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 *

128 related articles for article (PubMed ID: 29624232)

  • 1. A rare large mutation involving two exons of the SP-B gene in an infant with severe respiratory distress.
    Takcı Ş; Anuk-İnce D; Louha M; Couderc R; Çakar N; Köseoğlu RD; Ateş Ö
    Turk J Pediatr; 2017; 59(4):483-486. PubMed ID: 29624232
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary surfactant protein B deficiency resulting from a novel mutation.
    Somaschini M; Wert S; Mangili G; Colombo A; Nogee L
    Intensive Care Med; 2000 Jan; 26(1):97-100. PubMed ID: 10663288
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency.
    Tredano M; van Elburg RM; Kaspers AG; Zimmermann LJ; Houdayer C; Aymard P; Hull WM; Whitsett JA; Elion J; Griese M; Bahuau M
    Hum Mutat; 1999; 14(6):502-9. PubMed ID: 10571948
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A major deletion in the surfactant protein-B gene causing lethal respiratory distress.
    Wegner DJ; Hertzberg T; Heins HB; Elmberger G; MacCoss MJ; Carlson CS; Nogee LM; Cole FS; Hamvas A
    Acta Paediatr; 2007 Apr; 96(4):516-20. PubMed ID: 17391469
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inherited disorders of neonatal lung diseases.
    Yurdakök M
    Turk J Pediatr; 2004; 46(2):105-14. PubMed ID: 15214737
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency.
    Brasch F; Schimanski S; Mühlfeld C; Barlage S; Langmann T; Aslanidis C; Boettcher A; Dada A; Schroten H; Mildenberger E; Prueter E; Ballmann M; Ochs M; Johnen G; Griese M; Schmitz G
    Am J Respir Crit Care Med; 2006 Sep; 174(5):571-80. PubMed ID: 16728712
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Surfactant protein B deficiency: a rare cause of respiratory failure in a Lebanese newborn.
    Ferzli G; Yunis KA; Mroueh S
    Ann Saudi Med; 2006; 26(1):69-70. PubMed ID: 16521884
    [No Abstract]   [Full Text] [Related]  

  • 8. Surfactant proteins gene variants in premature newborn infants with severe respiratory distress syndrome.
    Somaschini M; Presi S; Ferrari M; Vergani B; Carrera P
    J Perinatol; 2018 Apr; 38(4):337-344. PubMed ID: 29255193
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Surfactant protein B deficiency and gene mutations for neonatal respiratory distress syndrome in China Han ethnic population.
    Yin X; Meng F; Wang Y; Xie L; Kong X; Feng Z
    Int J Clin Exp Pathol; 2013; 6(2):267-72. PubMed ID: 23330012
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Surfactant protein A and B genetic variants in respiratory distress syndrome in singletons and twins.
    Marttila R; Haataja R; Guttentag S; Hallman M
    Am J Respir Crit Care Med; 2003 Nov; 168(10):1216-22. PubMed ID: 12947025
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Allelic heterogeneity in hereditary surfactant protein B (SP-B) deficiency.
    Nogee LM; Wert SE; Proffit SA; Hull WM; Whitsett JA
    Am J Respir Crit Care Med; 2000 Mar; 161(3 Pt 1):973-81. PubMed ID: 10712351
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Surfactant-associated proteins B and C: molecular biology and physiologic properties].
    Gortner L; Hilgendorff A
    Z Geburtshilfe Neonatol; 2004 Jun; 208(3):91-7. PubMed ID: 15229816
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Relationship between R236C site in exon 7 of SP-B gene and respiratory distress syndrome in Han newborns in western Inner Mongolia].
    Wang J; Mei H; Liu CZ; Zhang YY; Liu CL; Song D; Zhang YH
    Zhongguo Dang Dai Er Ke Za Zhi; 2016 Sep; 18(9):802-805. PubMed ID: 27655533
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Pulmonary surfactant protein adenosine triphosphate-binding-cassette-A3 gene composite mutations in infant congenital interstitial lung disease: report of a case and review of literature].
    Xie N; Chen DH; Lin YN; Wu SZ; Gu YY; Zeng QS; Zhai YY; Yang LY; Xu JX
    Zhonghua Er Ke Za Zhi; 2016 Oct; 54(10):761-766. PubMed ID: 27784479
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Surfactant protein B deficiency caused by a novel mutation involving multiple exons of the SP-B gene.
    Schuerman FA; Griese M; Gille JP; Brasch F; Noorduyn LA; van Kaam AH
    Eur J Med Res; 2008 Jun; 13(6):281-6. PubMed ID: 18558554
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: relationship to SFTPB.
    Tredano M; Griese M; de Blic J; Lorant T; Houdayer C; Schumacher S; Cartault F; Capron F; Boccon-Gibod L; Lacaze-Masmonteil T; Renolleau S; Delaisi B; Elion J; Couderc R; Bahuau M
    Am J Med Genet A; 2003 Jun; 119A(3):324-39. PubMed ID: 12784301
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unexplained neonatal respiratory distress due to congenital surfactant deficiency.
    Somaschini M; Nogee LM; Sassi I; Danhaive O; Presi S; Boldrini R; Montrasio C; Ferrari M; Wert SE; Carrera P
    J Pediatr; 2007 Jun; 150(6):649-53, 653.e1. PubMed ID: 17517255
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic disorders of surfactant homeostasis.
    Whitsett JA; Wert SE; Xu Y
    Biol Neonate; 2005; 87(4):283-7. PubMed ID: 15985750
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic influences and neonatal lung disease.
    Hallman M; Haataja R
    Semin Neonatol; 2003 Feb; 8(1):19-27. PubMed ID: 12667827
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic disorders of surfactant homeostasis.
    Whitsett JA
    Paediatr Respir Rev; 2006; 7 Suppl 1():S240-2. PubMed ID: 16798578
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.