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Publications

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

Export 7 results:
Author Title Type [ Year(Asc)]
Filters: Keyword is Siblings  [Clear All Filters]
2017
Sfontouris, I. A., Kolibianakis E. M., Lainas G. T., Petsas G. K., Tarlatzis B. C., & Lainas T. G. (2017).  Blastocyst Development in a Single Medium Compared to Sequential Media: A Prospective Study With Sibling Oocytes.. Reprod Sci. 24(9), 1312-1318.
Sfontouris, I. A., Kolibianakis E. M., Lainas G. T., Venetis C. A., Petsas G. K., Tarlatzis B. C., et al. (2017).  Blastocyst utilization rates after continuous culture in two commercial single-step media: a prospective randomized study with sibling oocytes.. J Assist Reprod Genet. 34(10), 1377-1383.
Kimiskidis, V. K., Papaliagkas V., Papagiannopoulos S., Zafeiriou D., Kazis D., Tsatsali-Foroglou E., et al. (2017).  Investigation of the motor system in two siblings with Canavan's disease: a combined transcranial magnetic stimulation (TMS) - diffusion tensor imaging (DTI) study.. Metab Brain Dis. 32(2), 307-310.
Christoforidis, A., Skordis N., Fanis P., Dimitriadou M., Sevastidou M., Phelan M. M., et al. (2017).  A novel MKRN3 nonsense mutation causing familial central precocious puberty.. Endocrine. 56(2), 446-449.
Pavlidou, E., Ramachandran V., Govender V., Wilson C., Das R., Vlachou V., et al. (2017).  A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus-Merzbacher disease: A new MRI finding.. Brain Dev. 39(3), 271-274.
2015
Kostopoulos, I. V., Tsakiridou A. A., Pavlidis D., Megalakaki A., & Papadhimitriou S. I. (2015).  Familial chronic lymphocytic leukemia in two siblings with ATM/13q14 deletion and a similar pattern of clonal evolution.. Blood Cancer J. 5, e322.
2012
Vakalopoulos, I., Kampantais S., Dimopoulos P., Papastavros C., & Katsikas V. (2012).  Treatment of obstructive uropathy in one of three young brothers suffering from Gorlin-Cohen syndrome: a case report.. BMC Urol. 12, 2.

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