Zádori, Dénes and Füvesi, Judit and Timár, Erzsébet and Horváth, Emese and Bencsik, Renáta and Szepfalusi, Noémi and Must, Anita and Vécsei, László and Molnár, Mária Judit and Klivényi, Péter (2017) The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family with Alzheimer Disease : A Phenomenological Study. ALZHEIMER DISEASE & ASSOCIATED DISORDERS, 31 (4). pp. 343-345. ISSN 0893-0341
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Official URL: https://doi.org/10.1097/WAD.0000000000000206
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | short term memory; seizure; priority journal; physical examination; phenomenology; nuclear magnetic resonance imaging; myoclonus; missense mutation; mini mental state examination; Middle Aged; mental deterioration; memory disorder; MEMORY; medical history; language disability; immobility; Hungarian (citizen); human; genetic screening; FRACTURE; Female; family history; dysphasia; disorders of higher cerebral function; clinical article; case report; ARTICLE; apraxia of speech; Adult; Val717Phe mutation; PHENOTYPE; HEREDITARY; AMYLOID PRECURSOR PROTEIN; Alzheimer disease |
| Subjects: | R Medicine / orvostudomány > RC Internal medicine / belgyógyászat > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry / idegkórtan, neurológia, pszichiátria |
| SWORD Depositor: | MTMT SWORD |
| Depositing User: | MTMT SWORD |
| Date Deposited: | 17 Sep 2018 07:50 |
| Last Modified: | 17 Sep 2018 07:50 |
| URI: | http://real.mtak.hu/id/eprint/84146 |
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