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 *

177 related articles for article (PubMed ID: 33359301)

  • 1. Three Infants with Pathogenic Variants in the ABCA3 Gene: Presentation, Treatment, and Clinical Course.
    Si X; Steffes LC; Schymick JC; Hazard FK; Tracy MC; Cornfield DN
    J Pediatr; 2021 Apr; 231():278-283.e2. PubMed ID: 33359301
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype-phenotype correlations for infants and children with ABCA3 deficiency.
    Wambach JA; Casey AM; Fishman MP; Wegner DJ; Wert SE; Cole FS; Hamvas A; Nogee LM
    Am J Respir Crit Care Med; 2014 Jun; 189(12):1538-43. PubMed ID: 24871971
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel ABCA3 mutations as a cause of respiratory distress in a term newborn.
    Gonçalves JP; Pinheiro L; Costa M; Silva A; Gonçalves A; Pereira A
    Gene; 2014 Jan; 534(2):417-20. PubMed ID: 24269975
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A New
    Mitsiakos G; Tsakalidis C; Karagianni P; Gialamprinou D; Chatziioannidis I; Papoulidis I; Tsanakas I; Soubasi V
    Medicina (Kaunas); 2019 Jul; 55(7):. PubMed ID: 31331098
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Null ABCA3 in humans: large homozygous ABCA3 deletion, correlation to clinical-pathological findings.
    Carrera P; Ferrari M; Presi S; Ventura L; Vergani B; Lucchini V; Cogo PE; Carnielli VP; Somaschini M; Tagliabue P
    Pediatr Pulmonol; 2014 Mar; 49(3):E116-20. PubMed ID: 24420869
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.
    Wambach JA; Wegner DJ; Heins HB; Druley TE; Mitra RD; Hamvas A; Cole FS
    J Pediatr; 2014 Jun; 164(6):1316-21.e3. PubMed ID: 24657120
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinical analysis of heterozygous ABCA3 mutations in children].
    Xu X; Liu E; Luo Z; Luo J; Fu Z
    Zhonghua Er Ke Za Zhi; 2014 Apr; 52(4):244-7. PubMed ID: 24915907
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ultrastructural and molecular analysis in fatal neonatal interstitial pneumonia caused by a novel ABCA3 mutation.
    Bruder E; Hofmeister J; Aslanidis C; Hammer J; Bubendorf L; Schmitz G; Rufle A; Bührer C
    Mod Pathol; 2007 Oct; 20(10):1009-18. PubMed ID: 17660803
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Biologic characterization of ABCA3 variants in lung tissue from infants and children with ABCA3 deficiency.
    Xu KK; Wegner DJ; Geurts LC; Heins HB; Yang P; Hamvas A; Eghtesady P; Sweet SC; Sessions Cole F; Wambach JA
    Pediatr Pulmonol; 2022 May; 57(5):1325-1330. PubMed ID: 35170262
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome.
    Wambach JA; Yang P; Wegner DJ; Heins HB; Kaliberova LN; Kaliberov SA; Curiel DT; White FV; Hamvas A; Hackett BP; Cole FS
    Am J Respir Cell Mol Biol; 2016 Nov; 55(5):716-721. PubMed ID: 27374344
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.
    Wambach JA; Wegner DJ; Depass K; Heins H; Druley TE; Mitra RD; An P; Zhang Q; Nogee LM; Cole FS; Hamvas A
    Pediatrics; 2012 Dec; 130(6):e1575-82. PubMed ID: 23166334
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease.
    Saugstad OD; Hansen TW; Rønnestad A; Nakstad B; Tølløfsrud PA; Reinholt F; Hamvas A; Coles FS; Dean M; Wert SE; Whitsett JA; Nogee LM
    Acta Paediatr; 2007 Feb; 96(2):185-90. PubMed ID: 17429902
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. ABCA3 deficiency: neonatal respiratory failure and interstitial lung disease.
    Bullard JE; Wert SE; Nogee LM
    Semin Perinatol; 2006 Dec; 30(6):327-34. PubMed ID: 17142158
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. ABCA3 gene mutations in newborns with fatal surfactant deficiency.
    Shulenin S; Nogee LM; Annilo T; Wert SE; Whitsett JA; Dean M
    N Engl J Med; 2004 Mar; 350(13):1296-303. PubMed ID: 15044640
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pulmonary nodules in a newborn with ATP-binding cassette transporter A3 (ABCA3) mutations.
    Uchida DA; Wert SE; Nogee LM; Carroll TR; Chatfield BA
    Pediatrics; 2011 May; 127(5):e1347-51. PubMed ID: 21464189
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ABCA3 mutation-induced congenital pulmonary surfactant deficiency: A case report.
    Lei C; Wan C; Liu C
    Medicine (Baltimore); 2024 Mar; 103(13):e37622. PubMed ID: 38552044
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole exome sequencing identifies a novel variant in ABCA3 in an individual with fatal congenital surfactant protein deficiency.
    Bozkurt HB; Şahin Y
    Turk J Pediatr; 2021; 63(4):703-707. PubMed ID: 34449154
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.