Research Topics
| Hamid MehenniSummaryAffiliation: University of Geneva Country: Switzerland Publications
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Detail Information
Publications
An unexpected Cowden syndrome case found among members of a large familial adenomatous polyposis kindredHamid Mehenni
Department of Cell Biology, University of Geneva, Switzerland
Eur J Gastroenterol Hepatol 17:1407-12. 2005..Genetic testing is a powerful tool that can provide a definitive diagnosis for FAP. However, not all polyposes in the FAP family are adenomatous polyposes...
Cancer risks in LKB1 germline mutation carriersH Mehenni
Unité de Gastroentérologie et Hépatologie, Centre Médico chirurgical de Plainpalais et Département de Biologie Cellulaire, Universite de Geneve, Switzerland
Gut 55:984-90. 2006..This syndrome is associated with an increased risk of malignancies in different organs but there is a lack of data on cancer range and risk in LKB1 germline mutation carriers...
Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndromeHamid Mehenni
Centre Médico Chirurgical Rond Point Plainpalais et Département de biologie cellulaire, Unité de recherche des maladies prédisposant aux cancers gastro intestinaux, Universite de Geneve, Geneve, Switzerland
Dig Dis Sci 52:1924-33. 2007....
LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromesHamid Mehenni
Departement de Biologie Cellulaire, Universite de Geneve, 1211 Geneve 4, Switzerland
Hum Mol Genet 14:2209-19. 2005....
