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Items: 12

1.

Haemophilia A: health and economic burden of a rare disease in Portugal.

Café A, Carvalho M, Crato M, Faria M, Kjollerstrom P, Oliveira C, Pinto PR, Salvado R, Dos Santos AA, Silva C.

Orphanet J Rare Dis. 2019 Sep 4;14(1):211. doi: 10.1186/s13023-019-1175-5.

2.

Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia.

Nicolau M, Vargas S, Silva M, Coelho A, Ferreira E, Mendonça J, Vieira L, Kjöllerström P, Maia R, Silva R, Dias A, Ferreira T, Morais A, Soares IM, Lavinha J, Faustino P.

Ann Hematol. 2019 Sep 2. doi: 10.1007/s00277-019-03783-y. [Epub ahead of print]

PMID:
31478061
3.

Refractory immune hemolytic anemia in an immunocompetent infant with cytomegalovirus infection.

Loureiro B, Batalha S, Rocha E, Maia R, Kjöllerström P.

Pediatr Blood Cancer. 2019 Aug;66(8):e27791. doi: 10.1002/pbc.27791. Epub 2019 May 2. No abstract available.

PMID:
31045313
4.

Retinopathy and bone marrow failure revealing Coats plus syndrome.

Painho T, Conceição C, Kjöllerström P, Batalha S.

BMJ Case Rep. 2018 Mar 9;2018. pii: bcr-2018-224477. doi: 10.1136/bcr-2018-224477. No abstract available.

PMID:
29523622
5.

Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia.

Ferrão J, Silva M, Gonçalves L, Gomes S, Loureiro P, Coelho A, Miranda A, Seuanes F, Reis AB, Pina F, Maia R, Kjöllerström P, Monteiro E, Lacerda JF, Lavinha J, Gonçalves J, Faustino P.

Ann Hematol. 2017 Nov;96(11):1921-1929. doi: 10.1007/s00277-017-3090-y. Epub 2017 Sep 8.

PMID:
28887661
6.

Pantoea Species Bacteremia in a Child With Sickle Cell Disease: Looking for a Culprit.

Oliveira MI, Batalha S, Gouveia C, Maia R, Kjöllerstrom P.

J Pediatr Hematol Oncol. 2017 Aug;39(6):e307-e308. doi: 10.1097/MPH.0000000000000819.

PMID:
28267078
7.

Hemorheological alterations in sickle cell anemia and their clinical consequences - The role of genetic modulators.

Silva M, Vargas S, Coelho A, Dias A, Ferreira T, Morais A, Maia R, Kjöllerström P, Lavinha J, Faustino P.

Clin Hemorheol Microcirc. 2016;64(4):859-866. doi: 10.3233/CH-168048.

PMID:
27814292
8.

Sickle cell anemia - Nitric oxide related genetic modifiers of hematological and biochemical parameters.

Aguiar L, Matos A, Gil Â, Afonso C, Almeida S, Braga L, Lavinha J, Kjollerstrom P, Faustino P, Bicho M, Inácio Â.

Clin Hemorheol Microcirc. 2016;64(4):957-963. doi: 10.3233/CH-168008.

PMID:
27802215
9.

Cutaneous hyperpigmentation and cobalamin deficiency.

Machado R, Furtado F, Kjöllerström P, Cunha F.

Br J Haematol. 2016 Sep;174(6):834. doi: 10.1111/bjh.14242. Epub 2016 Jul 19. No abstract available.

PMID:
27433789
10.

Genotype-phenotype correlation in a cohort of Portuguese patients comprising the entire spectrum of VWD types: impact of NGS.

Fidalgo T, Salvado R, Corrales I, Pinto SC, Borràs N, Oliveira A, Martinho P, Ferreira G, Almeida H, Oliveira C, Marques D, Gonçalves E, Diniz M, Antunes M, Tavares A, Caetano G, Kjöllerström P, Maia R, Sevivas TS, Vidal F, Ribeiro L.

Thromb Haemost. 2016 Jul 4;116(1):17-31. doi: 10.1160/TH15-07-0604. Epub 2016 Mar 17.

PMID:
26988807
11.

Prolonged thrombocytopenia in a child with severe neonatal alloimmune reaction and Noonan syndrome.

Salva I, Batalha S, Maia R, Kjollerstrom P.

Platelets. 2016 Jun;27(4):381-2. doi: 10.3109/09537104.2015.1107034. Epub 2015 Nov 24.

PMID:
26599469
12.

Linezolid in the treatment of multidrug-resistant/extensively drug-resistant tuberculosis in paediatric patients: experience of a paediatric infectious diseases unit.

Kjöllerström P, Brito MJ, Gouveia C, Ferreira G, Varandas L.

Scand J Infect Dis. 2011 Jul;43(6-7):556-9. doi: 10.3109/00365548.2011.564649. Epub 2011 Mar 10.

PMID:
21391771

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