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PUBMED FOR HANDHELDS

Journal Abstract Search

325 related items for PubMed ID: 17557942

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  • 5. 50 years ago in the Journal of Pediatrics: A note on studies of salt excretion in sweat: relationships between rate, conductivity, and electrolyte composition of sweat from patients with cystic fibrosis and from control subjects. Gibson, LE, di Sant’Agnese, PA. J Pediatr 1963;62:855-67.
    Gonska T.
    J Pediatr; 2013 Jun; 162(6):1187. PubMed ID: 23708418
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  • 6. Mislocalization of delta F508 CFTR in cystic fibrosis sweat gland.
    Kartner N, Augustinas O, Jensen TJ, Naismith AL, Riordan JR.
    Nat Genet; 1992 Aug; 1(5):321-7. PubMed ID: 1284548
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  • 8. Low abundance of sweat duct Cl- channel CFTR in both healthy and cystic fibrosis athletes with exceptionally salty sweat during exercise.
    Brown MB, Haack KK, Pollack BP, Millard-Stafford M, McCarty NA.
    Am J Physiol Regul Integr Comp Physiol; 2011 Mar; 300(3):R605-15. PubMed ID: 21228336
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  • 12. Higher bioelectric potentials due to decreased chloride absorption in the sweat glands of patients with cystic fibrosis.
    Quinton PM, Bijman J.
    N Engl J Med; 1983 May 19; 308(20):1185-9. PubMed ID: 6843595
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  • 13. [From gene to disease; from defective chloride ion transport to cystic fibrosis].
    Scheffer H, van den Ouweland AM, Veeze HJ.
    Ned Tijdschr Geneeskd; 2001 Apr 07; 145(14):686-7. PubMed ID: 11530706
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  • 15. Screening for cystic fibrosis: the importance of using the correct tools.
    Shah U, Moatter T.
    J Ayub Med Coll Abbottabad; 2006 Apr 07; 18(1):7-10. PubMed ID: 16773960
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  • 16. Functional interaction of CFTR and ENaC in sweat glands.
    Reddy MM, Quinton PM.
    Pflugers Arch; 2003 Jan 07; 445(4):499-503. PubMed ID: 12548396
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  • 17. The importance of sweat testing for older siblings of patients with cystic fibrosis identified by newborn screening.
    Munck A, Houssin E, Roussey M.
    J Pediatr; 2009 Dec 07; 155(6):928-930.e1. PubMed ID: 19914431
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  • 20. The changing face of the exocrine pancreas in cystic fibrosis: the correlation between pancreatic status, pancreatitis and cystic fibrosis genotype.
    Augarten A, Ben Tov A, Madgar I, Barak A, Akons H, Laufer J, Efrati O, Aviram M, Bentur L, Blau H, Paret G, Wilschanski M, Kerem BS, Yahav Y.
    Eur J Gastroenterol Hepatol; 2008 Mar 07; 20(3):164-8. PubMed ID: 18301294
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