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- Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
- In vivo angle dysgenesis in PHACE syndrome with developmental glaucomaToshit Varshney, Sai Vineeth Maddu, Kanchangouri Satpute, Dewang AngmoBMJ Case Reports CP Aug 2024, 17 (8) e255434; DOI: 10.1136/bcr-2023-255434
- Subcutaneous panniculitis-like T-cell lymphoma and lupus erythematosus profundus: a diagnostic dilemmaMun Leng Lee, Puo Nen Lim, Jane Colgan, John R GoodladBMJ Case Reports CP Jun 2024, 17 (6) e255592; DOI: 10.1136/bcr-2023-255592
- Severe non-hepatic hyperammonaemic encephalopathy in an immunocompromised adolescent with enterocolitisAdrienne Elizabeth Borrie, Meghan Pike, Stephanie Villeneuve, Neeraj VermaBMJ Case Reports CP Jun 2024, 17 (6) e256225; DOI: 10.1136/bcr-2023-256225
- Bilateral optic disc collaterals secondary to high-flow dural arteriovenous fistula: a diagnostic dilemmaSampada Dattatray Kulkarni Irlekar, Ramesh Kekunnaya, Virender SachdevaBMJ Case Reports CP May 2024, 17 (5) e253192; DOI: 10.1136/bcr-2022-253192
- Radiographical bony lesions after discontinuation of immunosuppressant therapy: bone involvement in sarcoidosisChristopher Pullins, Cyril Varghese, Sethu Sandeep Koneru, Jesse D BracamonteBMJ Case Reports CP Apr 2024, 17 (4) e255611; DOI: 10.1136/bcr-2023-255611
- Recurrent leishmaniasis infection isolated in the pleural fluidHina Qiam, Emily Lowe, Adriel Heilong Fung, Prasanna SankaranBMJ Case Reports CP Mar 2024, 17 (3) e256632; DOI: 10.1136/bcr-2023-256632
- Familial recurrent molar pregnancy: positive for KHDC3L gene mutationAbhipsa Rath, Pruthwiraj Sethi, Saubhagya Kumar Jena, Subarna MitraBMJ Case Reports CP Nov 2023, 16 (11) e254435; DOI: 10.1136/bcr-2022-254435
- Spontaneous muscle haematoma in a patient with cirrhosisLakshmanan Suja, Nanthakumar Logithasan, Narayanasamy Senthil, Archa Anna AnilBMJ Case Reports CP Nov 2023, 16 (11) e254525; DOI: 10.1136/bcr-2022-254525
- Sclerosing encapsulating peritonitis causing fatal bowel obstructionKylie Nabata, Akie Watanabe, Heather StuartBMJ Case Reports CP Nov 2023, 16 (11) e255625; DOI: 10.1136/bcr-2023-255625
- Rare case of central congenital hypothyroidism due to a TSHβ mutation presenting with macro-orchidismMadhura Bharat Karguppikar, Nadia Schoenmakers, Vaman Khadilkar, Anuradha KhadilkarBMJ Case Reports CP Nov 2023, 16 (11) e252796; DOI: 10.1136/bcr-2022-252796
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