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Rare disease
- Adult-onset Still’s disease with concurrent thrombotic thrombocytopenic purpura: case report and literature reviewRyohei Kato, Tomoyuki Ikeuchi, Katsuyuki Tomita, Akira YamasakiBMJ Case Reports CP Sep 2020, 13 (9) e235786; DOI: 10.1136/bcr-2020-235786
- Successful surgical resection of a rare case of a giant sacral chordoma: a multidisciplinary featSafwan Omar Alomari, Shadi Bsat, Mohammad Khalife, Ghassan SkafBMJ Case Reports CP Sep 2020, 13 (9) e235045; DOI: 10.1136/bcr-2020-235045
- Down syndrome with co-occurring Marfan syndromeMiao Wei, Natasha Lepore, Kelli Paulsen, Jonathan D SantoroBMJ Case Reports CP Sep 2020, 13 (9) e235988; DOI: 10.1136/bcr-2020-235988
- Solitary extramedullary plasmacytoma of the larynx: a rare cause of dysphoniaHannes Hermann Brandt, Steffi Johanna Brockmeier, Nora TetterBMJ Case Reports CP Sep 2020, 13 (9) e234478; DOI: 10.1136/bcr-2020-234478
- Adrenal medullary hyperplasia mimicking pheochromocytomaAnnalisa Montebello, Michelle Ann Ceci, Sandro VellaBMJ Case Reports CP Sep 2020, 13 (9) e236209; DOI: 10.1136/bcr-2020-236209
- Primary leptomeningeal T-cell lymphoblastic lymphoma: a rare cause of chronic meningitisArunmozhimaran Elavarasi, Rohit Bhatia, Sudheer Arava, Lalit KumarBMJ Case Reports CP Sep 2020, 13 (9) e236491; DOI: 10.1136/bcr-2020-236491
- Eosinophilic colitis: an infrequent disease with difficult diagnoseJavier Páramo-Zunzunegui, Ignacio Ortega-Fernandez, Silvia Benito-Barbero, Laura Rubio-LópezBMJ Case Reports CP Sep 2020, 13 (9) e235804; DOI: 10.1136/bcr-2020-235804
- Congenital dysfibrinogenaemia presented with preterm premature rupture of the membranes and vaginal bleedingZaker I Schwabkey, Farrell C Sheehan, Courtney Bellomo, Mihir RavalBMJ Case Reports CP Sep 2020, 13 (9) e235961; DOI: 10.1136/bcr-2020-235961
- Bickerstaff’s brainstem encephalitis associated with anti-GM1 and anti-GD1a antibodiesJonathan Cleaver, Richard James, Gurjit Chohan, Paul LyonsBMJ Case Reports CP Sep 2020, 13 (9) e236545; DOI: 10.1136/bcr-2020-236545
- Primary haemochromatosis resulting in dilated cardiomyopathy arising out of mutation in HJV gene in Indian patients: a rare scenarioAbhishek Goyal, Bishav Mohan, Kavita Saggar, Gurpreet Singh WanderBMJ Case Reports CP Sep 2020, 13 (9) e235650; DOI: 10.1136/bcr-2020-235650
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