Výsledky vyhledávání - "Anemia, sickle cell/diagnosis"

Processing of positive newborn screening results: a qualitative exploration of current practice in England

Autor: Louise Moody, Stephen Morris, Mandy Bryon, Jane Chudleigh, Rachel S Carling, Kevin W Southern, Ellinor K. Olander, Fiona Ulph, Alan Simpson, Holly Chinnery, Pru Holder

Publikováno v: BMJ Open
BMJ Open, Vol 10, Iss 12 (2020)
Chudleigh, J, Chinnery, H, Holder, P, Carling, R S, Southern, K, Olander, E, Moody, L, Morris, S, Ulph, F, Bryon, M & Simpson, A 2020, ' Processing of positive newborn screening results : a qualitative exploration of current practice in England ', BMJ Open, vol. 10, no. 12, e044755, pp. 1-11 . https://doi.org/10.1136/bmjopen-2020-044755

ObjectiveTo explore current communication practices for positive newborn screening results from the newborn bloodspot screening (NBS) laboratory to clinicians to highlight differences, understand how the pathways are implemented in practice, identify

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4137d6ea686f8b72aea1cb410fc5386
https://doi.org/10.1136/bmjopen-2020-044755

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Brazilian Guidelines for transcranial doppler in children and adolescents with sickle cell disease

Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Vol 33, Iss 1, Pp 43-48 (2011)
Revista Brasileira de Hematologia e Hemoterapia
Revista Brasileira de Hematologia e Hemoterapia v.33 n.1 2011
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Revista Brasileira de Hematologia e Hemoterapia, Volume: 33, Issue: 1, Pages: 43-48, Published: FEB 2011

BACKGROUND: Sickle cell disease is the most common monogenic hereditary disease in Brazil. Although strokes are one of the main causes of morbidity and mortality in these patients, the use of transcranial Doppler to identify children at risk is not u

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::910b0340197eed3f8f1c46dead49a1db
https://doi.org/10.5581/1516-8484.20110014

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The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC disease

Autor: A Osei, Swee Lay Thein, Emma Drasar, Anke Hannemann, David C. Rees, John S. Gibson, Sanjay Tewari

Publikováno v: Rees, D C, Thein, S L, Osei, A, Drasar, E, Tewari, S, Hannemann, A & Gibson, J S 2015, ' The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC disease ', Haematologica, vol. 100, no. 5, pp. 595-600 . https://doi.org/10.3324/haematol.2014.120402

HbSC disease is the second commonest form of sickle cell disease, with poorly understood pathophysiology and few treatments. We studied the role of K-Cl cotransport activity in determining clinical and laboratory features, and investigated its potent

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::783794b60fd3243dd229ba22ebbb764e
https://www.repository.cam.ac.uk/handle/1810/254438

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Quality of life of individuals with sickle cell disease followed at referral centers in Alagoas, Brazil

Autor: Rosana Brandão Vilela, Jairo Calado Cavalcante, Fernando Antônio Tenório Nunes, Diego Lisboa Araújo, Bruno Fernandes Cavalcante, Matheus de Melo Lôbo

Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Volume: 34, Issue: 6, Pages: 442-446, Published: 2012
Revista Brasileira de Hematologia e Hemoterapia v.34 n.6 2012
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Revista Brasileira de Hematologia e Hemoterapia
Revista Brasileira de Hematologia e Hemoterapia, Vol 34, Iss 6, Pp 442-446 (2012)

BACKGROUND: Sickle cell disease is a genetic, hereditary and chronic disease that affects the health of its carriers and might impair their health-related quality of life. OBJECTIVE: The aim of the current study was to assess the health-related quali

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afac74240d5f8504381f1242f42270b8
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842012000600014&lng=en&tlng=en

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Early prenatal diagnosis by celocentesis

Autor: Makrydimas, G., Georgiou, I., Bouba, I., Lolis, D., Nicolaides, K. H.

BACKGROUND: Celocentesis is the ultrasound-guided aspiration of fluid from the extra-amniotic cavity at 7-8 weeks of gestation. This paper reports on the clinical application of celocentesis for early prenatal diagnosis. METHODS: Celocentesis was suc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10561::159d7ae1e6da7ee9da36e23927af8a49
http://olympias.lib.uoi.gr/jspui/handle/123456789/22284

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Brazilian Guidelines for transcranial doppler in children and adolescents with sickle cell disease.

Autor: Lobo CL; Instituto Estadual de Hematologia Arthur de Siqueira Cavalcanti (HEMORIO), Rio de Janeiro (RJ), Brazil., Cançado RD, Leite AC, Dos Anjos AC, Pinto AC, Matta AP, Silva CM, Silva GS, Friedrisch JR, Braga JA, Lange MC, Figueiredo MS, Rugani MÁ, Veloso O, Moura PG, Cortez PI, Adams R, Gualandro SF, de Castilho SL, Thomé U, Zetola VF

Publikováno v: Revista brasileira de hematologia e hemoterapia [Rev Bras Hematol Hemoter] 2011; Vol. 33 (1), pp. 43-8.

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