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Items: 5

1.

Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responses.

Spencer S, Köstel Bal S, Egner W, Lango Allen H, Raza SI, Ma CA, Gürel M, Zhang Y, Sun G, Sabroe RA, Greene D, Rae W, Shahin T, Kania K, Ardy RC, Thian M, Staples E, Pecchia-Bekkum A, Worrall WPM, Stephens J, Brown M, Tuna S, York M, Shackley F, Kerrin D, Sargur R, Condliffe A, Tipu HN, Kuehn HS, Rosenzweig SD, Turro E, Tavaré S, Thrasher AJ, Jodrell DI, Smith KGC, Boztug K, Milner JD, Thaventhiran JED.

J Exp Med. 2019 Jun 24. pii: jem.20190344. doi: 10.1084/jem.20190344. [Epub ahead of print]

PMID:
31235509
2.

Low gammaglobulin subclass 2 levels in paediatric cystic fibrosis patients followed over a 2-year period.

Garside JP, Kerrin DP, Brownlee KG, Gooi HC, Taylor JM, Conway SP.

Pediatr Pulmonol. 2007 Feb;42(2):125-30.

PMID:
17186508
3.

Immunoglobulin and IgG subclass levels in a regional pediatric cystic fibrosis clinic.

Garside JP, Kerrin DP, Brownlee KG, Gooi HC, Taylor JM, Conway SP.

Pediatr Pulmonol. 2005 Feb;39(2):135-40.

PMID:
15633199
4.

Homocystinuria presenting with sagittal sinus thrombosis in infancy.

Kerrin D, Murdoch Eaton D, Livingston J, Henderson M, Smith M.

J Child Neurol. 1996 Jan;11(1):70-1. No abstract available.

PMID:
8745393
5.

Community hospitals.

Kerrin D, Jones R.

J R Coll Gen Pract. 1989 Oct;39(327):434. No abstract available.

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