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Khaled Abu-Amero

Research Profile

Geographic Areas

Saudi Arabia

Chemicals & Drugs

DNA, Mitochondrial

Physiology

Living Beings

Arabs

Procedures

Concepts & Ideas

Disorders

Anatomy

Mitochondrion

Genes & Molecular Sequences

Single Nucleotide Polymorphism

Co-author Network

Publications

TOP 3
Ayman Alsulaiman; Khaled K Abu-Amero
Parent's attitude toward prenatal diagnosis and termination of pregnancy could be influenced by other factors rather than by the severity of the condition.
Khaled K Abu-Amero; Ibrahim Alorainy; Arif O Khan; Altaf A Kondkar; Darren T Oystreck; Mustafa A M Salih; Thomas Bosley
Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder.
Nancy Hanna; Robert Wollmann; Khaled K Abu-Amero; Rachida Bouhenni; Balaji Gupta; Deepak P Edward
Histopathologic changes in the extraocular muscle in centronuclear myopathy with a Dynamin 2 mutation.

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All Publications

2013: Ayman Alsulaiman; Khaled K Abu-Amero
Parent's attitude toward prenatal diagnosis and termination of pregnancy could be influenced by other factors rather than by the severity of the condition.
Prenatal diagnosis 2013;33(3):257-61.
2013: Khaled K Abu-Amero; Ibrahim Alorainy; Arif O Khan; Altaf A Kondkar; Darren T Oystreck; Mustafa A M Salih; Thomas Bosley
Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder.
Ophthalmic genetics 2013;34(1-2):90-6.
2013: Nancy Hanna; Robert Wollmann; Khaled K Abu-Amero; Rachida Bouhenni; Balaji Gupta; Deepak P Edward
Histopathologic changes in the extraocular muscle in centronuclear myopathy with a Dynamin 2 mutation.
Ophthalmic genetics 2013;34(1-2):83-6.
2013: Khaled K Abu-Amero; Martin Jaeger; Mihai G Netea; Theo Plantinga; Hisham Y Hassan
Genetic variation of TLR2 and TLR4 among the Saudi Arabian population: insight into the evolutionary dynamics of the Arabian Peninsula.
Genetic testing and molecular biomarkers 2013;17(2):166-9.
2013: Saleh A Al-Obeidan; Ahmed Mousa; Abid Naseem; Khaled K Abu-Amero; Essam A Osman
Efficacy and safety of non-penetrating deep sclerectomy surgery in Saudi patients with uncontrolled open angle glaucoma.
Saudi medical journal 2013;34(1):54-61.
2013: Mustafa A Salih; Sarar H Mohamed; Mohamed S Rashed; Mohamed A Sabry; Khaled K Abu-Amero; Ibrahim Alorainy; Eiman A Al-Yamani; Thomas M Bosley; Siham El-Akoum; Ali M Hellani
Preimplantation genetic diagnosis in isolated sulfite oxidase deficiency.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2013;40(1):109-12.
2012: Ayman Alsulaiman; Josephine M Green; Jenny Hewison; Khaled K Abu-Amero; Shenaz Ahmed; Janet Hirst
Attitudes to prenatal diagnosis and termination of pregnancy for 30 conditions among women in Saudi Arabia and the UK.
Prenatal diagnosis 2012;32(11):1109-13.
2012: Ali M Hellani; Hisham M Yousef; Siham M Akoum; Elias S Fadel; Khaled K Abu-Amero
Successful pregnancies after combined human leukocyte antigen direct genotyping and preimplantation genetic diagnosis utilizing multiple displacement amplification.
Saudi medical journal 2012;33(10):1059-64.
2012: Khaled K Abu-Amero; R Rand Allingham; Mohammad T Azad; Michael A Hauser; Essam A Osman; Saleh A Al-Obeidan
Lack of association between LOXL1 gene polymorphisms and primary open angle glaucoma in the Saudi Arabian population.
Ophthalmic genetics 2012;33(3):130-3.
2012: Dilek Colak; Namik Kaya; Jose Morales; Albandary Al-Bakheet; Banan AlYounes; Thomas M Bosley; Khaled K Abu-Amero
Genome-wide expression profiling of patients with primary open angle glaucoma.
Investigative ophthalmology & visual science 2012;53(9):5899-904.
2012: Yasser H Al-Faky; Turki Al-Turki; Thomas Bosley; Mustafa A M Salih; Khaled K Abu-Amero; Adel H Alsuhaibani
Prominent corneal nerves: a novel sign of lipoid proteinosis.
The British journal of ophthalmology 2012;96(7):935-40.
2012: Abdullah G Alotaibi; Samah M Fawazi; Badriah R Alenazy; Khaled K Abu-Amero
Outcomes of 3 hours part-time occlusion treatment combined with near activities among children with unilateral amblyopia.
Saudi medical journal 2012;33(4):395-8.
2012: Khaled K Abu-Amero; Altaf A Kondkar; Ahmed Mousa; Essam A Osman; Saleh A Al-Obeidan
Lack of association of SNP rs4236601 near CAV1 and CAV2 with POAG in a Saudi cohort.
Molecular vision 2012;18():1960-5.
2012: Khaled K Abu-Amero; Stephen Akafo; Jason Gibson; Ana M Gonzalez; Michael A Hauser; Yutao Liu; Gamal Mohamed; R Rand Allingham
Mitochondrial genetic background in Ghanaian patients with primary open-angle glaucoma.
Molecular vision 2012;18():1955-9.
2012: Khaled K Abu-Amero; Taif Anwar Azad; L Jay Katz; Marlene Moster; Jonathan Myers; George L Spaeth; Thomas M Bosley
Absence of altered expression of optineurin in primary open angle glaucoma patients.
Molecular vision 2012;18():1421-7.
2012: Khaled K Abu-Amero; Taif Anwar Azad; L Jay Katz; Marlene Moster; Jonathan Myers; George L Spaeth; Thomas M Bosley
Unaltered myocilin expression in the blood of primary open angle glaucoma patients.
Molecular vision 2012;18():1004-9.
2011: Khaled K Abu-Amero; Ali Hellani; Seema Kapoor; Sumit Monga; Thomas M Bosley
Horizontal gaze palsy and progressive scoliosis due to a deleterious mutation in ROBO3.
Ophthalmic genetics 2011;32(4):231-6.
2011: Khaled K Abu-Amero; Ibrahim Alorainy; Dario Catalano; Flavio Faletra; Paolo Gasparini; Ali M Hellani; Fulvio Parentin; Stefano Pensiero; Thomas M Bosley
Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations.
Ophthalmic genetics 2011;32(4):212-6.
2011: Ahmed A Al-Saleh; Ali Hellani; Khaled K Abu-Amero
Isolated foveal hypoplasia: report of a new case and detailed genetic investigation.
International ophthalmology 2011;31(2):117-20.
2011: Mustafa A Salih; Darren T Oystreck; Yasser H Al-Faky; Mohammad M Kabiraj; Mohamed I A Omer; Elamin M Subahi; David Beeson; Khaled K Abu-Amero; Thomas Bosley
Congenital myasthenic syndrome due to homozygous CHRNE mutations: report of patients in Arabia.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2011;31(1):42-7.
2011: Abdulelah A Al-Abdullah; Khaled K Abu-Amero; Ali Hellani; Hisham Alkhalidi; Thomas M Bosley
Choroid plexus papilloma metastases to both cerebellopontine angles mimicking neurofibromatosis type 2.
Journal of neurology 2011;258(3):504-6.
2011: Khaled K Abu-Amero; R Rand Allingham; Michael A Hauser; Ahmed Mousa; Essam A Osman; Joshua Wheeler; Benjamin Whigham; Saleh A Al-Obeidan
Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.
Molecular vision 2011;17():2911-9.
2011: Khaled K Abu-Amero; Altaf A Kondkar; Ahmed Mousa; Essam A Osman; Saleh A Al-Obeidan
Decreased total antioxidants status in the plasma of patients with pseudoexfoliation glaucoma.
Molecular vision 2011;17():2769-75.
2011: Khaled K Abu-Amero; Vicente M Cabrera; Ana M González; José M Larruga; Essam A Osman; Saleh A Al-Obeidan
Susceptibility to primary angle closure glaucoma in Saudi Arabia: the possible role of mitochondrial DNA ancestry informative haplogroups.
Molecular vision 2011;17():2171-6.
2011: Khaled K Abu-Amero; Vicente M Cabrera; Ana M González; José M Larruga; Essam A Osman; Saleh A Al-Obeidan
Mitochondrial DNA lineages of African origin confer susceptibility to primary open-angle glaucoma in Saudi patients.
Molecular vision 2011;17():1468-72.
2011: Khaled K Abu-Amero
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited.
Middle East African journal of ophthalmology 2011;18(1):17-23.
2011: Khaled K Abu-Amero
Ophthalmic genetics: moving forward.
Middle East African journal of ophthalmology 2011;18(1):1.
2011: Thomas M Bosley; Ali Hellani; George L Spaeth; Jonathan Myers; L Jay Katz; Marlene R Moster; Barry Milcarek; Khaled K Abu-Amero
Down-regulation of OPA1 in patients with primary open angle glaucoma.
Molecular vision 2011;17():1074-9.
2011: Khaled K Abu-Amero; Ali M Hellani; Sameer M Al Mansouri; Hatem Kalantan; Abdulrahman M Al-Muammar
High-resolution analysis of DNA copy number alterations in patients with isolated sporadic keratoconus.
Molecular vision 2011;17():822-6.
2011: Khaled K Abu-Amero; Hatem Kalantan; Abdulrahman M Al-Muammar
Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia.
Molecular vision 2011;17():667-72.
2011: Khaled K Abu-Amero; Vicente M Cabrera; José M Larruga; Essam A Osman; Ana M González; Saleh A Al-Obeidan
Eurasian and Sub-Saharan African mitochondrial DNA haplogroup influences pseudoexfoliation glaucoma development in Saudi patients.
Molecular vision 2011;17():543-7.
2011: Mustafa A Salih; Khaled K Abu-Amero; Saleh Alrasheed; Ibrahim A Alorainy; Lu Liu; John A McGrath; Lionel Van Maldergem; Yasser H Al-Faky; Adel H Alsuhaibani; Darren T Oystreck; Thomas M Bosley
Molecular and neurological characterizations of three Saudi families with lipoid proteinosis.
BMC medical genetics 2011;12():31.
2010: Thomas Bosley; Khaled K Abu-Amero
Assessing mitochondrial DNA nucleotide changes in spontaneous optic neuropathies.
Ophthalmic genetics 2010;31(4):163-72.
2010: Khaled K Abu-Amero; Ali Hellani; Mustafa A Salih; Ibrahim Alorainy; Ghassan Zidan; Kyle C Kern; Nancy L Sicotte; Thomas M Bosley
Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy.
Ophthalmic genetics 2010;31(3):147-54.
2010: Ali Hellani; Sarar Mohamed; Siham Al-Akoum; Thomas M Bosley; Khaled K Abu-Amero
A t(5;16)(p15.32;q23.3) generating 16q23.3 --> qter duplication and 5p15.32 --> pter deletion in two siblings with mental retardation, dysmorphic features, and speech delay.
American journal of medical genetics. Part A 2010;152A(6):1555-60.
2010: Khaled K Abu-Amero; Ali Hellani; Mustafa A Salih; Abdulkarim Al Hussain; Majed al Obailan; Ghassan Zidan; Ibrahim Alorainy; Thomas Bosley
Ophthalmologic abnormalities in a de novo terminal 6q deletion.
Ophthalmic genetics 2010;31(1):1-11.
2010: Khaled K Abu-Amero; Olyan M Al-Boudari; Ahmed Mousa; Ana M Gonzalez; Jose M Larruga; Vicente M Cabrera; Nduna Dzimiri
The mitochondrial DNA variant 16189T>C is associated with coronary artery disease and myocardial infarction in Saudi Arabs.
Genetic testing and molecular biomarkers 2010;14(1):43-7.
2010: Salem H Khalil; Khaled K Abu-Amero; Fahad Al Mohareb; NA Chaudhri
Molecular monitoring of response to imatinib (Glivec) in chronic myeloid leukemia patients: experience at a tertiary care hospital in Saudi Arabia.
Genetic testing and molecular biomarkers 2010;14(1):67-74.
2010: Khaled K Abu-Amero; Mohammad Jaber; Ali Hellani; Thomas Bosley
Genome-wide expression profile of LHON patients with the 11778 mutation.
The British journal of ophthalmology 2010;94(2):256-9.
2010: Henry S Schutta; Khaled K Abu-Amero; Thomas Bosley
Exceptions to the Valsalva doctrine.
Neurology 2010;74(4):329-35.
2010: Khaled K Abu-Amero; Essam A Osman; Ahmed S Dewedar; Silke Schmidt; R Rand Allingham; Saleh A Al-Obeidan
Analysis of LOXL1 polymorphisms in a Saudi Arabian population with pseudoexfoliation glaucoma.
Molecular vision 2010;16():2805-10.
2010: Khaled K Abu-Amero; Ali M Hellani; Mustafa A Salih; Mohammad Z Seidahmed; Tageldin S Elmalik; Ghassan Zidan; Thomas M Bosley
A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.
BMC medical genetics 2010;11():135.
2009: Ghazi A Alsbeih; Najla M Al-Harbi; Medhat M El-Sebaie; Nasser M Al-Rajhi; Khaled S Al-Hadyan; Khaled K Abu-Amero
Involvement of mitochondrial DNA sequence variations and respiratory activity in late complications following radiotherapy.
Clinical cancer research : an official journal of the American Association for Cancer Research 2009;15(23):7352-60.
2009: Ali Hellani; Siham Al-Akoum; Khaled K Abu-Amero
G6PD Mediterranean S188F codon mutation is common among Saudi sickle cell patients and increases the risk of stroke.
Genetic testing and molecular biomarkers 2009;13(4):449-52.
2009: Khaled K Abu-Amero; B Milcarek; Thomas Bosley
GSTM1 and GSTT1 deletion genotypes in various spontaneous optic neuropathies in Arabs.
The British journal of ophthalmology 2009;93(8):1101-4.
2009: Ali Hellani; Elias Fadel; Shaker El-Sadadi; Hamdan El-Sweilam; Ahmed El-Dawood; Khaled K Abu-Amero
Molecular spectrum of alpha-thalassemia mutations in microcytic hypochromic anemia patients from Saudi Arabia.
Genetic testing and molecular biomarkers 2009;13(2):219-21.
2009: Khaled K Abu-Amero; Hesham al Dhalaan; Zayed al Zayed; Ali Hellani; Thomas Bosley
Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations.
Journal of the neurological sciences 2009;276(1-2):22-6.
2009: Khaled K Abu-Amero; Hesham Al-Dhalaan; Saeed Bohlega; Ali Hellani; Robert W Taylor
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report.
Journal of medical case reports 2009;3():77.
2009: Ali Hellani; Nidal Almassri; Khaled K Abu-Amero
A novel mutation in the ADA gene causing severe combined immunodeficiency in an Arab patient: a case report.
Journal of medical case reports 2009;3():6799.
2009: Khaled K Abu-Amero; Ali Hellani; Ana M González; Jose M Larruga; Vicente M Cabrera; Peter A Underhill
Saudi Arabian Y-Chromosome diversity and its relationship with nearby regions.
BMC genetics 2009;10():59.
2009: Khaled K Abu-Amero; Ali Hellani; Patrick Bender; George L Spaeth; Jonathan Myers; L Jay Katz; Marlene Moster; Thomas Bosley
High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucoma.
Molecular vision 2009;15():1594-8.
2009: Hajer Ennafaa; Vicente M Cabrera; Khaled K Abu-Amero; Ana M González; mohamed ben amor; Rym Bouhaha; Nduna Dzimiri; Amel B Elgaaïed; José M Larruga
Mitochondrial DNA haplogroup H structure in North Africa.
BMC genetics 2009;10():8.
2009: Ali Hellani; Hiba Baghdadi; Nidal Dabbour; Nidal Almassri; Khaled K Abu-Amero
A novel PTCH1 germline mutation distinguishes basal cell carcinoma from basaloid follicular hamartoma: a case report.
Journal of medical case reports 2009;3():52.
2008: Thomas Bosley; Michael C Brodsky; Charles M Glasier; Khaled K Abu-Amero
Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities.
Investigative ophthalmology & visual science 2008;49(12):5250-6.
2008: Canny Sugiana; David J Pagliarini; Matthew McKenzie; Denise M Kirby; Renato Salemi; Khaled K Abu-Amero; Hans-Henrik M Dahl; Wendy M Hutchison; Katherine A Vascotto; Stacey M Smith; Robert F Newbold; John Christodoulou; Sarah Calvo; Vamsi K Mootha; Michael T Ryan; David R Thorburn
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease.
American journal of human genetics 2008;83(4):468-78.
2008: Ghazi Atiyeh Alsbeih; Medhat Mohamed El-Sebaie; Nasser Mohamed Al-Rajhi; Najla Mohamed Al-Harbi; Khaled Saleh Al-Hadyan; Muneera Hamad Al-Buhairi; Belal Ali Moftah; Mohammad Othman Al-Shabanah; Khaled K Abu-Amero
Association between XRCC1 G399A Polymorphism and Late Complications to Radiotherapy in Saudi Head and Neck Cancer Patients.
Journal of the Egyptian National Cancer Institute 2008;20(3):302-8.
2008: Khaled K Abu-Amero; Jose M Larruga; Ana M González; Thomas Bosley
The role of mitochondrial haplogroups in non-arteritic anterior ischemic optic neuropathy.
Ophthalmic genetics 2008;29(3):111-6.
2008: Saeed A Bohlega; Khaled K Abu-Amero
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs.
Saudi medical journal 2008;29(7):952-6.
2008: Thomas Bosley; Ibrahim A Alorainy; Mustafa A Salih; Hesham M Aldhalaan; Khaled K Abu-Amero; Darren T Oystreck; Max A Tischfield; Elizabeth C Engle; Robert P Erickson
The clinical spectrum of homozygous HOXA1 mutations.
American journal of medical genetics. Part A 2008;146A(10):1235-40.
2008: Zuhair N Al-Hassnan; Mohamed S Rashed; Osama Y Al-Dirbashi; Zoltan Patay; Zuhair Rahbeeni; Khaled K Abu-Amero
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with stroke-like imaging presentation: clinical, biochemical and molecular analysis.
Journal of the neurological sciences 2008;264(1-2):187-94.
2008: Khaled K Abu-Amero; Ali Hellani; Saeed Bohlega
Absence of mtDNA mutations in leukocytes of CADASIL patients.
BMC research notes 2008;1():16.
2008: Khaled K Abu-Amero; Jose Morales; Thomas Bosley; Gamal H Mohamed; Vicente M Cabrera
The role of mitochondrial haplogroups in glaucoma: a study in an Arab population.
Molecular vision 2008;14():518-22.
2008: Khaled K Abu-Amero; Jose Morales; Gamal H Mohamed; moncef osman; Thomas Bosley
Glutathione S-transferase M1 and T1 polymorphisms in Arab glaucoma patients.
Molecular vision 2008;14():425-30.
2008: Khaled K Abu-Amero; José M Larruga; Vicente M Cabrera; Ana M González
Mitochondrial DNA structure in the Arabian Peninsula.
BMC evolutionary biology 2008;8():45.
2008: Khaled K Abu-Amero; Thomas Bosley; Jose Morales
Analysis of nuclear and mitochondrial genes in patients with pseudoexfoliation glaucoma.
Molecular vision 2008;14():29-36.
2007: Khaled K Abu-Amero; Thomas Bosley
Reassessment of the pathologic significance of the 9438 mitochondrial DNA mutation associated with LHON.
Ophthalmic genetics 2007;28(4):229-30.
2007: Khaled K Abu-Amero; Jose Morales; Mazen N Osman; Thomas Bosley
Nuclear and mitochondrial analysis of patients with primary angle-closure glaucoma.
Investigative ophthalmology & visual science 2007;48(12):5591-6.
2007: Khaled K Abu-Amero; Thomas Bosley
Mitochondrial DNA abnormalities in NAION.
The British journal of ophthalmology 2007;91(11):1561.
2007: Thomas Bosley; Mustafa A Salih; Ibrahim Alorainy; Darren T Oystreck; M Nester; Khaled K Abu-Amero; Max A Tischfield; Elizabeth C Engle
Clinical characterization of the HOXA1 syndrome BSAS variant.
Neurology 2007;69(12):1245-53.
2007: Osama Y Al-Dirbashi; Khaled K Abu-Amero; Abdulrahman Alswaid; G F Hoffmann; Khalid Al-Qahtani; Mohamed S Rashed
LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 gene.
Journal of inherited metabolic disease 2007;30(4):611.
2007: Saeed Bohlega; Asmahan Al Shubili; Abdulrahman Edris; Abdulrahman Alreshaid; Thamer Alkhairallah; M Walid AlSous; Samir Farah; Khaled K Abu-Amero
CADASIL in Arabs: clinical and genetic findings.
BMC medical genetics 2007;8():67.
2007: Thomas Bosley; Cris S Constantinescu; Christopher R Tench; Khaled K Abu-Amero
Mitochondrial changes in leukocytes of patients with optic neuritis.
Molecular vision 2007;13():1516-28.
2007: Ana M González; José M Larruga; Khaled K Abu-Amero; Yufei Shi; José Pestano; Vicente M Cabrera
Mitochondrial lineage M1 traces an early human backflow to Africa.
BMC genomics 2007;8():223.
2007: Khaled K Abu-Amero; Futwan Al-Mohanna; Olayan M Al-Boudari; Gamal H Mohamed; Nduna Dzimiri
The interactive role of type 2 diabetes mellitus and E-selectin S128R mutation on susceptibility to coronary heart disease.
BMC medical genetics 2007;8():35.
2007: Khaled K Abu-Amero; Ana M González; José M Larruga; Thomas Bosley; Vicente M Cabrera
Eurasian and African mitochondrial DNA influences in the Saudi Arabian population.
BMC evolutionary biology 2007;7():32.
2006: Khaled K Abu-Amero; Pinar T Ozand; Hesham Al-Dhalaan
Novel mitochondrial DNA transversion mutation in transfer ribonucleic acid for leucine 2 (CUN) in a patient with the clinical features of MELAS.
Journal of child neurology 2006;21(11):971-2.
2006: Khaled K Abu-Amero; Thomas Bosley
Mitochondrial abnormalities in patients with LHON-like optic neuropathies.
Investigative ophthalmology & visual science 2006;47(10):4211-20.
2006: Thomas Bosley; Darren T Oystreck; Richard L Robertson; Abdulaziz al Awad; Khaled K Abu-Amero; Elizabeth C Engle
Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A.
Brain : a journal of neurology 2006;129(Pt 9):2363-74.
2006: Khaled K Abu-Amero; Thomas Bosley
Increased relative mitochondrial DNA content in leucocytes of patients with NAION.
The British journal of ophthalmology 2006;90(7):823-5.
2006: Khaled K Abu-Amero; Jose Morales; Thomas Bosley
Mitochondrial abnormalities in patients with primary open-angle glaucoma.
Investigative ophthalmology & visual science 2006;47(6):2533-41.
2006: Khaled K Abu-Amero; Tarek M Owaidah; M Al-Mahed
Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene.
Journal of thrombosis and haemostasis : JTH 2006;4(5):1152-3.
2006: Khaled K Abu-Amero; Ali S Alzahrani; Minjing Zou; Yufei Shi
Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome.
Oncogene 2006;25(5):677-84.
2006: Khaled K Abu-Amero; Olayan M Al-Boudari; Gamal H Mohamed; Nduna Dzimiri
E-selectin S128R polymorphism and severe coronary artery disease in Arabs.
BMC medical genetics 2006;7():52.
2006: Khaled K Abu-Amero; Olayan M Al-Boudari; Gamal H Mohamed; Nduna Dzimiri
T null and M null genotypes of the glutathione S-transferase gene are risk factor for CAD independent of smoking.
BMC medical genetics 2006;7():38.
2006: Khaled K Abu-Amero; Olayan M Al-Boudari; Gamal H Mohamed; Nduna Dzimiri
The Glu27 genotypes of the beta2-adrenergic receptor are predictors for severe coronary artery disease.
BMC medical genetics 2006;7():31.
2006: Khaled K Abu-Amero; Thomas Bosley
Prothrombotic and atherosclerotic risk factors lack significance in NAION patients harbouring mitochondrial DNA mutations.
The British journal of ophthalmology 2006;90(1):119-20.
2005: Khaled K Abu-Amero; Olayan M Al-Boudari; Gamal H Mohamed; Nduna Dzimiri
Beta 3 adrenergic receptor Trp64Arg polymorphism and manifestation of coronary artery disease in Arabs.
Human biology 2005;77(6):795-802.
2005: Khaled K Abu-Amero; Thomas Bosley
Detection of mitochondrial respiratory dysfunction in circulating lymphocytes using resazurin.
Archives of pathology & laboratory medicine 2005;129(10):1295-8.
2005: Khaled K Abu-Amero; Thomas Bosley; Saeed Bohlega; D McLean
Complex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation.
The British journal of ophthalmology 2005;89(10):1380-1.
2005: Khaled K Abu-Amero; Roger J Miles; Mahmoud Halablab
Cholesterol protects Acholeplasma laidlawii against oxidative damage caused by hydrogen peroxide.
Veterinary research communications 2005;29(5):373-80.
2005: Thomas Bosley; Mustafa A Salih; J C Jen; D D M Lin; Darren T Oystreck; Khaled K Abu-Amero; David B MacDonald; Zayed Al Zayed; Hesham Al-Dhalaan; Tulay Kansu; Bent Stigsby; R W Baloh
Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3.
Neurology 2005;64(7):1196-203.
2005: Khaled K Abu-Amero; Thomas Bosley; Saeed Bohlega; Erik Hansen
Mitochondrial T9957C mutation in association with NAION and seizures but not MELAS.
Ophthalmic genetics 2005;26(1):31-6.
2005: Khaled K Abu-Amero; Ali S Alzahrani; Minjing Zou; Yufei Shi
High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines.
Oncogene 2005;24(8):1455-60.
2004: Khaled K Abu-Amero; M Zou; Y Shi
Mitochondrial A135149 mutation without MELAS but in association with papillary thyroid carcinoma.
Clinical genetics 2004;66(6):569-70.
2004: Thomas Bosley; Khaled K Abu-Amero; Pinar T Ozand
Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy.
Neurology 2004;63(7):1305-8.
2004: Khaled K Abu-Amero; Tarek M Owaidah; Abduallah Al Jefri; Abdulaziz Al-Ghonaium; Ibrahim M Fawaz; Mohammed H Al-Hamed
A novel splice site mutation in the WAS gene causes Wiskott-Aldrich syndrome in two siblings of a Saudi family.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(7):599-603.
2004: Khaled K Abu-Amero; Mahmoud Halablab
Evaluation of the COBAS AMPLICOR MTB test for the detection of Mycobacterium tuberculosis complex.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-ṣiḥḥīyah li-sharq al-mutawassiṭ 2004;10(3):329-35.
2004: Khaled K Abu-Amero; Carol A Wyngaard; Nduna Dzimiri
Association of the platelet glycoprotein receptor IIIa (PlA1/PlA1) genotype with coronary artery disease in Arabs.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004;15(1):77-9.
2003: Ali N Al Odaib; Khaled K Abu-Amero; Pinar T Ozand; Ali M Al-Hellani
A new era for preventive genetic programs in the Arabian Peninsula.
Saudi medical journal 2003;24(11):1168-75.
2003: Khaled K Abu-Amero; Carol A Wyngaard; Nduna Dzimiri
Prevalence and role of methylenetetrahydrofolate reductase 677 C-->T and 1298 A-->C polymorphisms in coronary artery disease in Arabs.
Archives of pathology & laboratory medicine 2003;127(10):1349-52.
2003: Khaled K Abu-Amero
Human genetics information on the Web.
The journal of the Royal Society for the Promotion of Health 2003;123(2):102-4.
2003: Khaled K Abu-Amero; Carol A Wyngaard; Olayan M Al-Boudari; Marios Kambouris; Nduna Dzimiri
Lack of association of lipoprotein lipase gene polymorphisms with coronary artery disease in the Saudi Arab population.
Archives of pathology & laboratory medicine 2003;127(5):597-600.
2003: Khaled K Abu-Amero; Mohammed H Al-Hamed; Fatma S Al-Batniji
Homozygous protein C deficiency with purpura fulminans: report of a new case and a description of a novel mutation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2003;14(3):303-6.
2002: Khaled K Abu-Amero; Carol A Wyngaard; Marios Kambouris; Nduna Dzimiri
Prevalence of the 20210 G-->A prothrombin variant and its association with coronary artery disease in a Middle Eastern Arab population.
Archives of pathology & laboratory medicine 2002;126(9):1087-90.
2002: Khaled K Abu-Amero
Status of antituberculosis drug resistance in Saudi Arabia 1979-98.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-ṣiḥḥīyah li-sharq al-mutawassiṭ 2002;8(4-5):664-70.
2002: Khaled K Abu-Amero
Overview of the laboratory accreditation programme of the College of American Pathologists.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-ṣiḥḥīyah li-sharq al-mutawassiṭ 2002;8(4-5):654-63.
2002: Khaled K Abu-Amero
Tuberculosis information on the Web.
The journal of the Royal Society for the Promotion of Health 2002;122(2):82-5.
2002: Khaled K Abu-Amero
Review of the current status of drug-resistant tuberculosis in Saudi Arabia.
Annals of Saudi medicine 2002;22(3-4):236-8.
2002: Khaled K Abu-Amero; Mahmoud Halablab; Roger J Miles
Alternative to fluorescence assays to monitor fusion between Acholeplasma laidlawii cells and liposomes.
Letters in applied microbiology 2002;35(6):528-32.
2000: Khaled K Abu-Amero; E A Abu-Groun; Mahmoud Halablab; Roger J Miles
Kinetics and distribution of alcohol oxidising activity in Acholeplasma and Mycoplasma species.
FEMS microbiology letters 2000;183(1):147-51.