Ip WF - Search Results

1

Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurements.

Wilson DC, Ellis L, Zielenski J, Corey M, Ip WF, Tsui LC, Tullis E, Knowles MR, Durie PR. Wilson DC, et al. Among authors: ip wf. J Pediatr. 1998 Apr;132(4):596-9. doi: 10.1016/s0022-3476(98)70345-2. J Pediatr. 1998. PMID: 9580755

2

Exocrine pancreatic alterations in long-lived surviving cystic fibrosis mice.

Ip WF, Bronsveld I, Kent G, Corey M, Durie PR. Ip WF, et al. Pediatr Res. 1996 Aug;40(2):242-9. doi: 10.1203/00006450-199608000-00009. Pediatr Res. 1996. PMID: 8827772

3

Is fibrosing colonopathy an immune mediated disease?

Lee J, Ip W, Durie P. Lee J, et al. Arch Dis Child. 1997 Jul;77(1):66-70. doi: 10.1136/adc.77.1.66. Arch Dis Child. 1997. PMID: 9279159 Free PMC article.

4

Impact of protein deprivation on protein and DNA synthesis in the developing rat pancreas.

Ip WF, Beharry S, Durie PR. Ip WF, et al. Biol Neonate. 1998 Oct;74(4):294-303. doi: 10.1159/000014037. Biol Neonate. 1998. PMID: 9701652

5

Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar.

Ginzberg H, Shin J, Ellis L, Morrison J, Ip W, Dror Y, Freedman M, Heitlinger LA, Belt MA, Corey M, Rommens JM, Durie PR. Ginzberg H, et al. J Pediatr. 1999 Jul;135(1):81-8. doi: 10.1016/s0022-3476(99)70332-x. J Pediatr. 1999. PMID: 10393609

6

Serum pancreatic enzymes define the pancreatic phenotype in patients with Shwachman-Diamond syndrome.

Ip WF, Dupuis A, Ellis L, Beharry S, Morrison J, Stormon MO, Corey M, Rommens JM, Durie PR. Ip WF, et al. J Pediatr. 2002 Aug;141(2):259-65. doi: 10.1067/mpd.2002.125849. J Pediatr. 2002. PMID: 12183724 Clinical Trial.

7

Magnetic resonance imaging findings of the pancreas in patients with Shwachman-Diamond syndrome and mutations in the SBDS gene.

Toiviainen-Salo S, Raade M, Durie PR, Ip W, Marttinen E, Savilahti E, Mäkitie O. Toiviainen-Salo S, et al. J Pediatr. 2008 Mar;152(3):434-6. doi: 10.1016/j.jpeds.2007.12.013. J Pediatr. 2008. PMID: 18280855

8

Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis.

Gonska T, Ip W, Turner D, Han WS, Rose J, Durie P, Quinton P. Gonska T, et al. Thorax. 2009 Nov;64(11):932-8. doi: 10.1136/thx.2009.115295. Epub 2009 Sep 3. Thorax. 2009. PMID: 19734129

9

Evidence of a generalized defect of acinar cell function in Shwachman-Diamond syndrome.

Stormon MO, Ip WF, Ellis L, Schibli S, Rommens JM, Durie PR. Stormon MO, et al. Among authors: ip wf. J Pediatr Gastroenterol Nutr. 2010 Jul;51(1):8-13. doi: 10.1097/MPG.0b013e3181d67e78. J Pediatr Gastroenterol Nutr. 2010. PMID: 20512054

10

β-adrenergic sweat secretion as a diagnostic test for cystic fibrosis.

Quinton P, Molyneux L, Ip W, Dupuis A, Avolio J, Tullis E, Conrad D, Shamsuddin AK, Durie P, Gonska T. Quinton P, et al. Am J Respir Crit Care Med. 2012 Oct 15;186(8):732-9. doi: 10.1164/rccm.201205-0922OC. Epub 2012 Aug 2. Am J Respir Crit Care Med. 2012. PMID: 22859523

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