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An 18 megapixel 4.3″ 1443 ppi 120 Hz OLED display for wide field of view high acuity head mounted displays

Journal of the Society for Information Display, 2018-05, Vol.26 (5), p.314-324

2018

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510 PROGRESSION OF CHRONIC HEPATITIS B TO CIRRHOSIS AND HEPATOCELLULAR CARCINOMA BY AGE, SEX, DISEASE ACTIVITY, AND TREATMENT STATUS USING AASLD CRITERIA

Gastroenterology (New York, N.Y. 1943), 2021-05, Vol.160 (6), p.S-786-S-786

2021

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Abstract 1279: Development of a selective CDK2-E inhibitor in CCNE driven cancers

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.1279-1279

2021

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Abstract 2594: AI-powered radiomics model predicts immune checkpoint inhibitor-related pneumonitis (CIP) in advanced NSCLC patients

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.2594-2594

2024

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Abstract 2595: Accelerated and precise tumor segmentation in NSCLC: A comparative analysis of automated ClickSeg and manual annotation for radiomics

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.2595-2595

2024

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Abstract 7529: Harmonization radiomics model to predict immune checkpoint inhibitor-related pneumonitis (CIP) in non small cell lung cancer (NSCLC) in patients treated with immunotherapy

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.7529-7529

2024

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Abstract 7530: Harmonization radiomics models to predict tumor response in non-small cell lung cancer (NSCLC) patients treated with immunotherapy

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.7530-7530

2024

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Abstract 912: CheckpointPx, an interpretable radiology AI tool, predicts checkpoint blockade benefit independent of PDL1 status in non-small cell lung cancers (NSCLC): A multi-institutional validation study

Cancer research (Chicago, Ill.), 2024-03, Vol.84 (6_Supplement), p.912-912

2024

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Acute fetal ductal occlusion in lambs

American journal of obstetrics and gynecology, 1991-09, Vol.165 (3), p.775-778

1991

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Adenylyl Cyclase Type 5 Inhibition During Reperfusion Ameliorates Heart Failure Development

The FASEB journal, 2013-04, Vol.27 (S1)

2013

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Antenatal and Early Postnatal Antecedents of Parent-Reported Attention Problems at 2 Years of Age

The Journal of pediatrics, 2015, Vol.166 (1), p.20-25.e1

2015

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Bi-allelic mutations of LONP1 encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophy

Human molecular genetics, 2019-01, Vol.28 (2), p.290-306

2019

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Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability

American journal of human genetics, 2016-01, Vol.98 (1), p.202-209

2016

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Body Mass Index and Height in the Friedreich Ataxia Clinical Outcome Measures Study

Neurology. Genetics, 2021-12, Vol.7 (6), p.e638-e638

2021

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Channelopathies are a frequent cause of genetic ataxias associated with cerebellar atrophy (1719)

Neurology, 2020-04, Vol.94 (15_supplement)

2020

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Child Neurology: Progressive Cerebellar Atrophy and Retinal Dystrophy: Clues to an Ultrarare ACO2 -Related Neurometabolic Diagnosis

Neurology, 2023-10, Vol.101 (15)

2023

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Choice of Dose Level for a Randomized Clinical Trial of Low-Dose Bevacizumab vs Laser for Type 1 Retinopathy of Prematurity

JAMA ophthalmology, 2021-10, Vol.139 (10), p.1143

2021

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Clinical and genetic study of hereditary spastic paraplegia in Canada

Neurology. Genetics, 2017-02, Vol.3 (1), p.e122-e122

2017

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Complete deletion of the aprataxin gene: ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficit

Journal of neurology, neurosurgery and psychiatry, 2008-02, Vol.79 (2), p.234-236

2008

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Critically ill children during the 2009-2010 influenza pandemic in the United States

Pediatrics (Evanston), 2011-12, Vol.128 (6), p.e1450-e1458

2011

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Daratumumab Monotherapy for Patients with Relapsed or Refractory (R/R) Natural Killer/T-Cell Lymphoma (NKTCL), Nasal Type: Updated Results from an Open-Label, Single-Arm, Multicenter Phase 2 Study

Blood, 2019-11, Vol.134 (Supplement_1), p.1568-1568

2019

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Diagnosis, transport, and outcome in fetuses with left ventricular outflow tract obstruction

The Journal of thoracic and cardiovascular surgery, 1991-12, Vol.102 (6), p.841-848

1991

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Dizygotic twin pregnancy conceived with assisted reproductive technology associated with chromosomal anomaly, imprinting disorder, and monochorionic placentation

The Journal of pediatrics, 2005-04, Vol.146 (4), p.565-567

2005

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Early life antecedents of positive child health among 10-year-old children born extremely preterm

Pediatric research, 2019-12, Vol.86 (6), p.758-765

2019

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An 18 megapixel 4.3″ 1443 ppi 120 Hz OLED display for wide field of view high acuity head mounted displays

510 PROGRESSION OF CHRONIC HEPATITIS B TO CIRRHOSIS AND HEPATOCELLULAR CARCINOMA BY AGE, SEX, DISEASE ACTIVITY, AND TREATMENT STATUS USING AASLD CRITERIA

Abstract 1279: Development of a selective CDK2-E inhibitor in CCNE driven cancers

Abstract 2594: AI-powered radiomics model predicts immune checkpoint inhibitor-related pneumonitis (CIP) in advanced NSCLC patients

Abstract 2595: Accelerated and precise tumor segmentation in NSCLC: A comparative analysis of automated ClickSeg and manual annotation for radiomics

Abstract 7529: Harmonization radiomics model to predict immune checkpoint inhibitor-related pneumonitis (CIP) in non small cell lung cancer (NSCLC) in patients treated with immunotherapy

Abstract 7530: Harmonization radiomics models to predict tumor response in non-small cell lung cancer (NSCLC) patients treated with immunotherapy

Abstract 912: CheckpointPx, an interpretable radiology AI tool, predicts checkpoint blockade benefit independent of PDL1 status in non-small cell lung cancers (NSCLC): A multi-institutional validation study

Acute fetal ductal occlusion in lambs

Adenylyl Cyclase Type 5 Inhibition During Reperfusion Ameliorates Heart Failure Development

Antenatal and Early Postnatal Antecedents of Parent-Reported Attention Problems at 2 Years of Age

Bi-allelic mutations of LONP1 encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophy

Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability

Body Mass Index and Height in the Friedreich Ataxia Clinical Outcome Measures Study

Channelopathies are a frequent cause of genetic ataxias associated with cerebellar atrophy (1719)

Child Neurology: Progressive Cerebellar Atrophy and Retinal Dystrophy: Clues to an Ultrarare ACO2 -Related Neurometabolic Diagnosis

Choice of Dose Level for a Randomized Clinical Trial of Low-Dose Bevacizumab vs Laser for Type 1 Retinopathy of Prematurity

Clinical and genetic study of hereditary spastic paraplegia in Canada

Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants

Complete deletion of the aprataxin gene: ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficit

Critically ill children during the 2009-2010 influenza pandemic in the United States

Daratumumab Monotherapy for Patients with Relapsed or Refractory (R/R) Natural Killer/T-Cell Lymphoma (NKTCL), Nasal Type: Updated Results from an Open-Label, Single-Arm, Multicenter Phase 2 Study

Diagnosis, transport, and outcome in fetuses with left ventricular outflow tract obstruction

Dizygotic twin pregnancy conceived with assisted reproductive technology associated with chromosomal anomaly, imprinting disorder, and monochorionic placentation

Early life antecedents of positive child health among 10-year-old children born extremely preterm

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