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Dislocation interactions at the grain boundary in FCC bicrystals: An atomistically-informed dislocation dynamics study

Acta materialia, 2022-01, Vol.223, p.117455, Article 117455

2022

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First report of the spectrum of δ-globin gene mutations in Omani subjects - identification of novel mutations

International journal of laboratory hematology, 2015-04, Vol.37 (2), p.238-243

2015

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Latent hardening/softening behavior in tension and torsion combined loadings of single crystal FCC micropillars

Acta materialia, 2020-05, Vol.190, p.58-69

2020

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Increased Vasoocclusive Crises in "O" Blood Group Sickle Cell Disease Patients: Association with Underlying Thrombospondin Levels

Mediterranean journal of hematology and infectious diseases, 2017, Vol.9 (1), p.e2017028-e2017028

2017

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Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS

International journal of laboratory hematology, 2014-08, Vol.36 (4), p.488-492

2014

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Effect of size and orientation on stability of dislocation networks upon torsion loading and unloading in FCC metallic micropillars

Acta materialia, 2021-08, Vol.214, p.117010, Article 117010

2021

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Sickle cell-haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study

International journal of laboratory hematology, 2007-08, Vol.29 (4), p.292-301

2007

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Intrinsic size dependent plasticity in BCC micro-pillars under uniaxial tension and pure torsion

Extreme Mechanics Letters, 2020-10, Vol.40 (C), p.100901, Article 100901

2020

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“My thinking has changed but beliefs have not”: Motivated reasoning in learning to teach abortion

Theory and research in social education, 2024-05, p.1-26

2024

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Prediction of dislocation - grain boundary interactions in FCC aluminum bicrystals using a modified continuum criterion and machine learning methods

Materialia, 2023-09, Vol.31, p.101874, Article 101874

2023

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First report of the spectrum of δ‐globin gene mutations in O mani subjects – identification of novel mutations

International journal of laboratory hematology, 2015-04, Vol.37 (2), p.238-243

2015

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Reduced protein C levels--a contributory factor for stroke in sickle cell disease

Thrombosis and haemostasis, 1998-04, Vol.79 (4), p.879-880

1998

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Multiscale Modeling of Dislocation and Grain Boundary Mechanics in Small Scale Metals

Gravell, Jamie D

2021

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Potential pitfalls in the diagnosis of H b Handsworth in areas with high prevalence of H b S

International journal of laboratory hematology, 2014-08, Vol.36 (4), p.488-492

2014

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Accidental detection of lupus anticoagulants in children

Annals of tropical paediatrics, 2001-09, Vol.21 (3), p.277-279

2001

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Intrinsic size dependent plasticity in BCC micro-pillars under uniaxial tension and pure torsion

Extreme Mechanics Letters, 2020-08, Vol.40 (C)

2020

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Folate deficiency and neurologic complications in elderly Omani patients

Saudi medical journal, 2000-10, Vol.21 (10), p.985

2000

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HbS-Oman heterozygote : A new dominant sickle syndrome

Blood, 1998-12, Vol.92 (11), p.4375-4382

1998

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HbS-Oman Heterozygote: A New Dominant Sickle Syndrome

Blood, 1998-12, Vol.92 (11), p.4375-4382

1998

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Long-term effects of nitrous oxide anaesthesia on laboratory and clinical parameters in elderly Omani patients: a randomized double-blind study

Journal of clinical pharmacy and therapeutics, 2000-08, Vol.25 (4), p.271-277

2000

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Genetic epidemiology of HbS in Oman: multicentric origin for the betaS gene

American journal of hematology, 2000-05, Vol.64 (1), p.39-46

2000

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Genetic epidemiology of HbS in Oman: Multicentric origin for the βS gene

American journal of hematology, 2000-05, Vol.64 (1), p.39-46

2000

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689 Reduced protein C levels-a contributory factor for stroke on sickle cell disease

Journal of pediatric hematology/oncology, 1998-07, Vol.20 (4), p.407

1998

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Folate deficiencyy and neurologic complications in elderly Omani patients

Neurosciences (Riyadh, Saudi Arabia), 2000-10, Vol.5 (4), p.256-257

2000

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Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS

International Journal of Laboratory Hematology, 2014, Vol.36 (4), p.488-492

2014

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Dislocation interactions at the grain boundary in FCC bicrystals: An atomistically-informed dislocation dynamics study

First report of the spectrum of δ-globin gene mutations in Omani subjects - identification of novel mutations

Latent hardening/softening behavior in tension and torsion combined loadings of single crystal FCC micropillars

Increased Vasoocclusive Crises in "O" Blood Group Sickle Cell Disease Patients: Association with Underlying Thrombospondin Levels

Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS

Effect of size and orientation on stability of dislocation networks upon torsion loading and unloading in FCC metallic micropillars

Sickle cell-haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study

Intrinsic size dependent plasticity in BCC micro-pillars under uniaxial tension and pure torsion

“My thinking has changed but beliefs have not”: Motivated reasoning in learning to teach abortion

Prediction of dislocation - grain boundary interactions in FCC aluminum bicrystals using a modified continuum criterion and machine learning methods

First report of the spectrum of δ‐globin gene mutations in O mani subjects – identification of novel mutations

Reduced protein C levels--a contributory factor for stroke in sickle cell disease

Multiscale Modeling of Dislocation and Grain Boundary Mechanics in Small Scale Metals

Potential pitfalls in the diagnosis of H b Handsworth in areas with high prevalence of H b S

Accidental detection of lupus anticoagulants in children

Intrinsic size dependent plasticity in BCC micro-pillars under uniaxial tension and pure torsion

Folate deficiency and neurologic complications in elderly Omani patients

HbS-Oman heterozygote : A new dominant sickle syndrome

HbS-Oman Heterozygote: A New Dominant Sickle Syndrome

Long-term effects of nitrous oxide anaesthesia on laboratory and clinical parameters in elderly Omani patients: a randomized double-blind study

Genetic epidemiology of HbS in Oman: multicentric origin for the betaS gene

Genetic epidemiology of HbS in Oman: Multicentric origin for the βS gene

689 Reduced protein C levels-a contributory factor for stroke on sickle cell disease

Folate deficiencyy and neurologic complications in elderly Omani patients

Potential pitfalls in the diagnosis of Hb Handsworth in areas with high prevalence of HbS

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