Zobrazeno 1 - 5
of 5
pro vyhledávání: '"X. W. van den Tweel"'
Autor:
P.C. (Piero) Giordano, J.P. van Wouwe, Rob Rodrigues Pereira, P.H. Verkerk, X. W. van den Tweel, M. Peters, Karin Fijnvandraat, F G Garre
Publikováno v:
Archives of disease in childhood, 95(10), 822-825. BMJ Publishing Group
Archives of Disease in Childhood, 95(10), 822-825
Archives of Disease in Childhood, 10, 95, 822-825
Archives of Disease in Childhood, 95(10), 822-825
Archives of Disease in Childhood, 10, 95, 822-825
Objectives To estimate the prevalence of children with sickle cell disease (SCD) in The Netherlands. To estimate the annual number of children newly diagnosed as having SCD and the proportion with diagnoses through neonatal screening To estimate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::338301ead30f65edf41f9c97ccee7495
https://dare.uva.nl/personal/pure/en/publications/onethird-of-the-new-paediatric-patients-with-sickle-cell-disease-in-the-netherlands-are-immigrants-and-do-not-benefit-from-neonatal-screening(73d20545-6664-46b0-b35b-190f33102d13).html
https://dare.uva.nl/personal/pure/en/publications/onethird-of-the-new-paediatric-patients-with-sickle-cell-disease-in-the-netherlands-are-immigrants-and-do-not-benefit-from-neonatal-screening(73d20545-6664-46b0-b35b-190f33102d13).html
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 151(45)
Timely recognition of clinical signs and symptoms of sickle cell disease remains of great importance because the neonatal PKU screening program in The Netherlands that was introduced in January 1st 2007 will not reach all children with this disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd9493fb1d6e9431af681e9c81fcdc9a
https://pubmed.ncbi.nlm.nih.gov/18062592
https://pubmed.ncbi.nlm.nih.gov/18062592
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 145(37)
Early detection of children with sickle cell disease, determination of carriership frequency as well as evaluation of the knowledge regarding this haemoglobinopathy in various ethnic risk groups.Prospective.From 1 November 1998 through to 31 October
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c87375e9933d75b595798c3eff17b394
https://pubmed.ncbi.nlm.nih.gov/11582643
https://pubmed.ncbi.nlm.nih.gov/11582643
Autor:
Seung Yup Lee, Cowdrick, Kyle R., Sanders, Bharat, Sathialingam, Eashani, McCracken, Courtney E., Lam, Wilbur A., Joiner, Clinton H., Buckley, Erin M.
Publikováno v:
Neurophotonics; Jul-Sep2019, Vol. 6 Issue 3, p1-7, 7p
Autor:
National Academies of Sciences, Engineering, and Medicine, Health and Medicine Division, Board on Population Health and Public Health Practice, Committee on Addressing Sickle Cell Disease: A Strategic Plan and Blueprint for Action, Rose Marie Martinez, Henrietta Awo Osei-Anto, Marie McCormick
Sickle cell disease (SCD) is a genetic condition that affects approximately 100,000 people in the United States and millions more globally. Individuals with SCD endure the psychological and physiological toll of repetitive pain as well as side effect