J. Nixon

发表

Monoclonal antibody therapy for the treatment of asthma and chronic obstructive pulmonary disease with eosinophilic inflammation

T. Mustelin, G. Anderson, R. Kolbeck, 2017, Pharmacology & therapeutics.

Signs and symptoms of childhood cancer: a guide for early recognition.

P. Panagopoulou, J. Nixon, Ionna Fragkandrea, 2013, American family physician.

ORAI1 Mutations with Distinct Channel Gating Defects in Tubular Aggregate Myopathy

W. Newman, E. Malfatti, N. Romero, 2017, Human mutation.

Does cytosine-thymine-guanine (CTG) expansion size predict cardiac events and electrocardiographic progression in myotonic dystrophy?

A. Kelion, J. Forfar, D. Hilton‐Jones, 2001, Heart.

Randomised controlled trial of methotrexate for chronic inflammatory demyelinating polyradiculoneuropathy (RMC trial): a pilot, multicentre study

M. Lucchetta, D. Pareyson, A. Schenone, 2009, The Lancet Neurology.

Interstitial deletion of 2q associated with craniosynostosis, ocular coloboma, and limb abnormalities: cytogenetic and molecular investigation.

A. Wilkie, Kim Smith, M. Oldridge, 1997, American journal of medical genetics.

Computerised tomography scans of the head in a district general hospital.

S. Malthouse, D. Bateman, J. Nixon, 1996, Journal of the Royal College of Physicians of London.

Metastatic breast cancer 42 years after bilateral subcutaneous mastectomies.

J. Probert, G. Braatvedt, M. Jameson, 1997, Clinical oncology (Royal College of Radiologists (Great Britain)).

Long-term day-case treatment of peripheral neuromuscular disease with intravenous immunoglobulin: the practice of a regional day-case service in Preston, Lancashire.

J. Nixon, Sam Jones, C. Mchugh, 2013, Clinical medicine.

Service provision of complex mutation analysis: a technical and economic appraisal using dystrophin point mutation analysis as an example

A. Seller, J. Hopkin, D. Cockburn, 2002, Clinical genetics.

Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy

F. Baas, E. Mercuri, F. Muntoni, 2019 .

Disease relapse in patients with stage I nonseminomatous germ cell tumor of the testis on active surveillance.

V. Harvey, J. Nixon, P. Thompson, 1988, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

An MRI and neuropathological study of a case of fatal status epilepticus

D. Bateman, T. Moss, J. Nixon, 2001, Seizure.

Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions

Robert W. Taylor, D. Turnbull, K. J. Krishnan, 2013, Neurology.

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

J. Flint, S. Knight, L. Kearney, 1998, Journal of medical genetics.

Murray Monoclonal antibody therapy for the treatment of asthma and chronic obstructive pulmonary disease with eosinophilic in fl ammation

T. Mustelin, G. Anderson, R. Kolbeck, 2016 .

ANO5 Gene Analysis in a Large Cohort of Patients with Anoctaminopathy: Confirmation of Male Prevalence and High Occurrence of the Common Exon 5 Gene Mutation

K. Bushby, F. Muntoni, A. Schapira, 2013, Human mutation.