Тешка комбинована имунодефицијенција (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Тешка комбинована имунодефицијенција" in Serbian language version.

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19nih.gov

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16doi.org

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8archive.org

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1web.archive.org

1^st place

1indiancountrynews.net

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1worldcat.org

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archive.org (Global: 6^th place; Serbian: 5^th place)

Geha, R. S.; Notarangelo, L. D.; Casanova, J. L.; et al. (октобар 2007). „Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee”. Journal of Allergy and Clinical Immunology. 120 (4): 776—94. PMC 2601718 . PMID 17952897. doi:10.1016/j.jaci.2007.08.053.
Rosen, F. S. (март 1997). „Severe combined immunodeficiency: a pediatric emergency”. J Pediatr. 130 (3): 345—6. PMID 9063405.
Li L, Moshous D, Zhou Y, et al. (2002). „A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans”. J. Immunol. 168 (12): 6323—9. PMID 12055248. doi:10.4049/jimmunol.168.12.6323.
Ochs, H. D.; Igo, R. P. (1973). „The NBT slide test: a simple screening method for detecting chronic granulomatous disease and female carriers”. J Pediatr. 83 (1): 77—82. PMID 4768939. doi:10.1016/S0022-3476(73)80316-6.
Punwani D, Zhang Y, Yu J, Cowan MJ, Rana S, Kwan A; et al. (децембар 2016). „Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B”. New England Journal of Medicine. 375 (22): 2165—2176. PMC 5215776 . PMID 27959755. doi:10.1056/NEJMoa1509164. .
Gennery, A; Cant, A (март 2001). „Diagnosis of severe combined immunodeficiency”. J Clin Pathol. 54 (3): 191—195. PMC 1731376 . PMID 11253129. doi:10.1136/jcp.54.3.191.
Puck JM. (октобар 2007). „Population-based newborn screening for severe combined immunodeficiency steps toward implementation”. Journal of Allergy and Clinical Immunology. 120 (4): 760—8. PMID 17931561. doi:10.1016/j.jaci.2007.08.043. .
Powell, J.F.; Hunter, J.R. (1956). „Adenosine deaminase and ribosidase in spores of Bacillus cereus”. Biochem. J. 62 (3): 381—387. PMC 1215926 . PMID 13303984. doi:10.1042/bj0620381. Непознати параметар |name-list-style= игнорисан (помоћ)

doi.org (Global: 2^nd place; Serbian: 4^th place)

Geha, R. S.; Notarangelo, L. D.; Casanova, J. L.; et al. (октобар 2007). „Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee”. Journal of Allergy and Clinical Immunology. 120 (4): 776—94. PMC 2601718 . PMID 17952897. doi:10.1016/j.jaci.2007.08.053.
Notarangelo, L. D. (фебруар 2010). „Primary immunodeficiencies”. Journal of Allergy and Clinical Immunology. 125 (2 Suppl 2): S182—94. PMID 20042228. doi:10.1016/j.jaci.2009.07.053.
Aloj G, Giardano G, Valentino L, Maio F, Gallo V, Esposito T, Naddei R, Cirillo E, Pignata C (2012). „Severe combined immunodeficiencies: New and Old Scenarios”. Int Rev Immunol. 31 (1): 43—65. PMID 22251007. doi:10.3109/08830185.2011.644607.
Li L, Moshous D, Zhou Y, et al. (2002). „A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans”. J. Immunol. 168 (12): 6323—9. PMID 12055248. doi:10.4049/jimmunol.168.12.6323.
Ochs, H. D.; Igo, R. P. (1973). „The NBT slide test: a simple screening method for detecting chronic granulomatous disease and female carriers”. J Pediatr. 83 (1): 77—82. PMID 4768939. doi:10.1016/S0022-3476(73)80316-6.
Punwani D, Zhang Y, Yu J, Cowan MJ, Rana S, Kwan A; et al. (децембар 2016). „Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B”. New England Journal of Medicine. 375 (22): 2165—2176. PMC 5215776 . PMID 27959755. doi:10.1056/NEJMoa1509164. .
Liao, C. Y.; Yu, H. W.; Cheng, C. N.; Chen, J. S.; Lin, C. W.; Chen, P. C.; et al. (2018). „A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing”. J Microbiol Immunol Infect. 53 (1): 99—105. PMID 29551298. doi:10.1016/j.jmii.2018.02.003.
Kim, H. Y.; Kim, Y. M.; Park, H. J. (фебруар 2017). „Disseminated BCG pneumonitis revealing severe combined immunodeficiencyxs in CHARGE syndrome”. Pediatr Pulmonol. 52 (2). doi:10.1002/ppul.23533.
Gennery, A; Cant, A (март 2001). „Diagnosis of severe combined immunodeficiency”. J Clin Pathol. 54 (3): 191—195. PMC 1731376 . PMID 11253129. doi:10.1136/jcp.54.3.191.
Puck JM. (октобар 2007). „Population-based newborn screening for severe combined immunodeficiency steps toward implementation”. Journal of Allergy and Clinical Immunology. 120 (4): 760—8. PMID 17931561. doi:10.1016/j.jaci.2007.08.043. .
Tsuji, Y.; Imai, K.; Kajiwara, M.; Aoki, Y.; Isoda, T.; Tomizawa, D.; Imai, M.; Ito, S.; Maeda, H.; Minegishi, Y.; Ohkawa, H.; Yata, J.; Sasaki, N.; Kogawa, K.; Nagasawa, M.; Morio, T.; Nonoyama, S.; Mizutani, S. (март 2006). „20 years experience of a single team”. Bone Marrow Transplant. 37 (5): 469—77. PMID 16435016. doi:10.1038/sj.bmt.1705273.
Garcia-Lloret M, McGhee S, Chatila TA (новембар 2008). „Immunoglobulin replacement therapy in children”. Immunol Allergy Clin North Am. 28 (4): 833—49. PMC 2585601 . PMID 18940577. doi:10.1016/j.iac.2008.07.001. , ix
Kaplan, N.O., Colowick, S.P. and Ciotti, M.M. (1952). „Enzymatic deamination of cytosine nucleosides”. J. Biol. Chem. 194 (2): 579—591. PMID 14927650. doi:10.1016/S0021-9258(18)55811-7 .
Powell, J.F.; Hunter, J.R. (1956). „Adenosine deaminase and ribosidase in spores of Bacillus cereus”. Biochem. J. 62 (3): 381—387. PMC 1215926 . PMID 13303984. doi:10.1042/bj0620381. Непознати параметар |name-list-style= игнорисан (помоћ)
Fischer, Alain; Hacein-Bey, Salima; Cavazzana-Calvo, Marina (2002). „Gene therapy of severe combined immunodeficiencies”. Nature Reviews Immunology. 2 (8): 615—621. ISSN 1474-1733. PMID 12154380. doi:10.1038/nri859.
Neven, B.; Leroy, S.; Decaluwe, H.; et al. (април 2009). „Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency”. Blood. 113 (17): 4114—24. PMID 19168787. doi:10.1182/blood-2008-09-177923.

indiancountrynews.net (Global: low place; Serbian: low place)

„News From Indian Country - A rare and once-baffling disease forces Navajo parents to cope”. Архивирано из оригинала 19. 4. 2012. г. Приступљено 1. 2. 2008.

nih.gov (Global: 4^th place; Serbian: 8^th place)

ncbi.nlm.nih.gov

National Center for Biotechnology Information (US). Genes and Disease [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1998-. Severe combined immunodeficiency. Available from: https://www.ncbi.nlm.nih.gov/books/NBK22254/
Geha, R. S.; Notarangelo, L. D.; Casanova, J. L.; et al. (октобар 2007). „Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee”. Journal of Allergy and Clinical Immunology. 120 (4): 776—94. PMC 2601718 . PMID 17952897. doi:10.1016/j.jaci.2007.08.053.
Notarangelo, L. D. (фебруар 2010). „Primary immunodeficiencies”. Journal of Allergy and Clinical Immunology. 125 (2 Suppl 2): S182—94. PMID 20042228. doi:10.1016/j.jaci.2009.07.053.
Rosen, F. S. (март 1997). „Severe combined immunodeficiency: a pediatric emergency”. J Pediatr. 130 (3): 345—6. PMID 9063405.
Aloj G, Giardano G, Valentino L, Maio F, Gallo V, Esposito T, Naddei R, Cirillo E, Pignata C (2012). „Severe combined immunodeficiencies: New and Old Scenarios”. Int Rev Immunol. 31 (1): 43—65. PMID 22251007. doi:10.3109/08830185.2011.644607.
Li L, Moshous D, Zhou Y, et al. (2002). „A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans”. J. Immunol. 168 (12): 6323—9. PMID 12055248. doi:10.4049/jimmunol.168.12.6323.
Ochs, H. D.; Igo, R. P. (1973). „The NBT slide test: a simple screening method for detecting chronic granulomatous disease and female carriers”. J Pediatr. 83 (1): 77—82. PMID 4768939. doi:10.1016/S0022-3476(73)80316-6.
Punwani D, Zhang Y, Yu J, Cowan MJ, Rana S, Kwan A; et al. (децембар 2016). „Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B”. New England Journal of Medicine. 375 (22): 2165—2176. PMC 5215776 . PMID 27959755. doi:10.1056/NEJMoa1509164. .
Fischer, A. (1992). „Severe combined immunodeficiencies”. Immunodefic Rev. 3 (2): 83—100. PMID 1554500.
Liao, C. Y.; Yu, H. W.; Cheng, C. N.; Chen, J. S.; Lin, C. W.; Chen, P. C.; et al. (2018). „A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing”. J Microbiol Immunol Infect. 53 (1): 99—105. PMID 29551298. doi:10.1016/j.jmii.2018.02.003.
Uribe, L.; Weinberg, K. I. (октобар 1998). „X-linked SCID and other defects of cytokine pathways”. Semin Hematol. 35 (4): 299—309. PMID 9801259.
Gennery, A; Cant, A (март 2001). „Diagnosis of severe combined immunodeficiency”. J Clin Pathol. 54 (3): 191—195. PMC 1731376 . PMID 11253129. doi:10.1136/jcp.54.3.191.
Puck JM. (октобар 2007). „Population-based newborn screening for severe combined immunodeficiency steps toward implementation”. Journal of Allergy and Clinical Immunology. 120 (4): 760—8. PMID 17931561. doi:10.1016/j.jaci.2007.08.043. .
Tsuji, Y.; Imai, K.; Kajiwara, M.; Aoki, Y.; Isoda, T.; Tomizawa, D.; Imai, M.; Ito, S.; Maeda, H.; Minegishi, Y.; Ohkawa, H.; Yata, J.; Sasaki, N.; Kogawa, K.; Nagasawa, M.; Morio, T.; Nonoyama, S.; Mizutani, S. (март 2006). „20 years experience of a single team”. Bone Marrow Transplant. 37 (5): 469—77. PMID 16435016. doi:10.1038/sj.bmt.1705273.
Garcia-Lloret M, McGhee S, Chatila TA (новембар 2008). „Immunoglobulin replacement therapy in children”. Immunol Allergy Clin North Am. 28 (4): 833—49. PMC 2585601 . PMID 18940577. doi:10.1016/j.iac.2008.07.001. , ix
Kaplan, N.O., Colowick, S.P. and Ciotti, M.M. (1952). „Enzymatic deamination of cytosine nucleosides”. J. Biol. Chem. 194 (2): 579—591. PMID 14927650. doi:10.1016/S0021-9258(18)55811-7 .
Powell, J.F.; Hunter, J.R. (1956). „Adenosine deaminase and ribosidase in spores of Bacillus cereus”. Biochem. J. 62 (3): 381—387. PMC 1215926 . PMID 13303984. doi:10.1042/bj0620381. Непознати параметар |name-list-style= игнорисан (помоћ)
Fischer, Alain; Hacein-Bey, Salima; Cavazzana-Calvo, Marina (2002). „Gene therapy of severe combined immunodeficiencies”. Nature Reviews Immunology. 2 (8): 615—621. ISSN 1474-1733. PMID 12154380. doi:10.1038/nri859.
Neven, B.; Leroy, S.; Decaluwe, H.; et al. (април 2009). „Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency”. Blood. 113 (17): 4114—24. PMID 19168787. doi:10.1182/blood-2008-09-177923.

web.archive.org (Global: 1^st place; Serbian: 1^st place)

„News From Indian Country - A rare and once-baffling disease forces Navajo parents to cope”. Архивирано из оригинала 19. 4. 2012. г. Приступљено 1. 2. 2008.

worldcat.org (Global: 5^th place; Serbian: 12^th place)

Fischer, Alain; Hacein-Bey, Salima; Cavazzana-Calvo, Marina (2002). „Gene therapy of severe combined immunodeficiencies”. Nature Reviews Immunology. 2 (8): 615—621. ISSN 1474-1733. PMID 12154380. doi:10.1038/nri859.

Тешка комбинована имунодефицијенција (Serbian Wikipedia)

archive.org (Global: 6th place; Serbian: 5th place)

doi.org (Global: 2nd place; Serbian: 4th place)