Тешка комбинована имунодефицијенција (Serbian Wikipedia)

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

refsWebsite

Global rank Serbian rank

17nih.gov

4^th place

8^th place

12doi.org

2^nd place

4^th place

3archive.org

6^th place

5^th place

1web.archive.org

1^st place

1indiancountrynews.net

low place

1worldcat.org

5^th place

12^th place

archive.org

Rosen FS (март 1997). „Severe combined immunodeficiency: a pediatric emergency”. J Pediatr. 130 (3): 345—6. PMID 9063405. .
Ochs HD, Igo RP (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.
Powell, J.F. & Hunter, J.R. (1956). „Adenosine deaminase and ribosidase in spores of Bacillus cereus”. Biochem. J. 62: 381—387. PMID 13303984.

doi.org

Geha RS, Notarangelo LD, Casanova JL, et al. Primary immunodeficiency diseases (октобар 2007). „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 LD (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. :S182-94.
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 HD, Igo RP (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. .
Tsuji Y, Imai K, Kajiwara M, et al. Hematopoietic stem cell transplantation for 30 patients with primary immunodeficiency diseases. 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
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. 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

„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

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 RS, Notarangelo LD, Casanova JL, et al. Primary immunodeficiency diseases (октобар 2007). „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 LD (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. :S182-94.
Rosen FS (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 HD, Igo RP (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. .
Uribe L, Weinberg KI (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, et al. Hematopoietic stem cell transplantation for 30 patients with primary immunodeficiency diseases. 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: 579—591. PMID 14927650.
Powell, J.F. & Hunter, J.R. (1956). „Adenosine deaminase and ribosidase in spores of Bacillus cereus”. Biochem. J. 62: 381—387. PMID 13303984.
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

„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

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. doi:10.1038/nri859.