Βαρεία συνδυασμένη ανοσοανεπάρκεια (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Βαρεία συνδυασμένη ανοσοανεπάρκεια" in Greek language version.

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24nih.gov

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19doi.org

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5web.archive.org

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4archive.org

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1indiancountrynews.net

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1worldcat.org

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1uthscsa.edu

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1michigan.gov

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1esgct.org

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1vetgen.com

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archive.org

Gennery, A; Cant, A (March 2001). «Diagnosis of severe combined immunodeficiency». J Clin Pathol 54 (3): 191–195. doi:10.1136/jcp.54.3.191. PMID 11253129. PMC 1731376. https://archive.org/details/sim_journal-of-clinical-pathology_2001-03_54_3/page/191.
«Gene therapy for severe combined immunodeficiency: are we there yet?".». J. Clin. Invest. 117 (6): 1456–1465. 2007. doi:10.1172/jci30953. PMID 17549248. PMC 1878528. https://archive.org/details/sim_journal-of-clinical-investigation_2007-06_117_6/page/1456.
«Children reared in a reverse isolation environment: effects on cognitive and emotional development». J. Autism Dev. Disord. 16 (4): 415–424. 1986. doi:10.1007/bf01531708. PMID 3804957. https://archive.org/details/sim_journal-of-autism-and-developmental-disorders_1986-12_16_4/page/415.
Owen, Judith· Punt, Jenni (2013). Kuby Immunology. New York: W.H. Freeman and Company.

ct.gov

cga.ct.gov

doi.org

dx.doi.org

«Educational paper: The expanding clinical and immunological spectrum of severe combined immunodeficiency». Eur J Pediatr 170 (5): 561–571. 2011. doi:10.1007/s00431-011-1452-3. PMID 21479529.
«Severe combined immunodeficiencies: New and Old Scenarios». Int Rev Immunol 31 (1): 43–65. 2012. doi:10.3109/08830185.2011.644607. PMID 22251007.
«Gene therapy of severe combined immunodeficiencies». J Gene Med 3 (3): 201–206. 2001. doi:10.1002/1521-2254(200105/06)3:3<201::AID-JGM195>3.0.CO;2-Z. PMID 11437325.
Buckley R (2003). «Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution». Annu Rev Immunol 22: 625–655. doi:10.1146/annurev.immunol.22.012703.104614. PMID 15032591.
Haq IJ; Steinberg LJ; Hoenig M και άλλοι. (2007). «GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes». Clin. Immunol. 124 (2): 165–9. doi:10.1016/j.clim.2007.04.013. PMID 17572155.
«Jak3, severe combined immunodeficiency, and a new class of immunosuppressive drugs». Immunol. Rev. 203: 127–42. 2005. doi:10.1111/j.0105-2896.2005.00220.x. PMID 15661026. https://zenodo.org/record/1230593.
Li L; Moshous D; Zhou Y και άλλοι. (2002). «A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans». J. Immunol. 168 (12): 6323–9. doi:10.4049/jimmunol.168.12.6323. PMID 12055248.
Gennery, A; Cant, A (March 2001). «Diagnosis of severe combined immunodeficiency». J Clin Pathol 54 (3): 191–195. doi:10.1136/jcp.54.3.191. PMID 11253129. PMC 1731376. https://archive.org/details/sim_journal-of-clinical-pathology_2001-03_54_3/page/191.
van der Burg, Mirjam; Mahlaoui, Nizar; Gaspar, Hubert Bobby; Pai, Sung-Yun (2019-09-18). «Universal Newborn Screening for Severe Combined Immunodeficiency (SCID)». Frontiers in Pediatrics 7: 373. doi:10.3389/fped.2019.00373. ISSN 2296-2360. PMID 31620409.
Buckley RH (2004). «Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution». Annu. Rev. Immunol. 22 (1): 625–655. doi:10.1146/annurev.immunol.22.012703.104614. PMID 15032591.
«Gene therapy of severe combined immunodeficiencies». Nat Rev Immunol 2 (8): 615–621. 2002. doi:10.1038/nri859. PMID 12154380.
«Gene therapy for severe combined immunodeficiency: are we there yet?".». J. Clin. Invest. 117 (6): 1456–1465. 2007. doi:10.1172/jci30953. PMID 17549248. PMC 1878528. https://archive.org/details/sim_journal-of-clinical-investigation_2007-06_117_6/page/1456.
«Children reared in a reverse isolation environment: effects on cognitive and emotional development». J. Autism Dev. Disord. 16 (4): 415–424. 1986. doi:10.1007/bf01531708. PMID 3804957. https://archive.org/details/sim_journal-of-autism-and-developmental-disorders_1986-12_16_4/page/415.
Van der Burg, M; Gennery, AR (2011). «Educational paper. The expanding clinical and immunological spectrum of severe combined immunodeficiency». Eur. J. Pediatr. 170 (5): 561–571. doi:10.1007/s00431-011-1452-3. PMID 21479529.
«Severe combined immunodeficiency: A national surveillance study». Pediatr Allergy Immunol 19 (4): 298–302. 2008. doi:10.1111/j.1399-3038.2007.00646.x. PMID 18221464.
«Severe combined immunodeficiency: A cohort of 40 patients». Pediatr Allergy Immunol 19 (4): 303–306. 2008. doi:10.1111/j.1399-3038.2007.00647.x. PMID 18093084.
«Immunophenotyping of severe combined immunodeficiency in Morocco». IBS J Sci 26 (4): 161–164. 2011. doi:10.1016/j.immbio.2011.05.002.
«IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease». Genomics 23 (1): 69–74. 1994. doi:10.1006/geno.1994.1460. PMID 7829104.
Perryman LE (2004). «Molecular pathology of severe combined immunodeficiency in mice, horses, and dogs». Vet. Pathol. 41 (2): 95–100. doi:10.1354/vp.41-2-95. PMID 15017021.

esgct.org

Press release Αρχειοθετήθηκε 2007-09-29 στο Wayback Machine. from the European Society of Gene Therapy

foal.org

FOAL.org, an organization promoting research into genetic lethal diseases in horse

indiancountrynews.net

«News From Indian Country - A rare and once-baffling disease forces Navajo parents to cope». Αρχειοθετήθηκε από το πρωτότυπο στις 19 Απριλίου 2012. Ανακτήθηκε στις 1 Μαρτίου 2008.

lww.com

journals.lww.com

"CONVERSION OF NORMAL RATS INTO SCID-LIKE ANIMALS BY MEANS OF BONE MARROW TRANSPLANTATION FROM SCID DONORS ALLOWS ENGRAFTMENT OF HUMAN PERIPHERAL BLOOD MONONUCLEAR CELLS"

michigan.gov

«MDCH Adds Severe Combined Immunodeficiency (SCID) to Newborn Screening».

nih.gov

ncbi.nlm.nih.gov

«Educational paper: The expanding clinical and immunological spectrum of severe combined immunodeficiency». Eur J Pediatr 170 (5): 561–571. 2011. doi:10.1007/s00431-011-1452-3. PMID 21479529.
«Severe combined immunodeficiencies: New and Old Scenarios». Int Rev Immunol 31 (1): 43–65. 2012. doi:10.3109/08830185.2011.644607. PMID 22251007.
«Gene therapy of severe combined immunodeficiencies». J Gene Med 3 (3): 201–206. 2001. doi:10.1002/1521-2254(200105/06)3:3<201::AID-JGM195>3.0.CO;2-Z. PMID 11437325.
Buckley R (2003). «Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution». Annu Rev Immunol 22: 625–655. doi:10.1146/annurev.immunol.22.012703.104614. PMID 15032591.
Haq IJ; Steinberg LJ; Hoenig M και άλλοι. (2007). «GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes». Clin. Immunol. 124 (2): 165–9. doi:10.1016/j.clim.2007.04.013. PMID 17572155.
«Jak3, severe combined immunodeficiency, and a new class of immunosuppressive drugs». Immunol. Rev. 203: 127–42. 2005. doi:10.1111/j.0105-2896.2005.00220.x. PMID 15661026. https://zenodo.org/record/1230593.
Li L; Moshous D; Zhou Y και άλλοι. (2002). «A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans». J. Immunol. 168 (12): 6323–9. doi:10.4049/jimmunol.168.12.6323. PMID 12055248.
Gennery, A; Cant, A (March 2001). «Diagnosis of severe combined immunodeficiency». J Clin Pathol 54 (3): 191–195. doi:10.1136/jcp.54.3.191. PMID 11253129. PMC 1731376. https://archive.org/details/sim_journal-of-clinical-pathology_2001-03_54_3/page/191.
van der Burg, Mirjam; Mahlaoui, Nizar; Gaspar, Hubert Bobby; Pai, Sung-Yun (2019-09-18). «Universal Newborn Screening for Severe Combined Immunodeficiency (SCID)». Frontiers in Pediatrics 7: 373. doi:10.3389/fped.2019.00373. ISSN 2296-2360. PMID 31620409.
Buckley RH (2004). «Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution». Annu. Rev. Immunol. 22 (1): 625–655. doi:10.1146/annurev.immunol.22.012703.104614. PMID 15032591.
«Gene therapy of severe combined immunodeficiencies». Nat Rev Immunol 2 (8): 615–621. 2002. doi:10.1038/nri859. PMID 12154380.
«Gene therapy for severe combined immunodeficiency: are we there yet?".». J. Clin. Invest. 117 (6): 1456–1465. 2007. doi:10.1172/jci30953. PMID 17549248. PMC 1878528. https://archive.org/details/sim_journal-of-clinical-investigation_2007-06_117_6/page/1456.
«Children reared in a reverse isolation environment: effects on cognitive and emotional development». J. Autism Dev. Disord. 16 (4): 415–424. 1986. doi:10.1007/bf01531708. PMID 3804957. https://archive.org/details/sim_journal-of-autism-and-developmental-disorders_1986-12_16_4/page/415.
Van der Burg, M; Gennery, AR (2011). «Educational paper. The expanding clinical and immunological spectrum of severe combined immunodeficiency». Eur. J. Pediatr. 170 (5): 561–571. doi:10.1007/s00431-011-1452-3. PMID 21479529.
«Severe combined immunodeficiency: A national surveillance study». Pediatr Allergy Immunol 19 (4): 298–302. 2008. doi:10.1111/j.1399-3038.2007.00646.x. PMID 18221464.
«Severe combined immunodeficiency: A cohort of 40 patients». Pediatr Allergy Immunol 19 (4): 303–306. 2008. doi:10.1111/j.1399-3038.2007.00647.x. PMID 18093084.
«IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease». Genomics 23 (1): 69–74. 1994. doi:10.1006/geno.1994.1460. PMID 7829104.
Perryman LE (2004). «Molecular pathology of severe combined immunodeficiency in mice, horses, and dogs». Vet. Pathol. 41 (2): 95–100. doi:10.1354/vp.41-2-95. PMID 15017021.

pubmedcentral.nih.gov

«Educational paper: The expanding clinical and immunological spectrum of severe combined immunodeficiency». Eur J Pediatr 170 (5): 561–571. 2011. doi:10.1007/s00431-011-1452-3. PMID 21479529.
Gennery, A; Cant, A (March 2001). «Diagnosis of severe combined immunodeficiency». J Clin Pathol 54 (3): 191–195. doi:10.1136/jcp.54.3.191. PMID 11253129. PMC 1731376. https://archive.org/details/sim_journal-of-clinical-pathology_2001-03_54_3/page/191.
van der Burg, Mirjam; Mahlaoui, Nizar; Gaspar, Hubert Bobby; Pai, Sung-Yun (2019-09-18). «Universal Newborn Screening for Severe Combined Immunodeficiency (SCID)». Frontiers in Pediatrics 7: 373. doi:10.3389/fped.2019.00373. ISSN 2296-2360. PMID 31620409.
«Gene therapy for severe combined immunodeficiency: are we there yet?".». J. Clin. Invest. 117 (6): 1456–1465. 2007. doi:10.1172/jci30953. PMID 17549248. PMC 1878528. https://archive.org/details/sim_journal-of-clinical-investigation_2007-06_117_6/page/1456.
Van der Burg, M; Gennery, AR (2011). «Educational paper. The expanding clinical and immunological spectrum of severe combined immunodeficiency». Eur. J. Pediatr. 170 (5): 561–571. doi:10.1007/s00431-011-1452-3. PMID 21479529.

nih.gov

Rohr, Karen (17 Απριλίου 2019). «Gene therapy restores immunity in infants with rare immunodeficiency disease». National Institutes of Health (NIH) (στα Αγγλικά). Ανακτήθηκε στις 4 Ιουνίου 2020.

uthscsa.edu

genes-r-us.uthscsa.edu

«National Newborn Screening Status Report» (PDF). Αρχειοθετήθηκε από το πρωτότυπο (PDF) στις 16 Νοεμβρίου 2019. Ανακτήθηκε στις 9 Μαΐου 2021.

vetgen.com

«"The New DNA Test for Severe Combined Immunodeficiency (SCID) in Arabian Horses"». Αρχειοθετήθηκε από το πρωτότυπο στις 27 Φεβρουαρίου 2021. Ανακτήθηκε στις 9 Μαΐου 2021.

web.archive.org

«News From Indian Country - A rare and once-baffling disease forces Navajo parents to cope». Αρχειοθετήθηκε από το πρωτότυπο στις 19 Απριλίου 2012. Ανακτήθηκε στις 1 Μαρτίου 2008.
«National Newborn Screening Status Report» (PDF). Αρχειοθετήθηκε από το πρωτότυπο (PDF) στις 16 Νοεμβρίου 2019. Ανακτήθηκε στις 9 Μαΐου 2021.
«Wisconsin First State in Nation to Screen All Newborns for Severe Combined Immune Deficiency (SCID) or "Bubble Boy Disease"». Αρχειοθετήθηκε από το πρωτότυπο στις 3 Μαρτίου 2009.
Press release Αρχειοθετήθηκε 2007-09-29 στο Wayback Machine. from the European Society of Gene Therapy
«"The New DNA Test for Severe Combined Immunodeficiency (SCID) in Arabian Horses"». Αρχειοθετήθηκε από το πρωτότυπο στις 27 Φεβρουαρίου 2021. Ανακτήθηκε στις 9 Μαΐου 2021.

wisc.edu

slh.wisc.edu

«Wisconsin First State in Nation to Screen All Newborns for Severe Combined Immune Deficiency (SCID) or "Bubble Boy Disease"». Αρχειοθετήθηκε από το πρωτότυπο στις 3 Μαρτίου 2009.

worldcat.org

van der Burg, Mirjam; Mahlaoui, Nizar; Gaspar, Hubert Bobby; Pai, Sung-Yun (2019-09-18). «Universal Newborn Screening for Severe Combined Immunodeficiency (SCID)». Frontiers in Pediatrics 7: 373. doi:10.3389/fped.2019.00373. ISSN 2296-2360. PMID 31620409.

zenodo.org

«Jak3, severe combined immunodeficiency, and a new class of immunosuppressive drugs». Immunol. Rev. 203: 127–42. 2005. doi:10.1111/j.0105-2896.2005.00220.x. PMID 15661026. https://zenodo.org/record/1230593.