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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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Rumpel Leede Sign

Mayo Clinic proceedings, 2022-07, Vol.97 (7), p.1230-1231

2022

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In Reply—Rumpel-Leede Sign: Consider Underlying Vitamin C Deficiency

Mayo Clinic proceedings, 2022-11, Vol.97 (11), p.2164-2165

2022

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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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Evaluation of the magnitude and location of Cam deformity using three dimensional CT analysis

The bone & joint journal, 2014-09, Vol.96-B (9), p.1167-1171

2014

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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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ADAMTS18 -related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome

Taiwan journal of ophthalmology, 2023-10, Vol.13 (4), p.540-542

Khan, Arif O

2023

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Topological data analysis quantifies biological nano-structure from single molecule localization microscopy

Bioinformatics, 2020-03, Vol.36 (5), p.1614-1621

2020

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Mechanisms of action of disease-modifying agents and brain volume changes in multiple sclerosis

Neurology, 2008-07, Vol.71 (2), p.136

2008

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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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Fundus autofluorescence imaging in hereditary retinal diseases

Acta ophthalmologica (Oxford, England), 2018-08, Vol.96 (5), p.e549-e561

2018

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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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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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Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

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

2016

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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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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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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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Minimally invasive periacetabular osteotomy using a modified Smith-Petersen approach: technique and early outcomes

The bone & joint journal, 2017-01, Vol.99-B (1), p.22-28

2017

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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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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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Cardiac Manifestations of Post-Acute COVID-19 Infection

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

2022

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

Rumpel Leede Sign

In Reply—Rumpel-Leede Sign: Consider Underlying Vitamin C Deficiency

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

Evaluation of the magnitude and location of Cam deformity using three dimensional CT analysis

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

ADAMTS18 -related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome

Topological data analysis quantifies biological nano-structure from single molecule localization microscopy

Mechanisms of action of disease-modifying agents and brain volume changes in multiple sclerosis

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

Fundus autofluorescence imaging in hereditary retinal diseases

Super-resolution imaging and quantification of megakaryocytes and platelets

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

Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

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

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

Recognizing the KCNV2 -Related Retinal Phenotype

Minimally invasive periacetabular osteotomy using a modified Smith-Petersen approach: technique and early outcomes

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

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

Cardiac Manifestations of Post-Acute COVID-19 Infection

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