| Artigo em revista |
- João Chaves; Bárbara Leal; Ana Sardoeira; Vanessa Carvalho; Raquel Samões; Joel Freitas; Rui Chorão; et al. "Different relationships
between epilepsy syndromes and autoimmune diseases". Epileptic Disorders 25 1 (2023): 33-44. http://dx.doi.org/10.1002/epd2.20048.
10.1002/epd2.20048
- Ricardo Martins-Ferreira; Bárbara Leal; João Chaves; Laura Ciudad; Raquel Samões; António Martins da Silva; Paulo Pinho Costa;
Esteban Ballestar. "Circulating cell-free DNA methylation mirrors alterations in cerebral patterns in epilepsy". Clinical
Epigenetics 14 1 (2022): http://dx.doi.org/10.1186/s13148-022-01416-2.
10.1186/s13148-022-01416-2
- Ricardo Martins-Ferreira; Bárbara Leal; João Chaves; Tianlu Li; Laura Ciudad; Rui Rangel; Agostinho Santos; et al. "Epilepsy
progression is associated with cumulative DNA methylation changes in inflammatory genes". Progress in Neurobiology
209 (2022): 102207-102207. https://doi.org/10.1016/j.pneurobio.2021.102207.
10.1016/j.pneurobio.2021.102207
- Leal, BG; Barros Barbosa, A; Ferreirinha, F; Chaves, J; Rangel, R; Santos, A; Carvalho, C; et al. "Mesial Temporal Lobe Epilepsy
(MTLE) Drug-Refractoriness Is Associated With P2X7 Receptors Overexpression in the Human Hippocampus and Temporal Neocortex
and May Be Predicted by Low Circulating Levels of miR-22". FRONTIERS IN CELLULAR NEUROSCIENCE (2022):
10.3389/fncel.2022.910662
- Ferreira, A.M.; Leal, B.; Ferreira, I.; Brás, S.; Moreira, I.; Samões, R.; Sousa, A.P.; et al. "Depression and anxiety in
multiple sclerosis patients: The role of genetic variability of interleukin 1ß". Multiple Sclerosis and Related Disorders
52 (2021): http://www.scopus.com/inward/record.url?eid=2-s2.0-85105808028&partnerID=MN8TOARS.
10.1016/j.msard.2021.102982
- Leal, B.; Carvalho, C.; Ferreira, A.M.; Nogueira, M.; Brás, S.; Silva, B.M.; Selores, M.; Costa, P.P.; Torres, T.. "Serum
Levels of miR-146a in Patients with Psoriasis". Molecular Diagnosis and Therapy 25 4 (2021): 475-485. http://www.scopus.com/inward/record.url?eid=2-s2.0-85105395705&partnerID=MN8TOARS.
10.1007/s40291-021-00531-9
- Martins-Ferreira R; Leal B; Costa PP; Ballestar E. "Microglial innate memory and epigenetic reprogramming in neurological
disorders.". Progress in neurobiology (2020): http://europepmc.org/abstract/med/33309803.
10.1016/j.pneurobio.2020.101971
- Chaves J; Martins-Ferreira R; Ferreira AM; Brás S; Carvalho C; Bettencourt A; Samões R; et al. "Immunogenetic protective factors
in Genetic Generalized Epilepsy.". Epilepsy research (2020): http://europepmc.org/abstract/med/32585211.
10.1016/j.eplepsyres.2020.106396
- Martins-Ferreira, R.; Chaves, J.; Carvalho, C.; Bettencourt, A.; Chorão, R.; Freitas, J.; Samões, R.; et al. "Circulating
microRNAs as potential biomarkers for genetic generalized epilepsies: a three microRNA panel". European Journal of Neurology
27 4 (2020): 660-666. http://dx.doi.org/10.1111/ene.14129.
Publicado • 10.1111/ene.14129
- Nuno Gomes; André Cerejeira; Elisabete Moreira; Catarina Costa; Paulo Pinho e Costa; Filomena Azevedo. "Rhinophyma or something
more?". International Journal of Dermatology (2020): https://doi.org/10.1111/ijd.14825.
10.1111/ijd.14825
- Chaves, João; Martins-Ferreira, Ricardo; Carvalho, Cláudia; Bettencourt, Andreia; Brás, Sandra; Chorão, Rui; Freitas, Joel;
et al. "Apolipoprotein E isoforms and susceptibility to genetic generalized epilepsies". International Journal of Neuroscience
(2020): 1-6. http://dx.doi.org/10.1080/00207454.2019.1709840.
Publicado • 10.1080/00207454.2019.1709840
- Martins E; Urbano J; Leite S; Pinto A; Garcia R; Bergantim R; Rodrigues-Pereira P; et al. "Cardiac Amyloidosis Associated
with Apolipoprotein A-IV Deposition Diagnosed by Mass Spectrometry-Based Proteomic Analysis.". European journal of case
reports in internal medicine (2019): http://europepmc.org/abstract/med/31893197.
10.12890/2019_001237
- Santos, Ernestina; Bettencourt, Andreia; Duarte, Sara; Gabriel, Denis; Oliveira, Vanessa; da Silva, Ana Martins; Costa, Paulo
Pinho; et al. "Refractory myasthenia gravis: Characteristics of a portuguese cohort". Muscle & Nerve 60 2 (2019): 188-191.
http://dx.doi.org/10.1002/mus.26507.
Publicado • 10.1002/mus.26507
- Tavares, Isabel; Oliveira, Márcia E.; Maia, Nuno; Moreira, Luciana; Castro Lacerda, Pedro; Santos, Josefina; Santos, Rosário;
Pinho Costa, Paulo; Lobato, Luísa. "Haplotype analysis of newly diagnosed Portuguese and Brazilian families with fibrinogen
amyloidosis caused by the FGA p.Glu545Val variant". Amyloid 26 sup1 (2019): 144-145. http://dx.doi.org/10.1080/13506129.2019.1582500.
Publicado • 10.1080/13506129.2019.1582500
- Tavares, Isabel; Silvano, José; Moreira, Luciana; Oliveira, Márcia E.; Silva, Roberto; Sampaio, Susana; Costa, Paulo Pinho;
Lobato, Luísa. "Short-term complications after renal transplantation in AFibE526V (p.Glu545Val) amyloidosis". Amyloid
26 sup1 (2019): 162-163. http://dx.doi.org/10.1080/13506129.2019.1583196.
Publicado • 10.1080/13506129.2019.1583196
- Costa, Paulo. "Estrogen Metabolism-Associated CYP2D6 and IL6-174G/C Polymorphisms in Schistosoma haematobium Infection".
International Journal of Molecular Sciences (2017): http://www.mdpi.com/1422-0067/18/12/2560.
10.3390/ijms18122560
- Leal B; Chaves J; Carvalho C; Rangel R; Santos A; Bettencourt A; Lopes J; et al. "Brain expression of inflammatory mediators
in Mesial Temporal Lobe Epilepsy patients.". Journal of neuroimmunology (2017): http://europepmc.org/abstract/med/29153613.
10.1016/j.jneuroim.2017.10.014
- Bárbara Leal; João Chaves; Cláudia Carvalho; Andreia Bettencourt; Joel Freitas; João Lopes; João Ramalheira; et al. "Age of
onset of mesial temporal lobe epilepsy with hippocampal sclerosis: the effect of apolipoprotein E and febrile seizures". International
Journal of Neuroscience 127 9 (2017): 800-804. https://doi.org/10.1080%2F00207454.2016.1264396.
10.1080/00207454.2016.1264396
- Costa, Paulo. "Serum 25-hydroxyvitamin D levels in multiple sclerosis patients from the north of Portugal.". The Journal
of steroid biochemistry and molecular biology (2017): http://europepmc.org/abstract/med/28951256.
10.1016/j.jsbmb.2017.09.016
- Costa, Paulo. "The vitamin D receptor gene FokI polymorphism and Multiple Sclerosis in a Northern Portuguese population.".
Journal of neuroimmunology (2017): http://europepmc.org/abstract/med/28601283.
10.1016/j.jneuroim.2017.05.005
- Costa, Paulo. "Unrecognized Fibrinogen A a-Chain Amyloidosis: Results From Targeted Genetic Testing.". American journal
of kidney diseases : the official journal of the National Kidney Foundation (2017): http://europepmc.org/abstract/med/28359658.
10.1053/j.ajkd.2017.01.048
- Costa, Paulo. "HLA and age of onset in myasthenia gravis.". Neuromuscular disorders : NMD (2017): http://europepmc.org/abstract/med/28495048.
10.1016/j.nmd.2017.04.002
- Costa, Paulo. "Immunogenetic Predisposing Factors for Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis.". The International
journal of neuroscience (2017): http://europepmc.org/abstract/med/28675059.
10.1080/00207454.2017.1349122
- Costa, Paulo. "Fibrinogen A alpha-chain amyloidosis: a non-negligible cause of chronic kidney disease in dialysis patients.".
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International
Society of Amyloidosis (2017): http://europepmc.org/abstract/med/28434302.
10.1080/13506129.2017.1281119
- Costa, Paulo. "Vitamin D supplementation effects on FoxP3 expression in T cells and FoxP3+/IL-17A ratio and clinical course
in systemic lupus erythematosus patients: a study in a Portuguese cohort.". Immunologic research (2017): http://europepmc.org/abstract/med/27423437.
10.1007/s12026-016-8829-3
- Costa, Paulo. "Serum 25-hydroxyvitamin D levels in a healthy population from the North of Portugal.". The Journal of steroid
biochemistry and molecular biology (2016): http://europepmc.org/abstract/med/27825978.
10.1016/j.jsbmb.2016.11.005
- Torres, T.; Bettencourt, N.; Ferreira, J.; Carvalho, C.; Mendonça, D.; Pinho-Costa, P.; Vasconcelos, C.; Selores, M.; Silva,
B.. "Influence of TNF-a gene polymorphisms in coronary artery calcification in psoriasis patients". Journal of the European
Academy of Dermatology and Venereology 30 1 (2016): 191-193. http://www.scopus.com/inward/record.url?eid=2-s2.0-84954531180&partnerID=MN8TOARS.
10.1111/jdv.12706
- Neves F; Abrantes J; Almeida T; de Matos AL; Costa PP; Esteves PJ. "Genetic characterization of interleukins (IL-1a, IL-1ß,
IL-2, IL-4, IL-8, IL-10, IL-12A, IL-12B, IL-15 and IL-18) with relevant biological roles in lagomorphs.". (2015): http://europepmc.org/abstract/med/26395994.
10.1177/1753425915606209
- Lacerda PC; Moreira L; Vitorino R; Costa PP. "Use of MALDI-TOF Mass Spectrometry to Assay the Transthyretin V30M Mutation
in Serum From a Liver Transplant Donor: A Case Report.". (2015): http://europepmc.org/abstract/med/25943235.
10.1097/TP.0000000000000658
- Carvalho C; Marinho A; Leal B; Bettencourt A; Boleixa D; Almeida I; Farinha F; et al. "Association between vitamin D receptor
(VDR) gene polymorphisms and systemic lupus erythematosus in Portuguese patients.". (2015): http://europepmc.org/abstract/med/25661837.
- Torres T; Bettencourt N; Ferreira J; Carvalho C; Mendonça D; Pinho-Costa P; Vasconcelos C; Selores M; Silva B. "Influence
of interleukin-6 gene polymorphisms in epicardial adipose tissue and coronary artery calcification in patients with psoriasis.".
(2015): http://europepmc.org/abstract/med/25040543.
10.1111/bjd.13271
- Bettencourt A; Carvalho C; Leal B; Brás S; Lopes D; Martins da Silva A; Santos E; et al. "The Protective Role of HLA-DRB1(*)13
in Autoimmune Diseases.". (2015): http://europepmc.org/abstract/med/26605347.
10.1155/2015/948723
- Neves F; Abrantes J; Almeida T; Costa PP; Esteves PJ. "Evolutionary Insights into IL17A in Lagomorphs.". (2015): http://europepmc.org/abstract/med/26788019.
10.1155/2015/367670
- Domingos J; Ferrão C; Ramalho J; Rodrigues T; Moreira B; Santos E; Bettencourt A; et al. "Characteristics of Neuro-Behcet's
Disease in a Case-Series from a Single Centre in Northern Portugal.". (2015): http://europepmc.org/abstract/med/25997636.
10.1159/000381210
- Beirão JM; Malheiro J; Lemos C; Beirão I; Costa P; Torres P. "Ophthalmological manifestations in hereditary transthyretin
(ATTR V30M) carriers: a review of 513 cases.". (2015): http://europepmc.org/abstract/med/26096568.
10.3109/13506129.2015.1015678
- Moreira L; Beirão JM; Beirão I; Pinho e Costa P. "Oligomeric TTR V30M aggregates compromise cell viability, erythropoietin
gene expression and promoter activity in the human hepatoma cell line Hep3B.". (2015): http://europepmc.org/abstract/med/26088020.
10.3109/13506129.2015.1007497
- Carvalho, C.; Marinho, A.; Leal, B.; Bettencourt, A.; Boleixa, D.; Almeida, I.; Farinha, F.; et al. "Association between vitamin
D receptor (VDR) gene polymorphisms and systemic lupus erythematosus in Portuguese patients". Lupus 24 8 (2015): 846-853.
http://www.scopus.com/inward/record.url?eid=2-s2.0-84930886919&partnerID=MN8TOARS.
10.1177/0961203314566636
- Silva, L.; Lopes, J.; Ramalheira, J.; Cunha, D.; Carvalho, C.; Bettencourt, A.; Brás, S.; et al. "Obstructive sleep apnoea
syndrome and HLA in the North of Portugal,Síndrome de apnea obstructiva del sueño y HLA en el norte de Portugal". Revista
de Neurologia 61 7 (2015): 301-307. http://www.scopus.com/inward/record.url?eid=2-s2.0-84942897710&partnerID=MN8TOARS.
10.33588/rn.6107.2015199
- Beirão JM; Malheiro J; Lemos C; Matos E; Beirão I; Pinho-Costa P; Torres P. "Impact of liver transplantation on the natural
history of oculopathy in Portuguese patients with transthyretin (V30M) amyloidosis.". (2014): http://europepmc.org/abstract/med/25475560.
10.3109/13506129.2014.989318
- Neves F; Abrantes J; Pinheiro A; Almeida T; Costa PP; Esteves PJ. "Convergent evolution of IL-6 in two leporids (Oryctolagus
and Pentalagus) originated an extended protein.". (2014): http://europepmc.org/abstract/med/25027474.
10.1007/s00251-014-0787-0
- Torres T; Bettencourt N; Ferreira J; Carvalho C; Mendonça D; Pinho-Costa P; Vasconcelos C; Selores M; Silva B. "Influence
of TNF-a gene polymorphisms in coronary artery calcification in psoriasis patients.". (2014): http://europepmc.org/abstract/med/25174782.
- Bettencourt A; Silva AM; Carvalho C; Leal B; Santos E; Costa PP; Silva BM. "The role of KIR2DS1 in multiple sclerosis--KIR
in Portuguese MS patients.". (2014): http://europepmc.org/abstract/med/24529855.
10.1016/j.jneuroim.2014.01.009
- Martins-da-Silva A; Lopes J; Ramalheira J; Carvalho C; Cunha D; Costa PP; Silva MB. "Usefulness of genetic characterization
of narcolepsy and hypersomnia on phenotype definition: a study in Portuguese patients.". (2014): http://europepmc.org/abstract/med/24399620.
10.33588/rn.5802.2013361
- Bettencourt A; Leal B; Carvalho C; Oliveira R; Martins Silva A; Vaz Patto J; Bastos M; et al. "CC chemokine receptor polymorphism
CCR5¿32 in Portuguese Behcet's disease patients.". (2014): http://europepmc.org/abstract/med/25268662.
- Carvalho, C.; Calvisi, S.L.; Leal, B.; Bettencourt, A.; Marinho, A.; Almeida, I.; Farinha, F.; et al. "CCR5-Delta32: implications
in SLE development". International journal of immunogenetics 41 3 (2014): 236-241. http://www.scopus.com/inward/record.url?eid=2-s2.0-85027939983&partnerID=MN8TOARS.
10.1111/iji.12094
- Beirão JM; Moreira LM; Oliveira JC; Menéres MJ; Pessoa BB; Matos ME; Costa PP; Torres PA; Beirão IB. "Aqueous humor erythropoietin
levels in open-angle glaucoma patients with and without TTR V30M familial amyloid polyneuropathy.". (2014): http://europepmc.org/abstract/med/25018619.
- Beirão, N.M.; Miranda, V.; Beirão, I.; Costa, P.P.; Torres, P.. "The use of intravitreal ranibizumab to treat neovascular
glaucoma because of retinal amyloid angiopathy in familial amyloidosis transthyretin v30m related". Retinal Cases and Brief
Reports 7 1 (2013): 114-116. http://www.scopus.com/inward/record.url?eid=2-s2.0-84878093576&partnerID=MN8TOARS.
10.1097/ICB.0b013e3182681259
- Kasperaviciute, D.; Catarino, C.B.; Matarin, M.; Leu, C.; Novy, J.; Tostevin, A.; Leal, B.; et al. "Epilepsy, hippocampal
sclerosis and febrile seizures linked by common genetic variation around SCN1A". Brain 136 10 (2013): 3140-3150. http://www.scopus.com/inward/record.url?eid=2-s2.0-84884838178&partnerID=MN8TOARS.
10.1093/brain/awt233
- Beirão, J.M.; Matos, M.E.; Beirão, I.B.; Costa, P.P.; Torres, P.A.; Beirão, João M.; Matos, Maria E.; et al. "Topical cyclosporine
for severe dry eye disease in liver-transplanted Portuguese patients with familial amyloidotic polyneuropathy (ATTRV30M)".
European Journal of Ophthalmology 23 2 (2013): 156-163. http://www.scopus.com/inward/record.url?eid=2-s2.0-84874171172&partnerID=MN8TOARS.
Publicado • 10.5301/ejo.5000197
- Beirão M; Matos E; Beirão I; Pinho-Costa P; Torres P. "No ocular involvement in familial amyloidotic polyneuropathy ATTR V30M
domino liver recipients.". (2012): http://europepmc.org/abstract/med/22443165.
10.1111/j.1432-2277.2012.01467.x
- Bettencourt A; Martins da Silva A; Pinho E Costa P; Martins Silva B. "Molecular genetic studies of multiple sclerosis in the
portuguese population.". (2012): http://europepmc.org/abstract/med/23079250.
- Bettencourt, A.; Martins Da Silva, A.; Pinho E Costa, P.; Martins Silva, B.. "Molecular genetic studies of multiple sclerosis
in the Portuguese population | Estudos genéticos em doentes Portugueses com esclerose múltipla". Acta Medica Portuguesa
25 4 (2012): 224-230. http://www.scopus.com/inward/record.url?eid=2-s2.0-84867909675&partnerID=MN8TOARS.
- Beirão, N.M.; Matos, M.E.; Meneres, M.J.; Beirão, I.M.; Costa, P.P.; Torres, P.A.. "Vitreous surgery impact in glaucoma development
in liver transplanted familial amyloidosis ATTR V30M Portuguese patients". Amyloid 19 3 (2012): 146-151. http://www.scopus.com/inward/record.url?eid=2-s2.0-84865218034&partnerID=MN8TOARS.
10.3109/13506129.2012.710669
- Beirão, J.M.; Moreira, L.V.; Lacerda, P.C.; Vitorino, R.P.; Beirão, I.B.; Torres, P.A.; Costa, P.P.. "Inability of mutant
transthyretin V30M to cross the blood-eye barrier". Transplantation 94 8 (2012): http://www.scopus.com/inward/record.url?eid=2-s2.0-84868139951&partnerID=MN8TOARS.
10.1097/TP.0b013e318269e6d1
- Beirão, M.; Matos, E.; Reis, R.; Beirão, I.; Costa, P.P.; Torres, P.. "Spatial visual contrast sensitivity in liver transplanted
Portuguese familial amyloidotic polyneuropathy (ATTR V30M) patients". Amyloid 19 3 (2012): 152-155. http://www.scopus.com/inward/record.url?eid=2-s2.0-84865205684&partnerID=MN8TOARS.
10.3109/13506129.2012.712075
- Beirão, M.; Matos, E.; Beirâo, I.; Costa, P.P.E.; Torres, P.. "Anticipation of presbyopia in Portuguese familial amyloidosis
ATTR V30M". Amyloid 18 3 (2011): 92-97. http://www.scopus.com/inward/record.url?eid=2-s2.0-80052190905&partnerID=MN8TOARS.
10.3109/13506129.2011.576719
- Tavares, I.; Lobato, L.; Moreira, L.; Santos, J.; Lacerda, P.; Pinheiro, J.; Costa, P.. "Long-term follow-up of patients with
hereditary fibrinogen A alpha-chain amyloidosis.". Amyloid : the international journal of experimental and clinical investigation
: the official journal of the International Society of Amyloidosis 18 Suppl 1 (2011): 216-217. http://www.scopus.com/inward/record.url?eid=2-s2.0-82255165417&partnerID=MN8TOARS.
10.3109/13506129.2011.627069
- Beirão, N.M.; Matos, E.; Beirão, I.; Costa, P.P.; Torres, P.. "Recurrence of vitreous amyloidosis and need of surgical reintervention
in portuguese patients with familial amyloidosis ATTR V30M". Retina 31 7 (2011): 1373-1377. http://www.scopus.com/inward/record.url?eid=2-s2.0-79961208874&partnerID=MN8TOARS.
10.1097/IAE.0b013e318203c0c2
- Duarte, R.; Carvalho, C.; Pereira, C.; Bettencourt, A.; Carvalho, A.; Villar, M.; Domingos, A.; et al. "HLA class II alleles
as markers of tuberculosis susceptibility and resistance | O papel do HLA classe II na susceptibilidade/resistência à tuberculose".
Revista Portuguesa de Pneumologia 17 1 (2011): 15-19. http://www.scopus.com/inward/record.url?eid=2-s2.0-79955665023&partnerID=MN8TOARS.
10.1016/S0873-2159(11)70005-8
- Bettencourt, A.; Silva, A.M.; Santos, E.; Gomes, S.; Mendonça, D.; Costa, P.P.; Faustino, P.; Silva, B.M.. "HFE gene polymorphisms
and severity in Portuguese patients with multiple sclerosis". European Journal of Neurology 18 4 (2011): 663-666. http://www.scopus.com/inward/record.url?eid=2-s2.0-79952725496&partnerID=MN8TOARS.
10.1111/j.1468-1331.2010.03109.x
- Duarte, R.; Carvalho, C.; Pereira, C.; Bettencourt, A.; Carvalho, A.; Villar, M.; Domingos, A.; et al. "HLA class II alleles
as markers of tuberculosis susceptibility and resistance,O papel do HLA classe II na susceptibilidade/resistência À tuberculose".
Revista Portuguesa de Pneumologia (English Edition) 17 1 (2011): 15-19. http://www.scopus.com/inward/record.url?eid=2-s2.0-85038619284&partnerID=MN8TOARS.
10.1016/S2173-5115(11)70005-7
- Tavares, I.; Lobato, L.; Moreira, L.; Santos, J.; Lacerda, P.; Pinheiro, J.; Costa, P.. "Long-term follow-up of patients with
hereditary fibrinogen A alpha-chain amyloidosis". Amyloid 18 SUPPL. 1 (2011): 221-222. http://www.scopus.com/inward/record.url?eid=2-s2.0-79960023250&partnerID=MN8TOARS.
10.3109/13506129.2011.574354
- Beirão, I.; Moreira, L.; Barandela, T.; Lobato, L.; Silva, P.; Gouveia, C.M.; Carneiro, F.; et al. "Erythropoietin production
by distal nephron in normal and familial amyloidotic adult human kidneys". Clinical Nephrology 74 5 (2010): 327-335.
http://www.scopus.com/inward/record.url?eid=2-s2.0-78649902510&partnerID=MN8TOARS.
- Silva, A.M.; Bettencourt, A.; Pereira, C.; Santos, E.; Carvalho, C.; Mendonça, D.; Costa, P.P.; Monteiro, L.; Martins, B..
"Protective role of the HLA-A*02 allele in Portuguese patients with multiple sclerosis". Multiple Sclerosis 15 6 (2009):
771-774. http://www.scopus.com/inward/record.url?eid=2-s2.0-66249137162&partnerID=MN8TOARS.
10.1177/1352458509104588
- Bettencourt, A.; Pereira, C.; Carvalho, L.; Carvalho, C.; Patto, J.V.; Bastos, M.; Silva, A.M.; et al. "New insights of HLA
class I association to Behçet's disease in Portuguese patients". Tissue Antigens 72 4 (2008): 379-382. http://www.scopus.com/inward/record.url?eid=2-s2.0-51649106008&partnerID=MN8TOARS.
10.1111/j.1399-0039.2008.01087.x
- Beirão, I.; Moreira, L.; Porto, G.; Lobato, L.; Fonseca, I.; Cabrita, A.; Costa, P.M.P.. "Low erythropoietin production in
familial amyloidosis TTR V30M is not related with renal congophilic amyloid deposition: A clinicopathologic study of twelve
cases". Nephron - Clinical Practice 109 2 (2008): http://www.scopus.com/inward/record.url?eid=2-s2.0-48249126810&partnerID=MN8TOARS.
10.1159/000142527
- Beirão, I.; Almeida, S.; Swinkels, D.; Costa, P.M.P.; Moreira, L.; Fonseca, I.; Freitas, C.; Cabrita, A.; Porto, G.. "Low
serum levels of prohepcidin, but not hepcidin-25, are related to anemia in familial amyloidosis TTR V30M". Blood Cells,
Molecules, and Diseases 41 2 (2008): 175-178. http://www.scopus.com/inward/record.url?eid=2-s2.0-48749088914&partnerID=MN8TOARS.
10.1016/j.bcmd.2008.04.008
- Beirão, I.; Lobato, L.; Costa, P.M.P.; Fonseca, I.; Silva, M.; Bravo, F.; Cabrita, A.; Porto, G.. "Liver transplantation and
anemia in familial amyloidosis ATTR V30M". Amyloid 14 1 (2007): 33-37. http://www.scopus.com/inward/record.url?eid=2-s2.0-33947645336&partnerID=MN8TOARS.
10.1080/13506120601116476
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alleles on susceptibility and outcome of a Portuguese Multiple Sclerosis population". Journal of the Neurological Sciences
258 1-2 (2007): 69-74. http://www.scopus.com/inward/record.url?eid=2-s2.0-34249880485&partnerID=MN8TOARS.
10.1016/j.jns.2007.02.033
- Pinho e Costa, P.. "A brief history of the Portuguese Amyloid Research Centre | Breve história do Centro de Estudos de Paramiloidose".
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| Resumo em conferência |
- Carvalho, C; Leal, B; Bettencourt, A; Costa, A; Bras, S; Ramalheira, JEDP; Lopes, JMCF; et al. "Killer cell immunoglobulin-like
receptor genes and sleep disorders in a Portuguese population". 2019.
- Leal, B; Bettencourt, A; Ferreira, AM; Carvalho, C; Moreira, I; Costa, PP; Da Silva, BM; Cavaco, S; Da Silva, AM. "IL1B rs16944
and depression symptoms in multiple sclerosis patients". 2017.
- Leal, B; Carvalho, C; Chaves, J; Bettencourt, A; Ferreira, R; Rangel, R; Santos, A; et al. "Inverse correlation between miR-22
serum levels and p2x7r-mediated inflammatory response in mesial temporal lobe epilepsy patients". 2017.
10.1016/j.jns.2017.08.295
- Bettencourt, A; Leal, B; Ferreira, M; Carvalho, C; Moreira, I; Santos, E; Costa, PP; et al. "Depression symptoms in multiple
sclerosis patients - The role of IL1B". 2017.
10.1016/j.jns.2017.08.691
- Bettencourt, A; Boleixa, D; Sousa, AL; Santos, E; Marinho, A; Oliveira, JC; Reis, J; et al. "Vitamin D levels and severity
in multiple sclerosis patients from the North of Portugal". 2016.
- Boleixa, D; Goncalves, A; Bettencourt, A; Leal, B; Carvalho, C; Bras, S; Mendes, A; et al. "Genetic variation in DRD3 and
impulse control disorders in Parkinson's disease". 2015.
- Leal, B; Carvalho, C; Chaves, JMM; Bettencourt, A; Freitas, J; Lopes, JMCF; Ramalheira, JEDP; et al. "Expression of miR146-a,
an inflammation-associated microRNA, in mesial temporal lobe epilepsy". 2015.
- Bettencourt, A; Silva, AM; Carvalho, C; Leal, B; Santos, E; Samoes, R; Costa, PP; Silva, BM. "Vitamin D status and vitamin
D receptor gene Fok1 and Taq1 polymorphisms in Portuguese patients with multiple sclerosis". 2014.
- Leal, B; Chaves, J; Barreira, AC; Carvalho, C; Bettencourt, A; Lopes, J; Ramalheira, J; et al. "Is serotonin transporter implicated
in mesial temporal lobe epilepsy development?". 2014.
- Chaves, J; Leal, B; Barreira, A; Carvalho, C; Bettencourt, A; Lopes, J; Ramalheira, J; et al. "SEROTONIN RECEPTORS IN MESIAL
TEMPORAL LOBE EPILEPSY". 2014.
- Leal, B; Zenatti, L; Rangel, R; Chaves, J; Carvalho, C; Bettencourt, A; Santos, A; et al. "ADENOSINERGIC SYSTEM IN MESIAL
TEMPORAL LOBE EPILEPSY". 2014.
- Ferreira, JCP; Torres, T; Carvalho, CA; Bettencourt, A; Leal, B; Vasconcelos, C; Costa, PP; Selores, M; Silva, BM. "Apoe isoforms
in patients with psoriasis". 2013.
- Ferreira, JP; Torres, T; Carvalho, C; Bettencourt, A; Leal, B; Vasconcelos, C; Costa, PP; Selores, M; Silva, BM. "IL-6 and
TNF-alpha polymorphisms in portuguese psoriatic patients". 2013.
- Martins da Silva, AM; Leal, B; Chaves, J; Carvalho, C; Bettencourt, A; Branco, RC; Ferreira, J; Costa, PP; Martins da Silva,
BM. "APOE ISOFORMS IN FOCAL EPILEPSIES: AN ASSOCIATION STUDY IN A PORTUGUESE POPULATION". 2013.
- Chaves, J; Leal, B; Carvalho, C; Bettencourt, A; Bras, S; Barreira, A; Boleixa, D; et al. "MESIAL TEMPORAL LOBE EPILEPSY AND
SEROTONIN: THE ROLE OF HTR2A RECEPTOR". 2013.
- Leal, B; Castelo Branco, RC; Rangel, R; Chaves, J; Carvalho, C; Bettencourt, A; Honavar, M; et al. "HUMAN HERPES VIRUS 6B
AND MESIAL TEMPORAL LOBE EPILEPSY WITH HIPPOCAMPAL SCLEROSIS (MTLE-HS): IS THERE A LINK?". 2013.
- Neves, F; Abrantes, J; Costa, PP; Esteves, PJ. "Comparative evolutionary analysis of IL6 in lagomorphs". 2013.
- Lopes, A; Fonseca, M; Almeida, I; Perneta, F; Bettencourt, A; Carvalho, C; Marinho, A; et al. "HLA-DRB1 ALLELES AND AUTOANTIBODY
PRODUCTION IN A PORTUGUESE SCLERODERMA COHORT". 2012.
- Bettencourt, A; Carvalho, C; Leal, B; Maia, S; Lopes, D; Fonseca, M; Almeida, I; et al. "ASSOCIATION OF HLA-DRB1 ALLELES AND
AUTOANTIBODY PRODUCTION IN A PORTUGUESE SCLERODERMA COHORT". 2012.
- Carvalho, C; Bettencourt, A; Leal, B; Fonseca, M; Lopes, D; Perneta, F; Pestana, J; et al. "STUDY OF KIR GENES IN PORTUGUESE
PATIENTS WITH SYSTEMIC SCLEROSIS". 2012.
- Martins Da Silva, AM; Branco, R; Leal, B; Rangel, R; Carvalho, C; Bettencourt, A; Chaves, J; et al. "ARE GLUTAMINE SINTHETASE
EXPRESSION LEVELS ASSOCIATED WITH MESIAL TEMPORAL LOBE EPILEPSY WITH HIPPOCAMPAL SCLEROSIS?". 2012.
- Leal, B; Branco, R; Rangel, R; Bettencourt, A; Carvalho, C; Chaves, J; Santos, A; et al. "EXCITATORY AMINO ACID TRANSPORTER-1
EXPRESSION IN HUMAN MESIAL TEMPORAL LOBE EPILEPSY WITH HIPPOCAMPAL SCLEROSIS". 2012.
- Chaves, J; Brito, C; Leal, B; Carvalho, C; Bettencourt, A; Branco, R; Martins Da Silva, AM; Costa, PP; Martins Da Silva, BM.
"INFLAMMATORY PROCESS AND MESIAL TEMPORAL LOBE EPILEPSY WITH EPILEPSY: THE ROLE OF IL-1 beta". 2012.
- Bettencourt, A; Silva, AM; Carvalho, C; Leal, B; Santos, E; Coutinho, E; Costa, PP; Silva, BM. "Fok1 vitamin D receptor gene
polymorphism is associated with multiple sclerosis in a Portuguese population". 2011.
- Silva, AM; Bettencourt, A; Ribeiro, A; Goncalves, A; Pinto, C; Moreira, I; Santos, E; et al. "Dementia in multiple sclerosis:
demographic, clinical and genetic features". 2011.
- Bettencourt, A; Silva, AM; Carvalho, C; Leal, B; Santos, E; Coutinho, E; Pinho e Costa, PPE; Silva, BM. "Vitamin D receptor
gene Fok1 polymorphism in Portuguese patients with multiple sclerosis". 2011.
- Martins Silva, AM; Bettencourt, A; Goncalves, A; Pinto, C; Santos, E; Moreira, I; Tavares, A; et al. "Does APOE-epsilon4 have
a detrimental effect in multiple sclerosis?". 2011.
- Branco, RC; Leal, B; Rangel, R; Chaves, J; Bettencourt, A; Carvalho, C; Lima, JL; et al. "EXPRESSION OF GLUTAMATE TRANSPORTERS
IN HUMAN MESIAL TEMPORAL LOBE EPILEPSY WITH HIPOCAMPPAL SCLEROSIS: A PRELIMINARY STUDY". 2011.
- Leal, B; Carvalho, C; Bettencourt, A; Carneiro, P; Cerveira, C; Vasconcelos, C; Barbosa, P; Costa, PP; Silva, BM. "Killer
immunoglobulin-like receptor genes and rheumatoid arthritis in a Portuguese population". 2011.
- Leal, B; Rangel, R; Carvalho, C; Moreira, L; Chaves, J; Silva, AM; Lima, JL; et al. "INFLAMMATION IN HUMAN MESIAL TEMPORAL
LOBE EPILEPSY WITH HIPPOCAMPAL SCLEROSIS: PRELIMINARY EVALUATION". 2010.
- Carvalho, C; Lopes, D; Bettencourt, A; Leal, B; Maia, S; Vita, P; Almeida, F; et al. "Natural killer cell function and disease
progression in Portuguese patients with HIV - an immunogenetic perspective". 2010.
- Bettencourt, A; Silva, AM; Carvalho, C; Coutinho, E; Santos, E; Pereira, C; Mendonca, D; Costa, PP; Silva, BM. "Killer immunoglobulin-like
receptor genes in Portuguese multiple sclerosis patients". 2010.
- Leal, B; Rangel, R; Carvalho, C; Moreira, L; Chaves, J; Silva, AM; Lima, JL; et al. "Inflammation in human mesial temporal
lobe epilepsy with hippocampal sclerosis: a preliminary evaluation". 2010.
- Leal, B; Carvalho, C; Bettencourt, A; Leuschner, P; Nery, F; Carneiro, P; Cerveira, C; et al. "CCR5 and rheumatoid arthritis:
is there an association?". 2010.
- Leal, B; Chaves, J; Carvalho, C; Bettencourt, A; Barros, M; Lopes, D; Silva, AM; et al. "MDR1 GENE POLYMORPHISMS AND DRUG-RESISTANT
EPILEPSY IN A PORTUGUESE POPULATION". 2010.
- Martins Da Silva, AM; Lacerda, P; Guedes, L; Lopes, J; Leal, B; Pinho e Costa, PPE; Martins da Silva, BM. "VARIATION OF JME
FAMILY PHENOTYPE ANTICIPATED BY PREVIOUS EEG CHARACTERIZATION: CLINICAL AND GENETIC EXPLORATION". 2009.
- Leal, B; Chaves, J; Carvalho, C; Bettencourt, A; Barros, M; Pereira, C; Costa, PP; et al. "Predictive genetic risk factors
for febrile seizures and mesial temporal lobe epilepsy". 2009.
- Carvalho, C; Duarte, R; Pereira, C; Bettencourt, A; Quintas, Z; Vilar, M; Domingos, A; Costa, PP; Silva, BM. "Is susceptibility
and protection to tuberculosis KIR dependent?". 2009.
- Rodrigues, P; Pereira, C; Bettencourt, A; Carvalho, C; Leal, B; Torres, T; Lobo, I; et al. "KIR genes and HLA-Cw*0602 in Portuguese
patients with Psoriasis vulgaris". 2009.
- Leal, B; Pereira, C; Carvalho, C; Bettencourt, A; Costa, PP; Leuschner, P; Nery, F; et al. "HLA-DRB1 and rheumatoid arthritis:
the anti-CCP antibodies effect". 2009.
- Bettencourt, A; Martins Silva, AM; Pereira, C; Coutinho, E; Santos, E; Carvalho, C; Mendonca, D; et al. "Killer cell immunoglobulin-like
receptors (KIR) genes and multiple sclerosis: possible roles in protection and susceptibility". 2009.
- Chaves, J; Bettencourt, A; Leal, B; Carvalho, C; Pereira, C; Costa, PP; Monteiro, L; et al. "ApoE polymorphisms and susceptibility
to mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS) in a Portuguese population". 2008.
- Bettencourt, A; Silva, AM; Santos, E; Pereira, C; Carvalho, C; Leal, B; Costa, PP; Monteiro, L; Silva, BM. "Role of HFE in
disease course and susceptibility in a group of Portuguese multiple sclerosis patients". 2008.
- Silva, A; Bettencourt, A; Santos, E; Coutinho, E; Pereira, C; Carvalho, C; Mendonca, D; et al. "No evidence of increased genetic
susceptibility to autoimmune diseases in Portuguese Multiple Sclerosis patients". 2008.
- Bettencourt, A; Silva, A; Pereira, C; Coutinho, E; Santos, E; Carvalho, C; Mendonca, D; et al. "Benign course in multiple
sclerosis: Association with autoimmunity and the protein tyrosine phosphatase (PTPN22) 1858C > T gene pollymorphism". 2008.
- Riedstra, S; Leite, G; Ferreira, C; Gomes, FB; Costa, PMP; Ferreira, JPM. "Optimization of the expression of single-chain
antibodies using different Escherichia coli systems". 2007.
10.1016/j.jbiotec.2007.07.457
- Pereira, C; Leal, B; Carvalho, C; Bettencourt, A; Machado, A; Casimiro, S; Silva, AM; et al. "Evidence for the presence of
a common protective DRB1 allele for aid in the Portuguese population". 2007.
- Bettencourt, A; Pereira, C; Silva, AM; Carvalho, C; Leal, B; Couto, AR; Quintas, Z; et al. "HLA-DRB1*15-DQB1*06 haplotype
and multiple sclerosis in Portuguese patients". 2007.
- Riedstra, S; Cerejo, L; Bras, S; Costa, PMP; Ferreira, JPM. "Optimization of the conditions for the expression of an anti-transthyretin
scFv in Pichia pastoris". 2007.
10.1016/j.biotec.2007.07.917
- Moreira, L; Lobato, L; Tavares, I; Matos, C; Carvalho, E; Pinheiro, J; Costa, PP. "Fibrinogen A alpha-chain Glu526V amyloidosis
in seven Portuguese families". 2006.
- Fonseca, I; Lobato, L; Santos, J; Beirao, I; Cunha, C; Oliveira, JC; Cabrita, A; Costa, PP. "Vitamin D deficiency and serum
levels of parathyroid hormone in Portuguese patients with familial amyloidotic polyneuropathy (FAP, TTR V30M)". 2006.
- Pereira, C; Chaves, J; Leal, B; Carvalho, A; Bettencourt, C; Costa, P; Monteiro, L; et al. "GABBR1 polymorphisms in portuguese
mesial temporal lobe epilepsy patients". 2006.
- Bettencourt, A; Pereira, C; Silva, AM; Carvalho, C; Quintas, Z; Costa, PP; Monteiro, L. "Protective influence on Multiple
Sclerosis by HLA-A*02: a study in the Portuguese population". 2006.
- Pereira, C; Silva, AM; Pinto, D; Bettencourt, A; Costa, PP; Koeleman, B; Silva, BM. "The role of PTPN22 1858T autoimmunity
risk variant in Multiple Sclerosis Portuguese population". 2006.
- Silva, AM; Bettencourt, A; Pereira, C; Carvalho, C; Casimiro, S; Costa, PP; Monteiro, L; Silva, BM. "HLA-A*02 allele as a
modulating factor in multiple sclerosis: Implications for susceptibility and severity". 2006.
- Pereira, C; Martins da Silva, A; Pinto, D; Bettencourt, A; Costa, P; Koeleman, B; Martins da Silva, B. "The role of PTPN22
1858T autoimmunity risk variant in a Portuguese multiple sclerosis population". 2006.
- Silva, AM; Pereira, C; Bettencourt, A; Carvalho, C; Casimiro, S; Quintas, Z; Costa, PP; Monteiro, L; Silva, BM. "Influence
of HLA-DRB1 in clinical course and disease severity in Portuguese MS patients". 2005.
- Pereira, C; Silva, AM; Carvalho, C; Bettencourt, A; Casimiro, S; Quintas, Z; Costa, PM; Monteiro, L; Silva, BM. "TNFA promoter
polymrphisms in Portuguese multiple sclerosis patients". 2005.
- Pereira, C; Pereira, O; Escada, R; Pinto, D; Selores, M; Carvalho, C; Costa, P; Massa, A; Silva, B. "HLA-CW*0602 and TNFa
in psoriasis patients". 2005.
- Pereira, C; Silva, AM; Carvalho, C; Bettencourt, A; Casimiro, S; Quintas, Z; Costa, PM; Monteiro, L; Silva, BM. "DR/DQ antigens
in papillary thyroid tumors". 2005.
- Carvalho, C; Pereira, C; Duarte, R; Casimiro, S; Quintas, Z; Costa, PP; Silva, BM. "Genetic susceptibility to tuberculosis:
Association with HLA class II and TNA-a alleles". 2005.
- Silva, AM; Pereira, C; Bettencourt, A; Carvalho, C; Lacerda, P; Costa, PP; Monteiro, L; da Silva, BM. "Genetic susceptibility
to multiple sclerosis in Portuguese patients: A study of HLA and non HLA genes". 2005.
- Pereira, C; Paulo, P; Costa, PPE; Barbot, C; Santos, M; Ramalheira, J; Lopes, J; et al. "Association studies with GABA[B]R1
polymorphisms and idiopathic generalised epilepsy in Portuguese patients". 2004.
- Paulo, P; Pereira, C; Carvalho, C; Costa, PP; Lima, J; Casimiro, S; Quintas, Z; Silva, AM; Martins, B. "GABA(B)R1 polymorphisms
and idiopathic generalized epilepsy in Portuguese patients". 2004.
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