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"subdocumento" => "fla" "cita" => "Rev Port Pneumol. 2008;14:747-68" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 2847 "formatos" => array:3 [ "EPUB" => 237 "HTML" => 1783 "PDF" => 827 ] ] "pt" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Artigo Original/Original Article</span>" "titulo" => "Prevalência da asma e da rinite em adolescentes de 13 anos do Porto, Portugal" "tienePdf" => "pt" "tieneTextoCompleto" => 0 "tieneResumen" => array:2 [ 0 => "pt" 1 => "en" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "747" "paginaFinal" => "768" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Prevalence of asthma and rhinitis in 13 year old adolescents in Porto, Portugal" ] ] "contieneResumen" => array:2 [ "pt" => true "en" => true ] "contienePdf" => array:1 [ "pt" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Helena Falcão, Elisabete Ramos, Agostinho Marques, Henrique Barros" "autores" => array:4 [ 0 => array:2 [ "nombre" => "Helena" "apellidos" => "Falcão" ] 1 => array:2 [ "nombre" => "Elisabete" "apellidos" => "Ramos" ] 2 => array:2 [ "nombre" => "Agostinho" "apellidos" => "Marques" ] 3 => array:2 [ "nombre" => "Henrique" "apellidos" => "Barros" ] ] ] ] ] "idiomaDefecto" => "pt" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0873215915302853?idApp=UINPBA00004E" "url" => "/08732159/0000001400000006/v1_201509151433/S0873215915302853/v1_201509151433/pt/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S087321591530283X" "issn" => "08732159" "doi" => "10.1016/S0873-2159(15)30283-X" "estado" => "S350" "fechaPublicacion" => "2008-11-01" "aid" => "1" "copyright" => "Sociedade Portuguesa de Pneumologia/SPP" "documento" => "simple-article" "crossmark" => 0 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "edi" "cita" => "Rev Port Pneumol. 2008;14:725-6" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 1931 "formatos" => array:3 [ "EPUB" => 200 "HTML" => 1043 "PDF" => 688 ] ] "pt" => array:9 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Editorial/Editorial</span>" "titulo" => "A <span class="elsevierStyleItalic">Revista Portuguesa de Pneumologia</span> no <span class="elsevierStyleItalic">Science Citation Index</span>" "tienePdf" => "pt" "tieneTextoCompleto" => 0 "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "725" "paginaFinal" => "726" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "The Portuguese Pulmonology Journal <span class="elsevierStyleItalic">on the</span> Science Citation Index" ] ] "contienePdf" => array:1 [ "pt" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Helena Donato" "autores" => array:1 [ 0 => array:2 [ "nombre" => "Helena" "apellidos" => "Donato" ] ] ] ] ] "idiomaDefecto" => "pt" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S087321591530283X?idApp=UINPBA00004E" "url" => "/08732159/0000001400000006/v1_201509151433/S087321591530283X/v1_201509151433/pt/main.assets" ] "pt" => array:15 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Artigo Original/Original Article</span>" "titulo" => "Estudo de polimorfismos genéticos do HLA (classes I e II) e do TNF-α em doentes com sarcoidose" "tieneTextoCompleto" => 0 "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "727" "paginaFinal" => "746" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "António Morais, Helena Alves, Bruno Lima, Luís Delgado, Ricardo Gonçalves, Sandra Tafulo" "autores" => array:6 [ 0 => array:3 [ "nombre" => "António" "apellidos" => "Morais" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">1</span>" "identificador" => "af0005" ] ] ] 1 => array:3 [ "nombre" => "Helena" "apellidos" => "Alves" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "af0010" ] ] ] 2 => array:3 [ "nombre" => "Bruno" "apellidos" => "Lima" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "af0010" ] ] ] 3 => array:3 [ "nombre" => "Luís" "apellidos" => "Delgado" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">3</span>" "identificador" => "af0015" ] ] ] 4 => array:3 [ "nombre" => "Ricardo" "apellidos" => "Gonçalves" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "af0010" ] ] ] 5 => array:3 [ "nombre" => "Sandra" "apellidos" => "Tafulo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "af0010" ] ] ] ] "afiliaciones" => array:3 [ 0 => array:3 [ "entidad" => "Serviço de Pneumologia do Hospital São João, Porto / Pulmonology Unit, Hospital São João, Porto" "etiqueta" => "1" "identificador" => "af0005" ] 1 => array:3 [ "entidad" => "Centro de Histocompatibilidade do Norte / Histocompatability Centre of the North" "etiqueta" => "2" "identificador" => "af0010" ] 2 => array:3 [ "entidad" => "Serviço de Imunologia da Faculdade de Medicina do Porto / Pulmonology Unit, Porto Faculty of Medicine" "etiqueta" => "3" "identificador" => "af0015" ] ] ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "HLA class I and II and TNF-α gene polymorphisms in sarcoidosis patients" ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2008-03-26" "fechaAceptado" => "2008-06-17" "PalabrasClave" => array:2 [ "pt" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palavras-chave" "identificador" => "xpalclavsec570052" "palabras" => array:3 [ 0 => "Sacordoise" 1 => "genética" 2 => "HLA" ] ] ] "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Key-words" "identificador" => "xpalclavsec570053" "palabras" => array:3 [ 0 => "Sarcoidosis" 1 => "genetics" 2 => "HLA" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "pt" => array:2 [ "titulo" => "Resumo" "resumen" => "<span id="as0005" class="elsevierStyleSection elsevierViewall"><p id="sp0005" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Introdução:</span> A susceptibilidade genética na ocorrência da sarcoidose é sugerida por alguns factores, nomeadamente pela observação de casos de agregação familiar e a associação da raça a diferentes tipos de incidência e gravidade da doença. Vários estudos têm evidenciado a associação da classe I e especialmente da classe II do sistema HLA com a susceptibilidade à sarcoidose.</p><p id="sp0010" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Objectivos:</span> Estudo dos polimorfismos genéticos da classe I e II do sistema HLA e do TNF-α num grupo de doentes com sarcoidose, nomeadamente a sua influência na susceptibilidade, apresentação clínica e evolução da doença.</p><p id="sp0015" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Material e métodos:</span> Foram incluídos 104 doentes com sarcoidose, tendo sido estudadas a apresentação clínica, funcional, radiológica e os resultados do LBA. Foram usados métodos de biologia molecular na genotipagem do HLA-A*, B*, C*, DRB1*, DQB1* e TNF-α. O ADN foi extraído do sangue periférico e foram usados os métodos PCR-SSP e PCR-<span class="elsevierStyleItalic">reverse hibridization</span>. As frequências alélicas foram comparadas com controlos da mesma região geográfica pelo teste χ<span class="elsevierStyleSup">2</span>, sendo usado o teste Kruskal-Wallis para variáveis contínuas.</p><p id="sp0020" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Resultados:</span> Comparativamente com os controlos, os doentes incluídos apresentavam frequências aumentadas de: B*08 (10,6% <span class="elsevierStyleItalic">vs</span> 6,1%), OR<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>1,8, IC<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1,1;3,1], p<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,02; DRB1*12 (4,3% <span class="elsevierStyleItalic">vs</span> 1,7%), OR<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2,63, IC<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1,1;6,1], p<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,03. Os doentes com eritema nodoso apresentaram aumento das frequências alélicas de DRB1*03 (28% <span class="elsevierStyleItalic">vs</span> 9,3%), RR<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2,39, IC<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1,5;3,8], p<span class="elsevierStyleInf">c</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,01 e DQB1*02 (38% <span class="elsevierStyleItalic">vs</span> 18%), RR<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2,1, IC<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1,3;3,3], p<span class="elsevierStyleInf">c</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,02. O alelo DQB1*03 está diminuído nos doentes que apresentam síndroma ventilatória obstrutiva, RR<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,53, IC<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[0,3;0,9], p<span class="elsevierStyleInf">c</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,05. O alelo DRB1*15 encontra-se significativamente associado quer à síndroma ventilatória restritiva quer à diminuição da transferência alveolocapilar (21,1% <span class="elsevierStyleItalic">vs</span> 6,6%), RR<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2,46, IC<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1,35;4,48], p<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,01 e (18,1% <span class="elsevierStyleItalic">vs</span> 3,8%), RR<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>1,87, p<span class="elsevierStyleInf">c</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,05, respectivamente. Por sua vez, o genótipo A/A <span class="elsevierStyleItalic">(high)</span> do TNF-α apresentou uma frequência aumentada (p<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0,04) nos doentes com eritema nodoso.</p><p id="sp0025" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Conclusões:</span> Os resultados obtidos adicionam evidência ao facto de, quer a classe I quer a classe II do sistema HLA influenciarem a susceptibilidade, o tipo de apresentação, o grau de gravidade e a evolução na sarcoidose. Por outro lado, o eritema nodoso parece relacionar-se com o genótipo de elevada produção de TNF-α, associação esta já anteriormente descrita.</p><p id="sp0030" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Rev Port Pneumol 2008; XIV (6</span>)<span class="elsevierStyleBold">: 727-746</span></p></span>" ] "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="as0010" class="elsevierStyleSection elsevierViewall"><p id="sp0035" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Introduction:</span> Several factors suggest a genetic predisposition to sarcoidosis, namely the recognition of race as a risk factor and the occurrence of familial clustering of cases. Several studies have reported an association of sarcoidosis and HLA class I and especially class II alleles in different populations.</p><p id="sp0040" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Aim:</span> HLA class I, class II and TNF-α genotyping in a group of sarcoidosis patients and its relation with clinical presentation and outcome.</p><p id="sp0045" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Material and methods:</span> A total of 104 sarcoidosis patients were included. Clinical presentation, functional, radiology, BAL findings and organ involvement were studied. HLA– A*, -B*, -C*, DRB1*, DQB1* and TNF-α were genotyped by molecular biology methods. DNA was extracted from peripheral blood and PCR-SSP and PCR-reverse hybridisation methods were used. Allele frequencies were compared with controls from the same region. The X<span class="elsevierStyleSup">2</span> test was used for discrete values and the Kruskal-Wallis test for continuous values.</p><p id="sp0050" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Results:</span> When patients were compared with controls we noticed increased frequencies of B*08 (10.6% <span class="elsevierStyleItalic">vs</span>. 6.1%), O.R.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>1.8, C.I.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1.1;3.1], p<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.02; DRB1*12 (4.3% <span class="elsevierStyleItalic">vs</span>. 1.7%), O.R.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2.63, C.I.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1.1;6.1], p<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.03. Patients with erythema nodosum have increased frequencies of the alleles DRB1*03 (28% <span class="elsevierStyleItalic">vs</span>. 9.3%), R.R.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2.39, C.I.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1.5;3.8], p<span class="elsevierStyleInf">c</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.01 and DQB1*02 (38% <span class="elsevierStyleItalic">vs</span>. 18%), R.R.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2.1, C.I.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1.3;3.3], p<span class="elsevierStyleInf">c</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.02. Allele DQB1*03 is decreased in patients with obstructive pattern R.R.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.53, C.I.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[0.3;0.9], p<span class="elsevierStyleInf">c</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.05. Allele DRB1*15 is related to restrictive pattern and reduced diffusion capacity (21.1% <span class="elsevierStyleItalic">vs</span>. 6.6%), R.R.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2.46, C.I.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>[1.35;4.48], p<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.01 and (18.1% <span class="elsevierStyleItalic">vs</span>. 3.8%), R.R.<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>1.87, p<span class="elsevierStyleInf">c</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.05 respectively. The TNF-α A/A (high) genotype is significantly associated with erythema nodosum (p<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.04).</p><p id="sp0055" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Conclusions:</span> These data add support to the genetic association of HLA class I and II with sarcoidosis in terms of susceptibility, type of presentation, severity and outcome. Moreover as previously described in other populations, the TNF-α A/A (high) genotype has a significant association with erythema nodosum.</p><p id="sp0060" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Rev Port Pneumol 2008; XIV (6): 727-746</span></p></span>" ] ] "lecturaRecomendada" => array:1 [ 0 => array:3 [ "vista" => "all" "titulo" => "<span class="elsevierStyleSectionTitle" id="st0025">Bibliografia / Bibliography</span>" "seccion" => array:1 [ 0 => array:2 [ "vista" => "all" "bibliografiaReferencia" => array:42 [ 0 => array:3 [ "identificador" => "bb0005" "etiqueta" => "1." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "ATS/ERS/ WASOG Statement on Sarcoidosis" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "G.W. Hunninghake" 1 => "U. Costabel" 2 => "M. Ando" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1164/ajrccm.160.2.ats4-99" "Revista" => array:6 [ "tituloSerie" => "Am J Respir Crit Care Med" "fecha" => "1999" "volumen" => "160" "paginaInicial" => "736" "paginaFinal" => "755" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/10430755" "web" => "Medline" ] ] ] ] ] ] ] ] 1 => array:3 [ "identificador" => "bb0010" "etiqueta" => "2." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Sarcoidosis" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "M.C. Iannuzzi" 1 => "B.A. Rybicki" 2 => "A.S. Teirstein" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1056/NEJMra071714" "Revista" => array:6 [ "tituloSerie" => "N Engl J Med" "fecha" => "2007" "volumen" => "357" "paginaInicial" => "2153" "paginaFinal" => "2165" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/18032765" "web" => "Medline" ] ] ] ] ] ] ] ] 2 => array:3 [ "identificador" => "bb0015" "etiqueta" => "3." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Sarcoidosis" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "R.P. Baughman" 1 => "E.E. Lower" 2 => "R. du Bois" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/S0140-6736(03)12888-7" "Revista" => array:5 [ "tituloSerie" => "Lancet" "fecha" => "2003" "volumen" => "361" "paginaInicial" => "1111" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/12672326" "web" => "Medline" ] ] ] ] ] ] ] ] 3 => array:3 [ "identificador" => "bb0020" "etiqueta" => "4." "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Genetics ofn sarcoidosis; candidate genes and genome scans" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "M.C. 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Original language: Portuguese
Year/Month | Html | Total | |
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2024 November | 8 | 6 | 14 |
2024 October | 44 | 31 | 75 |
2024 September | 43 | 21 | 64 |
2024 August | 50 | 47 | 97 |
2024 July | 31 | 38 | 69 |
2024 June | 22 | 29 | 51 |
2024 May | 38 | 33 | 71 |
2024 April | 27 | 32 | 59 |
2024 March | 33 | 33 | 66 |
2024 February | 30 | 38 | 68 |
2024 January | 18 | 31 | 49 |
2023 December | 16 | 30 | 46 |
2023 November | 29 | 27 | 56 |
2023 October | 13 | 27 | 40 |
2023 September | 28 | 37 | 65 |
2023 August | 22 | 21 | 43 |
2023 July | 19 | 36 | 55 |
2023 June | 22 | 19 | 41 |
2023 May | 19 | 27 | 46 |
2023 April | 23 | 28 | 51 |
2023 March | 21 | 21 | 42 |
2023 February | 24 | 31 | 55 |
2023 January | 32 | 27 | 59 |
2022 December | 19 | 26 | 45 |
2022 November | 37 | 47 | 84 |
2022 October | 34 | 32 | 66 |
2022 September | 16 | 71 | 87 |
2022 August | 40 | 64 | 104 |
2022 July | 22 | 41 | 63 |
2022 June | 13 | 41 | 54 |
2022 May | 30 | 48 | 78 |
2022 April | 17 | 29 | 46 |
2022 March | 32 | 33 | 65 |
2022 February | 32 | 44 | 76 |
2022 January | 24 | 54 | 78 |
2021 December | 21 | 43 | 64 |
2021 November | 20 | 40 | 60 |
2021 October | 27 | 59 | 86 |
2021 September | 22 | 44 | 66 |
2021 August | 13 | 25 | 38 |
2021 July | 34 | 27 | 61 |
2021 June | 15 | 28 | 43 |
2021 May | 26 | 42 | 68 |
2021 April | 55 | 39 | 94 |
2021 March | 32 | 24 | 56 |
2021 February | 43 | 24 | 67 |
2021 January | 25 | 15 | 40 |
2020 December | 17 | 18 | 35 |
2020 November | 40 | 21 | 61 |
2020 October | 16 | 21 | 37 |
2020 September | 50 | 41 | 91 |
2020 August | 38 | 25 | 63 |
2020 July | 42 | 27 | 69 |
2020 June | 28 | 23 | 51 |
2020 May | 40 | 31 | 71 |
2020 April | 49 | 24 | 73 |
2020 March | 33 | 17 | 50 |
2020 February | 30 | 22 | 52 |
2020 January | 35 | 23 | 58 |
2019 December | 37 | 15 | 52 |
2019 November | 41 | 12 | 53 |
2019 October | 31 | 19 | 50 |
2019 September | 30 | 17 | 47 |
2019 August | 55 | 19 | 74 |
2019 July | 39 | 20 | 59 |
2019 June | 33 | 20 | 53 |
2019 May | 40 | 27 | 67 |
2019 April | 49 | 24 | 73 |
2019 March | 44 | 10 | 54 |
2019 February | 49 | 12 | 61 |
2019 January | 56 | 23 | 79 |
2018 December | 20 | 9 | 29 |
2018 November | 9 | 0 | 9 |
2018 October | 30 | 10 | 40 |
2018 September | 15 | 5 | 20 |
2018 August | 40 | 22 | 62 |
2018 July | 35 | 26 | 61 |
2018 June | 42 | 16 | 58 |
2018 May | 47 | 18 | 65 |
2018 April | 60 | 30 | 90 |
2018 March | 25 | 31 | 56 |
2018 February | 24 | 15 | 39 |
2018 January | 16 | 14 | 30 |
2017 December | 34 | 14 | 48 |
2017 November | 31 | 18 | 49 |
2017 October | 26 | 21 | 47 |
2017 September | 23 | 13 | 36 |
2017 August | 24 | 9 | 33 |
2017 July | 24 | 6 | 30 |
2017 June | 19 | 24 | 43 |
2017 May | 32 | 12 | 44 |
2017 April | 16 | 16 | 32 |
2017 March | 24 | 19 | 43 |
2017 February | 16 | 7 | 23 |
2017 January | 12 | 2 | 14 |
2016 December | 9 | 5 | 14 |
2016 November | 7 | 5 | 12 |
2016 October | 12 | 4 | 16 |
2016 September | 6 | 9 | 15 |
2016 August | 2 | 1 | 3 |
2016 July | 5 | 4 | 9 |
2016 June | 0 | 1 | 1 |
2016 May | 1 | 14 | 15 |
2016 April | 2 | 3 | 5 |
2016 March | 2 | 3 | 5 |
2016 February | 3 | 3 | 6 |
2016 January | 8 | 5 | 13 |
2015 December | 8 | 2 | 10 |
2015 November | 3 | 4 | 7 |
2015 October | 2 | 1 | 3 |