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Terlipressin plus Albumin for the Treatment of Type 1 Hepatorenal Syndrome

The New England journal of medicine, 2021-03, Vol.384 (9), p.818-828

2021

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Functional Movement Screening: Predicting Injuries in Officer Candidates

Medicine and science in sports and exercise, 2011-12, Vol.43 (12), p.2224-2230

2011

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Chromosome 10q26-driven age-related macular degeneration is associated with reduced levels of HTRA1 in human retinal pigment epithelium

Proceedings of the National Academy of Sciences - PNAS, 2021-07, Vol.118 (30)

2021

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Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci

Human genomics, 2021-09, Vol.15 (1), p.60-15, Article 60

2021

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Levels of the HtrA1 Protein in Serum and Vitreous Humor Are Independent of Genetic Risk for Age-Related Macular Degeneration at the 10q26 Locus

Investigative ophthalmology & visual science, 2024-04, Vol.65 (4), p.34-34

2024

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Real electronic signal data from particle accelerator power systems for machine learning anomaly detection

Data in brief, 2022-08, Vol.43 (C), p.108473-108473, Article 108473

2022

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Editorial: terlipressin in patients with ACLF grade 3—too late? Authorsʼ reply

Alimentary pharmacology & therapeutics, 2023-01, Vol.57 (1), p.179-180

2023

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A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome

PLoS genetics, 2009-09, Vol.5 (9), p.e1000649

2009

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Operational data for fault prognosis in particle accelerators with machine learning

Data in brief, 2023-12, Vol.51 (C), p.109658-109658, Article 109658

2023

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Early Fault Detection in Particle Accelerator Power Electronics Using Ensemble Learning

International journal of prognostics and health management, 2023-01, Vol.14 (1)

2023

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Pesticide data program: 30 years of food residue data and trends

Journal of exposure science & environmental epidemiology, 2023-09, Vol.33 (5), p.805-812

2023

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Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization

The Journal of physiology, 2008-07, Vol.586 (14), p.3405-3423

2008

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Multi-module-based CVAE to predict HVCM faults in the SNS accelerator

Machine learning with applications, 2023-09, Vol.13 (5), p.100484, Article 100484

2023

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Verified Hepatorenal Syndrome Reversal As A Robust Multi-Component Primary End Point: The CONFIRM Study Trial Design

Open access journal of clinical trials, 2019-01, Vol.11, p.67-73

2019

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Terlipressin Treatment Is Associated With Reversal of Hepatorenal Syndrome in Patients With Alcoholic Hepatitis

Clinical gastroenterology and hepatology, 2023-12, Vol.21 (13), p.3455-3457.e3

2023

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Characterization of West African Crystalline Macular Dystrophy in the Ghanaian Population

Ophthalmology retina, 2022-08, Vol.6 (8), p.723-731

2022

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Decreased need for RRT in liver transplant recipients after pretransplant treatment of hepatorenal syndrome-type 1 with terlipressin

Liver transplantation, 2024-04, Vol.30 (4), p.347-355

2024

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Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions

Epilepsia (Copenhagen), 2009-07, Vol.50 (7), p.1752-1759

2009

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Gender affects the association between serum creatinine levels and clinical response to terlipressin in patients with hepatorenal syndrome type of acute kidney injury

Journal of hepatology, 2022-07, Vol.77, p.S611

2022

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Diverse Macular Dystrophy Phenotype Caused by a Novel Complex Mutation in the ELOVL4 Gene

Investigative ophthalmology & visual science, 2001-12, Vol.42 (13), p.3331-3336

2001

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SAT-348 - Earlier diagnosis of hepatorenal syndrome-acute kidney injury with updated guidelines-review of the Confirm trial

Journal of hepatology, 2023-06, Vol.78, p.S296-S296

2023

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Earlier diagnosis of hepatorenal syndrome-acute kidney injury with updated guidelines-review of the Confirm trial

Journal of hepatology, 2023-06, Vol.78, p.S296

2023

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A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

Annals of neurology, 1999-10, Vol.46 (4), p.671-678

1999

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Cobb Syndrome: A Case Report and Systematic Review of the Literature

Pediatric neurology, 2008-12, Vol.39 (6), p.423-425

2008

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Hepatopulmonary Syndrome With Progressive Hypoxemia as an Indication for Liver Transplantation: Case Reports and Literature Review

Mayo Clinic proceedings, 1997-01, Vol.72 (1), p.44-53

1997

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Terlipressin plus Albumin for the Treatment of Type 1 Hepatorenal Syndrome

Functional Movement Screening: Predicting Injuries in Officer Candidates

Chromosome 10q26-driven age-related macular degeneration is associated with reduced levels of HTRA1 in human retinal pigment epithelium

Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci

Levels of the HtrA1 Protein in Serum and Vitreous Humor Are Independent of Genetic Risk for Age-Related Macular Degeneration at the 10q26 Locus

Real electronic signal data from particle accelerator power systems for machine learning anomaly detection

Editorial: terlipressin in patients with ACLF grade 3—too late? Authorsʼ reply

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome

Operational data for fault prognosis in particle accelerators with machine learning

Early Fault Detection in Particle Accelerator Power Electronics Using Ensemble Learning

Pesticide data program: 30 years of food residue data and trends

Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization

Multi-module-based CVAE to predict HVCM faults in the SNS accelerator

Verified Hepatorenal Syndrome Reversal As A Robust Multi-Component Primary End Point: The CONFIRM Study Trial Design

Terlipressin Treatment Is Associated With Reversal of Hepatorenal Syndrome in Patients With Alcoholic Hepatitis

Characterization of West African Crystalline Macular Dystrophy in the Ghanaian Population

Decreased need for RRT in liver transplant recipients after pretransplant treatment of hepatorenal syndrome-type 1 with terlipressin

Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions

Gender affects the association between serum creatinine levels and clinical response to terlipressin in patients with hepatorenal syndrome type of acute kidney injury

Diverse Macular Dystrophy Phenotype Caused by a Novel Complex Mutation in the ELOVL4 Gene

SAT-348 - Earlier diagnosis of hepatorenal syndrome-acute kidney injury with updated guidelines-review of the Confirm trial

Earlier diagnosis of hepatorenal syndrome-acute kidney injury with updated guidelines-review of the Confirm trial

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

Cobb Syndrome: A Case Report and Systematic Review of the Literature

Hepatopulmonary Syndrome With Progressive Hypoxemia as an Indication for Liver Transplantation: Case Reports and Literature Review

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