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Review and qualitative analysis of submodule-level distributed power electronic solutions in PV power systems

Renewable & sustainable energy reviews, 2017-09, Vol.76, p.516-528

2017

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Revised Recommendations of the Consortium of MS Centers Task Force for a Standardized MRI Protocol and Clinical Guidelines for the Diagnosis and Follow-Up of Multiple Sclerosis

American journal of neuroradiology : AJNR, 2016-03, Vol.37 (3), p.394-401

2016

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Narrowing the Expertise Gap for Predicting Intracranial Aneurysm Hemodynamics: Impact of Solver Numerics versus Mesh and Time-Step Resolution

American journal of neuroradiology : AJNR, 2015-07, Vol.36 (7), p.1310-1316

2015

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Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

PloS one, 2015-09, Vol.10 (9), p.e0137973-e0137973

2015

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Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

PloS one, 2016-11, Vol.11 (11), p.e0162620-e0162620

2016

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Hierarchical and non-hierarchical mineralisation of collagen

Biomaterials, 2011-02, Vol.32 (5), p.1291-1300

2011

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Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome

American journal of human genetics, 2014-05, Vol.94 (5), p.755-759

2014

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Severity of SARS-CoV-2 infection is associated with high numbers of alveolar mast cells and their degranulation

Frontiers in immunology, 2022-09, Vol.13, p.968981-968981

2022

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FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Nature communications, 2016-04, Vol.7 (1), p.10953-10953, Article 10953

2016

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Cardiac Manifestations of Post-Acute COVID-19 Infection

Current cardiology reports, 2022-12, Vol.24 (12), p.1775-1783

2022

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Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish

American journal of human genetics, 2017-07, Vol.101 (1), p.23-36

2017

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Foliar application of triacontanol ameliorates heat stress through regulation of the antioxidant defense system and improves yield of eggplant

Brazilian journal of biology, 2024, Vol.84, p.e253696-10

2024

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Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

PloS one, 2016-12, Vol.11 (12), p.e0167562

2016

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Diagnosis, monitoring, and management of adverse events from immune checkpoint inhibitor therapy

Current oncology (Toronto), 2020-04, Vol.27 (Suppl 2), p.S43-50

2020

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Recognizing the KCNV2 -Related Retinal Phenotype

Ophthalmology (Rochester, Minn.), 2013-11, Vol.120 (11), p.e79-e80

Khan, Arif O., MD

2013

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Non‐Newtonian versus numerical rheology: Practical impact of shear‐thinning on the prediction of stable and unstable flows in intracranial aneurysms

International journal for numerical methods in biomedical engineering, 2017-07, Vol.33 (7), p.n/a

2017

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A phase I study of the safety and tolerability of olaparib (AZD2281, KU0059436) and dacarbazine in patients with advanced solid tumours

British journal of cancer, 2011-03, Vol.104 (5), p.750-755

2011

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Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

PloS one, 2017-03, Vol.12 (3), p.e0173719-e0173719

2017

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New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations

PloS one, 2013-10, Vol.8 (10), p.e76831-e76831

2013

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Refractory right ventricular myocarditis induced by immune checkpoint inhibitor despite therapy cessation and immune suppression

Cardio-oncology (London, England), 2023-03, Vol.9 (1), p.15-15, Article 15

2023

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Protein prenylation restrains innate immunity by inhibiting Rac1 effector interactions

Nature communications, 2019-09, Vol.10 (1), p.3975-13, Article 3975

2019

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Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

PloS one, 2017-01, Vol.12 (1), p.e0171403-e0171403

2017

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Mutations in LRPAP1 Are Associated with Severe Myopia in Humans

American journal of human genetics, 2013-08, Vol.93 (2), p.313-320

2013

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CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution

Scientific reports, 2017-08, Vol.7 (1), p.8450-9, Article 8450

2017

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A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian Peninsula

Scientific reports, 2017-05, Vol.7 (1), p.1411-10, Article 1411

2017

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Review and qualitative analysis of submodule-level distributed power electronic solutions in PV power systems

Revised Recommendations of the Consortium of MS Centers Task Force for a Standardized MRI Protocol and Clinical Guidelines for the Diagnosis and Follow-Up of Multiple Sclerosis

Narrowing the Expertise Gap for Predicting Intracranial Aneurysm Hemodynamics: Impact of Solver Numerics versus Mesh and Time-Step Resolution

Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

Hierarchical and non-hierarchical mineralisation of collagen

Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome

Severity of SARS-CoV-2 infection is associated with high numbers of alveolar mast cells and their degranulation

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Cardiac Manifestations of Post-Acute COVID-19 Infection

Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish

Foliar application of triacontanol ameliorates heat stress through regulation of the antioxidant defense system and improves yield of eggplant

Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

Diagnosis, monitoring, and management of adverse events from immune checkpoint inhibitor therapy

Recognizing the KCNV2 -Related Retinal Phenotype

Non‐Newtonian versus numerical rheology: Practical impact of shear‐thinning on the prediction of stable and unstable flows in intracranial aneurysms

A phase I study of the safety and tolerability of olaparib (AZD2281, KU0059436) and dacarbazine in patients with advanced solid tumours

Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations

Refractory right ventricular myocarditis induced by immune checkpoint inhibitor despite therapy cessation and immune suppression

Protein prenylation restrains innate immunity by inhibiting Rac1 effector interactions

Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

Mutations in LRPAP1 Are Associated with Severe Myopia in Humans

CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution

A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian Peninsula

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