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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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Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes

Genome research, 2013-02, Vol.23 (2), p.236-247

2013

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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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Typical Forms of Plans for Certain Investigative (Search) Actions

Вісник Харківського національного університету внутрішніх справ, 2020-06, Vol.89 (2), p.271-283

Khan, O. O.

2020

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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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Perspectives for Using the Programmatic Approach within the Activities of Law Enforcement Agencies of Ukraine

Вісник Харківського національного університету внутрішніх справ, 2019-12, Vol.87 (4), p.170-178

Khan, O. O.

2019

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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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Low-dose Btk inhibitors selectively block platelet activation by CLEC-2

Haematologica (Roma), 2021-01, Vol.106 (1), p.208-219

2021

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Methodology fundamentals for investigating violations of the laws and customs of war

Вісник Харківського національного університету внутрішніх справ, 2023-07, Vol.101 (2 (P. 1)), p.301-309

2023

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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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Super-resolution imaging and quantification of megakaryocytes and platelets

Platelets (Edinburgh), 2020-07, Vol.31 (5), p.559-569

2020

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Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function

Haematologica (Roma), 2022-01, Vol.107 (1), p.243-259

2022

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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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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

Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes

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

Typical Forms of Plans for Certain Investigative (Search) Actions

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

Perspectives for Using the Programmatic Approach within the Activities of Law Enforcement Agencies of Ukraine

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

Low-dose Btk inhibitors selectively block platelet activation by CLEC-2

Methodology fundamentals for investigating violations of the laws and customs of war

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

Super-resolution imaging and quantification of megakaryocytes and platelets

Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function

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

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