المؤلفون: ST Stinghen, R Pavese, LAL Souza, D Gorski, AV Pereira, CS Costa, JF Oliveira, GV Kucek, ERPH Folda

المصدر: Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S722- (2023)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2531137923014864; https://doaj.org/toc/2531-1379

URL الوصول: https://doaj.org/article/2b89df1d4eaf40d591a0485348e8df3f

المؤلفون: Boldt ABW; Laboratory of Human Molecular Genetics, Postgraduate Program in Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil.; Laboratory of Molecular Immunopathology, Postgraduate Program in Internal Medicine and Health Sciences, Department of Clinical Pathology, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil., Oliveira-Toré CF; Laboratory of Molecular Immunopathology, Postgraduate Program in Internal Medicine and Health Sciences, Department of Clinical Pathology, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil., Kretzschmar GC; Laboratory of Human Molecular Genetics, Postgraduate Program in Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil., Weinschutz Mendes H; Laboratory of Molecular Immunopathology, Postgraduate Program in Internal Medicine and Health Sciences, Department of Clinical Pathology, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil., Stinghen ST; Laboratory of Molecular Immunopathology, Postgraduate Program in Internal Medicine and Health Sciences, Department of Clinical Pathology, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil., Andrade FA; Laboratory of Molecular Immunopathology, Postgraduate Program in Internal Medicine and Health Sciences, Department of Clinical Pathology, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil., Bumiller-Bini V; Laboratory of Human Molecular Genetics, Postgraduate Program in Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil., Gonçalves LB; Laboratory of Molecular Immunopathology, Postgraduate Program in Internal Medicine and Health Sciences, Department of Clinical Pathology, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil., Braga ACM; Laboratory of Molecular Immunopathology, Postgraduate Program in Internal Medicine and Health Sciences, Department of Clinical Pathology, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil., Stahlke EVRS; Health State Department of Paraná, Curitiba, Brazil., Velavan TP; Institute of Tropical Medicine, Universitätsklinikum Tübingen, Tübingen, Germany.; Vietnamese-German Center for Medical Research, Hanoi, Vietnam.; Faculty of Medicine, Duy Tan University, Da Nang, Vietnam., Thiel S; Department of Biomedicine, Aarhus University, Aarhus, Denmark., de Messias-Reason IJT; Laboratory of Molecular Immunopathology, Postgraduate Program in Internal Medicine and Health Sciences, Department of Clinical Pathology, Hospital de Clínicas, Federal University of Paraná, Curitiba, Brazil.

المصدر: Frontiers in immunology [Front Immunol] 2021 Feb 11; Vol. 11, pp. 574457. Date of Electronic Publication: 2021 Feb 11 (Print Publication: 2020).

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101560960 Publication Model: eCollection Cited Medium: Internet ISSN: 1664-3224 (Electronic) Linking ISSN: 16643224 NLM ISO Abbreviation: Front Immunol Subsets: MEDLINE

مواضيع طبية MeSH: Coinfection/*genetics , Complement Pathway, Mannose-Binding Lectin/*genetics , Hepatitis B/*genetics , Leprosy/*genetics , Receptors, Complement/*genetics, Adult ; Aged ; Aged, 80 and over ; Coinfection/immunology ; Complement System Proteins/genetics ; Complement System Proteins/metabolism ; Female ; Genetic Association Studies ; Genetic Predisposition to Disease/genetics ; Genotype ; Haplotypes ; Hepatitis B/immunology ; Hepatitis B virus ; Humans ; Leprosy/immunology ; Male ; Middle Aged ; Mycobacterium leprae ; Polymorphism, Single Nucleotide ; Young Adult

المؤلفون: Kretzschmar GC; Laboratory of Human Molecular Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil., Oliveira LC; Laboratory of Human Molecular Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil., Nisihara RM; Laboratory of Molecular Immunopathology, Department of Clinical Pathology, Clinical Hospital, Federal University of Paraná, Curitiba, Brazil., Velavan TP; Institute of Tropical Medicine, Department of Human Parasitology, University of Tübingen, Tübingen, Germany.; Vietnamese- German Center for Medical Research, VG-CARE, Hanoi, Vietnam., Stinghen ST; Laboratory of Molecular Immunopathology, Department of Clinical Pathology, Clinical Hospital, Federal University of Paraná, Curitiba, Brazil., Stahlke ERS; State Department of Health of Paraná, Curitiba, Brazil., Petzl-Erler ML; Laboratory of Human Molecular Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil., Messias-Reason IJT; Laboratory of Molecular Immunopathology, Department of Clinical Pathology, Clinical Hospital, Federal University of Paraná, Curitiba, Brazil., Boldt ABW; Laboratory of Human Molecular Genetics, Department of Genetics, Federal University of Paraná, Curitiba, Brazil.; Laboratory of Molecular Immunopathology, Department of Clinical Pathology, Clinical Hospital, Federal University of Paraná, Curitiba, Brazil.

المصدر: PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2018 Aug 09; Vol. 12 (8), pp. e0006705. Date of Electronic Publication: 2018 Aug 09 (Print Publication: 2018).

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101291488 Publication Model: eCollection Cited Medium: Internet ISSN: 1935-2735 (Electronic) Linking ISSN: 19352727 NLM ISO Abbreviation: PLoS Negl Trop Dis Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Polymorphism, Genetic*, Leprosy/*genetics , Receptors, Complement 3b/*genetics, Adolescent ; Adult ; Aged ; Aged, 80 and over ; Brazil/epidemiology ; Case-Control Studies ; Female ; Haplotypes ; Humans ; Leprosy/epidemiology ; Male ; Middle Aged ; Young Adult

المؤلفون: Dionello CF; Laboratório de Imunopatologia, Departamento de Patologia Médica, Clinical Hospital of Federal University of Parana, Curitiba, Brazil., Rosa Utiyama SR; Laboratório de Imunopatologia, Departamento de Patologia Médica, Clinical Hospital of Federal University of Parana, Curitiba, Brazil., Radominski SC; Departamento de Medicina Interna, Clinical Hospital of Federal University of Parana, Curitiba, Brazil., Stahlke E; Setor de Dermatologia, Centro Regional de Especialidades Metropolitano de Curitiba, Curitiba, Brazil., Stinghen ST; Laboratório de Imunopatologia, Departamento de Patologia Médica, Clinical Hospital of Federal University of Parana, Curitiba, Brazil., de Messias-Reason IJ; Laboratório de Imunopatologia, Departamento de Patologia Médica, Clinical Hospital of Federal University of Parana, Curitiba, Brazil. iara.reason@hc.ufpr.br.

المصدر: International journal of rheumatic diseases [Int J Rheum Dis] 2016 Oct; Vol. 19 (10), pp. 1024-1031. Date of Electronic Publication: 2015 Aug 06.

نوع المنشور: Comparative Study; Journal Article

بيانات الدورية: Publisher: Wiley on behalf of the Asia Pacific League of Associations for Rheumatology Country of Publication: England NLM ID: 101474930 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1756-185X (Electronic) Linking ISSN: 17561841 NLM ISO Abbreviation: Int J Rheum Dis Subsets: MEDLINE

مواضيع طبية MeSH: Arthritis, Rheumatoid/*immunology , Immunoglobulin M/*blood , Leprosy/*immunology , Peptides, Cyclic/*immunology , Rheumatoid Factor/*blood, Adolescent ; Adult ; Aged ; Aged, 80 and over ; Arthritis, Rheumatoid/blood ; Arthritis, Rheumatoid/diagnosis ; Arthritis, Rheumatoid/ethnology ; Biomarkers/blood ; Brazil/epidemiology ; Case-Control Studies ; Female ; Humans ; Leprosy/blood ; Leprosy/diagnosis ; Leprosy/ethnology ; Logistic Models ; Male ; Middle Aged ; Odds Ratio ; Predictive Value of Tests ; Risk Factors ; Young Adult

المؤلفون: Custódio G; Pelé Pequeno Príncipe Research Institute, Avenida Silva Jardim, 1632, Água Verde, Curitiba, PR 80.250-200, Brazil., Parise GA, Kiesel Filho N, Komechen H, Sabbaga CC, Rosati R, Grisa L, Parise IZ, Pianovski MA, Fiori CM, Ledesma JA, Barbosa JR, Figueiredo FR, Sade ER, Ibañez H, Arram SB, Stinghen ST, Mengarelli LR, Figueiredo MM, Carvalho DC, Avilla SG, Woiski TD, Poncio LC, Lima GF, Pontarolo R, Lalli E, Zhou Y, Zambetti GP, Ribeiro RC, Figueiredo BC

المصدر: Journal of clinical oncology : official journal of the American Society of Clinical Oncology [J Clin Oncol] 2013 Jul 10; Vol. 31 (20), pp. 2619-26. Date of Electronic Publication: 2013 Jun 03.

نوع المنشور: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Society of Clinical Oncology Country of Publication: United States NLM ID: 8309333 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1527-7755 (Electronic) Linking ISSN: 0732183X NLM ISO Abbreviation: J Clin Oncol Subsets: MEDLINE

مواضيع طبية MeSH: Germ-Line Mutation*, Adrenal Cortex Neoplasms/*epidemiology , Adrenal Cortex Neoplasms/*genetics , Genetic Predisposition to Disease/*epidemiology , Genetic Testing/*methods , Tumor Suppressor Protein p53/*genetics, Adrenal Cortex Neoplasms/diagnosis ; Brazil/epidemiology ; Child ; Child, Preschool ; Early Detection of Cancer/methods ; Female ; Gene Expression Regulation ; Heterozygote ; Humans ; Incidence ; Infant, Newborn ; Male ; Neonatal Screening/methods ; Pedigree ; Risk Assessment ; Sex Distribution

المؤلفون: Boechat GA; Center for Molecular Genetics and Cancer Research in Children (CEGEMPAC), Agostinho Leão Júnior, Brazil., Stinghen ST, Custódio G, Pianovski MA, Figueiredo FR, Jenkins J, Zambetti GP, Ribeiro RC, Figueiredo BC

المصدر: Journal of pediatric hematology/oncology [J Pediatr Hematol Oncol] 2011 May; Vol. 33 (4), pp. e149-53.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 9505928 Publication Model: Print Cited Medium: Internet ISSN: 1536-3678 (Electronic) Linking ISSN: 10774114 NLM ISO Abbreviation: J Pediatr Hematol Oncol Subsets: MEDLINE

مواضيع طبية MeSH: Adrenal Cortex/*embryology , Adrenal Cortex/*metabolism , Adrenal Cortex Neoplasms/*metabolism , Adrenal Cortex Neoplasms/*pathology , Alkaline Phosphatase/*metabolism , Isoenzymes/*metabolism, Adrenal Cortex Neoplasms/genetics ; Apoptosis/physiology ; Child ; Female ; GPI-Linked Proteins/metabolism ; Germ-Line Mutation ; Humans ; Immunohistochemistry ; Male ; Tumor Suppressor Protein p53/genetics

المؤلفون: Zancanella P; Center for Molecular Genetics and Cancer Research-CEGEMPAC, Department of Pediatrics, Federal University of Paraná, and Division of Pediatric Oncology, Erasto Gaertner Hospital, Liga Paranaense de Combate ao Câncer, Curitiba, PR, CEP, Brazil., Pianovski MA, Oliveira BH, Ferman S, Piovezan GC, Lichtvan LL, Voss SZ, Stinghen ST, Callefe LG, Parise GA, Santana MH, Figueiredo BC

المصدر: Journal of pediatric hematology/oncology [J Pediatr Hematol Oncol] 2006 Aug; Vol. 28 (8), pp. 513-24.

نوع المنشور: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 9505928 Publication Model: Print Cited Medium: Print ISSN: 1077-4114 (Print) Linking ISSN: 10774114 NLM ISO Abbreviation: J Pediatr Hematol Oncol Subsets: MEDLINE

مواضيع طبية MeSH: Adrenal Cortex Neoplasms/*drug therapy , Adrenocortical Carcinoma/*drug therapy , Antineoplastic Combined Chemotherapy Protocols/*therapeutic use , Cisplatin/*administration & dosage , Doxorubicin/*administration & dosage , Etoposide/*administration & dosage , Mitotane/*administration & dosage, Administration, Oral ; Adrenal Cortex Neoplasms/diagnosis ; Adrenal Cortex Neoplasms/surgery ; Adrenocortical Carcinoma/diagnosis ; Adrenocortical Carcinoma/surgery ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Child ; Child, Preschool ; Cisplatin/adverse effects ; Disease Progression ; Dose-Response Relationship, Drug ; Doxorubicin/adverse effects ; Drug Administration Schedule ; Drug Monitoring/methods ; Drug Therapy, Combination ; Etoposide/adverse effects ; Female ; Follow-Up Studies ; Humans ; Male ; Mitotane/adverse effects ; Neoplasm Staging ; Prospective Studies ; Remission Induction ; Survival Rate ; Time Factors ; Treatment Outcome

المؤلفون: Stinghen ST; Centro de Genética Molecular e Pesquisa do Câncer em Crianças (CEGEMPAC), Curitiba, PR, CEP 80030-110, Brazil., Moura JF, Zancanella P, Rodrigues GA, Pianovski MA, Lalli E, Arnold DL, Minozzo JC, Callefe LG, Ribeiro RC, Figueiredo BC

المصدر: Journal of biomedicine & biotechnology [J Biomed Biotechnol] 2006; Vol. 2006 (5), pp. 56087.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Hindawi Pub. Corp Country of Publication: United States NLM ID: 101135740 Publication Model: Print Cited Medium: Print ISSN: 1110-7243 (Print) Linking ISSN: 11107243 NLM ISO Abbreviation: J Biomed Biotechnol Subsets: PubMed not MEDLINE

المؤلفون: Rosa KA; Hemocentro Unicamp, Campinas, SP, Brazil., Reid ME, Lomas-Francis C, Powell VI, Costa FF, Stinghen ST, Watanabe AM, Carboni EK, Baldon JP, Jucksch MM, Castilho L

المصدر: Transfusion [Transfusion] 2005 Nov; Vol. 45 (11), pp. 1796-8.

نوع المنشور: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Association Of Blood Banks Country of Publication: United States NLM ID: 0417360 Publication Model: Print Cited Medium: Print ISSN: 0041-1132 (Print) Linking ISSN: 00411132 NLM ISO Abbreviation: Transfusion Subsets: MEDLINE

مواضيع طبية MeSH: Mutation*, Rh-Hr Blood-Group System/*genetics, Adult ; Base Sequence ; Codon, Terminator ; Erythrocytes/immunology ; Erythrocytes/metabolism ; Exons ; Female ; Frameshift Mutation ; Gene Deletion ; Guanine ; Homozygote ; Humans ; Molecular Sequence Data ; Pedigree ; Rh-Hr Blood-Group System/blood ; Syndrome ; Transcription, Genetic