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Items: 11

1.

Integrated lipid clinics for adults and children with familial hypercholesterolaemia.

Garrett EL, Chodhari R.

BMJ. 2018 Jan 15;360:k75. doi: 10.1136/bmj.k75. No abstract available.

PMID:
29335316
2.

Letter re: Reducing emergency department visits utilizing a primary care asthma specialty clinic in a high risk patient population.

Braithwaite S, Coppel J, Everson L, Kearney J, Gibson L, Chodhari R.

J Asthma. 2018 Oct;55(10):1077-1078. doi: 10.1080/02770903.2017.1391284. Epub 2017 Nov 30. No abstract available.

PMID:
29035125
3.

Re: A dynamic approach for outpatient scheduling.

Lim C, Chodhari R.

J Med Econ. 2017 Nov;20(11):1126. doi: 10.1080/13696998.2017.1360311. Epub 2017 Aug 11. No abstract available.

PMID:
28745579
4.

Childhood Asthma: A Narrative Approach.

Gibson L, Kearney J, Everson L, Coppel J, Chodhari R.

Chest. 2016 Jan;149(1):282-3. doi: 10.1016/j.chest.2015.09.027. Epub 2016 Jan 6. No abstract available.

PMID:
26757289
5.

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.

Panizzi JR, Becker-Heck A, Castleman VH, Al-Mutairi DA, Liu Y, Loges NT, Pathak N, Austin-Tse C, Sheridan E, Schmidts M, Olbrich H, Werner C, Häffner K, Hellman N, Chodhari R, Gupta A, Kramer-Zucker A, Olale F, Burdine RD, Schier AF, O'Callaghan C, Chung EM, Reinhardt R, Mitchison HM, King SM, Omran H, Drummond IA.

Nat Genet. 2012 May 13;44(6):714-9. doi: 10.1038/ng.2277.

6.

Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.

Castleman VH, Romio L, Chodhari R, Hirst RA, de Castro SC, Parker KA, Ybot-Gonzalez P, Emes RD, Wilson SW, Wallis C, Johnson CA, Herrera RJ, Rutman A, Dixon M, Shoemark A, Bush A, Hogg C, Gardiner RM, Reish O, Greene ND, O'Callaghan C, Purton S, Chung EM, Mitchison HM.

Am J Hum Genet. 2009 Feb;84(2):197-209. doi: 10.1016/j.ajhg.2009.01.011. Epub 2009 Feb 5.

7.

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm.

Loges NT, Olbrich H, Fenske L, Mussaffi H, Horvath J, Fliegauf M, Kuhl H, Baktai G, Peterffy E, Chodhari R, Chung EM, Rutman A, O'Callaghan C, Blau H, Tiszlavicz L, Voelkel K, Witt M, Zietkiewicz E, Neesen J, Reinhardt R, Mitchison HM, Omran H.

Am J Hum Genet. 2008 Nov;83(5):547-58. doi: 10.1016/j.ajhg.2008.10.001. Epub 2008 Oct 23.

8.

Primary ciliary dyskinesia: current state of the art.

Bush A, Chodhari R, Collins N, Copeland F, Hall P, Harcourt J, Hariri M, Hogg C, Lucas J, Mitchison HM, O'Callaghan C, Phillips G.

Arch Dis Child. 2007 Dec;92(12):1136-40. Epub 2007 Jul 18. Review.

9.

Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation.

Zariwala MA, Leigh MW, Ceppa F, Kennedy MP, Noone PG, Carson JL, Hazucha MJ, Lori A, Horvath J, Olbrich H, Loges NT, Bridoux AM, Pennarun G, Duriez B, Escudier E, Mitchison HM, Chodhari R, Chung EM, Morgan LC, de Iongh RU, Rutland J, Pradal U, Omran H, Amselem S, Knowles MR.

Am J Respir Crit Care Med. 2006 Oct 15;174(8):858-66. Epub 2006 Jul 20.

10.

Cilia, primary ciliary dyskinesia and molecular genetics.

Chodhari R, Mitchison HM, Meeks M.

Paediatr Respir Rev. 2004 Mar;5(1):69-76. Review.

PMID:
15222957
11.

Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates.

Jeganathan D, Chodhari R, Meeks M, Faeroe O, Smyth D, Nielsen K, Amirav I, Luder AS, Bisgaard H, Gardiner RM, Chung EM, Mitchison HM.

J Med Genet. 2004 Mar;41(3):233-40. No abstract available.

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