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Items: 1 to 20 of 28

1.

Antimicrobial susceptibility of non-fermenting Gram-negative pathogens isolated from cystic fibrosis patients.

Díez-Aguilar M, Ekkelenkamp M, Morosini MI, Merino I, Caballero JD, Jones M, van Westreenen M, Tunney MM, Cantón R, Fluit AC.

Int J Antimicrob Agents. 2018 Sep 18. pii: S0924-8579(18)30260-7. doi: 10.1016/j.ijantimicag.2018.09.001. [Epub ahead of print]

PMID:
30240837
2.

Updates in vitamin D therapy in cystic fibrosis.

Le TN.

Curr Opin Endocrinol Diabetes Obes. 2018 Sep 18. doi: 10.1097/MED.0000000000000439. [Epub ahead of print]

PMID:
30239380
3.

Crohn's disease and cystic fibrosis: there is still a lot to learn.

Trigo Salado C, Leo Carnerero E, de la Cruz Ramírez MD.

Rev Esp Enferm Dig. 2018 Sep 21;110. doi: 10.17235/reed.2018.5725/2018. [Epub ahead of print]

PMID:
30238759
4.

Antibiotic multidrug resistance in the cystic fibrosis airway microbiome is associated with decreased diversity.

Hahn A, Burrell A, Fanous H, Chaney H, Sami I, Perez GF, Koumbourlis AC, Freishtat RJ, Crandall KA.

Heliyon. 2018 Sep 17;4(9):e00795. doi: 10.1016/j.heliyon.2018.e00795. eCollection 2018 Sep.

PMID:
30238064
5.

Ultra-low-dose chest CT without anesthesia in the assessment of pediatric pulmonary diseases.

Dorneles CM, Pacini GS, Zanon M, Altmayer S, Watte G, Barros MC, Marchiori E, Baldisserotto M, Hochhegger B.

J Pediatr (Rio J). 2018 Sep 17. pii: S0021-7557(18)30519-9. doi: 10.1016/j.jped.2018.07.010. [Epub ahead of print]

PMID:
30236593
6.

Cholangiopathies - Towards a molecular understanding.

Tam PKH, Yiu RS, Lendahl U, Andersson ER.

EBioMedicine. 2018 Sep 17. pii: S2352-3964(18)30310-4. doi: 10.1016/j.ebiom.2018.08.024. [Epub ahead of print] Review.

PMID:
30236451
7.

A splice site variant in INPP5E causes diffuse cystic renal dysplasia and hepatic fibrosis in dogs.

Dillard KJ, Hytönen MK, Fischer D, Tanhuanpää K, Lehti MS, Vainio-Siukola K, Sironen A, Anttila M.

PLoS One. 2018 Sep 20;13(9):e0204073. doi: 10.1371/journal.pone.0204073. eCollection 2018.

8.

Reply to: Use of Masks in Cystic Fibrosis Patients.

Wood ME, Stockwell RE, Bell SC.

Am J Respir Crit Care Med. 2018 Sep 20. doi: 10.1164/rccm.201808-1476LE. [Epub ahead of print] No abstract available.

PMID:
30235006
9.

Use of Masks in Cystic Fibrosis Patients.

Zuckerman JB, Saiman L.

Am J Respir Crit Care Med. 2018 Sep 20. doi: 10.1164/rccm.201807-1248LE. [Epub ahead of print] No abstract available.

PMID:
30235001
10.

Hepatic Steatosis is Prevalent following Orthotopic Liver Transplantation in Children with Cystic Fibrosis.

Cortes-Santiago N, Leung DH, Castro E, Finegold M, Wu H, Patel K.

J Pediatr Gastroenterol Nutr. 2018 Sep 18. doi: 10.1097/MPG.0000000000002154. [Epub ahead of print]

PMID:
30234762
11.

Dynamic prediction of survival in cystic fibrosis: A landmarking analysis using UK patient registry data.

Keogh RH, Seaman SR, Barrett JK, Taylor-Robinson D, Szczesniak R.

Epidemiology. 2018 Sep 17. doi: 10.1097/EDE.0000000000000920. [Epub ahead of print]

PMID:
30234550
12.

Description of rare mutations and a novel variant in Brazilian patients with Cystic Fibrosis: a case series from a referral center in the Bahia State.

Mota LR, de Melo Filho VM, de Castro LL, Garcia DF, Terse-Ramos R, Toralles MBP, de Lima RLLF, Souza EL.

Mol Biol Rep. 2018 Sep 19. doi: 10.1007/s11033-018-4361-y. [Epub ahead of print]

PMID:
30232781
13.

The role of small intestinal bacterial overgrowth in cystic fibrosis: a randomized case-controlled clinical trial with rifaximin.

Furnari M, De Alessandri A, Cresta F, Haupt M, Bassi M, Calvi A, Haupt R, Bodini G, Ahmed I, Bagnasco F, Giannini EG, Casciaro R.

J Gastroenterol. 2018 Sep 19. doi: 10.1007/s00535-018-1509-4. [Epub ahead of print]

PMID:
30232597
14.

Pseudomonas aeruginosa ExoS Induces Intrinsic Apoptosis in Target Host Cells in a Manner That is Dependent on its GAP Domain Activity.

Kaminski A, Gupta KH, Goldufsky JW, Lee HW, Gupta V, Shafikhani SH.

Sci Rep. 2018 Sep 19;8(1):14047. doi: 10.1038/s41598-018-32491-2.

15.

The Functions of the Mammalian Methionine Sulfoxide Reductase System and Related Diseases.

Jiang B, Moskovitz J.

Antioxidants (Basel). 2018 Sep 18;7(9). pii: E122. doi: 10.3390/antiox7090122. Review.

16.

Acquired CFTR Dysfunction and Radiographic Bronchiectasis in Current and Former Smokers: A Cross-Sectional Study.

Teerapuncharoen K, Wells JM, Raju SV, Raraigh KS, Atalar M, Cutting GR, Rasmussen L, Nath PH, Bhatt SP, Solomon GM, Dransfield MT, Rowe SM.

Ann Am Thorac Soc. 2018 Sep 19. doi: 10.1513/AnnalsATS.201805-325RL. [Epub ahead of print] No abstract available.

PMID:
30230364
17.

Intercellular Communication between Airway Epithelial Cells is Mediated by Exosome-Like Vesicles.

Gupta R, Radicioni G, Abdelwahab S, Dang H, Carpenter J, Chua M, Mieczkowski PA, Sheridan J, Randell SH, Kesimer M.

Am J Respir Cell Mol Biol. 2018 Sep 19. doi: 10.1165/rcmb.2018-0156OC. [Epub ahead of print]

PMID:
30230353
18.

Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation.

Holtkamp KCA, Henneman L, Gille JJP, Meijers-Heijboer H, Cornel MC, Lakeman P.

J Community Genet. 2018 Sep 18. doi: 10.1007/s12687-018-0388-y. [Epub ahead of print]

PMID:
30229537
19.

[Cystic fibrosis : A new disease pattern in adult medicine].

Staab D, Schwarz C.

Internist (Berl). 2018 Sep 18. doi: 10.1007/s00108-018-0498-y. [Epub ahead of print] Review. German.

PMID:
30229366
20.

Alcohol Use and Alcohol-Interactive Medications Among Medically Vulnerable Youth.

Weitzman ER, Magane KM, Wisk LE, Allario J, Harstad E, Levy S.

Pediatrics. 2018 Sep 18. pii: e20174026. doi: 10.1542/peds.2017-4026. [Epub ahead of print]

PMID:
30228168

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