Your search returned 89 results.

Results
	41.	Implementation of personalized medicine in Central-Eastern Europe: pitfalls and potentials based on citizen's attitude. [electronic resource] by Balicza, Peter Terebessy, Andras Grosz, Zoltan Varga, Noemi Agnes Gal, Aniko Fekete, Balint Andras Molnar, Maria Judit Publication details: The EPMA journal Mar 2018 In: The EPMA journal vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	[Internet-based biobank-registers in Hungary]. [electronic resource] by Vásárhelyi, Barna Bencsik, Péter Szmolenszky, Agnes Molnár, Mária Judit Gyorffy, Balázs Kosztolányi, György Tulassay, Tivadar Falus, András Producer: 20070807 In: Orvosi hetilap vol. 148 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Localization of SUCLA2 and SUCLG2 subunits of succinyl CoA ligase within the cerebral cortex suggests the absence of matrix substrate-level phosphorylation in glial cells of the human brain. [electronic resource] by Dobolyi, Arpád Bagó, Attila G Gál, Aniko Molnár, Mária J Palkovits, Miklós Adam-Vizi, Vera Chinopoulos, Christos Producer: 20151026 In: Journal of bioenergetics and biomembranes vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	How bioinformatics influences health informatics: usage of biomolecular sequences, expression profiles and automated microscopic image analyses for clinical needs and public health. [electronic resource] by Kuznetsov, Vladimir Lee, Hwee Kuan Maurer-Stroh, Sebastian Molnár, Maria Judit Pongor, Sandor Eisenhaber, Birgit Eisenhaber, Frank Producer: 20150331 In: Health information science and systems vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	[The absence of the common LRRK2 G2019S mutation in 120 young onset Hungarian Parkinon's disease patients]. [electronic resource] by Balicza, Péter Bereznai, Benjamin Takáts, Annamária Klivényi, Péter Dibó, György Hidasi, Eszter Balogh, István Molnár, Mária Judit Producer: 20121113 In: Ideggyogyaszati szemle vol. 65 Availability: No items available. Save to lists Add to cart (remove)
	46.	Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene [electronic resource] by Illés, Anett Balicza, Péter Gál, Anikó Pentelényi, Klára Csabán, Dóra Gézsi, András Molnár, Viktor Molnár, Mária Judit Producer: 20200526 In: Orvosi hetilap vol. 161 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation. [electronic resource] by Reményi, Viktória Inczédy-Farkas, Gabriella Gál, Anikó Bereznai, Benjamin Pál, Zsuzsanna Karcagi, Veronica Mechler, Ferenc Molnár, Mária Judit Producer: 20150401 In: Ideggyogyaszati szemle vol. 67 Availability: No items available. Save to lists Add to cart (remove)
	48.	Psychiatric symptoms of patients with primary mitochondrial DNA disorders. [electronic resource] by Inczedy-Farkas, Gabriella Remenyi, Viktoria Gal, Aniko Varga, Zsofia Balla, Petra Udvardy-Meszaros, Agnes Bereznai, Benjamin Molnar, Maria Judit Producer: 20120809 In: Behavioral and brain functions : BBF vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Validation of the Hungarian translation of Hospital Anxiety and Depression Scale. [electronic resource] by Muszbek, Katalin Szekely, Anna Balogh, Eva Mária Molnár, Mária Rohánszky, Magdolna Ruzsa, Agnes Varga, Katalin Szöllosi, Melinda Vadász, Piroska Producer: 20060804 In: Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	[Etiological factors of sensorineural hearing loss in children after cochlear implantation]. [electronic resource] by Kecskeméti, Nóra Gáborján, Anita Szőnyi, Magdolna Küstel, Marianna Baranyi, Ildikó Molnár, Mária Judit Tamás, László Gál, Anikó Szirmai, Ágnes Producer: 20191024 In: Orvosi hetilap vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population. [electronic resource] by Pál, Zsuzsanna Varga, Zsófia Semsei, Ágnes Reményi, Viktória Rózsa, Csilla Falus, András Illes, Zsolt Buzás, Edit Irén Molnar, Maria Judit Producer: 20120813 In: Human immunology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Prospect of preimplantation genetic diagnosis for heritable mitochondrial DNA diseases. [electronic resource] by Dean, Nicola L Battersby, Brendan J Ao, Asangla Gosden, Roger G Tan, Seang Lin Shoubridge, Eric A Molnar, Maria Judit Producer: 20040528 In: Molecular human reproduction vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	The prion protein in human neuromuscular diseases. [electronic resource] by Kovács, Gábor G Kalev, Ognian Gelpi, Ellen Haberler, Christine Wanschitz, Julia Strohschneider, Michaela Molnár, Mária J László, Lajos Budka, Herbert Producer: 20041124 In: The Journal of pathology vol. 204 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy. [electronic resource] by Gal, Aniko Inczedy-Farkas, Gabriella Pal, Endre Remenyi, Viktoria Bereznai, Benjamin Geller, Laszlo Szelid, Zsolt Merkely, Bela Molnar, Maria Judit Producer: 20150821 In: Clinical neuropathology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement. [electronic resource] by Balicza, Péter Grosz, Zoltán Molnár, Viktor Illés, Anett Csabán, Dora Gézsi, Andras Dézsi, Lívia Zádori, Dénes Vécsei, László Molnár, Mária Judit Publication details: Frontiers in genetics 2018 In: Frontiers in genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	56.	The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials. [electronic resource] by Illés, Anett Csabán, Dóra Grosz, Zoltán Balicza, Péter Gézsi, András Molnár, Viktor Bencsik, Renáta Gál, Anikó Klivényi, Péter Molnar, Maria Judit Publication details: Frontiers in genetics 2019 In: Frontiers in genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	Exclusive neuronal expression of SUCLA2 in the human brain. [electronic resource] by Dobolyi, Arpád Ostergaard, Elsebet Bagó, Attila G Dóczi, Tamás Palkovits, Miklós Gál, Aniko Molnár, Mária J Adam-Vizi, Vera Chinopoulos, Christos Producer: 20150828 In: Brain structure & function vol. 220 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients. [electronic resource] by Milley, György Máté Varga, Edina Timea Grosz, Zoltán Nemes, Csilla Arányi, Zsuzsanna Boczán, Judit Diószeghy, Péter Molnár, Mária Judit Gál, Anikó Producer: 20191014 In: Neuromuscular disorders : NMD vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family With Alzheimer Disease: A Phenomenological Study. [electronic resource] by Zádori, Dénes Füvesi, Judit Timár, Erzsébet Horváth, Emese Bencsik, Renáta Szépfalusi, Noémi Must, Anita Vécsei, László Molnár, Mária Judit Klivényi, Péter Producer: 20190708 In: Alzheimer disease and associated disorders vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	Broadening the phenotype of the TWNK gene associated Perrault syndrome. [electronic resource] by Fekete, Bálint Pentelényi, Klára Rudas, Gabor Gál, Anikó Grosz, Zoltán Illés, Anett Idris, Jimoh Csukly, Gabor Domonkos, Andor Molnar, Maria Judit Producer: 20200214 In: BMC medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 89 results.