| Title | Authors / Editors | Date |
unige:55982 |
A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene |
Ferreiro-girani, Ana; Monnier, Nicole; Romero, Norma B; Leroy, Jean-Paul; ... Guicheney, Pascale |
2002 |
unige:13254 |
Absence of the hemochromatosis gene Cys282Tyr mutation in three ethnic groups from Algeria (Mzab), Ethiopia, and Senegal |
Roth, M.; Giraldo, P.; Hariti, G.; Poloni, Estella S.; ... Coppin, H. |
1997 |
unige:109700 |
Diversamente migranti. La mobilità italiana in Algeria |
Fois, Marisa |
2018 |
unige:126784 |
Gli italiani in Algeria: immigrati o colonizzatori? |
Fois, Marisa |
2019 |
unige:87882 |
Identity, Politics and Nation: Algerian Nationalism and the ‘Berberist Crisis' of 1949 |
Fois, Marisa |
2016 |
unige:118514 |
Switzerland, decolonisation, and migration: The case of the Association of swiss despoiled of Algeria or overseas possessions |
Fois, Marisa |
2019 |
unige:25700 |
War exposure, 5-HTTLPR genotype and lifetime risk of depression |
Artero, Sylvaine; Touchon, Jacques; Dupuy, Anne-Marie; Malafosse, Alain; Ritchie, Karen |
2011 |