Lalatović, Staša

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  • Lalatović, Staša (2)
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Author's Bibliography

Stigma and its association with health-related quality of life in adults with epilepsy | Elsevier Enhanced Reader

Staša Lalatović; Maja Milovanović; Nadežda Krstić

TY  - JOUR
AU  - Staša Lalatović
AU  - Maja Milovanović
AU  - Nadežda Krstić
UR  - https://reader.elsevier.com/reader/sd/pii/S1525505022003237?token=5D0FBDE6C3D43653AEE49DEB441C49D0E46C3FFAD8307F3A35E262CCAEB64D15C24BA4622C1A9699AD019811ADB10D67&originRegion=eu-west-1&originCreation=20220905065244
UR  - http://rfasper.fasper.bg.ac.rs/handle/123456789/4748
AB  - Objective: To explore the presence of felt and enacted stigma in people with epilepsy (PWE), members of a self-governing epilepsy organization and to evaluate the influence of both types of stigma on healthrelated quality of life (HRQoL) in PWE. Methods: Participants were 55 PWE (age range: 18–53 years), members of a non-governmental organization (further ‘‘NGO”). The sociodemographic and epilepsy-related variables were collected through structured interviews designed for the purpose of the study. Felt stigma was assessed with the Epilepsy Stigma Scale (ESS) and enacted stigma with the Questionnaire for episodes of discrimination against PWE. Quality of Life in Epilepsy Inventory (QOLIE-31) (Serbian version) was used for the evaluation of HRQoL. Results: The mean ESS score was 33.93 ± 14.50. Felt stigma was significantly associated with the male gender and the number of antiepileptic drugs (AEDs). Participants’ mean score on the Questionnaire for episodes of discrimination was 2.80 ± 2.78. Enacted stigma was significantly correlated with male gender and number of AEDs, as well as with older age/longer duration of the disorder. Felt stigma scores were positively correlated with enacted stigma scores (p < 0.001), but only felt stigma scores were negatively related to QOLIE-31 overall score (p = 0.01). The combination of AEDs, seizure frequency, and felt stigma best explained the HRQoL in PWE (p < 0.001). Conclusion: Felt and enacted stigma are moderately related, but only felt stigma appears to be a significant predictor of the deteriorating HRQoL in this sample. Interventions targeting felt stigma should be considered a part of comprehensive epilepsy care as well as educating the wider community about epilepsy.
PB  - Elsevier [Commercial Publisher]
T2  - Epilepsy & Behavior
T1  - Stigma and its association with health-related quality of life in adults with epilepsy | Elsevier Enhanced Reader
EP  - 108874
VL  - 135
DO  - https://doi.org/10.1016/j.yebeh.2022.108874
ER  - 
@article{
author = "Staša Lalatović and Maja Milovanović and Nadežda Krstić",
abstract = "Objective: To explore the presence of felt and enacted stigma in people with epilepsy (PWE), members of a self-governing epilepsy organization and to evaluate the influence of both types of stigma on healthrelated quality of life (HRQoL) in PWE. Methods: Participants were 55 PWE (age range: 18–53 years), members of a non-governmental organization (further ‘‘NGO”). The sociodemographic and epilepsy-related variables were collected through structured interviews designed for the purpose of the study. Felt stigma was assessed with the Epilepsy Stigma Scale (ESS) and enacted stigma with the Questionnaire for episodes of discrimination against PWE. Quality of Life in Epilepsy Inventory (QOLIE-31) (Serbian version) was used for the evaluation of HRQoL. Results: The mean ESS score was 33.93 ± 14.50. Felt stigma was significantly associated with the male gender and the number of antiepileptic drugs (AEDs). Participants’ mean score on the Questionnaire for episodes of discrimination was 2.80 ± 2.78. Enacted stigma was significantly correlated with male gender and number of AEDs, as well as with older age/longer duration of the disorder. Felt stigma scores were positively correlated with enacted stigma scores (p < 0.001), but only felt stigma scores were negatively related to QOLIE-31 overall score (p = 0.01). The combination of AEDs, seizure frequency, and felt stigma best explained the HRQoL in PWE (p < 0.001). Conclusion: Felt and enacted stigma are moderately related, but only felt stigma appears to be a significant predictor of the deteriorating HRQoL in this sample. Interventions targeting felt stigma should be considered a part of comprehensive epilepsy care as well as educating the wider community about epilepsy.",
publisher = "Elsevier [Commercial Publisher]",
journal = "Epilepsy & Behavior",
title = "Stigma and its association with health-related quality of life in adults with epilepsy | Elsevier Enhanced Reader",
pages = "108874",
volume = "135",
doi = "https://doi.org/10.1016/j.yebeh.2022.108874"
}
Staša Lalatović, Maja Milovanović,& Nadežda Krstić.Stigma and its association with health-related quality of life in adults with epilepsy | Elsevier Enhanced Reader. in Epilepsy & Behavior
Elsevier [Commercial Publisher]., 135.
https://doi.org/https://doi.org/10.1016/j.yebeh.2022.108874
Staša Lalatović, Maja Milovanović, Nadežda Krstić. Stigma and its association with health-related quality of life in adults with epilepsy | Elsevier Enhanced Reader. in Epilepsy & Behavior.135:null-108874.
doi:https://doi.org/10.1016/j.yebeh.2022.108874 .
Staša Lalatović, Maja Milovanović, Nadežda Krstić, "Stigma and its association with health-related quality of life in adults with epilepsy | Elsevier Enhanced Reader" in Epilepsy & Behavior, 135,
https://doi.org/https://doi.org/10.1016/j.yebeh.2022.108874 . .

Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom

Lalatović, Staša; SavićParojčić, Aleksandra; Mentus-Kandić, Tatjana; Krstić, Nadežda

(Univerzitet u Beogradu – Fakultet za specijalnu edukaciju i rehabilitaciju/ University of Belgrade – Faculty of Special Education and Rehabilitation, 2021)

TY  - CONF
AU  - Lalatović, Staša
AU  - SavićParojčić, Aleksandra
AU  - Mentus-Kandić, Tatjana
AU  - Krstić, Nadežda
PY  - 2021
UR  - http://rfasper.fasper.bg.ac.rs/handle/123456789/3772
AB  - Uvod: Način na koji osobe sa epilepsijom percipiraju svoje porodice igra važnu ulogu u celokupnom toku epilepsije.
Cilj: Primarni cilj istraživanja bio je ispitati kako osobe sa epilepsijom opažaju funkcionisanje svojih porodica. Detaljnije, ispitivala se povezanost dužine tra- janja simptoma i porodičnih skala.
Metod: Uzorak su činila 22 pacijenta sa epileptičnim napadima. Radi dobijanja neophodnih podataka korišćena je modifikovana lista sociodemografskih poda- taka koja je sastavni deo upitnika FACES IV i Mek Masterov upitnik za proce- nu porodice (McMaster Family Assesment Device; FAD). FAD sadrži 60 pitanja, podeljenih u sedam skala: Rešavanje problema, Komunikacija, Uloge, Afektivna responzivnost, Afektivno uključivanje, Kontrola ponašanja i Opšte funkcionisanje.
Rezultati: Utvrđeno je da osobe sa epilepsijom opažaju porodično funkcionisa- nje kao disfunkcionalno na dimenziji Kontrola ponašanja (AS=2,08; SD=0,34; cut off skor=1,90). Muškarci percipiraju porodično funkcionisanje kao više disfunkcionalno u odnosu na žene na dve dimenzije porodičnog funkcionisa- nja – Komunikacija [t(20)=2,18; p<0,05; d=0,93] i Uloge [t(20)=2,77; p<0,05; d=1,18]. Pacijenti koji i dalje žive u primarnoj porodici percipiraju porodično funkcionisanje kao više disfunkcionalno na dimenziji Komunikacija, u odnosu na one koji su se odvojili od primarne porodice [t(20)=2,18; p<0,05; d=0,93].
Rezultati regresione analize pokazuju da skale Rešavanje problema, Afektivna responzivnost i Opšte funkcionisanje objašnjavaju 34,7% varijanse dužine tra- janja epileptičnih napada [R²=0,35; F(3,18)=3,19; p<0,05].
Zaključak: Istraživanje ističe značaj porodičnih varijabli  i  specifičnosti istih kod osoba sa epilepsijom, kao i važnost uključivanja cele porodice u proces lečenja pacijenta.
AB  - Introduction: The way people with epilepsy perceive their families plays an important role in the overall course of epilepsy.
Aim: The primary goal of the study was to examine how people with epilepsy perceive the functioning of their families. The relationship between symptom duration and family scales was examined in more detail.
Method: The sample consisted of 22 patients with epileptic seizures. To obtain the necessary data, a modified list of socio-demographic data was used, which is an integral part of the FACES IV questionnaire and the McMaster Family Assessment Device. The Family Assessment Device contains 60 questions, divided into seven scales: Problem Solving, Communication, Roles, Affective Responsibility, Affective Involvement, Behaviour Control, and General Functioning.
Results: It was found that people with epilepsy perceived family functioning as dysfunctional on the Behaviour Control dimension (M=2.08; SD=.34; cut off score=1.90). Men perceived family functioning as more dysfunctional than women in two dimensions of family functioning – Communication [t(20)=2.18; p<.05; d=.93] and Roles [t(20)=2.77, p<.05, d=1.18].Patients still living in the primary family perceived family functioning as more dysfunctional in the Communication dimension, compared to those who separated from the primary family [t(20)=2.18; p<.05; d=.93]. The results of regression analysis show that the scales Problem Solving, Affective Responsiveness and General Functioning explain 34.7% of the variance in the duration of epileptic seizures [R²=.35; F(3,18) =3.19; p<.05].
Conclusion: The research emphasizes the importance of family variables and their specificity in people with epilepsy, as well as the importance of including the whole family in the process of treating the patient.
PB  - Univerzitet u Beogradu – Fakultet za specijalnu edukaciju i rehabilitaciju/ University of Belgrade – Faculty of Special Education and Rehabilitation
C3  - Zbornik radova - 11. Međunarodni naučni skup „Specijalna edukacija i rehabilitacija danas“, Beograd, Srbija, 29–30.10.2021.
T1  - Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom
T1  - Exploring aspects of family functioning in subjects with epilepsy
EP  - 82
SP  - 75
UR  - https://hdl.handle.net/21.15107/rcub_rfasper_3772
ER  - 
@conference{
author = "Lalatović, Staša and SavićParojčić, Aleksandra and Mentus-Kandić, Tatjana and Krstić, Nadežda",
year = "2021",
abstract = "Uvod: Način na koji osobe sa epilepsijom percipiraju svoje porodice igra važnu ulogu u celokupnom toku epilepsije.
Cilj: Primarni cilj istraživanja bio je ispitati kako osobe sa epilepsijom opažaju funkcionisanje svojih porodica. Detaljnije, ispitivala se povezanost dužine tra- janja simptoma i porodičnih skala.
Metod: Uzorak su činila 22 pacijenta sa epileptičnim napadima. Radi dobijanja neophodnih podataka korišćena je modifikovana lista sociodemografskih poda- taka koja je sastavni deo upitnika FACES IV i Mek Masterov upitnik za proce- nu porodice (McMaster Family Assesment Device; FAD). FAD sadrži 60 pitanja, podeljenih u sedam skala: Rešavanje problema, Komunikacija, Uloge, Afektivna responzivnost, Afektivno uključivanje, Kontrola ponašanja i Opšte funkcionisanje.
Rezultati: Utvrđeno je da osobe sa epilepsijom opažaju porodično funkcionisa- nje kao disfunkcionalno na dimenziji Kontrola ponašanja (AS=2,08; SD=0,34; cut off skor=1,90). Muškarci percipiraju porodično funkcionisanje kao više disfunkcionalno u odnosu na žene na dve dimenzije porodičnog funkcionisa- nja – Komunikacija [t(20)=2,18; p<0,05; d=0,93] i Uloge [t(20)=2,77; p<0,05; d=1,18]. Pacijenti koji i dalje žive u primarnoj porodici percipiraju porodično funkcionisanje kao više disfunkcionalno na dimenziji Komunikacija, u odnosu na one koji su se odvojili od primarne porodice [t(20)=2,18; p<0,05; d=0,93].
Rezultati regresione analize pokazuju da skale Rešavanje problema, Afektivna responzivnost i Opšte funkcionisanje objašnjavaju 34,7% varijanse dužine tra- janja epileptičnih napada [R²=0,35; F(3,18)=3,19; p<0,05].
Zaključak: Istraživanje ističe značaj porodičnih varijabli  i  specifičnosti istih kod osoba sa epilepsijom, kao i važnost uključivanja cele porodice u proces lečenja pacijenta., Introduction: The way people with epilepsy perceive their families plays an important role in the overall course of epilepsy.
Aim: The primary goal of the study was to examine how people with epilepsy perceive the functioning of their families. The relationship between symptom duration and family scales was examined in more detail.
Method: The sample consisted of 22 patients with epileptic seizures. To obtain the necessary data, a modified list of socio-demographic data was used, which is an integral part of the FACES IV questionnaire and the McMaster Family Assessment Device. The Family Assessment Device contains 60 questions, divided into seven scales: Problem Solving, Communication, Roles, Affective Responsibility, Affective Involvement, Behaviour Control, and General Functioning.
Results: It was found that people with epilepsy perceived family functioning as dysfunctional on the Behaviour Control dimension (M=2.08; SD=.34; cut off score=1.90). Men perceived family functioning as more dysfunctional than women in two dimensions of family functioning – Communication [t(20)=2.18; p<.05; d=.93] and Roles [t(20)=2.77, p<.05, d=1.18].Patients still living in the primary family perceived family functioning as more dysfunctional in the Communication dimension, compared to those who separated from the primary family [t(20)=2.18; p<.05; d=.93]. The results of regression analysis show that the scales Problem Solving, Affective Responsiveness and General Functioning explain 34.7% of the variance in the duration of epileptic seizures [R²=.35; F(3,18) =3.19; p<.05].
Conclusion: The research emphasizes the importance of family variables and their specificity in people with epilepsy, as well as the importance of including the whole family in the process of treating the patient.",
publisher = "Univerzitet u Beogradu – Fakultet za specijalnu edukaciju i rehabilitaciju/ University of Belgrade – Faculty of Special Education and Rehabilitation",
journal = "Zbornik radova - 11. Međunarodni naučni skup „Specijalna edukacija i rehabilitacija danas“, Beograd, Srbija, 29–30.10.2021.",
title = "Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom, Exploring aspects of family functioning in subjects with epilepsy",
pages = "82-75",
url = "https://hdl.handle.net/21.15107/rcub_rfasper_3772"
}
Lalatović, S., SavićParojčić, A., Mentus-Kandić, T.,& Krstić, N.. (2021). Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom. in Zbornik radova - 11. Međunarodni naučni skup „Specijalna edukacija i rehabilitacija danas“, Beograd, Srbija, 29–30.10.2021.
Univerzitet u Beogradu – Fakultet za specijalnu edukaciju i rehabilitaciju/ University of Belgrade – Faculty of Special Education and Rehabilitation., 75-82.
https://hdl.handle.net/21.15107/rcub_rfasper_3772
Lalatović S, SavićParojčić A, Mentus-Kandić T, Krstić N. Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom. in Zbornik radova - 11. Međunarodni naučni skup „Specijalna edukacija i rehabilitacija danas“, Beograd, Srbija, 29–30.10.2021.. 2021;:75-82.
https://hdl.handle.net/21.15107/rcub_rfasper_3772 .
Lalatović, Staša, SavićParojčić, Aleksandra, Mentus-Kandić, Tatjana, Krstić, Nadežda, "Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom" in Zbornik radova - 11. Međunarodni naučni skup „Specijalna edukacija i rehabilitacija danas“, Beograd, Srbija, 29–30.10.2021. (2021):75-82,
https://hdl.handle.net/21.15107/rcub_rfasper_3772 .

Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom

Lalatović, Staša; Savić Parojčić, Aleksandra; Mentus Kandić, Tatjana; Krstić, Nadežda

(Univerzitet u Beogradu – Fakultet za specijalnu edukaciju i rehabilitaciju University of Belgrade – Faculty of Special Education and Rehabilitation, 2021)

TY  - CONF
AU  - Lalatović, Staša
AU  - Savić Parojčić, Aleksandra
AU  - Mentus Kandić, Tatjana
AU  - Krstić, Nadežda
PY  - 2021
UR  - http://rfasper.fasper.bg.ac.rs/handle/123456789/3606
AB  - Uvod: Način na koji osobe sa epilepsijom percipiraju svoje porodice igra važnu ulogu u celokupnom toku epilepsije.
Cilj: Primarni cilj istraživanja bio je ispitati kako osobe sa epilepsijom opažaju funkcionisanje svojih porodica. Detaljnije, ispitivala se povezanost dužine trajanja simptoma i porodičnih skala.
Metod: Uzorak su činila 22 pacijenta sa epileptičnim napadima. Radi dobijanja neophodnih podataka korišćena je modifikovana lista sociodemografskih podataka koja je sastavni deo upitnika FACES IV i Mek Masterov upitnik za procenu porodice (McMaster Family Assesment Device; FAD). FAD sadrži 60 pitanja, podeljenih u sedam skala: Rešavanje problema, Komunikacija, Uloge, Afektivna responzivnost, Afektivno uključivanje, Kontrola ponašanja i Opšte funkcionisanje.
Rezultati: Utvrđeno je da osobe sa epilepsijom opažaju porodično funkcionisanje kao disfunkcionalno na dimenziji Kontrola ponašanja (AS=2,08; SD=0,34; cut off skor=1,90). Muškarci percipiraju porodično funkcionisanje kao više disfunkcionalno u odnosu na žene na dve dimenzije porodičnog funkcionisanja – Komunikacija [t(20)=2,18; p<0,05; d=0,93] i Uloge [t(20)=2,77; p<0,05; d=1,18]. Pacijenti koji i dalje žive u primarnoj porodici percipiraju porodično funkcionisanje kao više disfunkcionalno na dimenziji Komunikacija, u odnosu na one koji su se odvojili od primarne porodice [t(20)=2,18; p<,05; d=0,93]. Rezultati regresione analize pokazuju da skale Rešavanje problema, Afektivna responzivnost i Opšte funkcionisanje objašnjavaju 34,7% varijanse dužine trajanja epileptičnih napada [R²=0,35; F(3,18)=3,19; p<0,05].
Zaključak: Istraživanje ističe značaj porodičnih varijabli i specifičnosti istih kod osoba sa epilepsijom, kao i važnost uključivanja cele porodice u proces lečenja pacijenta.
AB  - Introduction: The way people with epilepsy perceive their families plays an important role in the overall course of epilepsy.
Aim: The primary goal of the study was to examine how people with epilepsy perceive the functioning of their families. The relationship between symptom duration and family scales was examined in more detail.
Method: The sample consisted of 22 patients with epileptic seizures.
To obtain the necessary data, a modified list of socio-demographic data was used, which is an integral part of the FACES IV questionnaire and the McMaster Family Assessment Device. The Family Assessment Device contains 60 questions, divided into seven scales: Problem Solving, Communication, Roles, Affective Responsibility, Affective Involvement, Behaviour Control, and General Functioning.
Results: It was found that people with epilepsy perceived family functioning as dysfunctional on the Behaviour Control dimension (M=2.08; SD=.34; cut off score=1.90). Men perceived family functioning as more dysfunctional than women in two dimensions of family functioning – Communication [t(20)=2.18; p<.05; d=.93] and Roles [t(20)=2.77, p<.05, d=1.18]. Patients still living in the primary family perceived family functioning as more dysfunctional in the Communication dimension, compared to those who separated from the primary family [t(20)=2.18; p<.05; d=.93]. The results of regression analysis show that the scales Problem Solving, Affective Responsiveness and General Functioning explain 34.7% of the variance in the duration of epileptic seizures [R²=.35; F(3,18) =3.19; p<.05].
Conclusion: The research emphasizes the importance of family variables and their specificity in people with epilepsy, as well as the importance of including the whole family in the process of treating the patient.
PB  - Univerzitet u Beogradu – Fakultet za specijalnu edukaciju i rehabilitaciju University of Belgrade – Faculty of Special Education and Rehabilitation
C3  - Zbornik rezimea 11. Međunarodni naučni skup Specijalna edukacija i rehabilitacija danas Beograd, 29–30. oktobar 2021. godine
T1  - Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom
T1  - Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa
Epilepsijom
EP  - 37
SP  - 36
UR  - https://hdl.handle.net/21.15107/rcub_rfasper_3606
ER  - 
@conference{
author = "Lalatović, Staša and Savić Parojčić, Aleksandra and Mentus Kandić, Tatjana and Krstić, Nadežda",
year = "2021",
abstract = "Uvod: Način na koji osobe sa epilepsijom percipiraju svoje porodice igra važnu ulogu u celokupnom toku epilepsije.
Cilj: Primarni cilj istraživanja bio je ispitati kako osobe sa epilepsijom opažaju funkcionisanje svojih porodica. Detaljnije, ispitivala se povezanost dužine trajanja simptoma i porodičnih skala.
Metod: Uzorak su činila 22 pacijenta sa epileptičnim napadima. Radi dobijanja neophodnih podataka korišćena je modifikovana lista sociodemografskih podataka koja je sastavni deo upitnika FACES IV i Mek Masterov upitnik za procenu porodice (McMaster Family Assesment Device; FAD). FAD sadrži 60 pitanja, podeljenih u sedam skala: Rešavanje problema, Komunikacija, Uloge, Afektivna responzivnost, Afektivno uključivanje, Kontrola ponašanja i Opšte funkcionisanje.
Rezultati: Utvrđeno je da osobe sa epilepsijom opažaju porodično funkcionisanje kao disfunkcionalno na dimenziji Kontrola ponašanja (AS=2,08; SD=0,34; cut off skor=1,90). Muškarci percipiraju porodično funkcionisanje kao više disfunkcionalno u odnosu na žene na dve dimenzije porodičnog funkcionisanja – Komunikacija [t(20)=2,18; p<0,05; d=0,93] i Uloge [t(20)=2,77; p<0,05; d=1,18]. Pacijenti koji i dalje žive u primarnoj porodici percipiraju porodično funkcionisanje kao više disfunkcionalno na dimenziji Komunikacija, u odnosu na one koji su se odvojili od primarne porodice [t(20)=2,18; p<,05; d=0,93]. Rezultati regresione analize pokazuju da skale Rešavanje problema, Afektivna responzivnost i Opšte funkcionisanje objašnjavaju 34,7% varijanse dužine trajanja epileptičnih napada [R²=0,35; F(3,18)=3,19; p<0,05].
Zaključak: Istraživanje ističe značaj porodičnih varijabli i specifičnosti istih kod osoba sa epilepsijom, kao i važnost uključivanja cele porodice u proces lečenja pacijenta., Introduction: The way people with epilepsy perceive their families plays an important role in the overall course of epilepsy.
Aim: The primary goal of the study was to examine how people with epilepsy perceive the functioning of their families. The relationship between symptom duration and family scales was examined in more detail.
Method: The sample consisted of 22 patients with epileptic seizures.
To obtain the necessary data, a modified list of socio-demographic data was used, which is an integral part of the FACES IV questionnaire and the McMaster Family Assessment Device. The Family Assessment Device contains 60 questions, divided into seven scales: Problem Solving, Communication, Roles, Affective Responsibility, Affective Involvement, Behaviour Control, and General Functioning.
Results: It was found that people with epilepsy perceived family functioning as dysfunctional on the Behaviour Control dimension (M=2.08; SD=.34; cut off score=1.90). Men perceived family functioning as more dysfunctional than women in two dimensions of family functioning – Communication [t(20)=2.18; p<.05; d=.93] and Roles [t(20)=2.77, p<.05, d=1.18]. Patients still living in the primary family perceived family functioning as more dysfunctional in the Communication dimension, compared to those who separated from the primary family [t(20)=2.18; p<.05; d=.93]. The results of regression analysis show that the scales Problem Solving, Affective Responsiveness and General Functioning explain 34.7% of the variance in the duration of epileptic seizures [R²=.35; F(3,18) =3.19; p<.05].
Conclusion: The research emphasizes the importance of family variables and their specificity in people with epilepsy, as well as the importance of including the whole family in the process of treating the patient.",
publisher = "Univerzitet u Beogradu – Fakultet za specijalnu edukaciju i rehabilitaciju University of Belgrade – Faculty of Special Education and Rehabilitation",
journal = "Zbornik rezimea 11. Međunarodni naučni skup Specijalna edukacija i rehabilitacija danas Beograd, 29–30. oktobar 2021. godine",
title = "Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom, Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa
Epilepsijom",
pages = "37-36",
url = "https://hdl.handle.net/21.15107/rcub_rfasper_3606"
}
Lalatović, S., Savić Parojčić, A., Mentus Kandić, T.,& Krstić, N.. (2021). Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom. in Zbornik rezimea 11. Međunarodni naučni skup Specijalna edukacija i rehabilitacija danas Beograd, 29–30. oktobar 2021. godine
Univerzitet u Beogradu – Fakultet za specijalnu edukaciju i rehabilitaciju University of Belgrade – Faculty of Special Education and Rehabilitation., 36-37.
https://hdl.handle.net/21.15107/rcub_rfasper_3606
Lalatović S, Savić Parojčić A, Mentus Kandić T, Krstić N. Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom. in Zbornik rezimea 11. Međunarodni naučni skup Specijalna edukacija i rehabilitacija danas Beograd, 29–30. oktobar 2021. godine. 2021;:36-37.
https://hdl.handle.net/21.15107/rcub_rfasper_3606 .
Lalatović, Staša, Savić Parojčić, Aleksandra, Mentus Kandić, Tatjana, Krstić, Nadežda, "Ispitivanje aspekata porodičnog funkcionisanja kod osoba sa epilepsijom" in Zbornik rezimea 11. Međunarodni naučni skup Specijalna edukacija i rehabilitacija danas Beograd, 29–30. oktobar 2021. godine (2021):36-37,
https://hdl.handle.net/21.15107/rcub_rfasper_3606 .