| A novel mutation in PSEN1 (p. T119I) in an Argentine family with early-and late-onset Alzheimer's disease T Itzcovich, P Chrem-Méndez, S Vázquez, M Barbieri-Kennedy, M Niikado, ... Neurobiology of Aging 85, 155. e9-155. e12, 2020 | 23 | 2020 |
| Evaluation of cerebrospinal fluid neurofilament light chain as a routine biomarker in a memory clinic M Niikado, P Chrem-Méndez, T Itzcovich, M Barbieri-Kennedy, I Calandri, ... The Journals of Gerontology: Series A 74 (4), 442-445, 2019 | 23 | 2019 |
| Perry disease in an Argentine family due to the DCTN1 p. G67D variant E Silva, T Itzcovich, M Niikado, A Caride, E Fernández, JC Vázquez, ... Parkinsonism & related disorders 97, 63-64, 2022 | 3 | 2022 |
| Generation of a human induced pluripotent stem cell line from a familial Alzheimer's disease PSEN1 T119I patient L Isaja, MS Rodríguez-Varela, M Marazita, S Mucci, T Itzcovich, ... Stem Cell Research 53, 102325, 2021 | 3 | 2021 |
| Progranulin c. 709‐1g> a variant in an argentine family with behavioral variant frontotemporal dementia and semantic primary progressive aphasia M Niikado, I Calandri, M Barbieri Kennedy, T Itzcovich, HE Martinetto, ... Wiley, 2019 | 1 | 2019 |
| P4‐100: PSEN1 MUTATION (L166V) IN AN ARGENTINE CASE WITH FAMILIAL EARLY ONSET ALZHEIMER'S DISEASE AND AMYLOID ANGIOPATHY MB Kennedy, P Chrem, M Riudavets, T Itzcovich, M Niikado, H Martinetto, ... Alzheimer's & Dementia 15, P1313-P1313, 2019 | | 2019 |
| PSEN1 mutation (l166v) in an argentine case with familial early onset alzheimer's disease and amyloid angiopathy M Barbieri Kennedy, PA Chrem Mendez, MA Riudavets, T Itzcovich, ... Elsevier, 2019 | | 2019 |
| Rare missense variants in TREM2 and ABCA7 in a patient with sporadic early‐onset alzheimer's disease T Itzcovich, PA Chrem Mendez, S Vazquez, M Barbieri Kennedy, ... Wiley, 2019 | | 2019 |
