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Primary resistance to clarithromycin, metronidazole and amoxicillin of Helicobacter pylori isolated from Tunisian patients with peptic ulcers and gastritis: a prospective multicentre study

Annals of clinical microbiology and antimicrobials, 2010-08, Vol.9 (1), p.22-22

2010

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Intubation-Surfactant-Extubation Strategy in a Medical Resource-limited Department: A Prospective Study

Journal of tropical pediatrics (1980), 2016-04, Vol.62 (2), p.169-170

2016

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Arg924X homozygous mutation in insulin receptor gene in a Tunisian patient with Donohue syndrome

Journal of pediatric endocrinology & metabolism : JPEM, 2016-06, Vol.29 (6), p.753

2016

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Prevalence of celiac disease in Tunisia: mass-screening study in schoolchildren

European journal of gastroenterology & hepatology, 2007-08, Vol.19 (8), p.687-694

2007

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Celiac disease in Tunisian children: A second screening study using a "new generation" rapid test

Immunological investigations, 2013-01, Vol.42 (4), p.356-368

2013

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SLC26A3 gene mutations in Tunisian patients with congenital chloride diarrhea

Tunisie Medicale, 2016-01, Vol.94 (1), p.83-83

2016

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Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency

Blood, 2006-09, Vol.108 (6), p.1925-1931

2006

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Primary immunodeficiencies : Report of 33 Pediatric Tunisian cases

Tunisie Medicale, 2016-04, Vol.94 (4), p.320-325

2016

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Abstracts of the Conferences of the Sixteenth Francophone Meetings of Allergology Hammamet, 4-7 October 2017

Tunisie Medicale, 2017-08, Vol.95 (8-9), p.777-806

2017

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Cystic fibrosis: A report of 33 pediatric Tunisian cases

Tunisie Medicale, 2015-08, Vol.93 (8-9), p.569-573

2015

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Omenn syndrome: two case reports

Acta dermatovenerologica Croatica, 2013, Vol.21 (4), p.259-262

2013

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HLA class II polymorphism in children with coeliac disease in Tunisia: is there any influence on clinical manifestation?

European journal of gastroenterology & hepatology, 2009-11, Vol.21 (11), p.1286-1290

2009

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Cyclic vomiting syndrome in children

Tunisie Medicale, 2012-06, Vol.90 (6), p.501

2012

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Chylothorax: a complication of internal jugular vein catheterization in a premature newborn

Tunisie Medicale, 2011-03, Vol.89 (3), p.312

2011

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Compound Heterozygosity in the Novel Mutations W157R and T591K in the γ-Glutamyl Carboxylase Gene Causes Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency in a Tunisian Family

Blood, 2005-11, Vol.106 (11), p.2147-2147

2005

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Sternal cleft, a rare congenital anomaly. Report of the first Tunisian case

Tunisie Medicale, 2008-12, Vol.86 (12), p.1082

2008

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A novel mutation in infant hypophophatasia: a case report

Tunisie Medicale, 2007-05, Vol.85 (5), p.433

2007

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Crohnʼs Disease Lesions in the Upper Gastrointestinal Tract: Correlation Between Clinical, Radiological, Endoscopic, and Histological Features in Adolescents and Children

Journal of pediatric gastroenterology and nutrition, 1989-05, Vol.8 (4), p.442-446

1989

Volltextzugriff (PDF)

Deficient expression of leukocyte adhesion proteins. A new Tunisian case

Tunisie Medicale, 2006-07, Vol.84 (7), p.464

2006

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Acute leukoencephalitis in infant treated by high-dose corticosteroid. A case report

Tunisie Medicale, 2005-03, Vol.83 (3), p.172

2005

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Pulmonary alveolar proteinosis in two siblings. A case report

Tunisie Medicale, 2005-08, Vol.83 (8), p.488

2005

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Crohnʼs Disease Lesions in the Upper Gastrointestinal Tract: Correlation Between Clinical, Radiological, Endoscopic, and Histological Features in Adolescents and Children

Journal of pediatric gastroenterology and nutrition, 1989-05, Vol.8 (4), p.442-446

1989

Volltextzugriff (PDF)

Confirmation de la présence de Leishmania infantum MON-80 en tunisie

Bulletin de la Société de pathologie exotique, 1999-02, Vol.92 (1), p.29-30

1999

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Omenn Syndrome : Two Case Reports

Acta dermatovenerologica Croatica, 2014, Vol.21 (4)

2014

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Cyclic vomiting syndrome in children

La Tunisie medicale, 2012, Vol.90 (6), p.501-502

2012

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Primary resistance to clarithromycin, metronidazole and amoxicillin of Helicobacter pylori isolated from Tunisian patients with peptic ulcers and gastritis: a prospective multicentre study

Intubation-Surfactant-Extubation Strategy in a Medical Resource-limited Department: A Prospective Study

Arg924X homozygous mutation in insulin receptor gene in a Tunisian patient with Donohue syndrome

Prevalence of celiac disease in Tunisia: mass-screening study in schoolchildren

Celiac disease in Tunisian children: A second screening study using a "new generation" rapid test

SLC26A3 gene mutations in Tunisian patients with congenital chloride diarrhea

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency

Primary immunodeficiencies : Report of 33 Pediatric Tunisian cases

Abstracts of the Conferences of the Sixteenth Francophone Meetings of Allergology Hammamet, 4-7 October 2017

Cystic fibrosis: A report of 33 pediatric Tunisian cases

Omenn syndrome: two case reports

HLA class II polymorphism in children with coeliac disease in Tunisia: is there any influence on clinical manifestation?

Cyclic vomiting syndrome in children

Chylothorax: a complication of internal jugular vein catheterization in a premature newborn

Compound Heterozygosity in the Novel Mutations W157R and T591K in the γ-Glutamyl Carboxylase Gene Causes Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency in a Tunisian Family

Sternal cleft, a rare congenital anomaly. Report of the first Tunisian case

A novel mutation in infant hypophophatasia: a case report

Crohnʼs Disease Lesions in the Upper Gastrointestinal Tract: Correlation Between Clinical, Radiological, Endoscopic, and Histological Features in Adolescents and Children

Deficient expression of leukocyte adhesion proteins. A new Tunisian case

Acute leukoencephalitis in infant treated by high-dose corticosteroid. A case report

Pulmonary alveolar proteinosis in two siblings. A case report

Crohnʼs Disease Lesions in the Upper Gastrointestinal Tract: Correlation Between Clinical, Radiological, Endoscopic, and Histological Features in Adolescents and Children

Confirmation de la présence de Leishmania infantum MON-80 en tunisie

Omenn Syndrome : Two Case Reports

Cyclic vomiting syndrome in children

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