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Results: 1 to 20 of 151

Similar articles for PubMed (Select 9580754)

1.

The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel.

Rosenstein BJ, Cutting GR.

J Pediatr. 1998 Apr;132(4):589-95. Review.

PMID:
9580754
2.

Diagnostic problems in cystic fibrosis - specific characteristics of a group of infants and young children diagnosed positive through neonatal screening, in whom cystic fibrosis had not been diagnosed.

Woś H, Sankiewicz-Szkółka M, Więcek S, Kordys-Darmolińska B, Grzybowska-Chlebowczyk U, Kniażewska M.

Dev Period Med. 2015 Jan-Mar;19(1):25-31.

PMID:
26003067
3.

Association of sweat chloride concentration at time of diagnosis and CFTR genotype with mortality and cystic fibrosis phenotype.

McKone EF, Velentgas P, Swenson AJ, Goss CH.

J Cyst Fibros. 2015 Feb 3. pii: S1569-1993(15)00007-7. doi: 10.1016/j.jcf.2015.01.005. [Epub ahead of print]

PMID:
25660278
4.

Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn screening.

Munck A, Mayell SJ, Winters V, Shawcross A, Derichs N, Parad R, Barben J, Southern KW.

J Cyst Fibros. 2015 Jan 24. pii: S1569-1993(15)00003-X. doi: 10.1016/j.jcf.2015.01.001. [Epub ahead of print]

PMID:
25630966
5.

Rectal prolapse and cystic fibrosis.

El-Chammas KI, Rumman N, Goh VL, Quintero D, Goday PS.

J Pediatr Gastroenterol Nutr. 2015 Jan;60(1):110-2. doi: 10.1097/MPG.0000000000000546.

PMID:
25162364
6.

Exercise intolerance, malnutrition, abnormal sweat chloride levels, and two CFTR mutations: is it cystic fibrosis?

Com G, Uc A.

J Pediatr Health Care. 2015 Mar-Apr;29(2):201-4. doi: 10.1016/j.pedhc.2014.05.010. Epub 2014 Jul 22. No abstract available.

PMID:
25060775
7.

Cystic fibrosis presenting with persistent pneumonia --a case study of a 3-month-old adopted baby.

Lodh M, Joshi AK.

J Indian Med Assoc. 2013 Oct;111(10):699, 703.

PMID:
24968502
8.

Does integration of various ion channel measurements improve diagnostic performance in cystic fibrosis?

Ooi CY, Dupuis A, Gonska T, Ellis L, Ni A, Jarvi K, Martin S, Ray P, Steele L, Kortan P, Dorfman R, Solomon M, Zielenski J, Corey M, Tullis E, Durie P.

Ann Am Thorac Soc. 2014 May;11(4):562-70. doi: 10.1513/AnnalsATS.201311-412OC.

PMID:
24697796
9.

Diagnosis of cystic fibrosis in the kindred of an infant with CFTR-related metabolic syndrome: importance of follow-up that includes monitoring sweat chloride concentrations over time.

Williams SN, Nussbaum E, Chin TW, Do PC, Singh KE, Randhawa I.

Pediatr Pulmonol. 2014 Mar;49(3):E103-8. doi: 10.1002/ppul.22918. Epub 2013 Nov 4.

PMID:
24535988
10.

Is there evidence for correct diagnosis in cystic fibrosis registries?

Thomas M, Lemonnier L, Gulmans V, Naehrlich L, Vermeulen F, Cuppens H, Castellani C, Norek A, De Boeck K.

J Cyst Fibros. 2014 May;13(3):275-80. doi: 10.1016/j.jcf.2013.10.010. Epub 2013 Nov 22.

PMID:
24274930
11.

[Aquagenic palmoplantar keratoderma in children with cystic fibrosis].

Weil B, Chaillou E, Troussier F, Pelatan C, Chiffoleau M, Darviot E, Chevalier MC, Martin L, Giniès JL.

Arch Pediatr. 2013 Dec;20(12):1306-9. doi: 10.1016/j.arcped.2013.09.023. Epub 2013 Nov 5. French.

PMID:
24210985
12.

Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?

Ooi CY, Dupuis A, Ellis L, Jarvi K, Martin S, Ray PN, Steele L, Kortan P, Gonska T, Dorfman R, Solomon M, Zielenski J, Corey M, Tullis E, Durie P.

Thorax. 2014 Mar;69(3):254-60. doi: 10.1136/thoraxjnl-2013-203832. Epub 2013 Oct 21.

PMID:
24149827
13.

Relevance of nasal potential difference in diagnosis of cystic fibrosis among children.

Valiulis A, Skurvydienė I, Misevičienė V, Kasnauskienė J, Vaidelienė L, Utkus A.

Medicina (Kaunas). 2013;49(4):185-90.

14.

Diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator gene in patients suspected of having mild or atypical cystic fibrosis.

Dal'Maso VB, Mallmann L, Siebert M, Simon L, Saraiva-Pereira ML, Dalcin Pde T.

J Bras Pneumol. 2013 Mar-Apr;39(2):181-9. English, Portuguese.

15.

Atypical cystic fibrosis: identification in the primary care setting.

Schram CA.

Can Fam Physician. 2012 Dec;58(12):1341-5, e699-704. Review.

16.

Jejunoileal atresia and cystic fibrosis: don't miss it.

Siersma CL, Rottier BL, Hulscher JB, Bouman K, van Stuijvenberg M.

BMC Res Notes. 2012 Dec 7;5:677. doi: 10.1186/1756-0500-5-677.

17.

CF versus CRMS: diagnostic challenges in cystic fibrosis.

Temme R, Roggenbuck J, McNamara J.

Minn Med. 2012 Oct;95(10):42-4.

PMID:
23193705
18.

To sweat or not to sweat: is that enough to diagnose cystic fibrosis?

Laguna TA.

Am J Respir Crit Care Med. 2012 Oct 15;186(8):700-1. doi: 10.1164/rccm.201208-1510ED. No abstract available.

PMID:
23071183
19.

Cystic fibrosis infant care challenges in diagnosis and management in the era of newborn screening.

Padman R, Flathers K, Passi V.

Del Med J. 2012 May;84(5):149-55.

PMID:
22866385
20.

Misdiagnosis of cystic fibrosis: experience from Germany.

Naehrlich L, Bagheri-Behrouzi A; German CF quality assurance group.

J Cyst Fibros. 2013 Jan;12(1):68-73. doi: 10.1016/j.jcf.2012.06.008. Epub 2012 Jul 24.

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