E-LIB Suche - Ergebnisse für: Alorainy, Ibrahim A.

1

Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sial..:

Ali Alghamdi, Malak ; Benabdelkamel, Hicham ; Masood, Afshan...
Frontiers in Genetics. 13 (2022) - p. , 2022

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

2

Ancient founder mutation in RUBCN: a second unrelated famil..:

Seidahmed, Mohammed Z. ; Hamad, Muddathir H. ; AlBakheet, Albandary...
BMC Neurology. 20 (2020) 1 - p. , 2020

Link: https://doi.org/10.1186/..

3

Biallelic mutations in human DCC cause developmental split-..:

Jamuar, Saumya S ; Schmitz-Abe, Klaus ; D'Gama, Alissa M...
Nature Genetics. 49 (2017) 4 - p. 606-612 , 2017

Link: https://doi.org/10.1038/..

4

Hyperekplexia, microcephaly and simplified gyral pattern ca..:

Seidahmed, Mohammed Zain ; Salih, Mustafa A. ; Abdulbasit, Omer B....
BMC Neurology. 16 (2016) 1 - p. , 2016

Link: https://doi.org/10.1186/..

5

Gonadal mosaicism for ACTA1 gene masquerading as autosomal ..:

Seidahmed, Mohammed Zain ; Salih, Mustafa A. ; Abdelbasit, Omer Bashir...
American Journal of Medical Genetics Part A. 170 (2016) 8 - p. 2219-2221 , 2016

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

6

The association between petrous apex cephalocele and empty ..:

Jamjoom, Dima Z. ; Alorainy, Ibrahim A.
Surgical and Radiologic Anatomy. 37 (2015) 10 - p. 1179-1182 , 2015

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

7

Apparent discontinuity of the roof of the glenoid fossa on ..:

Al-Ekrish, Asma'a Abdurrahman ; Alorainy, Ibrahim A.
Oral Radiology. 32 (2015) 1 - p. 61-65 , 2015

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

8

Neurologic Injury in Isolated Sulfite Oxidase Deficiency:

Bosley, Thomas M. ; Alorainy, Ibrahim A. ; Oystreck, Darren T....
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 41 (2014) 1 - p. 42-48 , 2014

Link: https://doi.org/10.1017/..

9

Ocular Motility Disturbances in Orbitofacial Neurofibromato..:

Bosley, Thomas ; Alorainy, Ibrahim ; Morales, Jose..
Neurology. 82 (2014) 10_supplement - p. , 2014

Link: https://doi.org/10.1212/..

10

Neurologic Injury in Isolated Sulfite Oxidase Deficiency (P..:

Bosley, Thomas ; Alorainy, Ibrahim ; Oystreck, Darren..
Neurology. 82 (2014) 10_supplement - p. , 2014

Link: https://doi.org/10.1212/..

11

HOXA1 Mutations are Not Commonly Associated with Non-Syndro..:

Abu-Amero, Khaled K. ; Hagr, Abdulrahman al ; Almomani, Murad O....
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 41 (2014) 4 - p. 448-451 , 2014

Link: https://doi.org/10.1017/..

12

Ocular motility abnormalities in orbitofacial neurofibromat..:

Oystreck, Darren T. ; Alorainy, Ibrahim A. ; Morales, Jose...
Journal of American Association for Pediatric Ophthalmology and Strabismus. 18 (2014) 4 - p. 338-343 , 2014

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

13

Xq26.3 Microdeletion in a Male with Wildervanck Syndrome (P..:

Bosley, Thomas ; Kondkar, Altaf ; Alorainy, Ibrahim...
Neurology. 80 (2013) 7_supplement - p. , 2013

Link: https://doi.org/10.1212/..

14

Preimplantation Genetic Diagnosis in Isolated Sulfite Oxida..:

Salih, Mustafa A. ; Bosley, Thomas M. ; Alorainy, Ibrahim A....
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 40 (2013) 1 - p. 109-112 , 2013

Link: https://doi.org/10.1017/..

15

A novel syndrome of lethal familial hyperekplexia associate..:

Seidahmed, Mohammed Zein ; Salih, Mustafa A ; Abdulbasit, Omer B...
BMC Neurology. 12 (2012) 1 - p. , 2012

Link: https://doi.org/10.1186/..