Хипохидротична ектодермална дисплазија (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Хипохидротична ектодермална дисплазија" in Serbian language version.
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archive.org
- Tarjan, I.; Gabris, K.; Rozsa, N. (мај 2005). „Early prosthetic treatment of patients with ectodermal dysplasia: a clinical report.”. J Prosthet Dent. 93 (5): 419—24. PMID 15867750. doi:10.1016/j.prosdent.2005.01.012.
doi.org
- Rojas, Lida Velazque; Silva, Gisele Dalben da (2015-10-01). „Hypohidrotic ectodermal dysplasia: clinical and radiographic characteristics”. Revista Odontológica Mexicana (на језику: шпански). 19 (4): e249—e253. ISSN 1870-199X. doi:10.1016/j.rodmex.2015.10.016.
- The International Incontinentia Pigmenti (IP) Consortium; Smahi, Asmae; Courtois, G.; Vabres, P.; Yamaoka, S.; Heuertz, S.; Munnich, A.; Israël, A.; Heiss, Nina S.; Klauck, S. M.; Kioschis, P.; Wiemann, S.; Poustka, A.; Esposito, Teresa; Bardaro, T.; Gianfrancesco, F.; Ciccodicola, A.; d'Urso, M.; Woffendin, Hayley; Jakins, T.; Donnai, D.; Stewart, H.; Kenwrick, S. J.; Aradhya, Swaroop; Yamagata, T.; Levy, M.; Lewis, R. A.; Nelson, D. L. (мај 2000). „Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti”. Nature. 405 (6785): 466—72. Bibcode:2000Natur.405..466T. PMID 10839543. doi:10.1038/35013114. 25.
- Zonana, J.; Elder, M. E.; Schneider, L. C.; et al. (децембар 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).”. Am J Hum Genet. 67 (6): 1555—62. PMC 1287930
. PMID 11047757. doi:10.1086/316914. - Mues G, Bonds J, Xiang L, Vieira AR, Seymen F, Klein O; et al. (октобар 2014). „The WNT10A gene in ectodermal dysplasias and selective tooth agenesis”. Am J Med Genet A. 164 (10): 2455—2460. PMC 4167166 . PMID 24700731. doi:10.1002/ajmg.a.36520.A (10):2455-60
- Ali, R. H.; Habib, R; Ud-Din, N.; Khan, M. N.; Ansar, M; Ahmad, W. (август 2013). „Novel mutations in the gene HOXC13 underlying pure hair and nail ectodermal dysplasia in consanguineous families.”. Br J Dermatol. 169 (2): 478—80. PMID 23461661. doi:10.1111/bjd.12302.
- Nordgarden H, Storhaug K, Lyngstadaas SP, Jensen JL (октобар 2003). „Salivary gland function in persons with ectodermal dysplasias”. Eur J Oral Sci. 111 (5): 371—376. PMID 12974678. doi:10.1034/j.1600-0722.2003.00058.x.(5):371-6
- N. Alves, Oliveira RJd, N.F. Deana (2012). „Displasia ectodérmica hipohidrótica: un síndrome de interés para la odontología.”. Int J Odontostomatol. 6: 45—50. doi:10.4067/S0718-381X2012000100006. ,
- Rouse C, Siegfried E, Breer W, Nahass G (2004). „Hair and sweat glands in families with hypohidrotic ectodermal dysplasia: further characterization”. Arch Dermatol. 140 (7): 850—5. PMID 15262696. doi:10.1001/archderm.140.7.850. [Reference list]
- Jones, K. B.; Goodwin, A. F.; Landan, M; Seidel, K.; Tran, D. K.; Hogue J, Chavez M, Fete M, Yu W, Hussein T, Johnson R, Huttner K, Jheon AH, Klein OD (2013). „Characterization of X-linked hypohidrotic ectodermal dysplasia (XL-HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging”. Am J Med Genet A. 161 (7): 1585—1593. PMC 4414120 . PMID 23687000. doi:10.1002/ajmg.a.35959.
- Lexner, M. O.; Bardow, A; Hertz, J. M.; Nielsen, L. A.; Kreiborg, S. (2007). „Anomalies of tooth formation in hypohidrotic ectodermal dysplasia”. Int J Paediatr Dent. 17 (1): 10—18. PMID 17181574. doi:10.1111/j.1365-263X.2006.00801.x.
- Monreal, A. W.; Zonana, J.; Ferguson, B. (1998). „Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations”. Am J Hum Genet. 63 (2): 380—389. PMC 1377324 . PMID 9683615. doi:10.1086/301984.
- Chassaing N, Bourthoumieu S, Cossee M, Calvas P, Vincent MC (2006). „Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia”. Hum Mutat. 27 (3): 255—9. PMID 16435307. doi:10.1002/humu.20295. [Reference list]
- Monreal, A. W.; Ferguson, B. M.; Headon, D. J.; Street, S. L.; Overbeek, P. A.; Zonana, J. (1999). „Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia”. Nat Genet. 22 (4): 366—9. PMID 10431241. doi:10.1038/11937.
- Bohring A, Stamm T, Spaich C, Haase C, Spree K, Hehr U, Hoffmann M, Ledig S, Sel S, Wieacker P, Röpke A (2009). „WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes”. Am J Hum Genet. 85 (1): 97—105. PMC 2706962 . PMID 19559398. doi:10.1016/j.ajhg.2009.06.001.:97–105. [PMC free article] [PubMed] [Reference list]
- Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A (2011). „Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases”. Hum Mutat. 32 (1): 70—2. PMID 20979233. doi:10.1002/humu.21384. [Reference list]
- Theiler, M.; Frieden, I. J. (2016 Mar-Apr). „High-Potency Topical Steroids: An Effective Therapy for Chronic Scalp Inflammation in Rapp-Hodgkin Ectodermal Dysplasia”. Pediatr Dermatol. 33 (2): e84—7. PMID 26861896. doi:10.1111/pde.12784. Проверите вредност парамет(а)ра за датум:
|date=(помоћ) - Dhima M, Salinas TJ, Cofer SA, Rieck KL (2013). „Rehabilitation of medically complex ectodermal dysplasia with novel surgical and prosthodontic protocols”. Int J Oral Maxillofac Surg. 43 (3): 301—304. PMID 24035129. doi:10.1016/j.ijom.2013.08.004. Sep 12.
- Al-Ibrahim HA, Al-Hadlaq SM, Abduljabbar TS, Al-Hamdan KS, Abdin HA (јануар 2012). „Surgical and implant-supported fixed prosthetic treatment of a patient with ectodermal dysplasia: a case report.”. Spec Care Dentist. 32 (1): 1—5. PMID 22229591. doi:10.1111/j.1754-4505.2011.00222.x.
- Tarjan, I.; Gabris, K.; Rozsa, N. (мај 2005). „Early prosthetic treatment of patients with ectodermal dysplasia: a clinical report.”. J Prosthet Dent. 93 (5): 419—24. PMID 15867750. doi:10.1016/j.prosdent.2005.01.012.
- Lee, H. E.; Chang, I. K.; Im, M; Seo, Y. J.; Lee, J. H.; Lee, Y. (април 2013). „Topical minoxidil treatment for congenital alopecia in hypohidrotic ectodermal dysplasia”. J Am Acad Dermatol. 68 (4): e139—e140. PMID 23522427. doi:10.1016/j.jaad.2012.10.019.
- Melkote S, Dhurat RS, Palav A, Jerajani HR (фебруар 2009). „Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin”. Int J Dermatol. 48 (2): 184—185. PMID 19200200. doi:10.1111/j.1365-4632.2009.03907.x.(2):184-5.
- Klineberg I, Cameron A, Whittle T, Hobkirk J, Bergendal B, Maniere MC, et al. Rehabilitation of children with ectodermal dysplasia (2013 Jul-Aug). „Part 1: an international Delphi study.”. Int J Oral Maxillofac Implants. 28 (4): 1090—100. PMID 23869367. doi:10.11607/jomi.2980. Проверите вредност парамет(а)ра за датум:
|date=(помоћ). - Fete M, Hermann J, Behrens J, Huttner KM (октобар 2014). „X-linked hypohidrotic ectodermal dysplasia (XLHED): clinical and diagnostic insights from an international patient registry”. Am J Med Genet A. 164 (10): 2437—2442. PMID 24664614. doi:10.1002/ajmg.a.36436.A (10):2437-42.
elsevier.es
- Rojas, Lida Velazque; Silva, Gisele Dalben da (2015-10-01). „Hypohidrotic ectodermal dysplasia: clinical and radiographic characteristics”. Revista Odontológica Mexicana (на језику: шпански). 19 (4): e249—e253. ISSN 1870-199X. doi:10.1016/j.rodmex.2015.10.016.
harvard.edu
adsabs.harvard.edu
- The International Incontinentia Pigmenti (IP) Consortium; Smahi, Asmae; Courtois, G.; Vabres, P.; Yamaoka, S.; Heuertz, S.; Munnich, A.; Israël, A.; Heiss, Nina S.; Klauck, S. M.; Kioschis, P.; Wiemann, S.; Poustka, A.; Esposito, Teresa; Bardaro, T.; Gianfrancesco, F.; Ciccodicola, A.; d'Urso, M.; Woffendin, Hayley; Jakins, T.; Donnai, D.; Stewart, H.; Kenwrick, S. J.; Aradhya, Swaroop; Yamagata, T.; Levy, M.; Lewis, R. A.; Nelson, D. L. (мај 2000). „Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti”. Nature. 405 (6785): 466—72. Bibcode:2000Natur.405..466T. PMID 10839543. doi:10.1038/35013114. 25.
nih.gov
ncbi.nlm.nih.gov
- Wright, J. Timothy; Grange, Dorothy K.; Fete, Mary (1993), Adam, Margaret P.; Ardinger, Holly H., ур., Hypohidrotic Ectodermal Dysplasia, University of Washington, Seattle, PMID 20301291, Приступљено 2022-02-18
- The International Incontinentia Pigmenti (IP) Consortium; Smahi, Asmae; Courtois, G.; Vabres, P.; Yamaoka, S.; Heuertz, S.; Munnich, A.; Israël, A.; Heiss, Nina S.; Klauck, S. M.; Kioschis, P.; Wiemann, S.; Poustka, A.; Esposito, Teresa; Bardaro, T.; Gianfrancesco, F.; Ciccodicola, A.; d'Urso, M.; Woffendin, Hayley; Jakins, T.; Donnai, D.; Stewart, H.; Kenwrick, S. J.; Aradhya, Swaroop; Yamagata, T.; Levy, M.; Lewis, R. A.; Nelson, D. L. (мај 2000). „Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti”. Nature. 405 (6785): 466—72. Bibcode:2000Natur.405..466T. PMID 10839543. doi:10.1038/35013114. 25.
- Zonana, J.; Elder, M. E.; Schneider, L. C.; et al. (децембар 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).”. Am J Hum Genet. 67 (6): 1555—62. PMC 1287930 . PMID 11047757. doi:10.1086/316914.
- Mues G, Bonds J, Xiang L, Vieira AR, Seymen F, Klein O; et al. (октобар 2014). „The WNT10A gene in ectodermal dysplasias and selective tooth agenesis”. Am J Med Genet A. 164 (10): 2455—2460. PMC 4167166 . PMID 24700731. doi:10.1002/ajmg.a.36520.A (10):2455-60
- Ali, R. H.; Habib, R; Ud-Din, N.; Khan, M. N.; Ansar, M; Ahmad, W. (август 2013). „Novel mutations in the gene HOXC13 underlying pure hair and nail ectodermal dysplasia in consanguineous families.”. Br J Dermatol. 169 (2): 478—80. PMID 23461661. doi:10.1111/bjd.12302.
- Nordgarden H, Storhaug K, Lyngstadaas SP, Jensen JL (октобар 2003). „Salivary gland function in persons with ectodermal dysplasias”. Eur J Oral Sci. 111 (5): 371—376. PMID 12974678. doi:10.1034/j.1600-0722.2003.00058.x.(5):371-6
- Rouse C, Siegfried E, Breer W, Nahass G (2004). „Hair and sweat glands in families with hypohidrotic ectodermal dysplasia: further characterization”. Arch Dermatol. 140 (7): 850—5. PMID 15262696. doi:10.1001/archderm.140.7.850. [Reference list]
- Jones, K. B.; Goodwin, A. F.; Landan, M; Seidel, K.; Tran, D. K.; Hogue J, Chavez M, Fete M, Yu W, Hussein T, Johnson R, Huttner K, Jheon AH, Klein OD (2013). „Characterization of X-linked hypohidrotic ectodermal dysplasia (XL-HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging”. Am J Med Genet A. 161 (7): 1585—1593. PMC 4414120 . PMID 23687000. doi:10.1002/ajmg.a.35959.
- Lexner, M. O.; Bardow, A; Hertz, J. M.; Nielsen, L. A.; Kreiborg, S. (2007). „Anomalies of tooth formation in hypohidrotic ectodermal dysplasia”. Int J Paediatr Dent. 17 (1): 10—18. PMID 17181574. doi:10.1111/j.1365-263X.2006.00801.x.
- Monreal, A. W.; Zonana, J.; Ferguson, B. (1998). „Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations”. Am J Hum Genet. 63 (2): 380—389. PMC 1377324 . PMID 9683615. doi:10.1086/301984.
- Chassaing N, Bourthoumieu S, Cossee M, Calvas P, Vincent MC (2006). „Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia”. Hum Mutat. 27 (3): 255—9. PMID 16435307. doi:10.1002/humu.20295. [Reference list]
- Monreal, A. W.; Ferguson, B. M.; Headon, D. J.; Street, S. L.; Overbeek, P. A.; Zonana, J. (1999). „Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia”. Nat Genet. 22 (4): 366—9. PMID 10431241. doi:10.1038/11937.
- Bohring A, Stamm T, Spaich C, Haase C, Spree K, Hehr U, Hoffmann M, Ledig S, Sel S, Wieacker P, Röpke A (2009). „WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes”. Am J Hum Genet. 85 (1): 97—105. PMC 2706962 . PMID 19559398. doi:10.1016/j.ajhg.2009.06.001.:97–105. [PMC free article] [PubMed] [Reference list]
- Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A (2011). „Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases”. Hum Mutat. 32 (1): 70—2. PMID 20979233. doi:10.1002/humu.21384. [Reference list]
- Theiler, M.; Frieden, I. J. (2016 Mar-Apr). „High-Potency Topical Steroids: An Effective Therapy for Chronic Scalp Inflammation in Rapp-Hodgkin Ectodermal Dysplasia”. Pediatr Dermatol. 33 (2): e84—7. PMID 26861896. doi:10.1111/pde.12784. Проверите вредност парамет(а)ра за датум:
|date=(помоћ) - Dhanrajani, P. J.; Jiffry, A. O. (март 1998). „Management of ectodermal dysplasia: a literature review.”. Dent Update. 25 (2): 73—5. PMID 9791211.
- Dhima M, Salinas TJ, Cofer SA, Rieck KL (2013). „Rehabilitation of medically complex ectodermal dysplasia with novel surgical and prosthodontic protocols”. Int J Oral Maxillofac Surg. 43 (3): 301—304. PMID 24035129. doi:10.1016/j.ijom.2013.08.004. Sep 12.
- Al-Ibrahim HA, Al-Hadlaq SM, Abduljabbar TS, Al-Hamdan KS, Abdin HA (јануар 2012). „Surgical and implant-supported fixed prosthetic treatment of a patient with ectodermal dysplasia: a case report.”. Spec Care Dentist. 32 (1): 1—5. PMID 22229591. doi:10.1111/j.1754-4505.2011.00222.x.
- Aydinbelge M, Gumus HO, Sekerci AE, Demetoglu U, Etoz OA (2013 Sep-Oct). „Implants in children with hypohidrotic ectodermal dysplasia: an alternative approach to esthetic management: case report and review of the literature.”. Pediatr Dent. 35 (5): 441—6. PMID 24290558. Проверите вредност парамет(а)ра за датум:
|date=(помоћ) - Tarjan, I.; Gabris, K.; Rozsa, N. (мај 2005). „Early prosthetic treatment of patients with ectodermal dysplasia: a clinical report.”. J Prosthet Dent. 93 (5): 419—24. PMID 15867750. doi:10.1016/j.prosdent.2005.01.012.
- El Osta Chaiban R, Chaiban W (децембар 2011). „Ectodermal dysplasia: dental management and benefits, a case report.”. Eur J Paediatr Dent. 12 (4): 282—4. PMID 22185258..
- Lee, H. E.; Chang, I. K.; Im, M; Seo, Y. J.; Lee, J. H.; Lee, Y. (април 2013). „Topical minoxidil treatment for congenital alopecia in hypohidrotic ectodermal dysplasia”. J Am Acad Dermatol. 68 (4): e139—e140. PMID 23522427. doi:10.1016/j.jaad.2012.10.019.
- Melkote S, Dhurat RS, Palav A, Jerajani HR (фебруар 2009). „Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin”. Int J Dermatol. 48 (2): 184—185. PMID 19200200. doi:10.1111/j.1365-4632.2009.03907.x.(2):184-5.
- Klineberg I, Cameron A, Whittle T, Hobkirk J, Bergendal B, Maniere MC, et al. Rehabilitation of children with ectodermal dysplasia (2013 Jul-Aug). „Part 1: an international Delphi study.”. Int J Oral Maxillofac Implants. 28 (4): 1090—100. PMID 23869367. doi:10.11607/jomi.2980. Проверите вредност парамет(а)ра за датум:
|date=(помоћ). - Fete M, Hermann J, Behrens J, Huttner KM (октобар 2014). „X-linked hypohidrotic ectodermal dysplasia (XLHED): clinical and diagnostic insights from an international patient registry”. Am J Med Genet A. 164 (10): 2437—2442. PMID 24664614. doi:10.1002/ajmg.a.36436.A (10):2437-42.
orpha.net
- „Orphanet: Suche / Krankheit”. www.orpha.net. Приступљено 2022-02-24.
worldcat.org
- Rojas, Lida Velazque; Silva, Gisele Dalben da (2015-10-01). „Hypohidrotic ectodermal dysplasia: clinical and radiographic characteristics”. Revista Odontológica Mexicana (на језику: шпански). 19 (4): e249—e253. ISSN 1870-199X. doi:10.1016/j.rodmex.2015.10.016.