi.org/10.6084/..

3

Efficacy of interferon beta-1a plus remdesivir compared wit..:

Kalil, Andre C ; Mehta, Aneesh K ; Patterson, Thomas F...
qt2cn0p0cr. , 2021

Link: https://escholarship.org..

4

Genotype-phenotype correlation in CLCN4-related development..:

Sahly, Ahmed N. ; Sierra-Marquez, Juan ; Bungert-Plümke, Stefanie...
Human Genetics. 143 (2024) 5 - p. 667-681 , 2024

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

5

Defining the Genetic Landscape of Congenital Mirror Movemen..:

Collins Hutchinson, Meagan L. ; St‐Onge, Judith ; Schlienger, Sabrina...
Movement Disorders. 39 (2024) 2 - p. 400-410 , 2024

Link: https://doi.org/10.1002/..

6

Epilepsy surgery outcomes in patients with GATOR1 gene comp..:

Sahly, Ahmed N ; Whitney, Robyn ; Costain, Gregory...
Seizure: European Journal of Epilepsy. 107 (2023) - p. 13-20 , 2023

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

7

The epileptology of Wiedemann-Steiner syndrome: Electroclin..:

Sahly, Ahmed N. ; Srour, Myriam ; Buhas, Daniela..
European Journal of Paediatric Neurology. 44 (2023) - p. 46-50 , 2023

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

8

SUDEP risk and autonomic dysfunction in genetic epilepsies:

Sahly, Ahmed N. ; Shevell, Michael ; Sadleir, Lynette G..
Autonomic Neuroscience. 237 (2022) - p. 102907 , 2022

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

9

MT‐TA pathogenic variants may cause developmental and epile..:

Sahly, Ahmed N. ; Buhas, Daniela ; Myers, Kenneth A.
American Journal of Medical Genetics Part A. 188 (2022) 10 - p. 3135-3138 , 2022

Link: https://doi.org/10.1002/..

10

Identification of a Rare Exon 19 Skipping Mutation in ALMS1..:

Saadah, Omar I. ; Banaganapalli, Babajan ; Kamal, Naglaa M....
Frontiers in Pediatrics. 9 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

11

Whole exome sequencing identifies rare biallelic ALMS1 miss..:

Kamal, Naglaa M. ; Sahly, Ahmed N. ; Banaganapalli, Babajan...
Saudi Journal of Biological Sciences. 27 (2020) 1 - p. 271-278 , 2020

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

12

Severe DNM1 encephalopathy with dysmyelination due to recur..:

Sahly, Ahmed N. ; Krochmalnek, Eric ; St-Onge, Judith..
Human Genetics. 139 (2020) 12 - p. 1575-1578 , 2020

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

13

Expanded Somatic Mutation Spectrum of MED12 Gene in Uterine..:

Ajabnoor, Ghada M. A. ; Mohammed, Nesma Amin ; Banaganapalli, Babajan...
Frontiers in Genetics. 9 (2018) - p. , 2018

Link: https://doi.org/10.3389/..

14

Whole exome sequencing of a consanguineous family identifie..:

Al-Aama, Jumana Yousuf ; Shaik, Noor Ahmad ; Banaganapalli, Babajan...
PLOS ONE. 12 (2017) 5 - p. e0176664 , 2017

Link: https://doi.org/10.1371/..

15

Labour outcomes with defibulation at delivery in immigrant ..:

Rouzi, Abdulrahim A. ; Berg, Rigmor C ; Al-Wassia, Heidi...
Swiss Medical Weekly. 150 (2020) 3536 - p. w20326 , 2020

Link: https://doi.org/10.4414/..