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Keith J. Johnson

University of Glasgow
Imperial College London

64

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3103

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Clinical Validation of a Blood-Based Predictive Test for Stratification of Response to Tumor Necrosis Factor Inhibitor Therapies in Rheumatoid Arthritis Patients

2020
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Sa1564 – The Dash to Educate on Nash: Does Medical Education Improve Physician Knowledge?

2019 Gastroenterology
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LGMD AUTOSOMAL RESSESSIVE AND DOMINANT

2018 Neuromuscular Disorders
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An international collaboration applying targeted whole exome sequencing to detect causative variants in 1001 patients affected by limb-girdle weakness of unknown origin

2018 Neuromuscular Disorders
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P.443 - Identification and characterisation of ATP2A1 variants through whole exome sequencing

2017 Neuromuscular Disorders
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LMX1B mutations as an unexpected cause of hereditary focal segmental glomerulosclerosis without extra-renal involvement

2013
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Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene

2006 Revista De Biologia Tropical
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A physical map of the genomic region on mouse chromosome 3 containing the hindshaker (hsh) mutation

2004 Genomics
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Abnormal contractile activity and calcium cycling in cardiac myocytes isolated from dmpk knockout mice

2003 Physiological Genomics
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Miotomía congénita: Caracterización clínica de una familia costarricense afectada por la Enfermedad de Thomsen

2003
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