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Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

American journal of human genetics, 2014-01, Vol.94 (1), p.144-152

2014

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Deep Learning Automation of Kidney, Liver, and Spleen Segmentation for Organ Volume Measurements in Autosomal Dominant Polycystic Kidney Disease

Tomography (Ann Arbor), 2022-07, Vol.8 (4), p.1804-1819

2022

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Pulmonary Embolism in Hospitalized Patients with COVID-19: A Multicenter Study

Radiology, 2021-12, Vol.301 (3), p.E426-E433

2021

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Prescribing in Type 2 Diabetes Patients With and Without Cardiovascular Disease History: A Descriptive Analysis in the UK CPRD

Clinical therapeutics, 2021-02, Vol.43 (2), p.320-335

2021

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Effect of Averaging Measurements From Multiple MRI Pulse Sequences on Kidney Volume Reproducibility in Autosomal Dominant Polycystic Kidney Disease

Journal of magnetic resonance imaging, 2023-10, Vol.58 (4), p.1153-1160

2023

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Test Retest Reproducibility of Organ Volume Measurements in ADPKD Using 3D Multimodality Deep Learning

Academic radiology, 2024-03, Vol.31 (3), p.889-899

2024

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Long-Term Cost-Effectiveness Analyses of Empagliflozin Versus Oral Semaglutide, in Addition to Metformin, for the Treatment of Type 2 Diabetes in the UK

Diabetes therapy, 2020-09, Vol.11 (9), p.2041-2055

2020

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Regenerative Therapies in Ischemic Stroke Recovery

Raza, Syed Shadab

1, 2022

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Novel homozygous mutations in the EVC and EVC2 genes in two consanguineous families segregating autosomal recessive Ellis-van Creveld syndrome

Clinical dysmorphology, 2016-01, Vol.25 (1), p.1-6

2016

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Exosomal miR-141-3p from PDLSCs Alleviates High Glucose-Induced Senescence of PDLSCs by Activating the KEAP1-NRF2 Signaling Pathway

Stem cells international, 2023-05, Vol.2023, p.7136819-24

2023

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Fiscal policy and economic growth in Sub-Saharan Africa: Do governance indicators matter?

PloS one, 2023-11, Vol.18 (11), p.e0293188-e0293188

2023

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Integration degree of China's the new development pattern of dual circulation and industrial green development

PloS one, 2023-07, Vol.18 (7), p.e0288160-e0288160

2023

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United States and Pakistan in the 21st Century: Geostrategy and Geopolitics in South Asia

Raza, Syed Tahseen

1, 2021

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Geopolitics of the Pakistan-Afghanistan Borderland

1, 2021

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A novel recessive mutation in the gene ELOVL4 causes a neuro-ichthyotic disorder with variable expressivity

BMC medical genetics, 2014-02, Vol.15 (1), p.25-25, Article 25

2014

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Tidal Volume and Positive End-expiratory Pressure and Postoperative Hypoxemia during General Anesthesia: A Single-center Multiple Crossover Factorial Cluster Trial

Anesthesiology (Philadelphia), 2022-10, Vol.137 (4), p.406-417

2022

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A web-based scoping review assessing the influence of smoking and smoking cessation on antidiabetic drug meabolism: implications for medication efficacy

Frontiers in pharmacology, 2024-06, Vol.15, p.1406860

2024

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Machine-learning-based Web system for the prediction of chronic kidney disease progression and mortality

PLOS digital health, 2023-01, Vol.2 (1), p.e0000188

2023

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Intragenic deletion mutation in the gene desmoglein 4 underlies autosomal recessive hypotrichosis in six consanguineous families

Journal of Taibah University Medical Sciences, 2016-06, Vol.11 (3), p.203-210

2016

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DP-CTGAN: Differentially Private Medical Data Generation Using CTGANs

Artificial Intelligence in Medicine, p.178-188

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Artificial Intelligence in Medicine: 20th International Conference on Artificial Intelligence in Medicine, AIME 2022, Halifax, NS, Canada, June 14-17, 2022, Proceedings

1, 2022

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TTS-GAN: A Transformer-Based Time-Series Generative Adversarial Network

Artificial Intelligence in Medicine, p.133-143

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BCR-ABL Independent Resistance Mechanisms to Chronic Myeloid Leukemia

Canadian Journal of Clinical Nutrition, 2023-06, Vol.11 (2), p.102-117

2023

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Advance Understanding of Epidemiological Factors Responsible for Ischemic Stroke

Canadian Journal of Clinical Nutrition, 2023-06, Vol.11 (2), p.112-132

2023

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Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

Deep Learning Automation of Kidney, Liver, and Spleen Segmentation for Organ Volume Measurements in Autosomal Dominant Polycystic Kidney Disease

Pulmonary Embolism in Hospitalized Patients with COVID-19: A Multicenter Study

Prescribing in Type 2 Diabetes Patients With and Without Cardiovascular Disease History: A Descriptive Analysis in the UK CPRD

Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responses

Effect of Averaging Measurements From Multiple MRI Pulse Sequences on Kidney Volume Reproducibility in Autosomal Dominant Polycystic Kidney Disease

Test Retest Reproducibility of Organ Volume Measurements in ADPKD Using 3D Multimodality Deep Learning

Long-Term Cost-Effectiveness Analyses of Empagliflozin Versus Oral Semaglutide, in Addition to Metformin, for the Treatment of Type 2 Diabetes in the UK

Regenerative Therapies in Ischemic Stroke Recovery

Novel homozygous mutations in the EVC and EVC2 genes in two consanguineous families segregating autosomal recessive Ellis-van Creveld syndrome

Exosomal miR-141-3p from PDLSCs Alleviates High Glucose-Induced Senescence of PDLSCs by Activating the KEAP1-NRF2 Signaling Pathway

Fiscal policy and economic growth in Sub-Saharan Africa: Do governance indicators matter?

Integration degree of China's the new development pattern of dual circulation and industrial green development

United States and Pakistan in the 21st Century: Geostrategy and Geopolitics in South Asia

Geopolitics of the Pakistan-Afghanistan Borderland

A novel recessive mutation in the gene ELOVL4 causes a neuro-ichthyotic disorder with variable expressivity

Tidal Volume and Positive End-expiratory Pressure and Postoperative Hypoxemia during General Anesthesia: A Single-center Multiple Crossover Factorial Cluster Trial

A web-based scoping review assessing the influence of smoking and smoking cessation on antidiabetic drug meabolism: implications for medication efficacy

Machine-learning-based Web system for the prediction of chronic kidney disease progression and mortality

Intragenic deletion mutation in the gene desmoglein 4 underlies autosomal recessive hypotrichosis in six consanguineous families

DP-CTGAN: Differentially Private Medical Data Generation Using CTGANs

Artificial Intelligence in Medicine: 20th International Conference on Artificial Intelligence in Medicine, AIME 2022, Halifax, NS, Canada, June 14-17, 2022, Proceedings

TTS-GAN: A Transformer-Based Time-Series Generative Adversarial Network

BCR-ABL Independent Resistance Mechanisms to Chronic Myeloid Leukemia

Advance Understanding of Epidemiological Factors Responsible for Ischemic Stroke

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