Articles with "case unusual" as a keyword



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A case of unusual mild clinical presentation of COVID-19 vaccine-induced immune thrombotic thrombocytopenia with splanchnic vein thrombosis

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Published in 2021 at "Annals of Hepatology"

DOI: 10.1016/j.aohep.2021.100590

Abstract: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive… read more here.

Keywords: covid vaccine; case unusual; mild clinical; clinical presentation ... See more keywords
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A case of unusual localized cutaneous mucinosis

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Published in 2019 at "Clinical and Experimental Dermatology"

DOI: 10.1111/ced.13940

Abstract: Cutaneous mucinosis is an umbrella term for a group of heterogeneous disorders caused by abnormal accumulation of mucin, either localized to the skin or associated with systemic involvement. Mucin is a normal component of the… read more here.

Keywords: case unusual; dermatology; localized cutaneous; cutaneous mucinosis ... See more keywords
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A Case of Unusual Drug Screening Results.

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Published in 2017 at "Clinical chemistry"

DOI: 10.1373/clinchem.2016.264507

Abstract: A 27-year-old man was found unconscious in his car by police. He was taken to an outside hospital where results of his serum alcohol and initial urine drug screen were reportedly negative. On arrival to… read more here.

Keywords: case unusual; reference interval; reference; drug screening ... See more keywords
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Case 3: An Unusual Case of Transient Neonatal Encephalopathy.

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Published in 2019 at "NeoReviews"

DOI: 10.1542/neo.20-8-e472

Abstract: A 7-day-old female neonate presents to a local hospital with lethargy, grunting, fast breathing, and abnormal movements after a short history of poor feeding overnight. She was born at 39 weeks’ gestation via cesarean section… read more here.

Keywords: case unusual; neonatal encephalopathy; transient neonatal; unusual case ... See more keywords
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[Mitochondrial DNA depletion syndrome-13: a case with an unusual onset].

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Published in 2019 at "Revista de neurologia"

DOI: 10.33588/rn.6910.2019221

Abstract: Síndrome de depleción de ADN mitocondrial tipo 13: un caso con un inicio poco común. read more here.

Keywords: case unusual; dna depletion; depletion syndrome; unusual onset ... See more keywords