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Multi-label learning for identifying co-occurring class code smells

Computing, 2024-08, Vol.106 (8), p.2585-2612

2024

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Application of Deep Learning for Code Smell Detection: Challenges and Opportunities

SN computer science, 2024-06, Vol.5 (5), p.614, Article 614

2024

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A multi-label classification approach for detecting test smells over java projects

Journal of King Saud University. Computer and information sciences, 2022-11, Vol.34 (10), p.8692-8701

2022

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Improving the Identification of Code Smells by Combining Structural and Semantic Information

Neural Information Processing, p.296-304

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Deep Representation Learning for Code Smells Detection using Variational Auto-Encoder

2019 International Joint Conference on Neural Networks (IJCNN), 2019, p.1-8

2019

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Robustness of a Complex System: Double-Stage Gearing System, with GPC and MC Methods

Advances in Materials, Mechanics and Manufacturing III, 2024, p.141-151

2024

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Study of a Car Suspension System Under Uncertainties

Advances in Materials, Mechanics and Manufacturing III, 2024, p.152-159

2024

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Uncertainty Consideration for Second Shaft Dynamic Behavior of a Double Stage Gearbox

Design and Modeling of Mechanical Systems - V, 2022, p.179-187

2022

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Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation

Frontiers in endocrinology (Lausanne), 2021-07, Vol.12, p.684018-684018

2021

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Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism

Journal of assisted reproduction and genetics, 2019-06, Vol.36 (6), p.1273-1280

2019

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Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency

Journal of clinical medicine, 2022-12, Vol.11 (24), p.7525

2022

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Congenital hypopituitarism in familial Turner syndrome cases caused by a highly prevalent PROP1 gene mutation in Tunisia

Endocrine and metabolic science, 2024-03, Vol.14, p.100160, Article 100160

2024

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Cardiothyreosis: Epidemiological, clinical and therapeutic approach

Clinical Medicine Insights. Cardiology, 2023-01, Vol.17, p.11795468231152042-11795468231152042

2023

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Case report: Management challenges of late diagnosed 17‐alpha hydroxylase deficiency

Clinical case reports, 2023-02, Vol.11 (2), p.e6962-n/a

2023

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Diabetes Distress and Illness Perceptions in Tunisian Type 2 Diabetes Patients

Diabetes, metabolic syndrome and obesity, 2023-11, Vol.16, p.3547-3556

2023

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Diagnosis and management of pituitary apoplexy: a Tunisian data

Chinese neurosurgical journal, 2023-07, Vol.9 (1), p.17-17, Article 17

2023

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Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population

Canadian journal of physiology and pharmacology, 2018-11, Vol.96 (11), p.1171

2018

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Early prediction of Student academic performance based on Machine Learning algorithms: A case study of bachelor’s degree students in KSA

Education and information technologies, 2023-12

2023

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A Framework for GDPR Compliance in Big Data Systems

Risks and Security of Internet and Systems, p.211-226

Volltextzugriff (PDF)

Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assay

Gene, 2017-07, Vol.620, p.10-14

2017

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A Rare Cause of Refractory Chronic Diarrhea and Cachexia: A Case Report

Iranian journal of public health, 2020-02, Vol.49 (2), p.386-388

2020

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Insulinoma with equivocal imaging

Endocrinology, diabetes & metabolism case reports, 2023-04, Vol.2023 (2)

2023

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Design Patterns for Self-Adaptive RTE Systems Specification

International Journal of Reconfigurable Computing, 2014-01, Vol.2014 (2014), p.1-21

2014

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Répercussions métaboliques et cardiovasculaires de la substitution glucocorticoïde au cours de la maladie d’Addison

The Pan African medical journal, 2018, Vol.30 (251)

2018

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Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinoma

Cancer biomarkers : section A of Disease markers, 2010-01, Vol.8 (1), p.43

2010

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Multi-label learning for identifying co-occurring class code smells

Application of Deep Learning for Code Smell Detection: Challenges and Opportunities

A multi-label classification approach for detecting test smells over java projects

Improving the Identification of Code Smells by Combining Structural and Semantic Information

Deep Representation Learning for Code Smells Detection using Variational Auto-Encoder

Robustness of a Complex System: Double-Stage Gearing System, with GPC and MC Methods

Study of a Car Suspension System Under Uncertainties

Uncertainty Consideration for Second Shaft Dynamic Behavior of a Double Stage Gearbox

Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation

Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism

Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency

Congenital hypopituitarism in familial Turner syndrome cases caused by a highly prevalent PROP1 gene mutation in Tunisia

Cardiothyreosis: Epidemiological, clinical and therapeutic approach

Case report: Management challenges of late diagnosed 17‐alpha hydroxylase deficiency

Diabetes Distress and Illness Perceptions in Tunisian Type 2 Diabetes Patients

Diagnosis and management of pituitary apoplexy: a Tunisian data

Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population

Early prediction of Student academic performance based on Machine Learning algorithms: A case study of bachelor’s degree students in KSA

A Framework for GDPR Compliance in Big Data Systems

Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assay

A Rare Cause of Refractory Chronic Diarrhea and Cachexia: A Case Report

Insulinoma with equivocal imaging

Design Patterns for Self-Adaptive RTE Systems Specification

Répercussions métaboliques et cardiovasculaires de la substitution glucocorticoïde au cours de la maladie d’Addison

Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinoma

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