UB Paderborn / Katalog / Suche / in CDI

A cost-effectiveness analysis of PHiD-CV compared to PCV13 in a national immunization program setting in Tunisia

Human vaccines & immunotherapeutics, 2022-11, Vol.18 (5), p.2079305-2079305

2022

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Interrelationships between cadmium, zinc and antioxidants in the liver of the rat exposed orally to relatively high doses of cadmium and zinc

Ecotoxicology and environmental safety, 2011-10, Vol.74 (7), p.2099-2104

2011

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Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

The American journal of the medical sciences, 2012-11, Vol.344 (5), p.363-373

2012

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Prevalence of Helicobacter pylori vacA, cagA, iceA and oipA genotypes in Tunisian patients

Annals of clinical microbiology and antimicrobials, 2010-03, Vol.9 (1), p.10-10

2010

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Antioxidant enzymes activities in obese Tunisian children

Nutrition journal, 2013-01, Vol.12 (1), p.18-18, Article 18

2013

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West syndrome and mosaic trisomy 13: A case report

Paediatrica Indonesiana, 2018-05, Vol.58 (3), p.146-50

2018

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Maternally Inherited Leigh Syndrome: T8993G Mutation in a Tunisian Family

Pediatric neurology, 2009-06, Vol.40 (6), p.437-442

2009

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Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients

Journal of human genetics, 2007-03, Vol.52 (3), p.262-270

2007

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Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities

Clinical Pediatric Endocrinology, 2010, Vol.19(4), pp.109-113

2010

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Localization of tissue transglutaminase and N (epsilon)-(gamma) -glutamyl lysine in duodenal cucosa during the development of mucosal atrophy in coeliac disease

Virchows Archiv : an international journal of pathology, 2005-06, Vol.446 (6), p.613-618

2005

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Fertility outcome in male and female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Middle East Fertility Society journal, 2014-06, Vol.19 (2), p.89-95

2014

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A new mutation in exon 3 of the SCL39A4 gene in a Tunisian family with severe acrodermatitis enteropathica

Nutrition (Burbank, Los Angeles County, Calif.), 2006-10, Vol.22 (10), p.1067-1070

2006

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High frequency of W1327X mutation in glycogen storage disease type III patients from central Tunisia

Annales de biologie clinique (Paris), 2012-11, Vol.70 (6), p.648-650

2012

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History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation

Mitochondrial DNA. Part A. DNA mapping, sequencing, and analysis, 2016-09, Vol.27 (5), p.3194-3198

2016

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Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Indian journal of endocrinology and metabolism, 2012-11, Vol.16 (6), p.939-946

2012

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Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis

Indian journal of endocrinology and metabolism, 2013-01, Vol.17 (1), p.121-127

2013

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Polymorphism in transporter antigen peptides gene (TAP1) associated with atopy in Tunisians

Journal of allergy and clinical immunology, 1997-02, Vol.99 (2), p.216-223

1997

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Rotavirus Strain Diversity in the Centre Coast of Tunisia from 2000 through 2003

The Journal of infectious diseases, 2010-09, Vol.202 (Supplement-1), p.S252-S257

2010

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Rotavirus Strain Diversity in the Centre Coast of Tunisia from 2000 through 2003: Rotavirus Infection in Africa: Epidemiology, Burden of Disease, and Strain Diversity

The Journal of infectious diseases, 2010, Vol.202

2010

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Enterovirus meningitis in Tunisia (Monastir, Mahdia, 2011–2013): identification of virus variants cocirculating in France

Diagnostic microbiology and infectious disease, 2016-02, Vol.84 (2), p.116-122

2016

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Trace element status and fatty acids metabolism during healthy ageing: An example of a population from the Tunisian eastern coast

Experimental gerontology, 2012-03, Vol.47 (3), p.243-249

2012

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Pentosidine: Can be Related to the Etiology of Chronic Kidney Disease?

International Journal of Diabetology & Vascular Disease Research, 2014-03, Vol.2 (2), p.49-53

2014

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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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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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A cost-effectiveness analysis of PHiD-CV compared to PCV13 in a national immunization program setting in Tunisia

Interrelationships between cadmium, zinc and antioxidants in the liver of the rat exposed orally to relatively high doses of cadmium and zinc

Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012)

Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

Prevalence of Helicobacter pylori vacA, cagA, iceA and oipA genotypes in Tunisian patients

Antioxidant enzymes activities in obese Tunisian children

West syndrome and mosaic trisomy 13: A case report

Maternally Inherited Leigh Syndrome: T8993G Mutation in a Tunisian Family

Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients

Congenital Adrenal Hyperplasia and Brain Magnetic Resonance Imaging Abnormalities

Localization of tissue transglutaminase and N (epsilon)-(gamma) -glutamyl lysine in duodenal cucosa during the development of mucosal atrophy in coeliac disease

Fertility outcome in male and female patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

A new mutation in exon 3 of the SCL39A4 gene in a Tunisian family with severe acrodermatitis enteropathica

High frequency of W1327X mutation in glycogen storage disease type III patients from central Tunisia

History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation

Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis

Polymorphism in transporter antigen peptides gene (TAP1) associated with atopy in Tunisians

Rotavirus Strain Diversity in the Centre Coast of Tunisia from 2000 through 2003

Rotavirus Strain Diversity in the Centre Coast of Tunisia from 2000 through 2003: Rotavirus Infection in Africa: Epidemiology, Burden of Disease, and Strain Diversity

Enterovirus meningitis in Tunisia (Monastir, Mahdia, 2011–2013): identification of virus variants cocirculating in France

Trace element status and fatty acids metabolism during healthy ageing: An example of a population from the Tunisian eastern coast

Pentosidine: Can be Related to the Etiology of Chronic Kidney Disease?

Genetic diseases in the Tunisian population

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

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