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Letters to the Editor
03 September 2021
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Author(s):
“A bruised reed shall he not break”: John Miles’s portraits of patients at the Royal Edinburgh Asylum. Part 1.
03 September 2021
This is the first of two papers which examine a series of portraits of patients at the Royal Edinburgh Asylum (REA) which were
Author(s):

Allan Beveridge1, Daisy Cunynghame2
Reactive arthritis: a clinical review
03 September 2021
Reactive arthritis (ReA) is a form of inflammatory arthritis triggered by a remote antecedent infection, usually in the genitou
Author(s):

Ameen Jubber1, Arumugam Moorthy1,2
Connecting and connectivity: providing video consulting in care homes in Wales
03 September 2021
Background During the COVID-19 pandemic, care home residents and staff were identified as being at risk of inf
Author(s):

Gemma Johns1, Sara Khalil2, Jess Williams3, Morgan Lees4, Lynne Hockey5, Mike Ogonovsky6, Alka Ahuja7
de Winter pattern: An important electrocardiographic sign not to be missed
03 September 2021
None
Author(s):

Yoon Kee Siow1, Dhani Darshan Francis2, Anwar Irawan Ruhani3, Siti Khairani Zainal Abidin4,
Ching Soong Khoo5
Tumefactive demyelination: a clinico-radiological dilemma
03 September 2021
None
Author(s):

Swati Kumar,1 Amlan Kusum Datta,2 Uddalak Chakraborty,3 Alak Pandit,4 Biman Kanti Ray5
Why so blue? The blood gas has the clue…
03 September 2021
None
Author(s):

John P Thomas1, Yat MA Hung2, Prasanna Sankaran3
Fascicular oculomotor nerve palsy due to a strategic midbrain infarction: the ‘eyes’ have it
03 September 2021
None
Author(s):

Ashin Varghese1, Boby Varkey Maramattom2
Severe intracranial atherosclerotic disease presenting as symptomatic isolated convexity subarachnoid haemorrhage
03 September 2021
Isolated convexity cortical subarachnoid haemorrhage (cSAH) is a rare form of non-traumatic subarachnoid haemorrhage localised
Author(s):

Ahmad Muhammad,1,2 Satya Narayana Patro,3,4 Suhail Hussain,5 Memon Noor Illahi,6,7 Khawaja Hassan Haroon8,9
“Please see this man with a 69-year history of hypoglycaemia”
03 September 2021
Mutations in the HNF4A gene are associated with hyperinsulinaemic hypoglycaemia in infants, frequently evolving into relative d
Author(s):

Robert M Gifford1–3, Evgenia Foteinopoulou4, Mark WJ Strachan5
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