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First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations

BMC medical genetics, 2017-11, Vol.18 (1), p.134-134, Article 134

2017

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Genome Tunisia Project: paving the way for precision medicine in North Africa

Genome medicine, 2024-08, Vol.16 (1), p.104-19

2024

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New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene

BMC medical genomics, 2021-06, Vol.14 (1), p.160-8, Article 160

2021

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Man-O-War simulator: a Low-cost manikin for training on chest tube management

African Journal of Emergency Medicine, 2023-06, Vol.13 (2), p.39-41

2023

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A rare homozygous p.Arg87Trp variant of the GBA gene in Gaucher disease: A case report

Clinical case reports, 2022-05, Vol.10 (5), p.e05846-n/a

2022

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Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities

Diagnostics (Basel), 2022-09, Vol.12 (10), p.2375

2022

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Stroke knowledge among emergency centre visitors: A cross-sectional multicenter survey

African Journal of Emergency Medicine, 2021-03, Vol.11 (1), p.10-14

2021

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Fuzzy VA-Files for multi-label image annotation based on visual content of regions

Signal, image and video processing, 2018-07, Vol.12 (5), p.877-884

2018

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Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature

Molecular genetics & genomic medicine, 2021-10, Vol.9 (10), p.e1796-n/a

2021

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The phenotypic spectrum in a patient with Glycine to Serine mutation in the COL2A1 gene: overview study

AIMS molecular science, 2021-03, Vol.8 (1), p.76-85

2021

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Envenimation scorpionique: aspects cliniques et thérapeutiques

Pan African Medical Journal Conference Proceedings, 2018, Vol.2

Rejeb, Imen

2018

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Use of sodium polystyrene sulfonate in an acute-on-chronic lithium poisoned patient: A case report

Journal of acute disease, 2016-03, Vol.5 (2), p.162-164

2016

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Diagnosis of chronic myeloid leukemia from acute intracerebral hemorrhage: A case report

Journal of acute disease, 2015-08, Vol.4 (3), p.252-254

2015

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Mucopolysaccharidosis type VII as a cause of recurrent Non-Immune Hydrops Fetalis: The first Tunisian case confirmed by Next-Generation Sequencing

Clinica chimica acta, 2021-02, Vol.513, p.68-70

2021

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Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes TP63 and CNGB3

Ophthalmic genetics, 2024-02, Vol.45 (1), p.84-94

2024

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Factors predicting early outcome in patients admitted at emergency department with severe head trauma

Journal of acute disease, 2015-03, Vol.4 (1), p.68-72

2015

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Image Retrieval Using Spatial Dominant Color Descriptor

2017 IEEE/ACS 14th International Conference on Computer Systems and Applications (AICCSA), 2017, p.788-795

2017

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Tunisian DREEM: Nursing Students’ Perception of the Learning Environment

Open journal of nursing, 2022, Vol.12 (11), p.745-757

2022

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A novel WFS1 variant associated with severe diabetic retinopathy in Wolfram syndrome type 1

Ophthalmic genetics, 2023-06, Vol.44 (3), p.304-312

2023

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Molecular genetics & genomic medicine, 2021-11, Vol.9 (10)

2021

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Molecular genetics & genomic medicine, 2021-10, Vol.9 (10)

2021

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Molecular genetics & genomic medicine, 2021-10, Vol.9 (10), p.n/a

2021

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Molecular genetics & genomic medicine, 2021-10, Vol.9 (10)

2021

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Prediction Value of the Canadian CT Head Rule and the New Orleans Criteria for Positive Head CT Scan and Acute Neurosurgical Procedures in Minor Head Trauma: A Multicenter External Validation Study

First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations

Genome Tunisia Project: paving the way for precision medicine in North Africa

New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene

Man-O-War simulator: a Low-cost manikin for training on chest tube management

A rare homozygous p.Arg87Trp variant of the GBA gene in Gaucher disease: A case report

Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities

Stroke knowledge among emergency centre visitors: A cross-sectional multicenter survey

Fuzzy VA-Files for multi-label image annotation based on visual content of regions

Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature

The phenotypic spectrum in a patient with Glycine to Serine mutation in the COL2A1 gene: overview study

Envenimation scorpionique: aspects cliniques et thérapeutiques

Use of sodium polystyrene sulfonate in an acute-on-chronic lithium poisoned patient: A case report

Diagnosis of chronic myeloid leukemia from acute intracerebral hemorrhage: A case report

Mucopolysaccharidosis type VII as a cause of recurrent Non-Immune Hydrops Fetalis: The first Tunisian case confirmed by Next-Generation Sequencing

Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes TP63 and CNGB3

Factors predicting early outcome in patients admitted at emergency department with severe head trauma

Image Retrieval Using Spatial Dominant Color Descriptor

Tunisian DREEM: Nursing Students’ Perception of the Learning Environment

A novel WFS1 variant associated with severe diabetic retinopathy in Wolfram syndrome type 1

Mosaic parental germline mutations causing recurrent forms of malformations of cortical development

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