Suchergebnisse - "Csabán, Dóra"

PubPharm (16)

1

GBA-associated Parkinson's disease in Hungary : clinical features and genetic insights

enthalten in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2023

von Szlepák, T. | Kossev, A. | Csabán, D. | +7

2

Genetic landscape of early-onset dementia in Hungary

enthalten in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2022

von Csaban, D. | Illes, A. | Renata, T. | +9

3

Genetic landscape of early-onset dementia in Hungary

enthalten in: Neurological sciences | 2022

von Csaban, D. | Illes, A. | Renata, T. | +9

4

Genetic landscape of early-onset dementia in Hungary

enthalten in: Neurological sciences | 2022

von Csaban, D. | Illes, A. | Renata, T. | +9

5

Genetic landscape of early-onset dementia in Hungary

enthalten in: Neurological sciences | 2022

von Csaban, D. | Illes, A. | Renata, T. | +9

6

Non-malignant, non-infectious lymphoproliferation : challenges in the diagnosis and treatment of autoimmune lymphoproliferative syndrome

enthalten in: Orvosi hetilap | 2022

von Molnár, E. | Kovács, G. | Varga, L. | +7

7

The Role of the Rare Variants in the Genes Encoding the Alpha-Ketoglutarate Dehydrogenase in Alzheimer's Disease

enthalten in: Life (Basel, Switzerland) | 2021

von Csaban, D. | Pentelenyi, K. | Toth-Bencsik, R. | +4

8

Positive association and future perspectives of mitochondrial DNA copy number and telomere length - a pilot twin study

enthalten in: Archives of medical science : AMS | 2021

von Melicher, D. | Illés, A. | Littvay, L. | +8

9

Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability

enthalten in: Neurology. Genetics | 2020

von Balicza, P. | Bencsik, R. | Lengyel, A. | +7

10

Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement

enthalten in: Orphanet journal of rare diseases | 2020

von Stengl, R. | Bors, A. | Ágg, B. | +10