Background: Malnutrition is a lack of proper nutrition associated with different chronic diseases, comorbidities, frailty, and a higher prevalence of morbidity and mortality. Aim: The aim of the study was to determine the most appropriate items that reflect nutrition status in this population group and incorporate them into the nutrition risk screening and malnutrition assessment tool. Methods: A cross-sectional validation study was conducted in Bosnia and Herzegovina among 300 individuals older than 65 years. An eight-step approach that included correspondence analysis, generation of the pool item, content validity, internal consistency, construct validity, criterion validity, face validity, and reliability was performed. Results: Correspondence analyses were performed using the contingency table's low-dimensional graphical representation of the rows and columns. After identifying nutrition status assessment-related topics via correspondence analyses, a literature review was performed to determine additional items. The assessment tool's accuracy was measured against clinical judgement as a reference standard. To test face validity of the tool, cognitive interviewing was used. Responses were analyzed and necessary changes were made. The final version of the tool included 14 items. Possible range score on the assessment tool was 0-21. Lower scores indicated nutrition risk. The screening and assessment tool showed acceptable validity and internal consistency.

• MeSH
• hodnocení rizik metody   MeSH
• hodnocení stavu výživy * MeSH
• lidé MeSH
• nutriční stav MeSH
• podvýživa prevence a kontrola   MeSH
• průřezové studie MeSH
• senioři * MeSH
• statistika jako téma MeSH
• Check Tag
• lidé MeSH
• mužské pohlaví MeSH
• senioři * MeSH
• ženské pohlaví MeSH
• Publikační typ
• validační studie MeSH
• Geografické názvy
• Bosna a Hercegovina MeSH

Poruchy autistického spektra jsou pervazivní vývojové poruchy. Ovlivněny jsou tak v podstatě všechny složky vývoje již od raného věku. Rodiče si všímají odlišností ze- jména v sociální oblasti, děti často nesdílejí pozornost, nekomunikují a nesdělují svoje potřeby a přání. Již ve věku 18 měsíců se dělá screening M-CHAT-R, který může zachytit nápadnosti ve vývoji (možné neurovývojové poruchy) a pediatr může rodiče směřovat k odborníkům – klinickým psychologům zaměřujícím se na práci s dětmi s PAS (poruchou autistického spektra), pedopsychiatrovi, dětskému neurologovi či specializovanému klinickému logopedovi. V tomto článku vám představíme kazuistiku s diferenciální diagnostikou odlišující PAS od dalších vývojových poruch (zejména vývojové dysfázie) a zaměřenou na stanovení stupně symptomů v kontextu poruch autistického spektra. Je to jedna z typických diferenciálních diagnostik, které na Soukromé klinice LOGO, s.r.o. děláme.

Autism Spectrum Disorders are pervasive developmental disorders. This means that they influence almost all areas of early development. Parents can see differences mainly in the social area. Children with ASD do not share activities, do not communicate their needs and wishes. At the age of 18 months, parents fill in the M-CHAT-R screening, which is sensitive to possible neurodevelopmental problems. A paediatrician can send the child to specialists in ASD diagnosis - clinical psychologist, child psychiatrist, neurologist and clinical speech therapist. In this article, we introduce you to a case study with differential diagnoses, showing the differences between Autism Spectrum Disorders and other developmental diseases (especially specific developmental disorders of speech and language). The focus is on the determination of the autistic symptoms level. This is one of the typical differential diagnoses we carry out at LOGO Clinic.

• MeSH
• kognitivní dysfunkce diagnóza   MeSH
• komunikační poruchy diagnóza   MeSH
• lidé MeSH
• poruchy autistického spektra * diagnóza   psychologie   MeSH
• předškolní dítě MeSH
• psychologické testy MeSH
• stereotypní chování MeSH
• vývojové poruchy řeči diagnóza   MeSH
• vývojové poruchy u dětí diagnóza   MeSH
• Check Tag
• lidé MeSH
• mužské pohlaví MeSH
• předškolní dítě MeSH
• Publikační typ
• kazuistiky MeSH

Cíl: Montrealský kognitivní test (MoCA) je jednou z nejpoužívanějších screeningových zkoušek kognice u dospělých osob, pro něž existují normy pro českou populaci. Varianta MoCA-22, která je určena pro osoby s poruchami zraku či imobilitou horních končetin, se dá administrovat i po telefonu. Tato studie přináší české normy MoCA-22. Materiál a metodika: Soubor (n = 1 049) se skládá z účastníků čtyř studií provedených v ČR. Zařazeny byly osoby ve věku 19–98 let, bez neurodegenerativního, psychiatrického či jiného závažného onemocnění. Data pro MoCA-22 byla odvozena z dat získaných vyšetřením standardní verzí MoCA. V souladu se zavedenou klinickou praxí i statistickou analýzou jsou soubor a odvozené normy rozděleny na tři věkové kategorie: 19–50 let, 51–74 let, 75 a více let. Výsledky: Pro výše uvedené věkové kategorie dále rozdělené dle dosaženého vzdělání (nižší, vyšší) předkládáme průměrné skóry i odhadované percentilové hranice. Výkon v MoCA-22 je ovlivněn dosaženým vzděláním a věkem, ale nikoli pohlavím. Pro úpravu výsledků dle demografických faktorů proto poskytujeme i regresní rovnici. Závěr: Normativní údaje pro MoCA-22 rozšíří klinické instrumentárium v Česku a umožní adekvátní screening kognice u osob, jež jsou zdravotním stavem limitovány při využití standardních metod.

Aim: The Montreal Cognitive Assessment (MoCA) is one of the most widely used cognitive screening tests in adults with reference standards for the Czech population. The MoCA-22 variant is designed for individuals with visual impairment or upper limb immobility and can be administered over the telephone. This study presents the Czech MoCA-22 normative standards. Materials and methods: The sample (N = 1,049) consists of participants from four studies conducted in the Czech Republic. The subjects included were aged 19–98 years, and were without neurodegenerative, psychiatric, or other serious illness. Data for the MoCA-22 were derived from data obtained by the standard version of MoCA. Following established clinical practice and statistical analysis, the population and derived norms are divided into three age categories: 19–50 years, 51–74 years, and 75 years and older. Results: For these age categories above, which were further subdivided by educational status (lower, higher), we present mean scores and estimated percentile thresholds. Performance in the MoCA-22 is affected by demoraphic factors, such as educational status and age but not sex, as reflected by the regression equation. Conclusions: Normative data for MoCA-22 will complement the clinical armamentarium in Czechia and allow adequate cognitive screening in people whose health status limits them when using standard methods.

• Klíčová slova
• Montrealský kognitivní test (MoCA),
• MeSH
• klinická studie jako téma MeSH
• kognitivní poruchy diagnóza   MeSH
• lidé MeSH
• neuropsychologické testy * normy   MeSH
• osoby upoutané na lůžko MeSH
• telefon MeSH
• telemedicína MeSH
• zrakově postižení MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• práce podpořená grantem MeSH

The disease currently known as frontotemporal dementia (FTD) has undergone a complex evolution from its first description by Arnold Pick and later by Alois Alzheimer, through the first clinicopathological criteria introduced by David Neary and David Mann, to its current nomenclatural perception as a complex clinicopathological entity. Currently, Frontotemporal lobar degeneration is viewed as a heterogeneous syndrome caused by progressive degeneration of the frontal and temporal lobes of the brain. Clinically, it can manifest as three syndromes of frontotemporal dementia (behavioral variant of FTD, progressive non-fluent aphasia and semantic dementia) but also as so-called "overlap" syndromes involving corticobasal degeneration and progressive supranuclear palsy. Its prevalence is about 10 % among all dementias and 40 % among dementias with onset between 45 and 65 years of age. The clinical manifestation of the different subtypes varies, the common denominator being behavioral disturbances and impairment of fatic, gnostic and executive functions. Mnestic and visuo-spatial functions, although preserved for a relatively long time, are superimposed by personality disintegration, fatic, gnostic and executive dysfunction. Compared with Alzheimer's disease, it generally has an earlier age of onset, a more rapid course and more devastating impairment of individual cognitive domains. FTD has a heritability of more than 30 % according to current knowledge. The main genes involved are MAPT, C9orf72 and GRN. More rarely affected genes are VCP, TDP-43, FUS and CHMP2B. In our article, we focus on the genetics of FTD and the clinic-genetic-pathological correlations. We also aim to provide a plastic picture of how individual mutations affect the molecular mechanisms of neurodegeneration.

• MeSH
• epigeneze genetická genetika   MeSH
• frontotemporální demence * diagnóza   genetika   klasifikace   MeSH
• genetické testování metody   MeSH
• lidé MeSH
• primární progresivní nonfluentní afázie diagnóza   genetika   MeSH
• progranuliny genetika   MeSH
• proteiny tau genetika   MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• přehledy MeSH

BACKGROUND: The rapid increase in cannabis use during pregnancy-up by 170 % between 2009 and 2016-raises pressing concerns about its effects on fetal health, particularly on the delicate monoamine system within the fetoplacental unit, which is crucial for placental function and neurodevelopment. OBJECTIVE: This systematic review explores the impact of prenatal cannabinoid exposure on the monoamine system within the fetoplacental unit, with a focus on its implications for fetal development through the lens of the Developmental Origins of Health and Disease (DOHaD) framework. METHODS: A comprehensive search across multiple databases initially retrieved 18,252 papers. After rigorous screening, only 16 animal studies and 4 human studies met the inclusion criteria. Findings were synthesized to evaluate the effects of prenatal cannabis exposure on neurotransmitter regulation, receptor function, and gene expression. RESULTS: Although no studies directly addressed the monoamine system in the placenta, animal models revealed significant disruptions in neurotransmitter regulation and neurodevelopmental changes following prenatal cannabis exposure. Human studies suggested potential cognitive and behavioral risks for offspring exposed in utero. CONCLUSION: This review exposes a critical gap in the literature on cannabis' effects on the placental monoamine system. While evidence points to notable neurodevelopmental risks, the scarcity of focused research underscores the need for further investigation to fully understand the implications of prenatal cannabis exposure.

• MeSH
• biogenní monoaminy metabolismus   MeSH
• kanabinoidy * metabolismus   MeSH
• lidé MeSH
• placenta * metabolismus   účinky léků   MeSH
• těhotenství MeSH
• vývoj plodu účinky léků   MeSH
• zpožděný efekt prenatální expozice * metabolismus   MeSH
• zvířata MeSH
• Check Tag
• lidé MeSH
• těhotenství MeSH
• ženské pohlaví MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• přehledy MeSH
• systematický přehled MeSH

Kognitívna porucha (KP) po ischemickej cievnej mozgovej príhode (CMP) je častým fenoménom. U niektorých pacientov môže KP pretrvávať aj dlhý čas po prekonanej CMP, čo sa v anglickej literatúre označuje ako PCSI - post stroke cognitive impairment. Ide o osobitnú nozologickú jednotku, ktorú je potrebné začať diagnostikovať už počas hospitalizácie, no definitívnu diagnózu je možné vykonať až následne kontrolným vyšetrením kognitívnych funkcií s odstupom šesť mesiacov od CMP. Článok prináša aktuálny prehľad o diagnostike, predikcii a terapii PSCI ako osobitnej nozologickej jednotky.

Cognitive impairment (CI) after stroke is a frequent phenomenon. In some patients, CI can persist for a long time after overcoming stroke, which is referred to in the English literature as PCSI - post stroke cognitive impairment. It is a special nosological entity that needs to be diagnosed already during hospitalization, but a definitive diagnosis can only be made subsequently by a control examination of cognitive functions six months after stroke. The following article provides an up-to-date overview of the diagnosis, prediction and therapy of PSCI as a special nosological unit.

• MeSH
• cévní mozková příhoda * diagnóza   komplikace   patofyziologie   MeSH
• demence diagnóza   etiologie   MeSH
• diferenciální diagnóza MeSH
• kognitivní dysfunkce * diagnóza   etiologie   farmakoterapie   patofyziologie   MeSH
• lidé MeSH
• management nemoci MeSH
• neurozobrazování klasifikace   metody   MeSH
• testy pro posouzení mentálních funkcí a demence MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• práce podpořená grantem MeSH
• přehledy MeSH

BACKGROUND: Individuals with adverse pregnancy outcomes have an increased risk of cerebrovascular disease, but the association between adverse pregnancy outcomes and cognitive impairment and dementia is less well established. We aimed to synthesise, combine, and assess the growing body of data examining the associations between adverse pregnancy outcomes and mild cognitive impairment and dementia in parous women. METHODS: In this systematic review and meta-analysis, we searched PubMed (MEDLINE), Web of Science, and Embase from database inception up to July 18, 2024, with no language restrictions, for observational studies or clinical trials that reported mild cognitive impairment or dementia as outcomes and included female individuals or women who had an adverse pregnancy outcome, including hypertensive disorders of pregnancy, gestational diabetes, stillbirth, fetal growth restriction, preterm birth, or placental abruption. We excluded studies of men, nulliparous women, women with pre-pregnancy conditions associated with impaired cognition, and studies examining cognitive impairment within 6 months of pregnancy. Database searches were supplemented by manual review of the reference lists of included studies. If studies met eligibility criteria but did not have sufficient data for meta-analysis (ie, did not report a summary statistic or a hazard ratio [HR] for outcome estimation), they were included in the systematic review and excluded from the meta-analysis. After removing duplicates, two investigators independently screened titles and abstracts using Covidence software, with potentially eligible studies undergoing full-text review by the same reviewers, with further review by a third reviewer and disagreements resolved by discussion and group consensus. Study quality was assessed and summary statistics extracted by two reviewers independently. The primary outcomes of our study were mild cognitive impairment, all-cause dementia, Alzheimer's disease, and vascular dementia. Heterogeneity was measured using the Q test and I2 statistic, and we used random-effects models with inverse-variance weighting to assess the association between adverse pregnancy outcome and primary outcomes with sufficient meta-analysable data via pooled adjusted HRs and 95% CIs. The study protocol was registered with PROSPERO, CRD42023453511. FINDINGS: Of 11 251 publications identified, 15 studies (including 7 347 202 participants) met inclusion criteria for the systematic review, and 11 studies (6 263 431 participants) had sufficient data for meta-analysis. A history of any adverse pregnancy outcome was associated with higher risk of all-cause dementia (adjusted HR 1·32 [95% CI 1·17-1·49]; I2= 80%), Alzheimer's disease (1·26 [1·04-1·53]; I2=63%), and vascular dementia (1·94 [1·70-2·21]; I2=0%). A history of any hypertensive disorder of pregnancy was significantly associated with all-cause dementia (1·32 [1·11-1·57]; I2=74%) and vascular dementia (1·78 [1·46-2·17]; I2=0%), but not Alzheimer's disease (1·24 [0·98-1·57]; I2=66%). Stillbirth was not significantly associated with higher risk of all-cause dementia (1·26 [95% CI 0·93-1·71]; I2=62%). In individual studies, similar effect directions were observed for preterm birth and fetal growth restriction, but data were insufficient for meta-analysis. INTERPRETATION: Given their increased risk of dementia, women with a history of adverse pregnancy outcomes should be evaluated for additional dementia risk factors and monitored closely for any signs of cognitive decline. Furthermore, to obtain more reliable findings, future studies should measure both exposures and outcomes prospectively and objectively. FUNDING: National Institutes of Health, National Institute of Neurological Disorders and Stroke, National Institute on Aging, and National Heart, Lung and Blood Institute.

• MeSH
• demence * epidemiologie   psychologie   MeSH
• kognitivní dysfunkce * epidemiologie   psychologie   MeSH
• lidé MeSH
• těhotenství MeSH
• výsledek těhotenství * epidemiologie   psychologie   MeSH
• Check Tag
• lidé MeSH
• těhotenství MeSH
• ženské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH
• metaanalýza MeSH
• systematický přehled MeSH

Cíl: Cílem výzkumu bylo posouzení kognitivních funkcí u seniorů v domovech pro seniory prostřednictvím standardizovaných testů – Montrealský kognitivní test (MoCA) a Pojmenování obrázků a jejich vybavení (POBAV). Metodika: Výzkum zahrnoval 76 klientů ze tří domovů pro seniory. Hodnocení kognitivních funkcí bylo provedeno standardizovanými testy MoCA a POBAV (ježková verze). Statistické zpracování bylo provedeno na hladině významnosti a = 0,05. Výsledky: Průměrný skór v MoCA byl 20 bodů, průměrné výsledky u POBAV byly 3/5. Normální kognitivní stav mělo dle MoCA (při hraničním skóre ≤ 24 bodů) 21 % seniorů a dle POBAV dosáhlo normy 25 % dotázaných. U obou testů MoCA a POBAV nebyl zjištěn statisticky významný rozdíl v úrovni kognitivních funkcí v závislosti na pohlaví, vzdělání ani na délce pobytu v domově pro seniory. Byl však prokázán statisticky významný rozdíl v úrovni kognitivních funkcí v závislosti na věku, kognitivním tréninku i na kondičním cvičení a bylo zjištěno, že osoby absolvující kognitivní trénink a kondiční cvičení dosahují v obou testech lepších výsledků. Byla potvrzena shoda v detekci kognitivní poruchy pomocí MoCA a POBAV v 97 % případů. Mezi testy MoCA a POBAV byla zjištěna významná korelace. Pearsonův korelační koeficient mezi testy MoCA a POBAV – Chyby v pojmenování obrázků, znázorňuje negativní korelaci –0,625 (p < 0,001). Pearsonův korelační koeficient mezi testy MoCA a POBAV – Správně vybavené obrázky, představuje pozitivní korelaci 0,86 (p < 0,001). Závěr: Časný záchyt a monitoring kognitivního deficitu pomocí screeningových testů by měly být nedílnou součástí při poskytování dlouhodobé péče u seniorů. Test POBAV je vhodnou volbou pro včasný záchyt kognitivního deficitu a může sloužit jako srovnatelná alternativa testu MoCA.

Aim: The aim of the research was to assess cognitive functions of elderly people in nursing homes using standardized tests – Montreal Cognitive Assessment (MoCA) and Picture Naming and Immediate Recall (PICNIR). Methodology: The study included 76 clients from three nursing homes. The assessment of cognitive functions was carried out using the standardized tests MoCA and PICNIR (Hedgehog Version). Statistical processing was performed at a significance level of α = 0.05. Results: The average score in MoCA was 20 points, and the average results in PICNIR were 3/5. According to MoCA (with a threshold score of ≤ 24 points), 21% of elderly people had a normal cognitive state, and according to PICNIR, 25% of respondents reached the norm. No statistically significant difference in the level of cognitive functions was found in either the MoCA or PICNIR tests in relation to sex, education, or length of stay in the nursing home. However, a statistically significant difference in the level of cognitive functions was demonstrated in relation to age, cognitive training, and physical exercise, and it was found that individuals undergoing cognitive training and physical exercise achieved better results in both tests. A concordance in the detection of cognitive impairment using MoCA and PICNIR was confirmed in 97% of cases. A significant correlation was found between the MoCA and PICNIR tests. The Pearson correlation coefficient between MoCA and PICNIR – Mistakes in Naming demonstrated a negative correlation of –0.625 (P < 0.001). The Pearson correlation coefficient between MoCA and PICNIR – Correctly Recalled Picture Names indicated a positive correlation of 0.86 (P < 0.001). Conclusion: Early detection and monitoring of cognitive deficits using screening tests should be an integral part of providing long-term care for elderly people. The PICNIR test is a suitable choice for early detection of cognitive deficits and can serve as a comparable alternative to the MoCA test.

• MeSH
• domovy pro seniory statistika a číselné údaje   MeSH
• epidemiologické studie MeSH
• kognice MeSH
• korelace dat MeSH
• lidé MeSH
• neurokognitivní poruchy * diagnóza   epidemiologie   MeSH
• neuropsychologické testy * statistika a číselné údaje   MeSH
• senioři nad 80 let MeSH
• senioři MeSH
• testy pro posouzení mentálních funkcí a demence statistika a číselné údaje   MeSH
• Check Tag
• lidé MeSH
• mužské pohlaví MeSH
• senioři nad 80 let MeSH
• senioři MeSH
• ženské pohlaví MeSH

Neuropsychiatric symptoms (NPS) are common in hereditary ataxias as a part of the cerebellar cognitive affective syndrome. In Friedreich ataxia (FRDA), one of the most common hereditary ataxias, depressive symptoms were previously reported, but little is known about other NPS. We aimed to study the presence and severity of a broad range of NPS in individuals with FRDA and assess the relationship between the NPS and the disease severity, cognition, and quality of life and to examine the concordance between the NPS reported by the patients and by their informants. Mild Behavioral Impairment Checklist (MBI-C), a questionnaire designed for screening NPS in the early stages of neurodegenerative diseases, was administered to informants of individuals with FRDA and healthy controls and to people with FRDA themselves. Compared to healthy controls, patients with FRDA scored significantly higher in the total MBI-C score, emotion dysregulation domain (corresponding to depression and anxiety), and decreased motivation domain. When assessed by caregiver, the total MBI-C score and several NPS domains correlated with activities of daily living. Only psychotic symptoms were related to ataxia severity and general cognition. When endorsed by patients, only the relation between few MBI-C domains and quality of life was observed. We found slight to moderate agreement between informant-rated and patient-rated scores. NPS, particularly emotion dysregulation and decreased motivation, are common and clinically relevant in FRDA and should receive more attention due to their potential impact on quality of life and the possibility of therapeutic intervention.

• MeSH
• činnosti denního života MeSH
• deprese etiologie   MeSH
• dospělí MeSH
• Friedreichova ataxie * psychologie   komplikace   MeSH
• kognice MeSH
• kvalita života * MeSH
• lidé středního věku MeSH
• lidé MeSH
• mladý dospělý MeSH
• průzkumy a dotazníky MeSH
• studie případů a kontrol MeSH
• stupeň závažnosti nemoci MeSH
• úzkost MeSH
• Check Tag
• dospělí MeSH
• lidé středního věku MeSH
• lidé MeSH
• mladý dospělý MeSH
• mužské pohlaví MeSH
• ženské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH

BACKGROUND: The spread of tau pathology closely correlates with the disease course and cognitive decline in Alzheimer's disease (AD). Tau-targeting immunotherapies are being developed to stop the spread of tau pathology and thus halt disease progression. In this post hoc analysis of the ADAMANT clinical trial, we examined the performance of AADvac1, an active immunotherapy targeting the microtubule-binding region (MTBR) of tau, in a subgroup of participants with elevated plasma p-tau217, indicating AD-related neuropathological changes. METHODS: ADAMANT was a 24-month, randomized, placebo-controlled, parallel-group, double-blinded, multicenter, phase 2 clinical trial in subjects with mild AD. The trial participants were randomized 3:2 to receive six doses of AADvac1 or placebo at 4-week intervals, followed by five booster doses at 14-week intervals. The primary outcome was safety. The secondary outcomes were the Clinical Dementia Rating-Sum of Boxes (CDR-SB), the Alzheimer's Disease Cooperative Study - Activities of Daily Living score for Mild Cognitive Impairment 18-item version (ADCS-ADL-MCI-18), and immunogenicity. Volumetric MRI, plasma neurofilament light (NfL), and glial fibrillary acidic protein (GFAP) were exploratory outcomes. The inclusion criterion for this post-hoc analysis was a baseline plasma p-tau217 level above the cutoff for AD. RESULTS: Among 196 ADAMANT participants, 137 were positive for plasma p-tau217 (mean age 71.4 years, 59% women). AADvac1 was safe and well tolerated in this subgroup. AADvac1 reduced the rate of accumulation of log-plasma NfL by 56% and that of GFAP by 73%. The treatment differences in the CDR-SB and ADCS-ADL-MCI-18 scores favored AADvac1 but were not statistically significant. AADvac1 had no effect on whole-brain volume but nonsignificantly reduced the loss of brain cortical tissue in several regions. Importantly, the impact on the study outcomes was more pronounced in participants with higher anti-tau antibody levels. CONCLUSIONS: These results suggest that AADvac1 tau immunotherapy can reduce plasma biomarkers of neurodegeneration and neuroinflammation. These findings and possible observations on brain atrophy and cognition are hypothesis-generating and warrant further evaluation in a larger clinical trial. TRIAL REGISTRATION: EudraCT 2015-000630-30 (primary) and NCT02579252.

• MeSH
• aktivní imunoterapie metody   MeSH
• Alzheimerova nemoc * krev   terapie   imunologie   MeSH
• biologické markery krev   MeSH
• dvojitá slepá metoda MeSH
• lidé středního věku MeSH
• lidé MeSH
• proteiny tau * krev   MeSH
• senioři nad 80 let MeSH
• senioři MeSH
• testy pro posouzení mentálních funkcí a demence MeSH
• výsledek terapie MeSH
• Check Tag
• lidé středního věku MeSH
• lidé MeSH
• mužské pohlaví MeSH
• senioři nad 80 let MeSH
• senioři MeSH
• ženské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH
• klinické zkoušky, fáze II MeSH
• multicentrická studie MeSH
• randomizované kontrolované studie MeSH