Hypohidrotic ectodermal dysplasia (English Wikipedia)

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

refsWebsite

Global rank English rank

11nih.gov

4^th place

5doi.org

2^nd place

4worldcat.org

5^th place

2medlineplus.gov

1,581^st place

1,299^th place

2nfed.org

low place

2genome.gov

9,308^th place

8,899^th place

1cancer.gov

1,684^th place

1,350^th place

1clinicaltrials.gov

5,225^th place

4,062^nd place

1web.archive.org

1^st place

cancer.gov

"X-linked recessive inheritance". www.cancer.gov. 2012-07-20. Retrieved 2025-02-28.

clinicaltrials.gov

"Phase 2 Study to Evaluate Safety, Pharmacokinetics, Immunogenicity and Pharmacodynamics/Efficacy of EDI200 in Male Infants With X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) - Full Text View - ClinicalTrials.gov". Retrieved 2018-09-19.

doi.org

Mukkamala, Krishna; Gentile, Ronald C.; Willner, Judith; Tsang, Stephen (2010-12-01). "Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3". Ophthalmic Genetics. 31 (4): 178–182. doi:10.3109/13816810.2010.497529. ISSN 1381-6810. PMC 3056021. PMID 21067479.
Liu, Haochen; Su, Lanxin; Liu, Hangbo; Zheng, Jinglei; Feng, Hailan; Liu, Yang; Yu, Miao; Han, Dong (October 2022). "Rare X-Linked Hypohidrotic Ectodermal Dysplasia in Females Associated with Ectodysplasin-A Variants and the X-Chromosome Inactivation Pattern". Diagnostics. 12 (10): 2300. doi:10.3390/diagnostics12102300. ISSN 2075-4418. PMC 9600026. PMID 36291989.
Körber, Iris; Klein, Ophir; Morhart, Patrick; Faschingbauer, Florian; Grange, Dorothy; Clarke, Angus; Bodemer, Christine; Maitz, Silvia; Huttner, Kenneth (2020-04-06). "Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects". British Journal of Clinical Pharmacology. 86 (10): 2063–2069. doi:10.1111/bcp.14301. ISSN 1365-2125. PMC 7495278. PMID 32250462.
Schneider, Holm; Faschingbauer, Florian; Schuepbach-Mallepell, Sonia; Körber, Iris; Wohlfart, Sigrun; Dick, Angela; Wahlbuhl, Mandy; Kowalczyk-Quintas, Christine; Vigolo, Michele (2018-04-26). "Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia". New England Journal of Medicine. 378 (17): 1604–1610. doi:10.1056/NEJMoa1714322. ISSN 0028-4793. PMID 29694819.
Deshmukh, Seema; Prashanth, S (2012-12-05). "Ectodermal Dysplasia: A Genetic Review". International Journal of Clinical Pediatric Dentistry. 5 (3): 197–202. doi:10.5005/jp-journals-10005-1165. PMC 4155886. PMID 25206167.

genome.gov

"Autosomal Dominant Disorder". www.genome.gov. Retrieved 2025-02-28.
"Autosomal Recessive Disorder". www.genome.gov. Retrieved 2025-02-28.

medlineplus.gov

"Hypohidrotic ectodermal dysplasia: MedlinePlus Genetics". medlineplus.gov. Retrieved 2025-02-28.
"EDA gene: MedlinePlus Genetics". medlineplus.gov. Retrieved 2025-02-28.

nfed.org

"X-Linked Hypohidrotic Ectodermal Dysplasia | National Foundation for Ectodermal Dysplasias". National Foundation for Ectodermal Dysplasias. Archived from the original on 2018-04-29. Retrieved 2018-04-29.
"Babies With XLHED Treated In Utero | National Foundation for Ectodermal Dysplasias". National Foundation for Ectodermal Dysplasias. 2016-12-07. Retrieved 2018-04-29.

nih.gov

pubmed.ncbi.nlm.nih.gov

Mukkamala, Krishna; Gentile, Ronald C.; Willner, Judith; Tsang, Stephen (2010-12-01). "Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3". Ophthalmic Genetics. 31 (4): 178–182. doi:10.3109/13816810.2010.497529. ISSN 1381-6810. PMC 3056021. PMID 21067479.
Wright, J. Timothy; Grange, Dorothy K.; Fete, Mary (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Hypohidrotic Ectodermal Dysplasia", GeneReviews®, Seattle (WA): University of Washington, Seattle, PMID 20301291, retrieved 2025-02-28
Liu, Haochen; Su, Lanxin; Liu, Hangbo; Zheng, Jinglei; Feng, Hailan; Liu, Yang; Yu, Miao; Han, Dong (October 2022). "Rare X-Linked Hypohidrotic Ectodermal Dysplasia in Females Associated with Ectodysplasin-A Variants and the X-Chromosome Inactivation Pattern". Diagnostics. 12 (10): 2300. doi:10.3390/diagnostics12102300. ISSN 2075-4418. PMC 9600026. PMID 36291989.
Körber, Iris; Klein, Ophir; Morhart, Patrick; Faschingbauer, Florian; Grange, Dorothy; Clarke, Angus; Bodemer, Christine; Maitz, Silvia; Huttner, Kenneth (2020-04-06). "Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects". British Journal of Clinical Pharmacology. 86 (10): 2063–2069. doi:10.1111/bcp.14301. ISSN 1365-2125. PMC 7495278. PMID 32250462.
Schneider, Holm; Faschingbauer, Florian; Schuepbach-Mallepell, Sonia; Körber, Iris; Wohlfart, Sigrun; Dick, Angela; Wahlbuhl, Mandy; Kowalczyk-Quintas, Christine; Vigolo, Michele (2018-04-26). "Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia". New England Journal of Medicine. 378 (17): 1604–1610. doi:10.1056/NEJMoa1714322. ISSN 0028-4793. PMID 29694819.
Deshmukh, Seema; Prashanth, S (2012-12-05). "Ectodermal Dysplasia: A Genetic Review". International Journal of Clinical Pediatric Dentistry. 5 (3): 197–202. doi:10.5005/jp-journals-10005-1165. PMC 4155886. PMID 25206167.

ncbi.nlm.nih.gov

Mukkamala, Krishna; Gentile, Ronald C.; Willner, Judith; Tsang, Stephen (2010-12-01). "Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3". Ophthalmic Genetics. 31 (4): 178–182. doi:10.3109/13816810.2010.497529. ISSN 1381-6810. PMC 3056021. PMID 21067479.
Wright, J. Timothy; Grange, Dorothy K.; Fete, Mary (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Hypohidrotic Ectodermal Dysplasia", GeneReviews®, Seattle (WA): University of Washington, Seattle, PMID 20301291, retrieved 2025-02-28
Liu, Haochen; Su, Lanxin; Liu, Hangbo; Zheng, Jinglei; Feng, Hailan; Liu, Yang; Yu, Miao; Han, Dong (October 2022). "Rare X-Linked Hypohidrotic Ectodermal Dysplasia in Females Associated with Ectodysplasin-A Variants and the X-Chromosome Inactivation Pattern". Diagnostics. 12 (10): 2300. doi:10.3390/diagnostics12102300. ISSN 2075-4418. PMC 9600026. PMID 36291989.
Körber, Iris; Klein, Ophir; Morhart, Patrick; Faschingbauer, Florian; Grange, Dorothy; Clarke, Angus; Bodemer, Christine; Maitz, Silvia; Huttner, Kenneth (2020-04-06). "Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects". British Journal of Clinical Pharmacology. 86 (10): 2063–2069. doi:10.1111/bcp.14301. ISSN 1365-2125. PMC 7495278. PMID 32250462.
Deshmukh, Seema; Prashanth, S (2012-12-05). "Ectodermal Dysplasia: A Genetic Review". International Journal of Clinical Pediatric Dentistry. 5 (3): 197–202. doi:10.5005/jp-journals-10005-1165. PMC 4155886. PMID 25206167.

web.archive.org

"X-Linked Hypohidrotic Ectodermal Dysplasia | National Foundation for Ectodermal Dysplasias". National Foundation for Ectodermal Dysplasias. Archived from the original on 2018-04-29. Retrieved 2018-04-29.

worldcat.org

search.worldcat.org

Mukkamala, Krishna; Gentile, Ronald C.; Willner, Judith; Tsang, Stephen (2010-12-01). "Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3". Ophthalmic Genetics. 31 (4): 178–182. doi:10.3109/13816810.2010.497529. ISSN 1381-6810. PMC 3056021. PMID 21067479.
Liu, Haochen; Su, Lanxin; Liu, Hangbo; Zheng, Jinglei; Feng, Hailan; Liu, Yang; Yu, Miao; Han, Dong (October 2022). "Rare X-Linked Hypohidrotic Ectodermal Dysplasia in Females Associated with Ectodysplasin-A Variants and the X-Chromosome Inactivation Pattern". Diagnostics. 12 (10): 2300. doi:10.3390/diagnostics12102300. ISSN 2075-4418. PMC 9600026. PMID 36291989.
Körber, Iris; Klein, Ophir; Morhart, Patrick; Faschingbauer, Florian; Grange, Dorothy; Clarke, Angus; Bodemer, Christine; Maitz, Silvia; Huttner, Kenneth (2020-04-06). "Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects". British Journal of Clinical Pharmacology. 86 (10): 2063–2069. doi:10.1111/bcp.14301. ISSN 1365-2125. PMC 7495278. PMID 32250462.
Schneider, Holm; Faschingbauer, Florian; Schuepbach-Mallepell, Sonia; Körber, Iris; Wohlfart, Sigrun; Dick, Angela; Wahlbuhl, Mandy; Kowalczyk-Quintas, Christine; Vigolo, Michele (2018-04-26). "Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia". New England Journal of Medicine. 378 (17): 1604–1610. doi:10.1056/NEJMoa1714322. ISSN 0028-4793. PMID 29694819.