Rezultati - Latsoudis, Helen

Novel mutation of the PRNP gene of a clinical CJD case od Kotta, Konstantia, Paspaltsis, Ioannis, Bostantjopoulou, Sevasti, Latsoudis, Helen, Plaitakis, Andreas, Kazis, Dimitrios, Collinge, John, Sklaviadis, Theodoros

Polni tekst Polni tekst Polni tekst

Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene od Drosataki, Eleni, Maragkou, Sevasti, Dermitzaki, Kleio, Stavrakaki, Ioanna, Lygerou, Dimitra, Latsoudis, Helen, Pleros, Christos, Petrakis, Ioannis, Zaganas, Ioannis, Stylianou, Kostas

Polni tekst Polni tekst Polni tekst

Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset od Plaitakis, Andreas, Latsoudis, Helen, Kanavouras, Konstantinos, Ritz, Beate, Bronstein, Jeff M, Skoula, Irene, Mastorodemos, Vasileios, Papapetropoulos, Spyridon, Borompokas, Nikolas, Zaganas, Ioannis, Xiromerisiou, Georgia, Hadjigeorgiou, George M, Spanaki, Cleanthe

Polni tekst Polni tekst Polni tekst

Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism od Ross, Owen A., Spanaki, Cleanthe, Griffith, Alida, Lin, Chin-Hsien, Kachergus, Jennifer, Haugarvoll, Kristoffer, Latsoudis, Helen, Plaitakis, Andreas, Ferreira, Joaquim J., Sampaio, Cristina, Bonifati, Vincenzo, Wu, Ruey-Meei, Zabetian, Cyrus P., Farrer, Matthew J.

Polni tekst Polni tekst Polni tekst

Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients od Zaganas, Ioannis, Mastorodemos, Vasilios, Spilioti, Martha, Mathioudakis, Lambros, Latsoudis, Helen, Michaelidou, Kleita, Kotzamani, Dimitra, Notas, Konstantinos, Dimitrakopoulos, Konstantinos, Skoula, Irene, Ioannidis, Stefanos, Klothaki, Eirini, Erimaki, Sophia, Stavropoulos, Georgios, Vassilikos, Vassilios, Amoiridis, Georgios, Efthimiadis, Georgios, Evangeliou, Athanasios, Mitsias, Panayiotis

Polni tekst Polni tekst Polni tekst