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- Neonatal and paediatric intensive care
Neonatal and paediatric intensive care
- False elevation of serum cortisol in chemiluminescence immunoassay by Siemens Advia Centaur XP system in 21-hydroxylase deficiency: an ‘endocrine laboma’Neeti Agrawal, Partha Pratim Chakraborty, Anirban Sinha, Animesh MaitiBMJ Case Reports CP Sep 2020, 13 (9) e235450; DOI: 10.1136/bcr-2020-235450
- Duplication cyst with midgut volvulus in a neonate: an unusual presentationNitin G Pai, Santosh Prabhu, Pavithra Prabhakar, Vijay KumarBMJ Case Reports CP Aug 2020, 13 (8) e235526; DOI: 10.1136/bcr-2020-235526
- Premature infant with sudden respiratory distressAsmaa Elsaudi Nasr, Alhumaidy Mohamed Alsharaan, Jubara AlallahBMJ Case Reports CP Jun 2020, 13 (6) e234945; DOI: 10.1136/bcr-2020-234945
- Fetal congenital midaortic syndrome with unilateral renal artery stenosis prenatally presenting with polyhydramnios and postpartum as hyponatremic hypertensive syndromeSara Ardabili, Vincent Uerlings, Andrea Kaelin Agten, Markus HodelBMJ Case Reports CP May 2020, 13 (5) e234459; DOI: 10.1136/bcr-2020-234459
- Rare case of basilar artery aneurysm in a young childPeter Mallett, Sean Thomas O'Reilly, Ian Rennie, Mano Shanmuganathan, Andrew James ThompsonBMJ Case Reports CP Apr 2020, 13 (4) e233875; DOI: 10.1136/bcr-2019-233875
- Nosocomial pneumonia and sepsis caused by a rare organism Cedecea lapagei in an infant and a review of literatureViraraghavan Vadakkencherry Ramaswamy, Sanghamitra Gummadapu, Nori SuryanarayanaBMJ Case Reports CP Jul 2019, 12 (7) e229854; DOI: 10.1136/bcr-2019-229854
- Congenital protein C deficiency causing major arterial thrombosis in a neonateSanchari Chakravarty, Saugata Acharyya, Manas Kumar MahapatraBMJ Case Reports CP Jul 2019, 12 (7) e230034; DOI: 10.1136/bcr-2019-230034
- Contralateral effect of systemic absorption of low dose bevacizumab (Avastin) after unilateral intravitreal injection in severe retinopathy of prematurity (ROP)Ayad Shafiq, Roxane Hillier, Richard HearnBMJ Case Reports CP Mar 2020, 13 (3) e232359; DOI: 10.1136/bcr-2019-232359
- Phenotype and variations associated with the deletion of the 1q44 cytoband and the pathogenic duplication in the 9q32q34.3 cytobandsAna Gómez-Carpintero García, Ana Vidal Esteban, Amanda Bermejo Gómez, Ruth Camila Púa TorrejónBMJ Case Reports CP Mar 2020, 13 (3) e231938; DOI: 10.1136/bcr-2019-231938
- Severe haemolytic disease of a newborn with variant D mimicking blocked-D phenomenonSoumya Das, Shamee Shastry, Poornima B BaligaBMJ Case Reports CP Dec 2019, 12 (12) e231891; DOI: 10.1136/bcr-2019-231891
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