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 *

241 related articles for article (PubMed ID: 21034611)

  • 1. Evaluation and management of inherited disorders of surfactant metabolism.
    Hamvas A
    Chin Med J (Engl); 2010 Oct; 123(20):2943-7. PubMed ID: 21034611
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic testing in children with surfactant dysfunction.
    Turcu S; Ashton E; Jenkins L; Gupta A; Mok Q
    Arch Dis Child; 2013 Jul; 98(7):490-5. PubMed ID: 23625987
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic disorders of surfactant proteins.
    Hamvas A; Cole FS; Nogee LM
    Neonatology; 2007; 91(4):311-7. PubMed ID: 17575475
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inherited pulmonary surfactant metabolism disorders in Argentina: Differences between patients with SFTPC and ABCA3 variants.
    Balinotti JE; Mallie C; Maffey A; Colom A; Epaud R; de Becdelievre A; Fanen P; Delestrain C; Medín M; Teper A
    Pediatr Pulmonol; 2023 Feb; 58(2):540-549. PubMed ID: 36324278
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic disorders of surfactant dysfunction.
    Wert SE; Whitsett JA; Nogee LM
    Pediatr Dev Pathol; 2009; 12(4):253-74. PubMed ID: 19220077
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic mechanisms of surfactant deficiency.
    Nogee LM
    Biol Neonate; 2004; 85(4):314-8. PubMed ID: 15218289
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes.
    Hamvas A; Nogee LM; Wegner DJ; Depass K; Christodoulou J; Bennetts B; McQuade LR; Gray PH; Deterding RR; Carroll TR; Kammesheidt A; Kasch LM; Kulkarni S; Cole FS
    J Pediatr; 2009 Dec; 155(6):854-859.e1. PubMed ID: 19647838
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Population-based frequency of surfactant dysfunction mutations in a native Chinese cohort.
    Chen YJ; Wambach JA; DePass K; Wegner DJ; Chen SK; Zhang QY; Heins H; Cole FS; Hamvas A
    World J Pediatr; 2016 May; 12(2):190-5. PubMed ID: 26547207
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation.
    Bullard JE; Nogee LM
    Pediatr Res; 2007 Aug; 62(2):176-9. PubMed ID: 17597647
    [TBL] [Abstract][Full Text] [Related]  

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

  • 12. Surfactant composition and function in patients with ABCA3 mutations.
    Garmany TH; Moxley MA; White FV; Dean M; Hull WM; Whitsett JA; Nogee LM; Hamvas A
    Pediatr Res; 2006 Jun; 59(6):801-5. PubMed ID: 16641205
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. Surfactant proteins in pediatric interstitial lung disease.
    Griese M; Lorenz E; Hengst M; Schams A; Wesselak T; Rauch D; Wittmann T; Kirchberger V; Escribano A; Schaible T; Baden W; Schulze J; Krude H; Aslanidis C; Schwerk N; Kappler M; Hartl D; Lohse P; Zarbock R
    Pediatr Res; 2016 Jan; 79(1-1):34-41. PubMed ID: 26375475
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Altered surfactant homeostasis and recurrent respiratory failure secondary to TTF-1 nuclear targeting defect.
    Peca D; Petrini S; Tzialla C; Boldrini R; Morini F; Stronati M; Carnielli VP; Cogo PE; Danhaive O
    Respir Res; 2011 Aug; 12(1):115. PubMed ID: 21867529
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and review.
    Citti A; Peca D; Petrini S; Cutrera R; Biban P; Haass C; Boldrini R; Danhaive O
    Ultrastruct Pathol; 2013 Oct; 37(5):356-65. PubMed ID: 24047351
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ABCA3, a key player in neonatal respiratory transition and genetic disorders of the surfactant system.
    Peca D; Cutrera R; Masotti A; Boldrini R; Danhaive O
    Biochem Soc Trans; 2015 Oct; 43(5):913-9. PubMed ID: 26517903
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Lung diseases in children associated with inherited disorders of surfactant metabolism].
    Delestrain C; Flamein F; Jonard L; Couderc R; Guillot L; Fanen P; Epaud R
    Rev Pneumol Clin; 2013 Aug; 69(4):183-9. PubMed ID: 23856024
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Outcomes of Lung Transplantation for Infants and Children with Genetic Disorders of Surfactant Metabolism.
    Eldridge WB; Zhang Q; Faro A; Sweet SC; Eghtesady P; Hamvas A; Cole FS; Wambach JA
    J Pediatr; 2017 May; 184():157-164.e2. PubMed ID: 28215425
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.