E-LIB Suche - Ergebnisse für: Grosz, Zoltán

1

The improvement of motor symptoms in Huntington's disease d..:

Csehi, Reka ; Molnar, Viktor ; Fedor, Mariann...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

2

Genetic landscape of early-onset dementia in Hungary:

Csaban, Dora ; Illes, Anett ; Renata, Toth-Bencsik...
Neurological Sciences. 43 (2022) 9 - p. 5289-5300 , 2022

Link: https://doi.org/10.1007/..

3

Improving Mood and Cognitive Symptoms in Huntington's Disea..:

Molnar, Maria Judit ; Molnar, Viktor ; Fedor, Mariann...
Frontiers in Psychiatry. 12 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

4

A ritka betegségben szenvedő gyermekek átvezetése a felnőtt..:

Molnár, Mária Judit ; Cs. Sági, Judit ; Szabó, Léna.
Orvosi Hetilap. 163 (2022) 51 - p. 2021-2026 , 2022

Link: https://doi.org/10.1556/..

5

The Role of the Rare Variants in the Genes Encoding the Alp..:

Csaban, Dora ; Pentelenyi, Klara ; Toth-Bencsik, Renata...
Life. 11 (2021) 4 - p. 321 , 2021

Link: https://doi.org/10.3390/..

6

Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme A..:

Gal, Aniko ; Grosz, Zoltán ; Borsos, Beata...
Life. 11 (2021) 6 - p. 507 , 2021

Link: https://doi.org/10.3390/..

7

Efficacy of nusinersen in type 1, 2 and 3 spinal muscular a..:

Szabó, Léna ; Gergely, Anita ; Jakus, Rita...
European Journal of Paediatric Neurology. 27 (2020) - p. 37-42 , 2020

Link: https://doi.org/10.1016/..

8

The Challenge of Genetic Counselling in Early Onset Parkins..:

Molnar, Maria ; Balicza, Peter ; Csaban, Dora...
Neurology. 94 (2020) 15_supplement - p. , 2020

Link: https://doi.org/10.1212/..

9

The Role of Genetic Testing in the Clinical Practice and Re..:

Illés, Anett ; Csabán, Dóra ; Grosz, Zoltán...
Frontiers in Genetics. 10 (2019) - p. , 2019

Link: https://doi.org/10.3389/..

10

Broadening the phenotype of the TWNK gene associated Perrau..:

Fekete, Bálint ; Pentelényi, Klára ; Rudas, Gabor...
BMC Medical Genetics. 20 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..

11

Implementation of personalized medicine in Central-Eastern ..:

Balicza, Peter ; Terebessy, Andras ; Grosz, Zoltan...
EPMA Journal. 9 (2018) 1 - p. 103-112 , 2018

Link: https://doi.org/10.1007/..

12

NKX2-1 New Mutation Associated With Myoclonus, Dystonia, an..:

Balicza, Péter ; Grosz, Zoltán ; Molnár, Viktor...
Frontiers in Genetics. 9 (2018) - p. , 2018

Link: https://doi.org/10.3389/..

13

Genotypic and phenotypic spectrum of the most common causat..:

Milley, György Máté ; Varga, Edina Timea ; Grosz, Zoltán...
Neuromuscular Disorders. 28 (2018) 1 - p. 38-43 , 2018

Link: https://doi.org/10.1016/..

14

Genetic Background of the Hereditary Spastic Paraplegia Phe..:

Molnar, Maria ; Balicza, Peter ; Grosz, Zoltan...
Neurology. 86 (2016) 16_supplement - p. , 2016

Link: https://doi.org/10.1212/..

15

Three novel mutations and genetic epidemiology analysis of ..:

Milley, Gyorgy Mate ; Varga, Edina Timea ; Grosz, Zoltan...
Neuromuscular Disorders. 26 (2016) 10 - p. 706-711 , 2016

Link: https://doi.org/10.1016/..