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Development of a Longitudinal Research Curriculum for Pediatric Emergency Medicine Fellowship

The western journal of emergency medicine, 2022-01, Vol.23 (1), p.26-29

2022

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Psychosocial and Financial Burden of Therapy in USA Patients with Pulmonary Arterial Hypertension

Diseases, 2020-06, Vol.8 (2), p.22

2020

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Early intervention in the management of pulmonary arterial hypertension: clinical and economic outcomes

ClinicoEconomics and outcomes research, 2017-01, Vol.9, p.731-739

2017

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Genomic Observations of a Rare/Pathogenic SMAD3 Variant in Loeys⁻Dietz Syndrome 3 Confirmed by Protein Informatics and Structural Investigations

Medicina (Kaunas, Lithuania), 2019-05, Vol.55 (5), p.137

2019

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Examination of Molecular Effects of MYLK Deletion in a Patient with Extensive Aortic, Carotid, and Abdominal Dissections That Underlie the Genetic Dysfunction

Case reports in medicine, 2020-08, Vol.2020, p.1-7

2020

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Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm

Case reports in genetics, 2018, Vol.2018, p.6780494-4

2018

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Characterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular Modeling

Case reports in genetics, 2020-01, Vol.2020, p.3256539-7

2020

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Abstract 43: Feasibility of a Virtual Assistant for Patients’ Frequently Asked Questions: An Unexplored Artificial Intelligence Application in Plastic Surgery

Plastic and reconstructive surgery. Global open, 2019-04, Vol.7 (4S), p.31-32

2019

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Acute pulmonary embolism in patients with obstructive sleep apnea: frequency, hospital outcomes, and recurrence

Journal of clinical sleep medicine, 2020-07, Vol.16 (7), p.1029-1036

2020

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Hyperleukocytosis With Chronic Lymphocytic Leukemia Express Non-Variant Phenotype and Genotype

American journal of clinical pathology, 2014-10, Vol.142 (suppl_1), p.A093-A093

2014

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Do physicians know when to refer patients for genetic testing?

Journal of genetic counseling, 2024-08, Vol.33 (4), p.786-792

2024

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227. Prevalence, Comorbidities and Expenditures of S. aureus Bacteremia in Liver Transplant Recipients: A 2012–2016 Nationwide Analysis

Open forum infectious diseases, 2019-10, Vol.6 (Supplement_2), p.S131-S132

2019

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Ketorolac Injections for Musculoskeletal Conditions: A Narrative Review

Clinical medicine & research, 2024-03, Vol.22 (1), p.19-27

2024

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Artificial Intelligent Virtual Assistant for Plastic Surgery Patient's Frequently Asked Questions: A Pilot Study

Annals of plastic surgery, 2020-04, Vol.84 (4), p.e16

2020

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Health IT Usability Focus Section: Data Use and Navigation Patterns among Medical ICU Clinicians during Electronic Chart Review

Applied clinical informatics, 2017-10, Vol.8 (4), p.1117-1126

2017

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Cost-Utility of Routine Testing in Chronic Urticaria/Angioedema: A Cohort Study

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2019-11, Vol.7 (8), p.2823-2832

2019

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Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy

Ophthalmic genetics, 2020-11, Vol.41 (6), p.563-569

2020

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Early intervention in the management of pulmonary arterial hypertension: clinical and economic outcomes

ClinicoEconomics and outcomes research, 2017-01, Vol.9, p.731

2017

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Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm

Case reports in genetics, 2018, Vol.2018, p.6780494-6780494

2018

Volltextzugriff (PDF)

Examination of Molecular Effects of MYLK Deletion in a Patient with Extensive Aortic, Carotid, and Abdominal Dissections That Underlie the Genetic Dysfunction

Case reports in medicine, 2020, Vol.2020, p.5108052-5108052

2020

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Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy

Ophthalmic Genetics, 2020, Vol.41 (6), p.563-569

2020

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Characterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular Modeling

Case reports in genetics, 2020, Vol.2020, p.3256539-3256539

2020

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Microscale Investigation of Urban Heat Island (UHI) in Annaba City: Unveiling Factors and Mitigation Strategies

Sustainability, 2024-01, Vol.16 (2), p.747

2024

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In-silico study reveals immunological signaling pathways, their genes, and potential herbal drug targets in ovarian cancer

Informatics in medicine unlocked, 2020, Vol.20, p.100422, Article 100422

2020

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Six-Minute Walk Test Improved Forearm Skin Blood Flow in Tunisian Obese Women

Obesity (Silver Spring, Md.), 2012-09, Vol.20 (9), p.1773-1779

2012

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Development of a Longitudinal Research Curriculum for Pediatric Emergency Medicine Fellowship

Psychosocial and Financial Burden of Therapy in USA Patients with Pulmonary Arterial Hypertension

Early intervention in the management of pulmonary arterial hypertension: clinical and economic outcomes

Genomic Observations of a Rare/Pathogenic SMAD3 Variant in Loeys⁻Dietz Syndrome 3 Confirmed by Protein Informatics and Structural Investigations

Examination of Molecular Effects of MYLK Deletion in a Patient with Extensive Aortic, Carotid, and Abdominal Dissections That Underlie the Genetic Dysfunction

Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm

Characterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular Modeling

Abstract 43: Feasibility of a Virtual Assistant for Patients’ Frequently Asked Questions: An Unexplored Artificial Intelligence Application in Plastic Surgery

Acute pulmonary embolism in patients with obstructive sleep apnea: frequency, hospital outcomes, and recurrence

Hyperleukocytosis With Chronic Lymphocytic Leukemia Express Non-Variant Phenotype and Genotype

Do physicians know when to refer patients for genetic testing?

227. Prevalence, Comorbidities and Expenditures of S. aureus Bacteremia in Liver Transplant Recipients: A 2012–2016 Nationwide Analysis

Ketorolac Injections for Musculoskeletal Conditions: A Narrative Review

Artificial Intelligent Virtual Assistant for Plastic Surgery Patient's Frequently Asked Questions: A Pilot Study

Health IT Usability Focus Section: Data Use and Navigation Patterns among Medical ICU Clinicians during Electronic Chart Review

Cost-Utility of Routine Testing in Chronic Urticaria/Angioedema: A Cohort Study

Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy

Early intervention in the management of pulmonary arterial hypertension: clinical and economic outcomes

Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm

Examination of Molecular Effects of MYLK Deletion in a Patient with Extensive Aortic, Carotid, and Abdominal Dissections That Underlie the Genetic Dysfunction

Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy

Characterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular Modeling

Microscale Investigation of Urban Heat Island (UHI) in Annaba City: Unveiling Factors and Mitigation Strategies

In-silico study reveals immunological signaling pathways, their genes, and potential herbal drug targets in ovarian cancer

Six-Minute Walk Test Improved Forearm Skin Blood Flow in Tunisian Obese Women

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