M. Guédiche

发表

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

K. Monastiri, H. Ben Cheikh, E. Kerkeni, 2007, Croatian medical journal.

A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients

M. Barbouche, M. Ben-ali, S. Barsaoui, 2016, Journal of Clinical Immunology.

Molecular epidemiology of human astrovirus and adenovirus serotypes 40/41 strains related to acute diarrhea in Tunisian children

N. Sakly, P. Pothier, A. de Rougemont, 2009, Journal of medical virology.

[Dual chamber pacing in hypertrophic obstructive cardiomyopathy].

W. Fehri, F. Azzouzi, H. Haouala, 1996, La Tunisie medicale.

Osteoprotegerin as a marker of cardiovascular risk in children and adolescents with type 1 diabetes

M. Najjar, F. Neffati, M. Guédiche, 2017, Pediatric diabetes.

Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith–Wiedemann syndrome as a sporadic adrenocortical tumor

M. Gribaa, A. Zakhama, A. Saâd, 2014, Applied & translational genomics.

Infantile Scurvy: Two Case Reports

M. Najjar, M. Guédiche, M. Golli, 2010, International journal of pediatrics.

Can paraoxonase 1 polymorphisms (L55 M and Q192 R) protect children with type 1 diabetes against lipid abnormalities?

M. Najjar, F. Neffati, J. Rejeb, 2014, Journal of clinical lipidology.

Relationship between GII.3 norovirus infections and blood group antigens in young children in Tunisia.

P. Pothier, A. de Rougemont, M. Aouni, 2015, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

Paraoxonase 1 polymorphisms (L55M and Q192R) as a genetic marker of diabetic nephropathy in youth with type 1 diabetes.

M. Najjar, F. Neffati, W. Douki, 2015, Endokrynologia Polska.

Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations.

M. Nilges, S. Abdelhak, S. Boubaker, 2006, Molecular genetics and metabolism.

A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients

M. Barbouche, M. Ben-ali, S. Barsaoui, 2016, Journal of Clinical Immunology.

[Profile of antimicrobial resistance of agents causing urinary tract infections in children].

M. Guédiche, A. Messaoudi, L. Ghedira Besbes, 2004, La Tunisie medicale.

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

M. Aouni, J. Bailly, H. Peigue-Lafeuille, 2016, Diagnostic microbiology and infectious disease.

[Infantile visceral leishmaniasis: difficult diagnosis in cases complicated by hemophagocytosis].

M. Bejaoui, A. Khelif, M. Guédiche, 1996, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

First molecular detection of Aichi virus in sewage and shellfish samples in the Monastir region of Tunisia

N. Sakly, P. Pothier, M. Aouni, 2010, Archives of Virology.

[Pneumococcal meningitis mortality in children. Prognostic factors in a series of 73 cases].

F. Thabet, B. Tabarki, M. Guédiche, 2007, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[Coxiella burnetti infectious endocarditis. Apropos of a case].

W. Fehri, H. Haouala, M. Guédiche, 1997, Annales de cardiologie et d'angeiologie.

Acute Infantile Gastroenteritis Associated with Human Enteric Viruses in Tunisia

N. Sakly, P. Pothier, A. de Rougemont, 2008, Journal of Clinical Microbiology.

Detection and Genomic Characterization of Aichi Viruses in Stool Samples from Children in Monastir, Tunisia

N. Sakly, P. Pothier, M. Aouni, 2009, Journal of Clinical Microbiology.

[Idiopathic steroid-resistant nephrotic syndrome in child : study of 20 cases].

A. Zakhama, S. Boussetta, M. Hachicha, 2011, La Tunisie medicale.

Cerebral Sinovenous Thrombosis in a Child with Idiopathic Nephrotic Syndrome

M. Guédiche, A. Gabsi, S. Haddad, 2011, Case reports in nephrology.

Molecular Epidemiology of Norovirus Gastroenteritis Investigated Using Samples Collected from Children in Tunisia during a Four-Year Period: Detection of the Norovirus Variant GGII.4 Hunter as Early as January 2003

N. Sakly, P. Pothier, M. Aouni, 2008, Journal of Clinical Microbiology.

Congenital Pulmonary Alveolar Proteinosis

M. Guédiche, C. Ben Meriem, S. Hammami, 2013, Case Reports in Pediatrics.

Nail-Patella Syndrome Associated with Short Stature: A Case Series

S. Chouchene, S. Hammami, L. Ghedira-Besbes, 2010, Case reports in medicine.

β-Ketothiolase (2-methylacetoacetyl-CoA thiolase) deficiency: A frequent disease in Tunisia?

N. Kaabachi, K. Monastiri, M. Guédiche, 1999, Journal of Inherited Metabolic Disease.

IMMUNE THROMBOCYTOPENIC PURPURE AND COELIAC DISEASE

M. Guédiche, S. Chouchane, S. Hammami, 2011, Journal of paediatrics and child health.