Pub Date : 2021-03-01DOI: 10.4274/jpr.galenos.2020.10692
A. Erdem, B. Etensel, M. Yazıcı, Sezen Karaca Özkısacık
{"title":"Diagnostic Evaluation of Foreign Body Aspiration in Children","authors":"A. Erdem, B. Etensel, M. Yazıcı, Sezen Karaca Özkısacık","doi":"10.4274/jpr.galenos.2020.10692","DOIUrl":"https://doi.org/10.4274/jpr.galenos.2020.10692","url":null,"abstract":"","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"8 1","pages":"49-54"},"PeriodicalIF":0.3,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47507498","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-03-01DOI: 10.4274/JPR.GALENOS.2020.47750
A. Tosun, Beste Kıpçak Yüzbaşı, A. Akyol
Introduction Tuberous sclerosis complex (TSC) is an autosomal dominant inherited genetic disease in which multiple organ involvement is characterized by common hamartomas in many organs especially including the brain, skin, heart, eye, kidney, lung and liver. TSC is due to programmed hyperplasia of ectodermal and mesodermal cells, which is characterized by epilepsy, adenoma sebaceum and mental retardation. It has a variable age of onset and variable clinical severity. About 2/3 of these cases are formed via spontaneous mutation. Due to mutations in the TSC1 (9q34) and TSC2 (16p13.3) genes respectively, the functions of the hamartin and tuberin proteins encoded by these genes are impaired. The mammalian target of hamartin-tuberin proteins is to
{"title":"Review of Tuberous Sclerosis Complex: A Single Center Experience","authors":"A. Tosun, Beste Kıpçak Yüzbaşı, A. Akyol","doi":"10.4274/JPR.GALENOS.2020.47750","DOIUrl":"https://doi.org/10.4274/JPR.GALENOS.2020.47750","url":null,"abstract":"Introduction Tuberous sclerosis complex (TSC) is an autosomal dominant inherited genetic disease in which multiple organ involvement is characterized by common hamartomas in many organs especially including the brain, skin, heart, eye, kidney, lung and liver. TSC is due to programmed hyperplasia of ectodermal and mesodermal cells, which is characterized by epilepsy, adenoma sebaceum and mental retardation. It has a variable age of onset and variable clinical severity. About 2/3 of these cases are formed via spontaneous mutation. Due to mutations in the TSC1 (9q34) and TSC2 (16p13.3) genes respectively, the functions of the hamartin and tuberin proteins encoded by these genes are impaired. The mammalian target of hamartin-tuberin proteins is to","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"8 1","pages":"75-81"},"PeriodicalIF":0.3,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46934756","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-03-01DOI: 10.4274/JPR.GALENOS.2020.17894
Ülkühan Öztoprak, E. Aksoy, Özlem Yayıcı Köken, Ayşegül Danış, Ayşe Seçil Ekşioğlu, N. Tuygun, D. Yüksel
Results: A total of 326 children (166 girls, 160 boys; age range 1 to 17.8 years) with CO poisoning were identified. Their ages ranged from 1 to 17.8 years, with a mean of 8.3±4.8 years. Improperly vented coal or wood stoves were the most common (80.7%) cause of intoxication. The most common presenting symptoms were nausea/vomiting and headache. Seizure was seen in 32 patients (9.8%). Two patients died and the mortality was 0.6%. All patients received normobaric oxygen therapy until their carboxyhemoglobin (COHb) levels were decreased below 2% and their symptoms resolved. One hundred of the 326 patients (30.7%) also were treated with hyperbaric oxygen (HBO) therapy as indicated by the signs and symptoms or COHb levels. Brain imaging was performed in 19 patients (thirteen magnetic resonance imaging and six computerized tomography), and was normal in 15. Acute brain stem demyelination related to water pipe smoking developed in one patient. All patients showed complete recovery without neurological sequelae except one who had mild right hemiparesis at discharge.
{"title":"Clinical Characteristics and Neurological Findings of Pediatric Patients with Acute Carbon Monoxide Intoxication","authors":"Ülkühan Öztoprak, E. Aksoy, Özlem Yayıcı Köken, Ayşegül Danış, Ayşe Seçil Ekşioğlu, N. Tuygun, D. Yüksel","doi":"10.4274/JPR.GALENOS.2020.17894","DOIUrl":"https://doi.org/10.4274/JPR.GALENOS.2020.17894","url":null,"abstract":"Results: A total of 326 children (166 girls, 160 boys; age range 1 to 17.8 years) with CO poisoning were identified. Their ages ranged from 1 to 17.8 years, with a mean of 8.3±4.8 years. Improperly vented coal or wood stoves were the most common (80.7%) cause of intoxication. The most common presenting symptoms were nausea/vomiting and headache. Seizure was seen in 32 patients (9.8%). Two patients died and the mortality was 0.6%. All patients received normobaric oxygen therapy until their carboxyhemoglobin (COHb) levels were decreased below 2% and their symptoms resolved. One hundred of the 326 patients (30.7%) also were treated with hyperbaric oxygen (HBO) therapy as indicated by the signs and symptoms or COHb levels. Brain imaging was performed in 19 patients (thirteen magnetic resonance imaging and six computerized tomography), and was normal in 15. Acute brain stem demyelination related to water pipe smoking developed in one patient. All patients showed complete recovery without neurological sequelae except one who had mild right hemiparesis at discharge.","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"8 1","pages":"20-28"},"PeriodicalIF":0.3,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42681089","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-03-01DOI: 10.4274/JPR.GALENOS.2020.90377
Nuriye Tarakçı, F. H. Yılmaz, H. Altunhan
Ad dress for Cor res pon den ce Nuriye Tarakçı MD, Necmettin Erbakan University, Meram Faculty of Medicine, Department of Neonatology, Konya, Turkey Phone: +90 532 739 09 34 E-mail: nuriyetarakci@hotmail.com ORCID: orcid.org/0000-0003-2444-4725 Re cei ved: 10.01.2020 Ac cep ted: 18.06.2020 Introduction The number of refugees who leave their home country due to civil wars in Middle Eastern countries has been increasing gradually over the years. In parallel with low socioeconomic status, unhealthy living conditions and an increased birth rate among these immigrants, health issues are also increasing. There have been many studies that investigated the perinatal status of the global immigrant population, and their findings revealed that having an immigrant status is related to insufficient antenatal care, perinatal mortality, prematurity, low birth weight (BW) and congenital anomalies (1-4). In addition to individual/patientassociated factors in host and immigrant populations, inequality and variability in healthcare access are factors that contribute to the poor perinatal outcomes of the immigrant population.
广告服装为Cor res pon den ce Nuriye tarakmd, Necmettin Erbakan大学，Meram医学院，新生儿科，科尼亚，土耳其电话:+90 532 739 09 34 E-mail: nuriyetarakci@hotmail.com ORCID: orcid.org/0000-0003-2444-4725接收:10.01.2020 Ac接收:18.06.2020引言由于中东国家的内战而离开祖国的难民人数近年来逐渐增加。在这些移民中，除了社会经济地位低、生活条件不健康和出生率增加之外，健康问题也在增加。有许多研究调查了全球移民人口的围产期状况，他们的研究结果表明，拥有移民身份与产前护理不足、围产期死亡率、早产、低出生体重(BW)和先天性异常有关(1-4)。除了东道国和移民人口中的个人/患者相关因素外，医疗保健机会的不平等和可变性也是导致移民人口围产期结局不佳的因素。
{"title":"Neonatal Outcomes of Immigrant and Turkish Preterm Infants Treated in a Level-3 Neonatal Intensive Care Unit: A Retrospective Study","authors":"Nuriye Tarakçı, F. H. Yılmaz, H. Altunhan","doi":"10.4274/JPR.GALENOS.2020.90377","DOIUrl":"https://doi.org/10.4274/JPR.GALENOS.2020.90377","url":null,"abstract":"Ad dress for Cor res pon den ce Nuriye Tarakçı MD, Necmettin Erbakan University, Meram Faculty of Medicine, Department of Neonatology, Konya, Turkey Phone: +90 532 739 09 34 E-mail: nuriyetarakci@hotmail.com ORCID: orcid.org/0000-0003-2444-4725 Re cei ved: 10.01.2020 Ac cep ted: 18.06.2020 Introduction The number of refugees who leave their home country due to civil wars in Middle Eastern countries has been increasing gradually over the years. In parallel with low socioeconomic status, unhealthy living conditions and an increased birth rate among these immigrants, health issues are also increasing. There have been many studies that investigated the perinatal status of the global immigrant population, and their findings revealed that having an immigrant status is related to insufficient antenatal care, perinatal mortality, prematurity, low birth weight (BW) and congenital anomalies (1-4). In addition to individual/patientassociated factors in host and immigrant populations, inequality and variability in healthcare access are factors that contribute to the poor perinatal outcomes of the immigrant population.","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"8 1","pages":"14-19"},"PeriodicalIF":0.3,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46295528","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-03-01DOI: 10.4274/JPR.GALENOS.2020.14471
Gülçin Özalp Gerçeker, Murat Bektaş
The ratio of childhood obesity has doubled in the last 30 years (4). The ratio of obese children and adolescents in the US was 16.9% (5). According to the investigation report on monitoring the growth of school children (6-10-year-old age group) project in Turkey by the General Directorate of Basic Health Services of the Turkish Ministry of Health (6) 8.5% of children were obese and the ratios of overweight children in cities and rural areas were 16.3% and 11.9%, respectively. There is a global increase in the prevalence of obesity and being overweight in children and adolescents. Researchers have the important task to investigate the causes of obesity such as sedentarism, emotional eating, parents, and children’s awareness about obesity. Demir and Bektas (7) reported that eating behaviors and parental feeding styles affect the occurrence of obesity in childhood. Parents may influence their children’s eating behaviors and result in high levels of disinhibited emotional eating in early adolescents (8). There are only a small number of studies that investigate the relationship between emotional eating and obesity in children (9,10).
{"title":"Relationship Among Obesity Awareness, Emotional Eating, and Obesity in Middle School Children","authors":"Gülçin Özalp Gerçeker, Murat Bektaş","doi":"10.4274/JPR.GALENOS.2020.14471","DOIUrl":"https://doi.org/10.4274/JPR.GALENOS.2020.14471","url":null,"abstract":"The ratio of childhood obesity has doubled in the last 30 years (4). The ratio of obese children and adolescents in the US was 16.9% (5). According to the investigation report on monitoring the growth of school children (6-10-year-old age group) project in Turkey by the General Directorate of Basic Health Services of the Turkish Ministry of Health (6) 8.5% of children were obese and the ratios of overweight children in cities and rural areas were 16.3% and 11.9%, respectively. There is a global increase in the prevalence of obesity and being overweight in children and adolescents. Researchers have the important task to investigate the causes of obesity such as sedentarism, emotional eating, parents, and children’s awareness about obesity. Demir and Bektas (7) reported that eating behaviors and parental feeding styles affect the occurrence of obesity in childhood. Parents may influence their children’s eating behaviors and result in high levels of disinhibited emotional eating in early adolescents (8). There are only a small number of studies that investigate the relationship between emotional eating and obesity in children (9,10).","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"8 1","pages":"55-61"},"PeriodicalIF":0.3,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46859399","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-02-22DOI: 10.4274/JPR.GALENOS.2020.59354
Esra Işık, H. Mehdiyeva, Bilçağ Akgün, T. Köse, K. Kavaklı, F. Özkınay, T. Atik
Aim: Previous studies have reported inhibitor development (ID) risk in those patients who have hemophilia A (HA) with missense mutations to be 3-10%. We investigated the association between ID risk and various features of missense mutations; including the impact directly related to amino acid group change. Materials and Methods: Missense mutations in the F8 gene, clinical findings of the patients including severity of HA, and ID status were obtained from the F8 gene variant database (http://www.factorviii-db.org/). Twenty amino acids were then classified into groups according to their side chains. All information regarding each specific mutation, as well as any impact of the mutation on the amino acid group change, was recorded. Additionally, localization (at which domain) of any changed amino acid in the F8 protein was noted. Combined Annotation Dependent Depletion (CADD), Rare Exome Variant Ensemble Learner (REVEL), Mendelian Clinically Applicable Pathogenicity and Deleterious Annotation using Neural Networks scores were applied to identify a significant cut-off value indicative of ID. Results: Three variations were identified that could be considered as useful in the prediction of ID in mild HA. The first being that among mild HA patients, 7.9% (n=70/883) with mutations causing no amino acid group changes showed ID. This rate, however, was only 2.9% in patients with mutations leading to amino acid group changes. Secondly; in patients with mutations causing no amino acid group changes affecting A2, A3 and C2 domains, ID risk was found to be higher than in patients with mutations leading to amino acid group changes. Thirdly; an association between ID and CADD and REVEL scores was observed. Conclusion: In mild HA patients, the characteristics of missense mutations in terms of amino acid group changes, and CADD and REVEL scores could be of considerable utility in the prediction of ID risk.
{"title":"A Novel Molecular Indicator for Inhibitor Development in Haemophilia A","authors":"Esra Işık, H. Mehdiyeva, Bilçağ Akgün, T. Köse, K. Kavaklı, F. Özkınay, T. Atik","doi":"10.4274/JPR.GALENOS.2020.59354","DOIUrl":"https://doi.org/10.4274/JPR.GALENOS.2020.59354","url":null,"abstract":"Aim: Previous studies have reported inhibitor development (ID) risk in those patients who have hemophilia A (HA) with missense mutations to be 3-10%. We investigated the association between ID risk and various features of missense mutations; including the impact directly related to amino acid group change. Materials and Methods: Missense mutations in the F8 gene, clinical findings of the patients including severity of HA, and ID status were obtained from the F8 gene variant database (http://www.factorviii-db.org/). Twenty amino acids were then classified into groups according to their side chains. All information regarding each specific mutation, as well as any impact of the mutation on the amino acid group change, was recorded. Additionally, localization (at which domain) of any changed amino acid in the F8 protein was noted. Combined Annotation Dependent Depletion (CADD), Rare Exome Variant Ensemble Learner (REVEL), Mendelian Clinically Applicable Pathogenicity and Deleterious Annotation using Neural Networks scores were applied to identify a significant cut-off value indicative of ID. Results: Three variations were identified that could be considered as useful in the prediction of ID in mild HA. The first being that among mild HA patients, 7.9% (n=70/883) with mutations causing no amino acid group changes showed ID. This rate, however, was only 2.9% in patients with mutations leading to amino acid group changes. Secondly; in patients with mutations causing no amino acid group changes affecting A2, A3 and C2 domains, ID risk was found to be higher than in patients with mutations leading to amino acid group changes. Thirdly; an association between ID and CADD and REVEL scores was observed. Conclusion: In mild HA patients, the characteristics of missense mutations in terms of amino acid group changes, and CADD and REVEL scores could be of considerable utility in the prediction of ID risk.","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":" ","pages":"0-0"},"PeriodicalIF":0.3,"publicationDate":"2021-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43526673","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-07-08DOI: 10.4274/jpr.galenos.2020.92678
F. Mojarad, M. Farhadian, S. Torkaman
{"title":"The Prevalence of Sports-related Dental Injuries and the Rate of Awareness of Mouthguard Use among Child Athletes","authors":"F. Mojarad, M. Farhadian, S. Torkaman","doi":"10.4274/jpr.galenos.2020.92678","DOIUrl":"https://doi.org/10.4274/jpr.galenos.2020.92678","url":null,"abstract":"","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"7 1","pages":"358-364"},"PeriodicalIF":0.3,"publicationDate":"2020-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44483726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-07-08DOI: 10.4274/jpr.galenos.2020.98470
Ayşe Kahraman, Gülçin Özalp Gerçeker, Figen Yardımcı, Elif Bilsin, Ş. Binay Yaz, Hamide Nur Çevik Özdemir, Atiye Karakul, Dilek Zengin, Seda Ardahan Sevgili, Merve Gümüş, Selma Akpınar, D. Başbakkal
{"title":"The Effect of a Nurse Education Program on Infiltration and Extravasation in Pediatric Patients at a University Hospital","authors":"Ayşe Kahraman, Gülçin Özalp Gerçeker, Figen Yardımcı, Elif Bilsin, Ş. Binay Yaz, Hamide Nur Çevik Özdemir, Atiye Karakul, Dilek Zengin, Seda Ardahan Sevgili, Merve Gümüş, Selma Akpınar, D. Başbakkal","doi":"10.4274/jpr.galenos.2020.98470","DOIUrl":"https://doi.org/10.4274/jpr.galenos.2020.98470","url":null,"abstract":"","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"7 1","pages":"309-315"},"PeriodicalIF":0.3,"publicationDate":"2020-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45915878","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-07-08DOI: 10.4274/jpr.galenos.2019.38278
Esra Işık, Bilçağ Akgün, T. Atik, F. Özkınay, Ö. Çoğulu
{"title":"Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings","authors":"Esra Işık, Bilçağ Akgün, T. Atik, F. Özkınay, Ö. Çoğulu","doi":"10.4274/jpr.galenos.2019.38278","DOIUrl":"https://doi.org/10.4274/jpr.galenos.2019.38278","url":null,"abstract":"","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"7 1","pages":"267-272"},"PeriodicalIF":0.3,"publicationDate":"2020-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41459399","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2020-07-08DOI: 10.4274/jpr.galenos.2019.75010
S. Shanbhag, R. Alva
1,000 live births. A million of these are due to neonatal infections. Neonatal sepsis is encountered in 1-10 per 1,000 live births in developed countries and is believed to be three times higher in developing countries (1). Premature rupture of membranes (PROM) is responsible for 5.2% of neonatal infections (2). ABS TRACT Aim: Premature rupture of membranes (PROM) is a significant risk factor for various adverse neonatal outcomes such as prematurity, respiratory distress, birth asphyxia and early onset neonatal sepsis. Due to the public health relevance of this topic and its higher burden on health care services, this study was carried out to the identify risk factors and predictors of neonatal outcomes among babies born to mothers with PROM.
{"title":"Early Neonatal Outcomes in Premature Rupture of Membranes Beyond Twenty-eight Weeks of Gestation in a Tertiary Care Hospital of Coastal Karnataka","authors":"S. Shanbhag, R. Alva","doi":"10.4274/jpr.galenos.2019.75010","DOIUrl":"https://doi.org/10.4274/jpr.galenos.2019.75010","url":null,"abstract":"1,000 live births. A million of these are due to neonatal infections. Neonatal sepsis is encountered in 1-10 per 1,000 live births in developed countries and is believed to be three times higher in developing countries (1). Premature rupture of membranes (PROM) is responsible for 5.2% of neonatal infections (2). ABS TRACT Aim: Premature rupture of membranes (PROM) is a significant risk factor for various adverse neonatal outcomes such as prematurity, respiratory distress, birth asphyxia and early onset neonatal sepsis. Due to the public health relevance of this topic and its higher burden on health care services, this study was carried out to the identify risk factors and predictors of neonatal outcomes among babies born to mothers with PROM.","PeriodicalId":42409,"journal":{"name":"Journal of Pediatric Research","volume":"7 1","pages":"273-278"},"PeriodicalIF":0.3,"publicationDate":"2020-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43828937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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