Typical MRI features of PLA2G6 mutation-related phospholipase-associated neurodegeneration (PLAN)/infantile neuroaxonal dystrophy (INAD)
10.1136/bcr-2021-242586
March 25, 2021
Paediatrics
Coexistence of medium chain acyl-CoA dehydrogenase deficiency (MCADD) and type 1 diabetes (T1D): a management challenge
10.1136/bcr-2020-239325
March 24, 2021
Focal congenital hyperinsulinism resulting from biallelic loss of function of KCNJ11 gene
10.1136/bcr-2020-240218
March 24, 2021
SARS-CoV-2 infection triggering recurrence of Kawasaki disease in a 10-year-old child
10.1136/bcr-2020-240972
March 24, 2021
Premature thelarche in an infant girl with failure to thrive related to dietary soy exposure
10.1136/bcr-2020-239651
March 23, 2021
Paediatric case of endobronchial foreign body migration to the gastrointestinal tract
10.1136/bcr-2020-240858
March 23, 2021
Poland syndrome: neonatal presentation with axillary
10.1136/bcr-2020-241395
March 22, 2021
Clinical presentation and improvised management of neonatal pneumothorax in the setting of a low-resource country: Conakry, Guinea
10.1136/bcr-2020-235801
March 22, 2021
Successful primary repair of oesophageal atresia and distal tracheo-oesophageal fistula in a 525 g neonate, the smallest reported in literature
10.1136/bcr-2020-239696
March 22, 2021
Recurrent apnoea and respiratory failure in an infant: congenital central hypoventilation syndrome with a novel PHOX2B gene variant
10.1136/bcr-2020-239633
March 19, 2021