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Paediatrics
- Erythromelalgia in a patient with feet erythema and cyanosisKhaled El Khatib, Zeina Gerges, Nagham AzarBMJ Case Reports CP Jan 2023, 16 (1) e253786; DOI: 10.1136/bcr-2022-253786
- Neonatal herpes simplex presenting as a zosteriform eruptionElizabeth Anderson, Emma Johns, Joseph Conlon, Ezzeldin SalehBMJ Case Reports CP Jan 2023, 16 (1) e252627; DOI: 10.1136/bcr-2022-252627
- Severe thrombocytopaenia induced by systemic lupus erythematosus presenting as haemorrhagic oral bullae in a paediatric patientAlec Giakas, Katherine Holder, Bernardo Galvan, James StallworthBMJ Case Reports CP Jan 2023, 16 (1) e251989; DOI: 10.1136/bcr-2022-251989
- Intravitreal aflibercept for idiopathic choroidal neovascularisation in paediatric ageAna Rita Viana, José Lemos, Mariana Almeida Oliveira, Carla TeixeiraBMJ Case Reports CP Jan 2023, 16 (1) e252270; DOI: 10.1136/bcr-2022-252270
- Delayed finding of congenital duodenal obstruction following congenital diaphragmatic hernia repairGeorge S Bethell, Dina Fouad, Enitan Ogundipe, Mohammed ChoudhryBMJ Case Reports CP Jan 2023, 16 (1) e253394; DOI: 10.1136/bcr-2022-253394
- Recognising side effects of antipsychotics in children with intellectual disabilitiesJessica Lee, Rosie Shepperd, Martin Smith, Geetha AnandBMJ Case Reports CP Jan 2023, 16 (1) e251974; DOI: 10.1136/bcr-2022-251974
- Effect of vibrostimulatory wearable technology on stereotyped behaviour in a child with autism and intellectual disabilityCristina Santamarina-Siurana, Vicente Cloquell-Ballester, Carmen Berenguer-Forner, Milagros Fuentes-AlberoBMJ Case Reports CP Dec 2022, 15 (12) e252181; DOI: 10.1136/bcr-2022-252181
- Spontaneous subdiaphragmatic bar migration after pectus excavatum treatmentAlexander Hamming, Hendt Versteegh, J Marco SchnaterBMJ Case Reports CP Dec 2022, 15 (12) e251757; DOI: 10.1136/bcr-2022-251757
- Congenital sodium diarrhoea caused by rare de novo activating guanylate cyclase mutationSurichhya Bajracharya, Duane Stich, James Berman, Vincent BiankBMJ Case Reports CP Dec 2022, 15 (12) e251632; DOI: 10.1136/bcr-2022-251632
- Growth hormone deficiency in a case of septo-optic-dysplasia due to SOX2 mutation: should we re-test patients during the transition period?Valentina Gasco, Patrizia Matarazzo, Luisa De Sanctis, Ezio GhigoBMJ Case Reports CP Dec 2022, 15 (12) e251897; DOI: 10.1136/bcr-2022-251897
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