Hypohidrotic ectodermal dysplasia with immune deficiency (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hypohidrotic ectodermal dysplasia with immune deficiency" in English language version.

refsWebsite

Global rank English rank

22nih.gov

4^th place

13doi.org

2^nd place

13worldcat.org

5^th place

9web.archive.org

1^st place

3medlineplus.gov

1,581^st place

1,299^th place

3semanticscholar.org

11^th place

8^th place

2cancer.gov

1,684^th place

1,350^th place

1orpha.net

3,537^th place

7,177^th place

1ashpublications.org

low place

1bmj.com

1,226^th place

1,421^st place

1nature.com

234^th place

397^th place

1sciencedirect.com

149^th place

178^th place

1omim.org

4,380^th place

4,305^th place

ashpublications.org

"X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival". ashpublications.org. June 2014. Archived from the original on 2022-01-21. Retrieved 2022-09-24.

bmj.com

adc.bmj.com

Carrol, E. D.; Gennery, A. R.; Flood, T. J.; Spickett, G. P.; Abinun, M. (2003-04-01). "Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO". Archives of Disease in Childhood. 88 (4): 340–341. doi:10.1136/adc.88.4.340. ISSN 0003-9888. PMC 1719512. PMID 12651765. Archived from the original on 2018-06-03. Retrieved 2022-09-24.

cancer.gov

"X-linked recessive inheritance". www.cancer.gov. 2011-02-02. Retrieved 2022-09-24.
"autosomal dominant inheritance". www.cancer.gov. 2011-02-02. Retrieved 2022-09-24.

doi.org

Döffinger, R.; Smahi, A.; Bessia, C.; Geissmann, F.; Feinberg, J.; Durandy, A.; Bodemer, C.; Kenwrick, S.; Dupuis-Girod, S.; Blanche, S.; Wood, P.; Rabia, S. H.; Headon, D. J.; Overbeek, P. A.; Le Deist, F. (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1061-4036. PMID 11242109. S2CID 24898789.
Kawai, Tomoki; Nishikomori, Ryuta; Heike, Toshio (2012-01-01). "Diagnosis and Treatment in Anhidrotic Ectodermal Dysplasia with Immunodeficiency". Allergology International. 61 (2): 207–217. doi:10.2332/allergolint.12-RAI-0446. ISSN 1323-8930. PMID 22635013.
Johnston, Alicia M.; Niemela, Julie; Rosenzweig, Sergio D.; Fried, Ari J.; Delmonte, Ottavia Maria; Fleisher, Thomas A.; Kuehn, Hyesun (August 2016). "A Novel Mutation in IKBKG/NEMO Leads to Ectodermal Dysplasia with Severe Immunodeficiency (EDA-ID)". Journal of Clinical Immunology. 36 (6): 541–543. doi:10.1007/s10875-016-0309-y. ISSN 1573-2592. PMC 5007618. PMID 27368913.
Mancini, Anthony J.; Lawley, Leslie P.; Uzel, Gulbu (2008-03-01). "X-Linked Ectodermal Dysplasia With Immunodeficiency Caused by NEMO Mutation: Early Recognition and Diagnosis". Archives of Dermatology. 144 (3): 342–346. doi:10.1001/archderm.144.3.342. ISSN 0003-987X. PMID 18347290.
Carrol, E. D.; Gennery, A. R.; Flood, T. J.; Spickett, G. P.; Abinun, M. (2003-04-01). "Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO". Archives of Disease in Childhood. 88 (4): 340–341. doi:10.1136/adc.88.4.340. ISSN 0003-9888. PMC 1719512. PMID 12651765. Archived from the original on 2018-06-03. Retrieved 2022-09-24.
Keller, Michael D.; Petersen, Maureen; Ong, Peck; Church, Joseph; Risma, Kimberly; Burham, Jon; Jain, Ashish; Stiehm, E. Richard; Hanson, Eric P.; Uzel, Gulbu; Deardorff, Matthew A.; Orange, Jordan S. (2011-11-08). "Hypohidrotic Ectodermal Dysplasia and Immunodeficiency with Coincident NEMO and EDA Mutations". Frontiers in Immunology. 2: 61. doi:10.3389/fimmu.2011.00061. ISSN 1664-3224. PMC 3341983. PMID 22566850.
Döffinger, Rainer; Smahi, Asma; Bessia, Christine; Geissmann, Frédéric; Feinberg, Jacqueline; Durandy, Anne; Bodemer, Christine; Kenwrick, Sue; Dupuis-Girod, Sophie; Blanche, Stéphane; Wood, Philip; Rabia, Smail Hadj; Headon, Denis J.; Overbeek, Paul A.; Le Deist, Françoise (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1546-1718. PMID 11242109. S2CID 24898789. Archived from the original on 2022-06-16. Retrieved 2022-09-24.
Jacobs, Marc D.; Harrison, Stephen C. (1998-12-11). "Structure of an IκBα/NF-κB Complex". Cell. 95 (6): 749–758. doi:10.1016/S0092-8674(00)81698-0. ISSN 0092-8674. PMID 9865693. S2CID 7003353.
Orange, Jordan S.; Brodeur, Scott R.; Jain, Ashish; Bonilla, Francisco A.; Schneider, Lynda C.; Kretschmer, Roberto; Nurko, Samuel; Rasmussen, Wendy L.; Köhler, Julia R.; Gellis, Stephen E.; Ferguson, Betsy M.; Strominger, Jack L.; Zonana, Jonathan; Ramesh, Narayanaswamy; Ballas, Zuhair K. (June 2002). "Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations". The Journal of Clinical Investigation. 109 (11): 1501–1509. doi:10.1172/JCI14858. ISSN 0021-9738. PMC 150995. PMID 12045264.
Janssen, Riny; van Wengen, Annelies; Hoeve, Marieke A.; ten Dam, Monique; van der Burg, Miriam; van Dongen, Jacques; van de Vosse, Esther; van Tol, Maarten; Bredius, Robbert; Ottenhoff, Tom H.; Weemaes, Corry; van Dissel, Jaap T.; Lankester, Arjan (2004-09-06). "The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes". The Journal of Experimental Medicine. 200 (5): 559–568. doi:10.1084/jem.20040773. ISSN 0022-1007. PMC 2212739. PMID 15337789.
Pai, Sung-Yun; Levy, Ofer; Jabara, Haifa H.; Glickman, Jonathan N.; Stoler-Barak, Liat; Sachs, Jessica; Nurko, Samuel; Orange, Jordan S.; Geha, Raif S. (December 2008). "Allogeneic transplantation successfully corrects immune defects, but not susceptibility to colitis, in a patient with nuclear factor-kappaB essential modulator deficiency". The Journal of Allergy and Clinical Immunology. 122 (6): 1113–1118.e1. doi:10.1016/j.jaci.2008.08.026. ISSN 1097-6825. PMC 6141239. PMID 18851875.
Zonana, J.; Elder, M. E.; Schneider, L. C.; Orlow, S. J.; Moss, C.; Golabi, M.; Shapira, S. K.; Farndon, P. A.; Wara, D. W.; Emmal, S. A.; Ferguson, B. M. (December 2000). "A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)". American Journal of Human Genetics. 67 (6): 1555–1562. doi:10.1086/316914. ISSN 0002-9297. PMC 1287930. PMID 11047757.
Courtois, Gilles; Smahi, Asma; Reichenbach, Janine; Döffinger, Rainer; Cancrini, Caterina; Bonnet, Marion; Puel, Anne; Chable-Bessia, Christine; Yamaoka, Shoji; Feinberg, Jacqueline; Dupuis-Girod, Sophie; Bodemer, Christine; Livadiotti, Susanna; Novelli, Francesco; Rossi, Paolo (October 2003). "A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency". The Journal of Clinical Investigation. 112 (7): 1108–1115. doi:10.1172/JCI18714. ISSN 0021-9738. PMC 198529. PMID 14523047.

medlineplus.gov

"Anhidrotic ectodermal dysplasia with immune deficiency: MedlinePlus Genetics". medlineplus.gov. Archived from the original on 2021-11-01. Retrieved 2022-09-24.
"IKBKG gene: MedlinePlus Genetics". medlineplus.gov. Archived from the original on 2021-10-19. Retrieved 2022-09-24.
"NFKBIA gene: MedlinePlus Genetics". medlineplus.gov. Archived from the original on 2021-04-20. Retrieved 2022-09-24.

nature.com

Döffinger, Rainer; Smahi, Asma; Bessia, Christine; Geissmann, Frédéric; Feinberg, Jacqueline; Durandy, Anne; Bodemer, Christine; Kenwrick, Sue; Dupuis-Girod, Sophie; Blanche, Stéphane; Wood, Philip; Rabia, Smail Hadj; Headon, Denis J.; Overbeek, Paul A.; Le Deist, Françoise (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1546-1718. PMID 11242109. S2CID 24898789. Archived from the original on 2022-06-16. Retrieved 2022-09-24.

nih.gov

pubmed.ncbi.nlm.nih.gov

Döffinger, R.; Smahi, A.; Bessia, C.; Geissmann, F.; Feinberg, J.; Durandy, A.; Bodemer, C.; Kenwrick, S.; Dupuis-Girod, S.; Blanche, S.; Wood, P.; Rabia, S. H.; Headon, D. J.; Overbeek, P. A.; Le Deist, F. (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1061-4036. PMID 11242109. S2CID 24898789.
Kawai, Tomoki; Nishikomori, Ryuta; Heike, Toshio (2012-01-01). "Diagnosis and Treatment in Anhidrotic Ectodermal Dysplasia with Immunodeficiency". Allergology International. 61 (2): 207–217. doi:10.2332/allergolint.12-RAI-0446. ISSN 1323-8930. PMID 22635013.
Johnston, Alicia M.; Niemela, Julie; Rosenzweig, Sergio D.; Fried, Ari J.; Delmonte, Ottavia Maria; Fleisher, Thomas A.; Kuehn, Hyesun (August 2016). "A Novel Mutation in IKBKG/NEMO Leads to Ectodermal Dysplasia with Severe Immunodeficiency (EDA-ID)". Journal of Clinical Immunology. 36 (6): 541–543. doi:10.1007/s10875-016-0309-y. ISSN 1573-2592. PMC 5007618. PMID 27368913.
Mancini, Anthony J.; Lawley, Leslie P.; Uzel, Gulbu (2008-03-01). "X-Linked Ectodermal Dysplasia With Immunodeficiency Caused by NEMO Mutation: Early Recognition and Diagnosis". Archives of Dermatology. 144 (3): 342–346. doi:10.1001/archderm.144.3.342. ISSN 0003-987X. PMID 18347290.
Carrol, E. D.; Gennery, A. R.; Flood, T. J.; Spickett, G. P.; Abinun, M. (2003-04-01). "Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO". Archives of Disease in Childhood. 88 (4): 340–341. doi:10.1136/adc.88.4.340. ISSN 0003-9888. PMC 1719512. PMID 12651765. Archived from the original on 2018-06-03. Retrieved 2022-09-24.
Keller, Michael D.; Petersen, Maureen; Ong, Peck; Church, Joseph; Risma, Kimberly; Burham, Jon; Jain, Ashish; Stiehm, E. Richard; Hanson, Eric P.; Uzel, Gulbu; Deardorff, Matthew A.; Orange, Jordan S. (2011-11-08). "Hypohidrotic Ectodermal Dysplasia and Immunodeficiency with Coincident NEMO and EDA Mutations". Frontiers in Immunology. 2: 61. doi:10.3389/fimmu.2011.00061. ISSN 1664-3224. PMC 3341983. PMID 22566850.
Döffinger, Rainer; Smahi, Asma; Bessia, Christine; Geissmann, Frédéric; Feinberg, Jacqueline; Durandy, Anne; Bodemer, Christine; Kenwrick, Sue; Dupuis-Girod, Sophie; Blanche, Stéphane; Wood, Philip; Rabia, Smail Hadj; Headon, Denis J.; Overbeek, Paul A.; Le Deist, Françoise (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1546-1718. PMID 11242109. S2CID 24898789. Archived from the original on 2022-06-16. Retrieved 2022-09-24.
Jacobs, Marc D.; Harrison, Stephen C. (1998-12-11). "Structure of an IκBα/NF-κB Complex". Cell. 95 (6): 749–758. doi:10.1016/S0092-8674(00)81698-0. ISSN 0092-8674. PMID 9865693. S2CID 7003353.
Orange, Jordan S.; Brodeur, Scott R.; Jain, Ashish; Bonilla, Francisco A.; Schneider, Lynda C.; Kretschmer, Roberto; Nurko, Samuel; Rasmussen, Wendy L.; Köhler, Julia R.; Gellis, Stephen E.; Ferguson, Betsy M.; Strominger, Jack L.; Zonana, Jonathan; Ramesh, Narayanaswamy; Ballas, Zuhair K. (June 2002). "Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations". The Journal of Clinical Investigation. 109 (11): 1501–1509. doi:10.1172/JCI14858. ISSN 0021-9738. PMC 150995. PMID 12045264.
Janssen, Riny; van Wengen, Annelies; Hoeve, Marieke A.; ten Dam, Monique; van der Burg, Miriam; van Dongen, Jacques; van de Vosse, Esther; van Tol, Maarten; Bredius, Robbert; Ottenhoff, Tom H.; Weemaes, Corry; van Dissel, Jaap T.; Lankester, Arjan (2004-09-06). "The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes". The Journal of Experimental Medicine. 200 (5): 559–568. doi:10.1084/jem.20040773. ISSN 0022-1007. PMC 2212739. PMID 15337789.
Pai, Sung-Yun; Levy, Ofer; Jabara, Haifa H.; Glickman, Jonathan N.; Stoler-Barak, Liat; Sachs, Jessica; Nurko, Samuel; Orange, Jordan S.; Geha, Raif S. (December 2008). "Allogeneic transplantation successfully corrects immune defects, but not susceptibility to colitis, in a patient with nuclear factor-kappaB essential modulator deficiency". The Journal of Allergy and Clinical Immunology. 122 (6): 1113–1118.e1. doi:10.1016/j.jaci.2008.08.026. ISSN 1097-6825. PMC 6141239. PMID 18851875.
Zonana, J.; Elder, M. E.; Schneider, L. C.; Orlow, S. J.; Moss, C.; Golabi, M.; Shapira, S. K.; Farndon, P. A.; Wara, D. W.; Emmal, S. A.; Ferguson, B. M. (December 2000). "A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)". American Journal of Human Genetics. 67 (6): 1555–1562. doi:10.1086/316914. ISSN 0002-9297. PMC 1287930. PMID 11047757.
Courtois, Gilles; Smahi, Asma; Reichenbach, Janine; Döffinger, Rainer; Cancrini, Caterina; Bonnet, Marion; Puel, Anne; Chable-Bessia, Christine; Yamaoka, Shoji; Feinberg, Jacqueline; Dupuis-Girod, Sophie; Bodemer, Christine; Livadiotti, Susanna; Novelli, Francesco; Rossi, Paolo (October 2003). "A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency". The Journal of Clinical Investigation. 112 (7): 1108–1115. doi:10.1172/JCI18714. ISSN 0021-9738. PMC 198529. PMID 14523047.

ncbi.nlm.nih.gov

Johnston, Alicia M.; Niemela, Julie; Rosenzweig, Sergio D.; Fried, Ari J.; Delmonte, Ottavia Maria; Fleisher, Thomas A.; Kuehn, Hyesun (August 2016). "A Novel Mutation in IKBKG/NEMO Leads to Ectodermal Dysplasia with Severe Immunodeficiency (EDA-ID)". Journal of Clinical Immunology. 36 (6): 541–543. doi:10.1007/s10875-016-0309-y. ISSN 1573-2592. PMC 5007618. PMID 27368913.
Carrol, E. D.; Gennery, A. R.; Flood, T. J.; Spickett, G. P.; Abinun, M. (2003-04-01). "Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO". Archives of Disease in Childhood. 88 (4): 340–341. doi:10.1136/adc.88.4.340. ISSN 0003-9888. PMC 1719512. PMID 12651765. Archived from the original on 2018-06-03. Retrieved 2022-09-24.
Keller, Michael D.; Petersen, Maureen; Ong, Peck; Church, Joseph; Risma, Kimberly; Burham, Jon; Jain, Ashish; Stiehm, E. Richard; Hanson, Eric P.; Uzel, Gulbu; Deardorff, Matthew A.; Orange, Jordan S. (2011-11-08). "Hypohidrotic Ectodermal Dysplasia and Immunodeficiency with Coincident NEMO and EDA Mutations". Frontiers in Immunology. 2: 61. doi:10.3389/fimmu.2011.00061. ISSN 1664-3224. PMC 3341983. PMID 22566850.
Orange, Jordan S.; Brodeur, Scott R.; Jain, Ashish; Bonilla, Francisco A.; Schneider, Lynda C.; Kretschmer, Roberto; Nurko, Samuel; Rasmussen, Wendy L.; Köhler, Julia R.; Gellis, Stephen E.; Ferguson, Betsy M.; Strominger, Jack L.; Zonana, Jonathan; Ramesh, Narayanaswamy; Ballas, Zuhair K. (June 2002). "Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations". The Journal of Clinical Investigation. 109 (11): 1501–1509. doi:10.1172/JCI14858. ISSN 0021-9738. PMC 150995. PMID 12045264.
Janssen, Riny; van Wengen, Annelies; Hoeve, Marieke A.; ten Dam, Monique; van der Burg, Miriam; van Dongen, Jacques; van de Vosse, Esther; van Tol, Maarten; Bredius, Robbert; Ottenhoff, Tom H.; Weemaes, Corry; van Dissel, Jaap T.; Lankester, Arjan (2004-09-06). "The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes". The Journal of Experimental Medicine. 200 (5): 559–568. doi:10.1084/jem.20040773. ISSN 0022-1007. PMC 2212739. PMID 15337789.
Pai, Sung-Yun; Levy, Ofer; Jabara, Haifa H.; Glickman, Jonathan N.; Stoler-Barak, Liat; Sachs, Jessica; Nurko, Samuel; Orange, Jordan S.; Geha, Raif S. (December 2008). "Allogeneic transplantation successfully corrects immune defects, but not susceptibility to colitis, in a patient with nuclear factor-kappaB essential modulator deficiency". The Journal of Allergy and Clinical Immunology. 122 (6): 1113–1118.e1. doi:10.1016/j.jaci.2008.08.026. ISSN 1097-6825. PMC 6141239. PMID 18851875.
Zonana, J.; Elder, M. E.; Schneider, L. C.; Orlow, S. J.; Moss, C.; Golabi, M.; Shapira, S. K.; Farndon, P. A.; Wara, D. W.; Emmal, S. A.; Ferguson, B. M. (December 2000). "A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)". American Journal of Human Genetics. 67 (6): 1555–1562. doi:10.1086/316914. ISSN 0002-9297. PMC 1287930. PMID 11047757.
Courtois, Gilles; Smahi, Asma; Reichenbach, Janine; Döffinger, Rainer; Cancrini, Caterina; Bonnet, Marion; Puel, Anne; Chable-Bessia, Christine; Yamaoka, Shoji; Feinberg, Jacqueline; Dupuis-Girod, Sophie; Bodemer, Christine; Livadiotti, Susanna; Novelli, Francesco; Rossi, Paolo (October 2003). "A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency". The Journal of Clinical Investigation. 112 (7): 1108–1115. doi:10.1172/JCI18714. ISSN 0021-9738. PMC 198529. PMID 14523047.

rarediseases.info.nih.gov

"Hypohidrotic ectodermal dysplasia with immune deficiency - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2022-05-01. Retrieved 2022-09-24.

omim.org

"Entry - #612132 - ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 2; EDAID2 - OMIM". omim.org. Archived from the original on 2022-08-14. Retrieved 2022-09-24.

orpha.net

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Hypohidrotic ectodermal dysplasia with immunodeficiency". www.orpha.net. Archived from the original on 2017-07-30. Retrieved 2022-09-24.{{cite web}}: CS1 maint: numeric names: authors list (link)

sciencedirect.com

"Hypohidrotic Ectodermal Dysplasia - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2022-09-24.

semanticscholar.org

api.semanticscholar.org

Döffinger, R.; Smahi, A.; Bessia, C.; Geissmann, F.; Feinberg, J.; Durandy, A.; Bodemer, C.; Kenwrick, S.; Dupuis-Girod, S.; Blanche, S.; Wood, P.; Rabia, S. H.; Headon, D. J.; Overbeek, P. A.; Le Deist, F. (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1061-4036. PMID 11242109. S2CID 24898789.
Döffinger, Rainer; Smahi, Asma; Bessia, Christine; Geissmann, Frédéric; Feinberg, Jacqueline; Durandy, Anne; Bodemer, Christine; Kenwrick, Sue; Dupuis-Girod, Sophie; Blanche, Stéphane; Wood, Philip; Rabia, Smail Hadj; Headon, Denis J.; Overbeek, Paul A.; Le Deist, Françoise (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1546-1718. PMID 11242109. S2CID 24898789. Archived from the original on 2022-06-16. Retrieved 2022-09-24.
Jacobs, Marc D.; Harrison, Stephen C. (1998-12-11). "Structure of an IκBα/NF-κB Complex". Cell. 95 (6): 749–758. doi:10.1016/S0092-8674(00)81698-0. ISSN 0092-8674. PMID 9865693. S2CID 7003353.

web.archive.org

"Anhidrotic ectodermal dysplasia with immune deficiency: MedlinePlus Genetics". medlineplus.gov. Archived from the original on 2021-11-01. Retrieved 2022-09-24.
RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Hypohidrotic ectodermal dysplasia with immunodeficiency". www.orpha.net. Archived from the original on 2017-07-30. Retrieved 2022-09-24.{{cite web}}: CS1 maint: numeric names: authors list (link)
"Hypohidrotic ectodermal dysplasia with immune deficiency - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2022-05-01. Retrieved 2022-09-24.
"X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival". ashpublications.org. June 2014. Archived from the original on 2022-01-21. Retrieved 2022-09-24.
Carrol, E. D.; Gennery, A. R.; Flood, T. J.; Spickett, G. P.; Abinun, M. (2003-04-01). "Anhidrotic ectodermal dysplasia and immunodeficiency: the role of NEMO". Archives of Disease in Childhood. 88 (4): 340–341. doi:10.1136/adc.88.4.340. ISSN 0003-9888. PMC 1719512. PMID 12651765. Archived from the original on 2018-06-03. Retrieved 2022-09-24.
"IKBKG gene: MedlinePlus Genetics". medlineplus.gov. Archived from the original on 2021-10-19. Retrieved 2022-09-24.
Döffinger, Rainer; Smahi, Asma; Bessia, Christine; Geissmann, Frédéric; Feinberg, Jacqueline; Durandy, Anne; Bodemer, Christine; Kenwrick, Sue; Dupuis-Girod, Sophie; Blanche, Stéphane; Wood, Philip; Rabia, Smail Hadj; Headon, Denis J.; Overbeek, Paul A.; Le Deist, Françoise (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1546-1718. PMID 11242109. S2CID 24898789. Archived from the original on 2022-06-16. Retrieved 2022-09-24.
"NFKBIA gene: MedlinePlus Genetics". medlineplus.gov. Archived from the original on 2021-04-20. Retrieved 2022-09-24.
"Entry - #612132 - ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 2; EDAID2 - OMIM". omim.org. Archived from the original on 2022-08-14. Retrieved 2022-09-24.

worldcat.org

search.worldcat.org

Döffinger, R.; Smahi, A.; Bessia, C.; Geissmann, F.; Feinberg, J.; Durandy, A.; Bodemer, C.; Kenwrick, S.; Dupuis-Girod, S.; Blanche, S.; Wood, P.; Rabia, S. H.; Headon, D. J.; Overbeek, P. A.; Le Deist, F. (March 2001). "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling". Nature Genetics. 27 (3): 277–285. doi:10.1038/85837. ISSN 1061-4036. PMID 11242109. S2CID 24898789.
Kawai, Tomoki; Nishikomori, Ryuta; Heike, Toshio (2012-01-01). "Diagnosis and Treatment in Anhidrotic Ectodermal Dysplasia with Immunodeficiency". Allergology International. 61 (2): 207–217. doi:10.2332/allergolint.12-RAI-0446. ISSN 1323-8930. PMID 22635013.
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