Analysis of nuclear and mitochondrial genes in patients with pseudoexfoliation glaucoma

por Abu-Amero, Khaled K., Bosley, Thomas M., Morales, Jose
Publicado 2008

Visual and neurologic sequelae of methanol poisoning in Saudi Arabia

por Galvez-Ruiz, Alberto, Elkhamary, Sahar M., Asghar, Nasira, Bosley, Thomas M.
Publicado 2015

Carotid Cavernous Fistula: Ophthalmological Implications

por Chaudhry, Imtiaz A., Elkhamry, Sahar M., Al-Rashed, Waleed, Bosley, Thomas M.
Publicado 2009

Glutathione S-transferase M1 and T1 polymorphisms
in Arab glaucoma patients

por Abu-Amero, Khaled K., Morales, Jose, Mohamed, Gamal H., Osman, Mazen N., Bosley, Thomas M.
Publicado 2008

The role of mitochondrial haplogroups in glaucoma: a study in an Arab population

por Abu-Amero, Khaled K., Morales, Jose, Bosley, Thomas M., Mohamed, Gamal H., Cabrera, Vicente M.
Publicado 2008

Eurasian and African mitochondrial DNA influences in the Saudi Arabian population

por Abu-Amero, Khaled K, González, Ana M, Larruga, Jose M, Bosley, Thomas M, Cabrera, Vicente M
Publicado 2007

Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder

por Abu-Amero, Khaled K., Kondkar, Altaf A., Hellani, Ali M., Bosley, Thomas M., Khan, Arif O.
Publicado 2016

A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation

por Abu-Amero, Khaled K, Hellani, Ali M, Salih, Mustafa A, Seidahmed, Mohammad Z, Elmalik, Tageldin S, Zidan, Ghassan, Bosley, Thomas M
Publicado 2010

Unaltered myocilin expression in the blood of primary open angle glaucoma patients

por Abu-Amero, Khaled K., Azad, Taif Anwar, Spaeth, George L., Myers, Jonathan, Katz, L. Jay, Moster, Marlene, Bosley, Thomas M.
Publicado 2012

Absence of altered expression of optineurin in primary open angle glaucoma patients

por Abu-Amero, Khaled K., Azad, Taif Anwar, Spaeth, George L., Myers, Jonathan, Katz, L. Jay, Moster, Marlene, Bosley, Thomas M.
Publicado 2012

High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucoma

por Abu-Amero, Khaled K., Hellani, Ali, Bender, Patrick, Spaeth, George L., Myers, Jonathan, Katz, L. Jay, Moster, Marlene, Bosley, Thomas M.
Publicado 2009

Down-regulation of OPA1 in patients with primary open angle glaucoma

por Bosley, Thomas M., Hellani, Ali, Spaeth, George L., Myers, Jonathan, Katz, L. Jay, Moster, Marlene R., Milcarek, Barry, Abu-Amero, Khaled K.
Publicado 2011

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis

por Salih, Mustafa A, Abu-Amero, Khaled K, Alrasheed, Saleh, Alorainy, Ibrahim A, Liu, Lu, McGrath, John A, Van Maldergem, Lionel, Al-Fakey, Yasser H, AlSuhaibani, Adel H, Oystreck, Darren T, Bosley, Thomas M
Publicado 2011

Mutation in GM2A Leads to a Progressive Chorea-dementia Syndrome

por Salih, Mustafa A., Seidahmed, Mohammed Z., El Khashab, Heba Y., Hamad, Muddathir H. A., Bosley, Thomas M., Burn, Sabrina, Myers, Angela, Landsverk, Megan L., Crotwell, Patricia L., Bilguvar, Kaya, Mane, Shrikant, Kruer, Michael C.
Publicado 2015

New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations

por Salih, Mustafa A., Mundwiller, Emeline, Khan, Arif O., AlDrees, Abdulmajeed, Elmalik, Salah A., Hassan, Hamdy H., Al-Owain, Mohammed, Alkhalidi, Hisham M. S., Katona, Istvan, Kabiraj, Mohammad M., Chrast, Roman, Kentab, Amal Y., Alzaidan, Hamad, Rodenburg, Richard J., Bosley, Thomas M., Weis, Joachim, Koenig, Michel, Stevanin, Giovanni, Azzedine, Hamid
Publicado 2013

Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations

por Salih, Mustafa A., Mundwiller, Emeline, Khan, Arif O., AlDrees, Abdulmajeed, Elmalik, Salah A., Hassan, Hamdy H., Al-Owain, Mohammed, Alkhalidi, Hisham M. S., Katona, Istvan, Kabiraj, Mohammad M., Chrast, Roman, Kentab, Amal Y., Alzaidan, Hamad, Rodenburg, Richard J., Bosley, Thomas M., Weis, Joachim, Koenig, Michel, Stevanin, Giovanni, Azzedine, Hamid
Publicado 2013

Biallelic Mutations In Human DCC Cause Developmental Split Brain Syndrome

por Jamuar, Saumya S., Schmitz-Abe, Klaus, D’Gama, Alissa M., Drottar, Marie, Chan, Wai-Man, Peeva, Maya, Servattalab, Sarah, Lam, Anh-Thu N., Delgado, Mauricio R., Clegg, Nancy J., Al Zayed, Zayed, Dogar, Mohammad Asif, Alorainy, Ibrahim A., Jamea, Abdullah Abu, Abu-Amero, Khaled, Griebel, May, Ward, Wendy, Lein, Ed S., Markianos, Kyriacos, Barkovich, A. James, Robson, Caroline D., Grant, P. Ellen, Bosley, Thomas M., Engle, Elizabeth C., Walsh, Christopher A., Yu, Timothy W.
Publicado 2017