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Influence of combined CYP3A4 and CYP3A5 single-nucleotide polymorphisms on tacrolimus exposure in kidney transplant recipients: a study according to the post-transplant phase

Pharmacogenomics, 2015-12, Vol.16 (18), p.2045-2054

2015

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Pericardial effusion with cardiac tamponade caused by a central venous catheter in a very low birth weight infant

The Pan African medical journal, 2016, Vol.25 (13), p.13-13

2016

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Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome

BMC pediatrics, 2018-08, Vol.18 (1), p.286-286, Article 286

2018

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Spontaneous Intestinal Perforation in a Very Low Birth Weight Infant: Successful Management by Peritoneal Needle Suction

Journal of neonatal surgery, 2016-07, Vol.5 (3), p.39-39

2016

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78 Transient neonatal Behçet’s disease: a case report

Rheumatology (Oxford, England), 2022-10, Vol.61 (Supplement_2)

2022

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Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family

Tunisie Medicale, 2015-03, Vol.93 (3), p.170-174

2015

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Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations

Journal of dermatological science, 2010-02, Vol.57 (2), p.144-146

2010

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Primary Pulmonary Hypertension Associated with Asymptomatic Methylmalonic Aciduria in a Child

Journal of the College of Physicians and Surgeons--Pakistan, 2019-06, Vol.29 (6), p.S43-S44

2019

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First description of the MEGDEHL syndrome in the Tunisian population via whole‐exome sequencing: Novel nonsense mutation in SERAC1 gene

International journal of developmental neuroscience, 2022-12, Vol.82 (8), p.736-747

2022

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Single-center experience of congenital disorders of glycosylation syndrome screening in Tunisia: A retrospective study over a 15-year period (2007–2021)

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2024-02, Vol.31 (2), p.124-128

2024

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A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease

Genetics in medicine, 2022-10, Vol.24 (10), p.2194-2203

2022

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Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients

Neuropediatrics, 2020-10, Vol.51 (5), p.349-353

2020

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Inborn Errors Of Metabolism In Neonatal Period: A Challenging Management In Tunisia

Tunisie Medicale, 2019-05, Vol.97 (5), p.681-684

2019

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Influence of combined

Pharmacogenomics, 2015-12, Vol.16 (18), p.2045-2054

2015

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ABCB1 and SLCO1B3 Gene Polymorphisms and Their Impact on Digoxin Pharmacokinetics in Atrial Fibrillation Patients among the Tunisian Population

Pharmacology, 2017-01, Vol.99 (5-6), p.250-258

2017

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Therapeutic drug monitoring of caffeine in preterm infants: Could saliva be an alternative to serum?

Therapie, 2017-12, Vol.72 (6), p.685-689

2017

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Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency

Biochimica et biophysica acta, 2011-05, Vol.1812 (5), p.619-624

2011

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Neonatalogist-performed echography in neonatology: a Tunisian experience

Tunisie Medicale, 2019-01, Vol.97 (1), p.122-127

2019

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Genetic diseases in the Tunisian population

American journal of medical genetics. Part A, 2011-01, Vol.155A (1), p.238-267

2011

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Transported neonates in Tunisia

Tunisie Medicale, 2018-12, Vol.96 (12), p.865-868

2018

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Extremely preterm infants in Tunisia: Where are we now?

Tunisie Medicale, 2018-08, Vol.96 (8-9), p.510-513

2018

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Interplay of socio-economic factors, consanguinity, fertility, and offspring mortality in Monastir, Tunisia

Croatian medical journal, 2007-10, Vol.48 (5), p.701-707

2007

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Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome

Biology and medicine, 2017-11, Vol.9 (6)

2017

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A novel CASR mutation in a Tunisian FHH/NSHPT family associated with a mental retardation

Molecular biology reports, 2012-03, Vol.39 (3), p.2395-2400

2012

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Influence of combined CYP3A4 and CYP3A5 single-nucleotide polymorphisms on tacrolimus exposure in kidney transplant recipients: a study according to the post-transplant phase

Pericardial effusion with cardiac tamponade caused by a central venous catheter in a very low birth weight infant

Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome

Spontaneous Intestinal Perforation in a Very Low Birth Weight Infant: Successful Management by Peritoneal Needle Suction

78 Transient neonatal Behçet’s disease: a case report

Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family

Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations

Primary Pulmonary Hypertension Associated with Asymptomatic Methylmalonic Aciduria in a Child

First description of the MEGDEHL syndrome in the Tunisian population via whole‐exome sequencing: Novel nonsense mutation in SERAC1 gene

Single-center experience of congenital disorders of glycosylation syndrome screening in Tunisia: A retrospective study over a 15-year period (2007–2021)

A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease

Turner Syndrome: results of the first Tunisian study group on Turner Syndrome (TuSGOT)

Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients

Inborn Errors Of Metabolism In Neonatal Period: A Challenging Management In Tunisia

Influence of combined

ABCB1 and SLCO1B3 Gene Polymorphisms and Their Impact on Digoxin Pharmacokinetics in Atrial Fibrillation Patients among the Tunisian Population

Therapeutic drug monitoring of caffeine in preterm infants: Could saliva be an alternative to serum?

Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency

Neonatalogist-performed echography in neonatology: a Tunisian experience

Genetic diseases in the Tunisian population

Transported neonates in Tunisia

Extremely preterm infants in Tunisia: Where are we now?

Interplay of socio-economic factors, consanguinity, fertility, and offspring mortality in Monastir, Tunisia

Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome

A novel CASR mutation in a Tunisian FHH/NSHPT family associated with a mental retardation

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