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344 results

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Page 1
Clinical relevance of erythrocyte ferritin in microcytic anemias.
Vagace JM, Peças A, Groiss J, Bento C, Ribeiro ML, Gervasini G. Vagace JM, et al. Among authors: ribeiro ml. Clin Chim Acta. 2015 Mar 10;442:1-5. doi: 10.1016/j.cca.2014.12.035. Epub 2015 Jan 3. Clin Chim Acta. 2015. PMID: 25562818 Free article.
Transient neonatal cyanosis associated with a new Hb F variant: Hb F viseu.
Bento C, Magalhães Maia T, Carvalhais I, Moita F, Abreu G, Relvas L, Pereira A, Farela Neves J, Ribeiro ML. Bento C, et al. Among authors: ribeiro ml. J Pediatr Hematol Oncol. 2013 Mar;35(2):e77-80. doi: 10.1097/MPH.0b013e3182667be3. J Pediatr Hematol Oncol. 2013. PMID: 22935660
Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?).
Bento C, Almeida H, Maia TM, Relvas L, Oliveira AC, Rossi C, Girodon F, Fernandez-Lago C, Aguado-Diaz A, Fraga C, Costa RM, Araújo AL, Silva J, Vitória H, Miguel N, Silveira MP, Martin-Nuñez G, Ribeiro ML. Bento C, et al. Among authors: ribeiro ml. Eur J Haematol. 2013 Oct;91(4):361-8. doi: 10.1111/ejh.12170. Epub 2013 Aug 20. Eur J Haematol. 2013. PMID: 23859443
Genetic basis of congenital erythrocytosis: mutation update and online databases.
Bento C, Percy MJ, Gardie B, Maia TM, van Wijk R, Perrotta S, Della Ragione F, Almeida H, Rossi C, Girodon F, Aström M, Neumann D, Schnittger S, Landin B, Minkov M, Randi ML, Richard S, Casadevall N, Vainchenker W, Rives S, Hermouet S, Ribeiro ML, McMullin MF, Cario H; ECE-Consortium; Chauveau A, Gimenez-Roqueplo AP, Bressac-de-Paillerets B, Altindirek D, Lorenzo F, Lambert F, Dan H, Gad-Lapiteau S, Catarina Oliveira A, Rossi C, Fraga C, Taradin G, Martin-Nuñez G, Vitória H, Diaz Aguado H, Palmblad J, Vidán J, Relvas L, Ribeiro ML, Luigi Larocca M, Luigia Randi M, Pedro Silveira M, Percy M, Gross M, Marques da Costa R, Beshara S, Ben-Ami T, Ugo V; ECE-Consortium. Bento C, et al. Among authors: ribeiro ml. Hum Mutat. 2014 Jan;35(1):15-26. doi: 10.1002/humu.22448. Epub 2013 Oct 22. Hum Mutat. 2014. PMID: 24115288
Severe neonatal jaundice due to a de novo glucose-6-phosphate dehydrogenase deficient mutation.
Del Orbe Barreto R, Arrizabalaga B, de la Hoz AB, Aragües P, Garcia-Ruiz JC, Arrieta A, Adán R, Manco L, Macedo-Ribeiro S, Bento C, Ribeiro ML. Del Orbe Barreto R, et al. Among authors: ribeiro ml. Int J Lab Hematol. 2016 Apr;38(2):e27-9. doi: 10.1111/ijlh.12455. Epub 2015 Dec 23. Int J Lab Hematol. 2016. PMID: 26693676 No abstract available.
344 results