Journal of Academy of Medical Sciences
Home | About the journal | Editorial board | Search | Ahead of print | Current issue | Archives
Subscribe | Submit article | Instructions | Subscribe | Contact us | Login 
 
  Users Online: 85 Home Print this page Email this page Small font sizeDefault font sizeIncrease font size  

 Table of Contents  
ORIGINAL ARTICLE
Year : 2012  |  Volume : 2  |  Issue : 3  |  Page : 110-114

Seasonality of viral hepatitis


Department of Medicine, Knappschafts Krankenhaus, Ruhr-University, Bochum, Germany

Date of Web Publication21-May-2014

Correspondence Address:
Dr. Auda Fares
Albert-Schlangen Str. 36, 50181 Bedburg
Germany
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2249-4855.132952

Rights and Permissions
  Abstract 

Viral hepatitis is an infection that has been reported to be present throughout the year, but some particular months are associated with higher incidences. The primary objective was to review and report on the current knowledge and evidence that exists on seasonality of different type of acute viral hepatitis world-wide in order to develop recommendations for future research, prevention and control. Materials and Methods: A systematic literature review was performed to identify all the primary reports and studies published during 1970-2012 on acute hepatitis A, B, C and E (AHA, AHB, AHC and AHE) in human subjects by searching PubMed, reference lists of major articles and correspondence with scientific experts. For each report or study included, the following information was extracted (as applicable to study): Location (country and setting), study population (number of cases, patients), seasonal or monthly rate and study duration. Results: There is no definite and consistent seasonal pattern has been observed on AHA; AHB; AHE and AHC, although evidence points towards spring and summer peak for hepatitis A, B, C and E. Multiple source of transmission such as; summer travel to an endemic area, swimming habits of the population in hot months, increase sexual contact, tattoo, poor hygiene and environmental sanitation and food habits (feco-oral transmission of viral hepatitis) probably exists and should be further investigated through analytical and epidemiological.

Keywords: Hepatitis, periodicity, seasons


How to cite this article:
Fares A. Seasonality of viral hepatitis. J Acad Med Sci 2012;2:110-4

How to cite this URL:
Fares A. Seasonality of viral hepatitis. J Acad Med Sci [serial online] 2012 [cited 2019 Dec 10];2:110-4. Available from: http://www.e-jams.org/text.asp?2012/2/3/110/132952


  Introduction Top


Acute viral hepatitis is a systemic infection affecting the liver predominantly. Almost all cases of acute viral hepatitis are caused by one of five viral agents: Hepatitis A virus (HAV), hepatitis B virus (HBV), hepatitis C virus (HCV), hepatitis D virus and hepatitis E virus (HEV). Hepatitis may occur with limited or no symptoms, but often leads to jaundice, anorexia and malaise. Clinically classified the hepatitis in two form acute and chronic; hepatitis is acute when it lasts less than 6 months and chronic when it persists longer.

HAV and HEV are acquired by consuming food and water contaminated by the virus (excreted in-patient's stool) by way of the fecal-oral. HBV, HCV are contagious by blood and blood products, also may be transmitted by sexual contact. Vaccine for hepatitis A and B is available, but no vaccine is available for hepatitis C or E.

Viral hepatitis infection has been reported to be present throughout the year, but some particular months are associated with higher incidences in most of the countries around the world. The exact reasons why hepatitis infection cases present in one season more than other are not completely understand. However, several researchers have suggested that the climatic and behavioral factors such as, summer travel to endemic area, swimming habits of the population in hot months, increase in sexual contact, tattoo, poor hygiene and environmental sanitation and food habits (feco-oral transmission of viral hepatitis) may play a significant role in the seasonal appearance of diseases. [1],[2],[3]

However, none have documented a systematic review process or specifically focused on global seasonal patterns of viral hepatitis. Our objectives were to determine the seasonal pattern of viral hepatitis and possible seasonal trigger factors. We systematically reviewed the scientific literature to give an overview of the evidence available from the last 42 years and make recommendations for future research and prevention and control.


  Materials and Methods Top


A systematic review of the literature was performed to identify all the primary reports and studies that have been published between January 1970 and September 2012, conducted on the prevalence and incidence of HAV, HBV, HCV and HEV infections in human subjects. The primary objective was to review and report on the current knowledge and evidence that exists on seasonality of different type of hepatitis world-wide. Studies were included if (i) they had been conducted continuously for a minimum of a full-year to cover all seasons, (ii) the primary outcome was a clinical and laboratory confirmed diagnosis of the diseases of interest in human subjects, (iii) the study reported case data temporally (day, week, month) (iv) the study was written in English and published in a peer reviewed journal, (v) study design did not include intervention trials or deals with chronic hepatitis and, (vi) diagnosis of viral hepatitis infection was laboratory-confirmed using recognized tests. If one of the four criteria was not met, the report was excluded. For each report or study included, the following information was extracted (as applicable to study): Location (country and setting), study population (number of cases, patients), seasonal or monthly rate and study duration.

The studies were identified by using electronic search of the United States National Library of Medicine and the National Institutes of Health Medical Database (PubMed) from its inception was conducted in September 2012. Search words used were: "Periodicity" and "Seasons" and "hepatitis". This list was extended by including also references from a recent review of hepatitis epidemiology and correspondence with scientific experts.

As a majority of the data in this review came from countries in the northern hemisphere, seasons were defined based on their occurrence in the Northern hemisphere: Winter (December-February), spring (March-May), summer (June-August) and autumn (September-November). For the countries located in the southern hemisphere like Brazil, data for December, January, February comprised the summer season; data for March, April and May the fall season; June, July and August the winter season; and September, October and November the spring season. [3] Due to lack of consistency among the statistical methods used in most of the studies and limitation of data provide. Therefore, it was not possible to do statistical analysis to integrate the results.


  Results Top


Across four type of viral hepatitis infection (HAV, HBV, HCV and HEV), a total of 210 titles and abstracts were screened for eligibility. Of these, 28 studies from 17 countries conducted across 1970 to 2012 met the selection criteria and contributed to the systematic review. Key data from these studies are summarized in [Table 1]. Two studies were included in this review does not contain information about the number of participants and the duration of studies were not available in three selected studies. Form a total of studies included in this review, 16 articles included results from patients with acute hepatitis A, eight studies reported on acute hepatitis B, 12 studies on acute hepatitis E (AHE) and four studies on AHE. The seasonal distribution of viral hepatitis A, B, C and E showed a variable peak around the year with most prominent peak in the spring and summer in most of the countries subjects. For the viral hepatitis B infection, found no evidence of seasonality in half of studies included in this review.
Table 1: Global seasonality of acute viral hepatitis

Click here to view



  Discussion Top


Based on data from 28 studies, irregular, cyclical patterns were observed for acute viral hepatitis, with most prominent peaks were shown in spring and summer for hepatitis A; B; C and E in some of the countries subjects. These findings has been explained by some authors as due to summer travel to an endemic area, swimming habits of the population in hot months, increase sexual contact, tattoo, poor hygiene and environmental sanitation, and food habits (faeco-oral transmission of viral hepatitis). [1],[2],[3] HAV and HEV are communicable by way of the fecal-oral. On the other hand, HBV, HCV are contagious by blood and blood products, also may be transmitted by sexual intercourse and household exposure to an infected contact, exposure to multiple partners and perinatal exposure, particularly for hepatitis C, but the efficiency of transmission in these settings appears to be low.

HAV is an extremely stable virus and can survive for 12 weeks to 10 months in water. [28],[29],[30] This stability accounts for the frequent occurrence of waterborne and shellfish-transmitted outbreaks. [27],[31],[32] In this regard, the virus is relatively resistant to heat or chemical inactivation and this situation allow the dissemination of HAV infection. Therefore, disruption of sanitation and water supplies was the most likely contributing factor for the seasonal occurrence of hepatitis A and E. A number of case reports have described water exposure as a possible risk factor for acquiring HEV infection: Swimming in a lake, [33] through exposure to water from a high-pressure hose and water sourced from a stream which ran adjacent to a free-range pig farm. [34] In The Netherlands 2/12 (17%) of monthly samples of river water used for drinking water production and recreation were found positive for HEV ribonucleic acid in two separate years. [35] Furthermore, the peak incidence of HAV infection in the coast of Rio de Janeiro in Brazil was found during the rainy season. These finding indicate that the HAV infections transmitted indirectly through rainfall because these rains usually fill up the rivers so they could overflow and the persons could be contaminated with these waters. Other possible explanation is the swim habits of the population studied. All of them usually frequented the beaches of the Rio de Janeiro. The coast of Rio de Janeiro is very large and the city has a lot of rivers and waterfalls. Persons that lived at Rio de Janeiro usually swim at the beaches and rivers of the city. During the rainy season, the heavy runoff could cause contamination of these waters leading to excess of HAV infection during this season. [3] The observation in some countries that the peak of the epidemic was during the winter months suggests that transmission of HAV and HEV is related to shellfish consumption. HAV infection is the most serious viral infection linked to shellfish consumption, causing a debilitating disease and, occasionally, death. The first documented outbreak of "infectious hepatitis" occurred in Sweden in 1955, when 629 cases were associated with raw oyster consumption. [36] Subsequently, many HAV-associated outbreaks have been reported world-wide. The most demonstrative one was the outbreak of HAV infection in Shanghai, China, in 1988, in which almost 300,000 cases were linked to the consumption of clams harvested from a sewage-polluted area. [37],[38] The fairly protracted incubation period (mean duration, 4 weeks) of HAV infection makes it very difficult to determine the association with a particular food vehicle in sporadic cases. Normally, the food will not be available for testing at the time of diagnosis. Thus, it can be safely assumed that HAV infection associated with shellfish consumption is probably underreported. In addition, as shellfish consumption was found to be possibly one of the risk factors involved in AHE acute hepatitis C (AHC) it is now suspected that exposure to sewage or wastewater may contribute to HEV endemicity. [39],[40]

Travel history and sexual activity, which is supposed to be higher in summer, may give us explanation regarding to the summer seasonal peak of acute viral hepatitis. In a study conducted in UK found that the higher sexual activity and unsafe sex coinciding with the summer vacation. Data relating to sexually transmitted infections and attendances for human immunodeficiency virus tests similarly show an increase in the months following Christmas and in late summer. [41]

Injection drug use is the primary mode of transmission for HCV and HBV infection in the developed world. In one study conducted in USA, seroprevalence of HCV and HBV infection among long-term injection drug users were 85.0% for HCV and 77.4% for HBV and 64.7%, 49.8%, among those who had injected for 1 year or less. [42] Interestingly, seasonality of illicit drug has been reported to be higher in winter than in summer among USA teens (12-17 years of age). In another study conducted in Australia by using arrest data found evidence of higher arrest rates for drug possession and use during the Australian fall and winter (April through July) and lower rates during the Australian spring (November and December). [43] Additionally, a recent longitudinal study of cocaine and cocaine metabolites in wastewater reveal a clear seasonal difference indicative of human seasonal cocaine use patterns. [44] This observation could be a help to explaining seasonal occurrence of HCV or HBV.

Regarding seasonal variation of the occurrence of hepatitis B, some authors detected a peak in either spring or summer, whereas, others found no seasonal peak. Vaccination against hepatitis B has been recommended in most of the countries for all newborns, infants and particular risk groups. This gives us an explanation for the reduction in the incidence of hepatitis B infection and consequently, reduce seasonal incidence peak in general. Furthermore, seasonal exposure to dietary aflatoxin has been reported to be associated with acutely and chronically HBV-infected patients with most prominent during April-July. [45],[46]

Finally, the incubation period from time of exposure to the onset of symptoms can range from 2 weeks to 6 months and infection can be self-limited or chronic. Therefore, theoretically people who are infected in autumn or winter can develop active hepatitis shortly after infections are on average diagnosed 1-6 months after the first onset of symptom, resulting in a higher number of notifications in spring and summer. Furthermore, the number of unnotified or viral carrier cases is not known. These factors are potential confounders in the study of viral hepatitis seasonality variation.

In summary, this first systematic review on the seasonal variability of human viral hepatitis found that there is no definite and consistent seasonal pattern has been observed on viral hepatitis, although evidence points toward spring and summer peak. Multiple sources of transmission are likely to exist and these need to be further defined so that specific and appropriate preventive measures can be implemented.

 
  References Top

1.Al-Naaimi AS, Turky AM, Khaleel HA, Jalil RW, Mekhlef OA, Kareem SA, et al. Predicting acute viral hepatitis serum markers (A and E) in patients with suspected acute viral hepatitis attending primary health care centers in Baghdad: A one year cross-sectional study. Glob J Health Sci 2012;4:172-83.  Back to cited text no. 1
    
2.Al-Nasrawi KK, Al Diwan JK, Al-Hadithi TS, Saleh AM. Viral hepatitis E outbreak in Al-Sadr city, Baghdad, Iraq. East Mediterr Health J 2010;16:1128-32.  Back to cited text no. 2
    
3.Villar LM, De Paula VS, Gaspar AM. Seasonal variation of hepatitis A virus infection in the city of Rio de Janeiro, Brazil. Rev Inst Med Trop Sao Paulo 2002;44:289-92.  Back to cited text no. 3
    
4.Talaat M, El-Sayed N, Kandeel A, Azab MA, Afifi S, Youssef FG, et al. Sentinel surveillance for patients with acute hepatitis in Egypt, 2001-04. East Mediterr Health J 2010;16:134-40.  Back to cited text no. 4
    
5.Han YN. Identification of acute self-limited hepatitis B among patients presenting with hepatitis B virus-related acute hepatitis: A hospital-based epidemiological and clinical study. J Int Med Res 2009;37:1952-60.  Back to cited text no. 5
[PUBMED]    
6.Inoue J, Ueno Y, Nagasaki F, Akahane T, Fukushima K, Kogure T, et al. Sporadic acute hepatitis E occurred constantly during the last decade in northeast Japan. J Gastroenterol 2009;44:329-37.  Back to cited text no. 6
    
7.Dalton HR, Stableforth W, Hazeldine S, Thurairajah P, Ramnarace R, Warshow U, et al. Autochthonous hepatitis E in Southwest England: A comparison with hepatitis A. Eur J Clin Microbiol Infect Dis 2008;27:579-85.  Back to cited text no. 7
    
8.Dalton HR, Thurairajah PH, Fellows HJ, Hussaini HS, Mitchell J, Bendall R, et al. Autochthonous hepatitis E in southwest England. J Viral Hepat 2007;14:304-9.  Back to cited text no. 8
    
9.Gharbi-Khelifi H, Sdiri K, Ferre V, Harrath R, Berthome M, Billaudel S, et al. A 1-year study of the epidemiology of hepatitis A virus in Tunisia. Clin Microbiol Infect 2007;13:25-32.  Back to cited text no. 9
    
10.Battikhi MN, Battikhi EG. The seroepidemiology of Hepatitis A virus in Amman, Jordan. New Microbiol 2004;27:215-20.  Back to cited text no. 10
    
11.Huang P, Ye G, Zhong J, Sha Q. Assessment of current epidemiological status of viral hepatitis in Guangdong Province, China. Southeast Asian J Trop Med Public Health 2002;33:832-6.  Back to cited text no. 11
    
12.Rakadjieva T, Stoilova J, Petrov A. A study on the basic epidemiological parameters of viral hepatitis A in the region of Plovdiv, Bulgaria. Folia Med (Plovdiv) 2002;44:11-4.  Back to cited text no. 12
    
13.Singh J, Prakash C, Gupta RS, Bora D, Jain DC, Datta KK. Epidemiology of endemic viral hepatitis in an urban area of India: A retrospective community study in Alwar. Bull World Health Organ 1997;75:463-8.  Back to cited text no. 13
    
14.Green MS, Block C, Slater PE. Rise in the incidence of viral hepatitis in Israel despite improved socioeconomic conditions. Rev Infect Dis 1989;11:464-9.  Back to cited text no. 14
    
15.Papaevangelou G, Roumeliotou-Karayannis A, Contoyannis P. Changing epidemiological characteristics of acute viral hepatitis in Greece. Infection 1982;10:1-4.  Back to cited text no. 15
[PUBMED]    
16.Follett EA, McMichael S. Acute hepatitis A infection in West Scotland. Scott Med J 1981;26:135-7.  Back to cited text no. 16
[PUBMED]    
17.Naumova EN, Jagai JS, Matyas B, DeMaria A Jr, MacNeill IB, Griffiths JK. Seasonality in six enterically transmitted diseases and ambient temperature. Epidemiol Infect 2007;135:281-92.  Back to cited text no. 17
    
18.Held L, Hofmann M, Höhle M, Schmid V. A two-component model for counts of infectious diseases. Biostatistics 2006;7:422-37.  Back to cited text no. 18
    
19.Stewart JS, Farrow LJ, Clifford RE, Lamb SG, Coghill NF, Lindon RL, et al. A three-year survey of viral hepatitis in West London. Q J Med 1978;47:365-84.  Back to cited text no. 19
[PUBMED]    
20.Krausz Y, Melamed S, Sandler SG, Eliakim M. A comparative study of hepatitis B and non-B in hospitalized adults in an endemic area. Isr J Med Sci 1977;13:9-14.  Back to cited text no. 20
[PUBMED]    
21.Mansuy JM, Abravanel F, Miedouge M, Mengelle C, Merviel C, Dubois M, et al. Acute hepatitis E in south-west France over a 5-year period. J Clin Virol 2009;44:74-7.  Back to cited text no. 21
    
22.Dalton HR, Stableforth W, Thurairajah P, Hazeldine S, Remnarace R, Usama W, et al. Autochthonous hepatitis E in Southwest England: Natural history, complications and seasonal variation, and hepatitis E virus IgG seroprevalence in blood donors, the elderly and patients with chronic liver disease. Eur J Gastroenterol Hepatol 2008;20:784-90.  Back to cited text no. 22
    
23.Zhu G, Qu Y, Jin N, Sun Z, Liu T, Lee H, et al. Seroepidemiology and molecular characterization of hepatitis E virus in Jilin, China. Infection 2008;36:140-6.  Back to cited text no. 23
    
24.Shrestha SM, Shrestha S, Tsuda F, Nishizawa T, Gotanda Y, Takeda N, et al. Molecular investigation of hepatitis E virus infection in patients with acute hepatitis in Kathmandu, Nepal. J Med Virol 2003;69:207-14.  Back to cited text no. 24
    
25.Zhuang H, Cao XY, Liu CB, Wang GM. Epidemiology of hepatitis E in China. Gastroenterol Jpn 1991;26 Suppl 3:135-8.  Back to cited text no. 25
    
26.Pal PK, Haldar A, Bhattacharya SK. An outbreak of viral hepatitis in a housing complex of north Calcutta. J Commun Dis 1994;26:88-91.  Back to cited text no. 26
    
27.Velázquez O, Stetler HC, Avila C, Ornelas G, Alvarez C, Hadler SC, et al. Epidemic transmission of enterically transmitted non-A, non-B hepatitis in Mexico, 1986-1987. JAMA 1990;263:3281-5.  Back to cited text no. 27
    
28.Biziagos E, Passagot J, Crance JM, Deloince R. Long-term survival of hepatitis A virus and poliovirus type 1 in mineral water. Appl Environ Microbiol 1988;54:2705-10.  Back to cited text no. 28
    
29.McCaustland KA, Bond WW, Bradley DW, Ebert JW, Maynard JE. Survival of hepatitis A virus in feces after drying and storage for 1 month. J Clin Microbiol 1982;16:957-8.  Back to cited text no. 29
[PUBMED]    
30.Sattar SA, Jason T, Bidawid S, Farber J. Foodborne spread of hepatitis A: Recent studies on virus survival, transfer and inactivation. Can J Infect Dis 2000;11:159-63.  Back to cited text no. 30
    
31.Leoni E, Bevini C, Degli Esposti S, Graziano A. An outbreak of intrafamiliar hepatitis A associated with clam consumption: Epidemic transmission to a school community. Eur J Epidemiol 1998;14:187-92.  Back to cited text no. 31
    
32.Yao G. Clinical spectrum and natural history of viral hepatitis A in a 1988 Shangai epidemic. In: Hollinger BN, Lemon SM, Margolis HS, editors. Viral Hepatitis and Liver Disease. Baltimore: Williams and Wilkins; 1991. p. 76-8.  Back to cited text no. 32
    
33.Moucari R, Bernuau J, Nicand E, Cazals-hatem D, Valla D, Marcellin P, et al. Acute hepatitis E with severe jaundice: Report of three cases. Eur J Gastroenterol Hepatol 2007;19:1012-5.  Back to cited text no. 33
    
34.Lockwood GL, Fernandez-Barredo S, Bendall R, Banks M, Ijaz S, Dalton HR. Hepatitis E autochthonous infection in chronic liver disease. Eur J Gastroenterol Hepatol 2008;20:800-3.  Back to cited text no. 34
    
35.Bouwknegt M, Rutjes S, de Roda Husman AM. Hepatits E virus genotype 3 sources in the Netherlands and potential transmission routes to humans. In: 4 th Med-Vet-Net Annual Scientific Meeting Abstract Book, St. Malo, France, 11-14 June 2008. p. 37.  Back to cited text no. 35
    
36.Roos B. Hepatitis epidemic transmitted by oysters. Sven Lakartidn 1956;53:989-1003.  Back to cited text no. 36
[PUBMED]    
37.Tang YW, Wang JX, Xu ZY, Guo YF, Qian WH, Xu JX. A serologically confirmed, case-control study, of a large outbreak of hepatitis A in China, associated with consumption of clams. Epidemiol Infect 1991;107:651-7.  Back to cited text no. 37
    
38.Halliday ML, Kang LY, Zhou TK, Hu MD, Pan QC, Fu TY, et al. An epidemic of hepatitis A attributable to the ingestion of raw clams in Shanghai, China. J Infect Dis 1991;164:852-9.  Back to cited text no. 38
    
39.Renou C, Moreau X, Pariente A, Cadranel JF, Maringe E, Morin T, et al. A national survey of acute hepatitis E in France. Aliment Pharmacol Ther 2008;27:1086-93.  Back to cited text no. 39
    
40.Potasman I, Paz A, Odeh M. Infectious outbreaks associated with bivalve shellfish consumption: A worldwide perspective. Clin Infect Dis 2002;35:921-8.  Back to cited text no. 40
    
41.Wellings K, Macdowall W, Catchpole M, Goodrich J. Seasonal variations in sexual activity and their implications for sexual health promotion. J R Soc Med 1999;92:60-4.  Back to cited text no. 41
    
42.Garfein RS, Vlahov D, Galai N, Doherty MC, Nelson KE. Viral infections in short-term injection drug users: The prevalence of the hepatitis C, hepatitis B, human immunodeficiency, and human T-lymphotropic viruses. Am J Public Health 1996;86:655-61.  Back to cited text no. 42
    
43.Robert HL, Alan RM. Seasonal Use of Marijuana and Cocaine by Arrestees in Anchorage, Alaska. Anchorage, Alaska: University of Alaska Anchorage; 2005.  Back to cited text no. 43
    
44.Mari F, Politi L, Biggeri A, Accetta G, Trignano C, Di Padua M, et al. Cocaine and heroin in waste water plants: A 1-year study in the city of Florence, Italy. Forensic Sci Int 2009;189:88-92.  Back to cited text no. 44
    
45.Villar S, Le Roux-Goglin E, Gouas DA, Plymoth A, Ferro G, Boniol M, et al. Seasonal variation in TP53 R249S-mutated serum DNA with aflatoxin exposure and hepatitis B virus infection. Environ Health Perspect 2011;119:1635-40.  Back to cited text no. 45
    
46.Wild CP, Yin F, Turner PC, Chemin I, Chapot B, Mendy M, et al. Environmental and genetic determinants of aflatoxin-albumin adducts in the Gambia. Int J Cancer 2000;86:1-7.  Back to cited text no. 46
    



 
 
    Tables

  [Table 1]


This article has been cited by
1 The Honolulu Liver Disease Cluster at the Medical Center: Its Mysteries and Challenges
Rolf Teschke,Axel Eickhoff
International Journal of Molecular Sciences. 2016; 17(4): 476
[Pubmed] | [DOI]
2 The mystery of the Hawaii liver disease cluster in summer 2013: A pragmatic and clinical approach to solve the problem
Rolf Teschke,Alexander Schwarzenboeck,Christian Frenzel,Johannes Schulze,Axel Eickhoff,Albrecht Wolff
Annals of Hepatology. 2016; 15(1): 91
[Pubmed] | [DOI]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
Introduction
Materials and Me...
Results
Discussion
References
Article Tables

 Article Access Statistics
    Viewed2432    
    Printed193    
    Emailed0    
    PDF Downloaded220    
    Comments [Add]    
    Cited by others 2    

Recommend this journal