Articles with "syndrome diagnosis" as a keyword



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Association Between Rates of Down Syndrome Diagnosis in States With vs Without 20-Week Abortion Bans From 2011 to 2018

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Published in 2023 at "JAMA Network Open"

DOI: 10.1001/jamanetworkopen.2023.3684

Abstract: Key Points Question Is there an association between rates of neonatal Down syndrome diagnosis in states that did vs did not enact 20-week abortion bans from 2011 to 2018? Findings In this cohort study of… read more here.

Keywords: 2011 2018; syndrome diagnosis; week; association rates ... See more keywords
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[Asymptomatic Brugada syndrome: From diagnosis to treatment].

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Published in 2017 at "Annales de cardiologie et d'angeiologie"

DOI: 10.1016/j.ancard.2017.09.021

Abstract: Brugada syndrome management may be a difficult question. This article reviews diagnosis, prognosis evaluation, current and investigated treatments. read more here.

Keywords: diagnosis; asymptomatic brugada; diagnosis treatment; brugada syndrome ... See more keywords
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Filling the gap in antiphospholipid syndrome diagnosis: a patient’s story

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Published in 2020 at "Lupus"

DOI: 10.1177/0961203320903810

Abstract: S Sciascia , M Radin , S Baldovino and D Roccatello Center for Research of Immunopathology and Rare DiseasesCoordinating Center of Piemonte and Valle d’Aosta Network for Rare Diseases, Department of Clinical and Biological Sciences,… read more here.

Keywords: antiphospholipid syndrome; gap antiphospholipid; syndrome diagnosis; patient story ... See more keywords
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Family Sense-Making After a Down Syndrome Diagnosis

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Published in 2020 at "Qualitative Health Research"

DOI: 10.1177/1049732320935836

Abstract: The script of parenting shifts when parents learn of their child’s Down syndrome diagnosis. To build a theory of the diagnostic experience and early family sense-making process, we interviewed 33 parents and nine grandparents living… read more here.

Keywords: family sense; syndrome diagnosis; sense making; diagnosis ... See more keywords
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[Gorlin-Goltz Syndrome: Diagnosis and Treatment Options].

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Published in 2017 at "Acta medica portuguesa"

DOI: 10.20344/amp.7521

Abstract: The Gorlin-Goltz syndrome is a rare autosomal dominant hereditary condition, with complete penetrance and variable expressivity. Characterized by the appearance of multiple basaliomas, and often the development of keratocyst, it can also express itself by… read more here.

Keywords: diagnosis treatment; treatment; goltz syndrome; syndrome diagnosis ... See more keywords
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Myeloproliferative Syndrome - A Diagnosis on the Border Between Medical Specialties

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Published in 2022 at "Internal Medicine"

DOI: 10.47363/jccsr/2022(4)227

Abstract: Abstract Background. Myeloproliferative disorders define a vast and heteregenous group of neoplastic entities, characterized by malignant proliferation of blood cells. These may affect multiple tissues, some of these malignancies involving organs in which there is… read more here.

Keywords: massive splenomegaly; diagnosis; myeloproliferative syndrome; syndrome diagnosis ... See more keywords