371 related articles for article (PubMed ID: 11841556)
21. [Netherton syndrome].
Serra-Guillén C; Torrelo A; Drake M; Armesto S; Fernández-Llaca H; Zambrano A
Actas Dermosifiliogr; 2006 Jun; 97(5):348-50. PubMed ID: 16956571
[TBL] [Abstract][Full Text] [Related]
22. Genetic analysis of a severe case of Netherton syndrome and application for prenatal testing.
Müller FB; Hausser I; Berg D; Casper C; Maiwald R; Jung A; Jung H; Korge BP
Br J Dermatol; 2002 Mar; 146(3):495-9. PubMed ID: 11952552
[TBL] [Abstract][Full Text] [Related]
23. An infant with Netherton syndrome and persistent pulmonary hypertension requiring extracorporeal membrane oxygenation.
Macknet CA; Morkos A; Job L; Garberoglio MC; Clark RD; Macknet KD; Peverini RL
Pediatr Dermatol; 2008; 25(3):368-72. PubMed ID: 18577046
[TBL] [Abstract][Full Text] [Related]
24. Association of SPINK5 gene polymorphisms with atopic dermatitis in the Japanese population.
Kato A; Fukai K; Oiso N; Hosomi N; Murakami T; Ishii M
Br J Dermatol; 2003 Apr; 148(4):665-9. PubMed ID: 12752122
[TBL] [Abstract][Full Text] [Related]
25. SPINK5, the defective gene in netherton syndrome, encodes multiple LEKTI isoforms derived from alternative pre-mRNA processing.
Tartaglia-Polcini A; Bonnart C; Micheloni A; Cianfarani F; Andrè A; Zambruno G; Hovnanian A; D'Alessio M
J Invest Dermatol; 2006 Feb; 126(2):315-24. PubMed ID: 16374478
[TBL] [Abstract][Full Text] [Related]
26. [Netherton syndrome: a type of infantile erythroderma with failure to thrive, immune deficiency, rickets. Report of 3 cases].
André E; Till M; Descargues P; Cordier MP; Fouilhoux A; Haftek M; Hovnanian A; Lachaux A
Arch Pediatr; 2005 Sep; 12(9):1364-7. PubMed ID: 15935629
[TBL] [Abstract][Full Text] [Related]
27. Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndrome.
Sprecher E; Tesfaye-Kedjela A; Ratajczak P; Bergman R; Richard G
Clin Exp Dermatol; 2004 Sep; 29(5):513-7. PubMed ID: 15347338
[TBL] [Abstract][Full Text] [Related]
28. SPINK5 gene mutation and decreased LEKTI activity in three Chinese patients with Netherton's syndrome.
Zhao Y; Ma ZH; Yang Y; Yang SX; Wu LS; Ding BL; Lin ZM; Wang AP; Bu DF; Tu P
Clin Exp Dermatol; 2007 Sep; 32(5):564-7. PubMed ID: 17608759
[TBL] [Abstract][Full Text] [Related]
29. A Japanese infant with localized ichthyosis linearis circumflexa on the palms and soles harbouring a compound heterozygous mutation in the SPINK5 gene.
Mizuno Y; Suga Y; Muramatsu S; Hasegawa T; Shimizu T; Ogawa H
Br J Dermatol; 2005 Sep; 153(3):661-3. PubMed ID: 16120162
[TBL] [Abstract][Full Text] [Related]
30. Netherton Syndrome in a Mother and Her Two Children.
DeMoss J; Cooper L; Felts C; Wittenberg G
S D Med; 2022 Dec; 75(12):554-556. PubMed ID: 36893349
[TBL] [Abstract][Full Text] [Related]
31. A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteins.
Di WL; Hennekam RC; Callard RE; Harper JI
Br J Dermatol; 2009 Aug; 161(2):404-12. PubMed ID: 19438860
[TBL] [Abstract][Full Text] [Related]
32. Netherton Syndrome Caused by Heterozygous Frameshift Mutation Combined with Homozygous c.1258A>G Polymorphism in
Moltrasio C; Romagnuolo M; Riva D; Colavito D; Ferrucci SM; Marzano AV; Tadini G; Brena M
Genes (Basel); 2023 May; 14(5):. PubMed ID: 37239440
[TBL] [Abstract][Full Text] [Related]
33. The Arid Melancholy-Netherton Syndrome With Protein Energy Malnutrition.
Jain SP; Jain PA; Pandey N
J Clin Diagn Res; 2016 Apr; 10(4):WD01-2. PubMed ID: 27190931
[TBL] [Abstract][Full Text] [Related]
34. A novel SPINK5 mutation and successful subcutaneous immunoglobulin replacement therapy in a child with Netherton syndrome.
Zelieskova M; Banovcin P; Kozar M; Kozarova A; Nudzajova Z; Jesenak M
Pediatr Dermatol; 2020 Nov; 37(6):1202-1204. PubMed ID: 32767583
[TBL] [Abstract][Full Text] [Related]
35. Ichthyosis Linearis Circumflexa as the Only Clinical Manifestation of Netherton Syndrome.
Guerra L; Fortugno P; Pedicelli C; Mazzanti C; Proto V; Zambruno G; Castiglia D
Acta Derm Venereol; 2015 Jul; 95(6):720-4. PubMed ID: 25710899
[TBL] [Abstract][Full Text] [Related]
36. A synonymous mutation in SPINK5 exon 11 causes Netherton syndrome by altering exonic splicing regulatory elements.
Fortugno P; Grosso F; Zambruno G; Pastore S; Faletra F; Castiglia D
J Hum Genet; 2012 May; 57(5):311-5. PubMed ID: 22377713
[TBL] [Abstract][Full Text] [Related]
37. Netherton Syndrome: A Genotype-Phenotype Review.
Sarri CA; Roussaki-Schulze A; Vasilopoulos Y; Zafiriou E; Patsatsi A; Stamatis C; Gidarokosta P; Sotiriadis D; Sarafidou T; Mamuris Z
Mol Diagn Ther; 2017 Apr; 21(2):137-152. PubMed ID: 27905021
[TBL] [Abstract][Full Text] [Related]
38. Two siblings affected by Netherton/Comèl syndrome. Diagnostic pathology and description of a new SPINK5 variant.
Schepis C; Siragusa M; Centofanti A; Vinci M; Calì F
Dermatol Online J; 2019 Jul; 25(7):. PubMed ID: 31450277
[TBL] [Abstract][Full Text] [Related]
39. Association between polymorphisms in the SPINK5 gene and atopic dermatitis in the Japanese.
Nishio Y; Noguchi E; Shibasaki M; Kamioka M; Ichikawa E; Ichikawa K; Umebayashi Y; Otsuka F; Arinami T
Genes Immun; 2003 Oct; 4(7):515-7. PubMed ID: 14551605
[TBL] [Abstract][Full Text] [Related]
40. Netherton syndrome: a case report and review of the literature.
Sun JD; Linden KG
Int J Dermatol; 2006 Jun; 45(6):693-7. PubMed ID: 16796630
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
