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Items: 1 to 20 of 4708

1.

Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.

De Boeck K, Weren M, Proesmans M, Kerem E.

Pediatrics. 2005 Apr;115(4):e463-9. Epub 2005 Mar 16.

PMID:
15772171
2.

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;20(3):164-8. doi: 10.1097/MEG.0b013e3282f36d04.

PMID:
18301294
3.

[Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].

Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E.

Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:6-9. Serbian.

PMID:
15637983
4.

Evaluation of fecal pancreatic elastase-1 as a measure of pancreatic exocrine function in children with cystic fibrosis.

Cade A, Walters MP, McGinley N, Firth J, Brownlee KG, Conway SP, Littlewood JM.

Pediatr Pulmonol. 2000 Mar;29(3):172-6.

PMID:
10686036
5.

European Epidemiologic Registry of Cystic Fibrosis (ERCF): comparison of major disease manifestations between patients with different classes of mutations.

Koch C, Cuppens H, Rainisio M, Madessani U, Harms H, Hodson M, Mastella G, Navarro J, Strandvik B, McKenzie S; Investigators of the ERCF.

Pediatr Pulmonol. 2001 Jan;31(1):1-12.

PMID:
11180668
6.

Early decline of pancreatic function in cystic fibrosis patients with class 1 or 2 CFTR mutations.

Walkowiak J, Sands D, Nowakowska A, Piotrowski R, Zybert K, Herzig KH, Milanowski A.

J Pediatr Gastroenterol Nutr. 2005 Feb;40(2):199-201.

PMID:
15699697
7.

Symptomatic pancreatitis in patients with cystic fibrosis.

Gooding I, Bradley E, Puleston J, Gyi KM, Hodson M, Westaby D.

Am J Gastroenterol. 2009 Jun;104(6):1519-23. doi: 10.1038/ajg.2009.127. Epub 2009 May 12.

PMID:
19491865
8.

Gastrointestinal, liver, and pancreatic involvement in adult patients with cystic fibrosis.

Modolell I, Alvarez A, Guarner L, De Gracia J, Malagelada JR.

Pancreas. 2001 May;22(4):395-9.

PMID:
11345141
9.

Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat tests.

Augarten A, Shmilovich H, Doolman R, Aviram M, Akons H, Ben Tur L, Blau H, Kerem E, Rivlin J, Sela BA, Szeinberg A, Yahav Y.

Pediatr Pulmonol. 2000 Oct;30(4):320-3.

PMID:
11015133
10.

Genotype and phenotype correlations in patients with cystic fibrosis and pancreatitis.

Durno C, Corey M, Zielenski J, Tullis E, Tsui LC, Durie P.

Gastroenterology. 2002 Dec;123(6):1857-64.

PMID:
12454843
11.

The changing face of the exocrine pancreas in cystic fibrosis: pancreatic sufficiency, pancreatitis and genotype.

Walkowiak J, Lisowska A, Blaszczyński M.

Eur J Gastroenterol Hepatol. 2008 Mar;20(3):157-60. doi: 10.1097/MEG.0b013e3282f36d16. Review.

PMID:
18301292
12.

Serum lipase after secretin stimulation detects mild pancreatic involvement in cystic fibrosis.

Walkowiak J, Nousia-Arvanitakis S, Lisowska A, Piotrowski R, Strzykala K, Bychowiec B, Songin T, Galli-Tsinopoulou A, Sands D, Pidonia I, Krawczynski M, Milanowski A, Herzig KH.

J Pediatr Gastroenterol Nutr. 2004 Apr;38(4):430-5.

PMID:
15085023
13.

Variability of fecal pancreatic elastase measurements in cystic fibrosis patients.

Meyts I, Wuyts W, Proesmans M, De Boeck K.

J Cyst Fibros. 2002 Dec;1(4):265-8.

14.

Fecal elastase: pancreatic status verification and influence on nutritional status in children with cystic fibrosis.

Cohen JR, Schall JI, Ittenbach RF, Zemel BS, Stallings VA.

J Pediatr Gastroenterol Nutr. 2005 Apr;40(4):438-44.

PMID:
15795591
15.

Longitudinal follow-up of exocrine pancreatic function in pancreatic sufficient cystic fibrosis patients using the fecal elastase-1 test.

Walkowiak J, Nousia-Arvanitakis S, Agguridaki C, Fotoulaki M, Strzykala K, Balassopoulou A, Witt M, Herzig KH.

J Pediatr Gastroenterol Nutr. 2003 Apr;36(4):474-8.

PMID:
12658038
16.

[Pancreatitis in cystic fibrosis: association with genotype and pancreatic status].

Sojo Aguirre A, Martínez Ezquerra N, Bousoño García C, García Novo MD, Heredia González S, Manzanares López-Manzanares J, Baranda García F, Vázquez Cordero C.

An Pediatr (Barc). 2011 Dec;75(6):401-8. doi: 10.1016/j.anpedi.2011.06.005. Epub 2011 Aug 4. Spanish.

17.

Clinical and genetic risk factors for cystic fibrosis-related liver disease.

Wilschanski M, Rivlin J, Cohen S, Augarten A, Blau H, Aviram M, Bentur L, Springer C, Vila Y, Branski D, Kerem B, Kerem E.

Pediatrics. 1999 Jan;103(1):52-7.

PMID:
9917439
18.
19.

Non-classic cystic fibrosis associated with D1152H CFTR mutation.

Burgel PR, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D, Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M, Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser D.

Clin Genet. 2010 Apr;77(4):355-64. doi: 10.1111/j.1399-0004.2009.01294.x. Epub 2009 Oct 15.

PMID:
19843100
20.

Systemic inflammatory mediators and cystic fibrosis genotype.

Augarten A, Paret G, Avneri I, Akons H, Aviram M, Bentur L, Blau H, Efrati O, Szeinberg A, Barak A, Kerem E, Yahav J.

Clin Exp Med. 2004 Oct;4(2):99-102.

PMID:
15672947

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