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Mitochondrial Abnormalities in Patients with Primary Open-Angle Glaucoma
Mitochondrial Abnormalities in Patients with Primary Open-Angle Glaucoma
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Mitochondrial Abnormalities in Patients with Primary Open-Angle Glaucoma

Abu-Amero, Khaled K ; Morales, Jose ; Bosley, Thomas M

Investigative ophthalmology & visual science, 2006-06, Vol.47 (6), p.2533-2541 [Periódico revisado por pares]

Rockville, MD: ARVO

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E-selectin S128R polymorphism and severe coronary artery disease in Arabs
E-selectin S128R polymorphism and severe coronary artery disease in Arabs
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E-selectin S128R polymorphism and severe coronary artery disease in Arabs

Abu-Amero, Khaled K ; Al-Boudari, Olayan M ; Mohamed, Gamal H ; Dzimiri, Nduna

BMC medical genetics, 2006-06, Vol.7 (1), p.52-52, Article 52 [Periódico revisado por pares]

England: BioMed Central Ltd

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3
High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines
High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines
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High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines

ABU-AMERO, Khaled K ; ALZAHRANI, Ali S ; MINJING ZOU ; YUFEI SHI

Oncogene, 2005-02, Vol.24 (8), p.1455-1460 [Periódico revisado por pares]

Basingstoke: Nature Publishing

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4
Mitochondrial Abnormalities in Patients with LHON-like Optic Neuropathies
Mitochondrial Abnormalities in Patients with LHON-like Optic Neuropathies
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Mitochondrial Abnormalities in Patients with LHON-like Optic Neuropathies

Abu-Amero, Khaled K ; Bosley, Thomas M

Investigative ophthalmology & visual science, 2006-10, Vol.47 (10), p.4211-4220 [Periódico revisado por pares]

Rockville, MD: ARVO

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5
The Glu27 genotypes of the beta2-adrenergic receptor are predictors for severe coronary artery disease
The Glu27 genotypes of the beta2-adrenergic receptor are predictors for severe coronary artery disease
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The Glu27 genotypes of the beta2-adrenergic receptor are predictors for severe coronary artery disease

Abu-Amero, Khaled K ; Al-Boudari, Olayan M ; Mohamed, Gamal H ; Dzimiri, Nduna

BMC medical genetics, 2006-03, Vol.7 (1), p.31-31, Article 31 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Detection of mitochondrial respiratory dysfunction in circulating lymphocytes using resazurin
Detection of mitochondrial respiratory dysfunction in circulating lymphocytes using resazurin
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Detection of mitochondrial respiratory dysfunction in circulating lymphocytes using resazurin

Abu-Amero, Khaled K ; Bosley, Thomas M

Archives of pathology & laboratory medicine (1976), 2005-10, Vol.129 (10), p.1295-1298 [Periódico revisado por pares]

United States: College of American Pathologists

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7
T null and M null genotypes of the glutathione S-transferase gene are risk factor for CAD independent of smoking
T null and M null genotypes of the glutathione S-transferase gene are risk factor for CAD independent of smoking
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T null and M null genotypes of the glutathione S-transferase gene are risk factor for CAD independent of smoking

Abu-Amero, Khaled K ; Al-Boudari, Olayan M ; Mohamed, Gamal H ; Dzimiri, Nduna

BMC medical genetics, 2006-04, Vol.7 (1), p.38-38 [Periódico revisado por pares]

England: BioMed Central Ltd

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8
Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy
Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy
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Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy

BOSLEY, Thomas M ; ABU-AMERO, Khaled K ; OZAND, Pinar T

Neurology, 2004-10, Vol.63 (7), p.1305-1308 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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9
Novel Mitochondrial DNA Transversion Mutation in Transfer Ribonucleic Acid for Leucine 2 (CUN) in a Patient With the Clinical Features of MELAS
Novel Mitochondrial DNA Transversion Mutation in Transfer Ribonucleic Acid for Leucine 2 (CUN) in a Patient With the Clinical Features of MELAS
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Novel Mitochondrial DNA Transversion Mutation in Transfer Ribonucleic Acid for Leucine 2 (CUN) in a Patient With the Clinical Features of MELAS

Abu-Amero, Khaled K. ; Ozand, Pinar T. ; Al-Dhalaan, Hesham

Journal of child neurology, 2006-11, Vol.21 (11), p.971-972 [Periódico revisado por pares]

Los Angeles, CA: Sage Publications

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10
Prevalence and role of methylenetetrahydrofolate reductase 677 C-->T and 1298 A-->C polymorphisms in coronary artery disease in Arabs
Prevalence and role of methylenetetrahydrofolate reductase 677 C-->T and 1298 A-->C polymorphisms in coronary artery disease in Arabs
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Prevalence and role of methylenetetrahydrofolate reductase 677 C-->T and 1298 A-->C polymorphisms in coronary artery disease in Arabs

Abu-Amero, Khaled K ; Wyngaard, Carol A ; Dzimiri, Nduna

Archives of pathology & laboratory medicine (1976), 2003-10, Vol.127 (10), p.1349-1352 [Periódico revisado por pares]

United States: College of American Pathologists

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