These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 15935629)

  • 1. [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]  

  • 2. The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosis.
    Sprecher E; Chavanas S; DiGiovanna JJ; Amin S; Nielsen K; Prendiville JS; Silverman R; Esterly NB; Spraker MK; Guelig E; de Luna ML; Williams ML; Buehler B; Siegfried EC; Van Maldergem L; Pfendner E; Bale SJ; Uitto J; Hovnanian A; Richard G
    J Invest Dermatol; 2001 Aug; 117(2):179-87. PubMed ID: 11511292
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Severe hypernatremic dehydration in an infant with Netherton syndrome.
    Stoll C; Alembik Y; Tchomakov D; Messer J; Heid E; Boehm N; Calvas P; Hovnanian A
    Genet Couns; 2001; 12(3):237-43. PubMed ID: 11693786
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families.
    Bitoun E; Chavanas S; Irvine AD; Lonie L; Bodemer C; Paradisi M; Hamel-Teillac D; Ansai S; Mitsuhashi Y; Taïeb A; de Prost Y; Zambruno G; Harper JI; Hovnanian A
    J Invest Dermatol; 2002 Feb; 118(2):352-61. PubMed ID: 11841556
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A case of a Japanese neonate with congenital ichthyosiform erythroderma diagnosed as Netherton syndrome.
    Mizuno Y; Suga Y; Haruna K; Muramatsu S; Hasegawa T; Kohroh K; Shimizu T; Komatsu N; Ogawa H; Ikeda S
    Clin Exp Dermatol; 2006 Sep; 31(5):677-80. PubMed ID: 16901309
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Netherton syndrome with extensive skin peeling and failure to thrive due to a homozygous frameshift mutation in SPINK5.
    Geyer AS; Ratajczak P; Pol-Rodriguez M; Millar WS; Garzon M; Richard G
    Dermatology; 2005; 210(4):308-14. PubMed ID: 15942217
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A compound heterozygous mutation of the SPINK5 gene in a Taiwanese boy with Netherton syndrome.
    Chao SC; Tsai YM; Lee JY
    J Formos Med Assoc; 2003 Jun; 102(6):418-23. PubMed ID: 12923596
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Netherton syndrome: report of two Taiwanese siblings with staphylococcal scalded skin syndrome and mutation of SPINK5.
    Chao SC; Richard G; Lee JY
    Br J Dermatol; 2005 Jan; 152(1):159-65. PubMed ID: 15656819
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Netherton syndrome in two Japanese siblings with a novel mutation in the SPINK5 gene: immunohistochemical studies of LEKTI and other epidermal molecules.
    Shimomura Y; Sato N; Kariya N; Takatsuka S; Ito M
    Br J Dermatol; 2005 Nov; 153(5):1026-30. PubMed ID: 16225619
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndrome.
    Hausser I; Anton-Lamprecht I
    Pediatr Dermatol; 1996; 13(3):183-99. PubMed ID: 8806118
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminases.
    Raghunath M; Tontsidou L; Oji V; Aufenvenne K; Schürmeyer-Horst F; Jayakumar A; Ständer H; Smolle J; Clayman GL; Traupe H
    J Invest Dermatol; 2004 Sep; 123(3):474-83. PubMed ID: 15304086
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. LEKTI demonstrable by immunohistochemistry of the skin: a potential diagnostic skin test for Netherton syndrome.
    Ong C; O'Toole EA; Ghali L; Malone M; Smith VV; Callard R; Harper JI
    Br J Dermatol; 2004 Dec; 151(6):1253-7. PubMed ID: 15606522
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe bilateral rachitic genu valgum in patients with nonbullous congenital ichthyosiform erythroderma: a report of two cases and review of literature.
    Bhagat SB; Bhagat SS; Sharma HK; Naik M; Amin P; Pandit J
    J Pediatr Orthop B; 2007 Nov; 16(6):423-8. PubMed ID: 17909341
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Netherton syndrome: mutation analysis of two Taiwanese families.
    Lin SP; Huang SY; Tu ME; Wu YH; Lin CY; Lin HY; Lee-Chen GJ
    Arch Dermatol Res; 2007 Jun; 299(3):145-50. PubMed ID: 17415575
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Netherton syndrome: A neonatal case with respiratory insufficiency.
    Okulu E; Tunc G; Erdeve O; Mumcu Y; Atasay B; Ince E; Arsan S
    Arch Argent Pediatr; 2018 Aug; 116(4):e609-e611. PubMed ID: 30016041
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.