Journal article |
- Pires, Carolina; Saramago, Ana; Moura, Margarida M.; Li, Jing; Donato, Sara; Marques, Inês J.; Belo, Hélio; et al. Corresponding
author: Cavaco, B.M.. "Identification of Germline FOXE1 and Somatic MAPK Pathway Gene Alterations in Patients with Malignant
Struma Ovarii, Cleft Palate and Thyroid Cancer". International Journal of Molecular Sciences 25 4 (2024): 1966. http://dx.doi.org/10.3390/ijms25041966.
Open access • Published • 10.3390/ijms25041966
- Pires, Carolina; Marques, Inês J.; Valério, Mariana; Saramago, Ana; Santo, Paulo E.; Santos, Sandra; Silva, Margarida; et
al. Corresponding author: Cavaco, B.M.. "CHEK2 germline variants identified in familial non-medullary thyroid cancer lead
to impaired protein structure and function". Journal of Biological Chemistry (2024): 105767. http://dx.doi.org/10.1016/j.jbc.2024.105767.
Open access • 10.1016/j.jbc.2024.105767
- Simões-Pereira, Joana; Saramago, Ana; Rodrigues, Ricardo; Pojo, Marta; Pires, Carolina; Horta, Mariana; López-Presa, Dolores;
et al. "Clinical and molecular characterisation of metastatic papillary thyroid cancer according to radioiodine therapy outcomes".
Endocrine (2023): http://dx.doi.org/10.1007/s12020-023-03633-y.
10.1007/s12020-023-03633-y
- Pita, Jaime M.; Raspé, Eric; Coulonval, Katia; Decaussin-Petrucci, Myriam; Tarabichi, Maxime; Dom, Geneviève; Libert, Frederick;
et al. "CDK4 phosphorylation status and rational use for combining CDK4/6 and BRAF/MEK inhibition in advanced thyroid carcinomas".
Frontiers in Endocrinology 14 (2023): http://dx.doi.org/10.3389/fendo.2023.1247542.
10.3389/fendo.2023.1247542
- Pinto, Ana Teresa; Pojo, Marta; Rodrigues, Ricardo; Sousa, Diana Pacheco; Matthiesen, Rune; Carvalho, Ana Sofia; Beck, Hans
C.; et al. "SPRY4 as a Potential Mediator of the Anti-Tumoral Role of Macrophages in Anaplastic Thyroid Cancer Cells". Cancers
15 17 (2023): 4387. http://dx.doi.org/10.3390/cancers15174387.
10.3390/cancers15174387
- Sara Lomelino Pinheiro; Ana Saramago; Branca Maria Cavaco; Carmo Martins; Valeriano Leite; Tiago Nunes da Silva. "Clinical
and molecular characterization of parathyroid carcinoma in multiple endocrine neoplasia type 1". Endocrine Connections
(2023): https://doi.org/10.1530/EC-22-0479.
10.1530/EC-22-0479
- Dias, Daniela; Damásio, Inês; Marques, Pedro; Simões, Helder; Rodrigues, Ricardo; Cavaco, Branca Maria; Leite, Valeriano.
"Metastatic follicular thyroid cancer with a longstanding responsiveness to gemcitabine plus oxaliplatin". European Thyroid
Journal 12 3 (2023): http://dx.doi.org/10.1530/etj-22-0227.
10.1530/etj-22-0227
- Ana Figueiredo; A. Saramago; B. M. Cavaco; J. Simões-Pereira; V. Leite. "Familial parathyroid tumours-comparison of clinical
profiles between syndromes". Journal of Endocrinological Investigation (2023): http://dx.doi.org/10.1007/s40618-023-02032-4.
10.1007/s40618-023-02032-4
- Tiago Nunes da Silva; Ricardo Rodrigues; Ana Saramago; Carolina Pires; Miguel Rito; Mariana Horta; Carmo Martins; Valeriano
Leite; Branca M Cavaco. "Target therapy for BRAF mutated anaplastic thyroid cancer: a clinical and molecular study". European
Journal of Endocrinology 188 1 (2023): http://dx.doi.org/10.1093/ejendo/lvac011.
10.1093/ejendo/lvac011
- Inês Lemos Damásio; Joana Simões-Pereira; Donato S; Horta M; Cavaco BM; Rito M; Gomes P; Leite V. "Entrectinib in the neoadjuvant
setting of anaplastic thyroid cancer: a case report.". European thyroid journal (2022): https://doi.org/10.1530/ETJ-22-0179.
10.1530/etj-22-0179
- Cunha, Clara; Pinheiro, Sara Lomelino; Donato, Sara; Tavares Bello, Carlos; Simões, Helder; Nunes Silva, Tiago; Prazeres,
Susana; et al. "Parathyroid carcinoma: Single centre experience". Clinical Endocrinology (2022): http://dx.doi.org/10.1111/cen.14684.
10.1111/cen.14684
- Padeira, G.; Cavaco, B.M; Virella, D.; Sá-Couto, H.; Afonso-Lopes, M.L.. "Clinical, Molecular Characterization and Long-Term
Follow-Up of a Patient with Neonatal Severe Hyperparathyroidism". 53 (2022): 440-446. https://pjp.spp.pt/article/view/24480.
Published
- Chaves, Carolina; Nunes da Silva, Tiago; Dias Pereira, Bernardo; Anselmo, João; Claro, Isabel; Cavaco, Branca M.; Saramago,
Ana; Leite, Valeriano. "A case report of multiple endocrine neoplasia type 1 and autoimmune disease". Medicine 100
49 (2021): e28145. http://dx.doi.org/10.1097/md.0000000000028145.
10.1097/md.0000000000028145
- Marques, Inês J.; Gomes, Inês; Pojo, Marta; Pires, Carolina; Moura, Margarida M.; Cabrera, Rafael; Santos, Catarina; et al.
"Identification of SPRY4 as a Novel Candidate Susceptibility Gene for Familial Nonmedullary Thyroid Cancer". Thyroid
31 9 (2021): 1366-1375. http://dx.doi.org/10.1089/thy.2020.0290.
10.1089/thy.2020.0290
- Simões-Pereira, Joana; C. Ferreira, Teresa; Limbert, Edward; Cavaco, Branca Maria; Leite, Valeriano. "Outcomes of Thyrotropin
Alfa Versus Levothyroxine Withdrawal-Aided Radioiodine Therapy for Distant Metastasis of Papillary Thyroid Cancer". Thyroid
(2021): http://dx.doi.org/10.1089/thy.2021.0013.
10.1089/thy.2021.0013
- Simões-Pereira, Joana; Mourinho, Nádia; Ferreira, Teresa C; Limbert, Edward; Cavaco, Branca Maria; Leite, Valeriano. "Avidity
and Outcomes of Radioiodine Therapy for Distant Metastasis of Distinct Types of Differentiated Thyroid Cancer". The Journal
of Clinical Endocrinology & Metabolism 106 10 (2021): e3911-e3922. http://dx.doi.org/10.1210/clinem/dgab436.
10.1210/clinem/dgab436
- Pires, Carolina; Marques, Inês Jorge; Dias, Daniela; Saramago, Ana; Leite, Valeriano; Cavaco, Branca Maria. "A pathogenic
variant in CHEK2 shows a founder effect in Portuguese Roma patients with thyroid cancer". Endocrine 73 3 (2021): 588-597.
http://dx.doi.org/10.1007/s12020-021-02660-x.
10.1007/s12020-021-02660-x
- Pojo, Marta; Sofia Fargoso; Sidónia Santos; Patricia Machado; Branca Maria Cavaco; Fátima Vaz. "APOL2: A New Candidate Gene
Associated with Hereditary Prostate Cancer". British Journal of Cancer Research 3 3 (2020): 401-406. https://makperiodicallibrary.com/britishjournalofcancerresearch/wp-content/uploads/2020/04/BJCR-152.pdf.
Published
- Campos, Catarina; Fragoso, Sofia; Luís, Rafael; Pinto, Filipe; Brito, Cheila; Esteves, Susana; Pataco, Margarida; et al. "High-Throughput
Sequencing Identifies 3 Novel Susceptibility Genes for Hereditary Melanoma". Genes 11 4 (2020): 403. http://dx.doi.org/10.3390/genes11040403.
10.3390/genes11040403
- Moura, M. M.; Cabrera, R. A.; Esteves, S.; Cavaco, B. M.; Soares, P.; Leite, V.. "Correlation of molecular data with histopathological
and clinical features in a series of 66 patients with medullary thyroid carcinoma". 3 3 (2020): 401-406.
Published • 10.1007/s40618-020-01456-6
- Pinto, Ana T.; Pojo, Marta; Simões-Pereira, Joana; Roque, Ruben; Saramago, Ana; Roque, Lúcia; Martins, Carmo; et al. "Establishment
and characterization of a new patient-derived anaplastic thyroid cancer cell line (C3948), obtained through fine-needle aspiration
cytology". Endocrine 66 2 (2019): 288-300. http://dx.doi.org/10.1007/s12020-019-02009-5.
10.1007/s12020-019-02009-5
- Sousa, Diana P.; Pojo, Marta; Pinto, Ana T.; Leite, Valeriano; Serra, Ana Teresa; Cavaco, Branca M.. "Nobiletin Alone or in
Combination with Cisplatin Decreases the Viability of Anaplastic Thyroid Cancer Cell Lines". Nutrition and Cancer 72
2 (2019): 352-363. http://dx.doi.org/10.1080/01635581.2019.1634745.
10.1080/01635581.2019.1634745
- Donato, Sara; Simões, Helder; Pinto, Ana Teresa; M. Cavaco, Branca; Leite, Valeriano. "SDHx-related pheochromocytoma/paraganglioma
– genetic, clinical, and treatment outcomes in a series of 30 patients from a single center". Endocrine 65 2 (2019):
408-415. http://dx.doi.org/10.1007/s12020-019-01953-6.
10.1007/s12020-019-01953-6
- Lopes-Ventura, S.; Pojo, M.; Matias, A. T.; Moura, M. M.; Marques, I. J.; Leite, V.; Cavaco, B. M.. "The efficacy of HRAS
and CDK4/6 inhibitors in anaplastic thyroid cancer cell lines". Journal of Endocrinological Investigation 42 5 (2018):
527-540. http://dx.doi.org/10.1007/s40618-018-0947-4.
10.1007/s40618-018-0947-4
- Simões-Pereira, J.; Moura, M. M.; Marques, I. J.; Rito, M.; Cabrera, R. A.; Leite, V.; Cavaco, B. M.. "The role of EIF1AX
in thyroid cancer tumourigenesis and progression". Journal of Endocrinological Investigation 42 3 (2018): 313-318.
http://dx.doi.org/10.1007/s40618-018-0919-8.
10.1007/s40618-018-0919-8
- Cavaco, Branca M; Canaff, Lucie; Nolin-Lapalme, Alexis; Vieira, Margarida; Silva, Tiago N; Saramago, Ana; Domingues, Rita;
et al. "Homozygous Calcium-Sensing Receptor Polymorphism R544Q Presents as Hypocalcemic Hypoparathyroidism". The Journal
of Clinical Endocrinology & Metabolism 103 8 (2018): 2879-2888. http://dx.doi.org/10.1210/jc.2017-02407.
10.1210/jc.2017-02407
- Cavaco, B.M.. "Identification of a novel CTR9 germline mutation in a family with Wilms tumor". (2018):
10.1016/j.ejmg.2017.12.010
- Cavaco, B.M.. "Genomic profiling reveals mutational landscape in parathyroid carcinomas". (2017):
10.1172/jci.insight.92061
- Marques, I.J.; Moura, M.M.; Cabrera, R.; Pinto, A.E.; Simões-Pereira, J.; Santos, C.; Menezes, F.D.; et al. "Identification
of somatic TERT promoter mutations in familial nonmedullary thyroid carcinomas". Clinical Endocrinology 87 4 (2017):
394-399. http://www.scopus.com/inward/record.url?eid=2-s2.0-85020539300&partnerID=MN8TOARS.
10.1111/cen.13375
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germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC)". Endocrine 49 1 (2015): 204-214.
http://www.scopus.com/inward/record.url?eid=2-s2.0-84938342196&partnerID=MN8TOARS.
10.1007/s12020-014-0470-0
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of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis
and mutational enrichment in kinases associated with cell migration and invasion". Journal of Clinical Endocrinology and
Metabolism 100 2 (2015): E360-E364. http://www.scopus.com/inward/record.url?eid=2-s2.0-84927566019&partnerID=MN8TOARS.
10.1210/jc.2014-3238
- Silva, A.L.; Carmo, F.; Moura, M.M.; Domingues, R.; Espadinha, C.; Leite, V.; Cavaco, B.; Bugalho, M.J.. "Identification and
characterization of two novel germline RET variants associated with medullary thyroid carcinoma". Endocrine 49 2 (2015):
366-372. http://www.scopus.com/inward/record.url?eid=2-s2.0-84929947736&partnerID=MN8TOARS.
10.1007/s12020-015-0559-0
- Moura, M.M.; Cavaco, B.M.; Leite, V.. "RAS proto-oncogene in medullary thyroid carcinoma". Endocrine-Related Cancer
22 5 (2015): R235-R252. http://www.scopus.com/inward/record.url?eid=2-s2.0-84942103878&partnerID=MN8TOARS.
10.1530/ERC-15-0070
- Cavaco, B.M.. "Novel Mutation in the CASR Gene (p.Leu123Ser) in a Case of Autosomal Dominant Hypocalcemia". (2015):
10.1055/s-0035-1554979
- Pita, J.M.; Figueiredo, I.F.; Moura, M.M.; Leite, V.; Cavaco, B.M.. "Cell cycle deregulation and TP53 and RAS mutations are
major events in poorly differentiated and undifferentiated thyroid carcinomas". Journal of Clinical Endocrinology and Metabolism
99 3 (2014): http://www.scopus.com/inward/record.url?eid=2-s2.0-84895822573&partnerID=MN8TOARS.
10.1210/jc.2013-1512
- Pinto, A.E.; Silva, G.L.; Henrique, R.; Menezes, F.D.; Teixeira, M.R.; Leite, V.; Cavaco, B.M.. "Familial vs sporadic papillary
thyroid carcinoma: A matched-case comparative study showing similar clinical/prognostic behaviour". European Journal of
Endocrinology 170 2 (2014): 321-327. http://www.scopus.com/inward/record.url?eid=2-s2.0-84893700531&partnerID=MN8TOARS.
10.1530/EJE-13-0865
- Melo, M.; Da Rocha, A.G.; Vinagre, J.; Batista, R.; Peixoto, J.; Tavares, C.; Celestino, R.; et al. "TERT promoter mutations
are a major indicator of poor outcome in differentiated thyroid carcinomas". Journal of Clinical Endocrinology and Metabolism
99 5 (2014): http://www.scopus.com/inward/record.url?eid=2-s2.0-84899908886&partnerID=MN8TOARS.
10.1210/jc.2013-3734
- Marques, P.; Santos, R.; Cavaco, B.; Leite, V.. "Chronic hypocalcemia due to anti-calcium sensing receptor antibodies | Hipocalcemia
crónica por anticorpos anti-recetor do cálcio". Acta Medica Portuguesa 27 3 (2014): 399-402. http://www.scopus.com/inward/record.url?eid=2-s2.0-84903764956&partnerID=MN8TOARS.
- Cavaco, B.M.. "Regulation of calcium metabolism in pseudohypoparathyroidism type 1b. From genotype to physiopathologyRegulação
do metabolismo do cálcio em pseudohipoparatiroidismo de tipo 1b. Do genótipo à fisiopatologia". (2014):
doi.org/10.1016/j.rpedm.2014.05.002
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Portuguese school children | Aporte do Iodo nas Crianças das Escolas em Portugal". Acta Medica Portuguesa 25 1 (2012):
29-36. http://www.scopus.com/inward/record.url?eid=2-s2.0-84865179915&partnerID=MN8TOARS.
- Domingues, R.; Tomaz, R.A.; Martins, C.; Nunes, C.; Bugalho, M.J.; Cavaco, B.M.. "Identification of the first germline HRPT2
whole-gene deletion in a patient with primary hyperparathyroidism". Clinical Endocrinology 76 1 (2012): 33-38. http://www.scopus.com/inward/record.url?eid=2-s2.0-83455163973&partnerID=MN8TOARS.
10.1111/j.1365-2265.2011.04184.x
- Tomaz, R.A.; Sousa, I.; Silva, J.G.; Santos, C.; Teixeira, M.R.; Leite, V.; Cavaco, B.M.. "FOXE1 polymorphisms are associated
with familial and sporadic nonmedullary thyroid cancer susceptibility". Clinical Endocrinology 77 6 (2012): 926-933.
http://www.scopus.com/inward/record.url?eid=2-s2.0-84869040208&partnerID=MN8TOARS.
10.1111/j.1365-2265.2012.04505.x
- Cavaco, B.M.; Santos, R.; Félix, A.; Carvalho, D.; Lopes, J.M.; Domingues, R.; Sirgado, M.; et al. "Identification of de novo
germline mutations in the HRPT2 gene in two apparently sporadic cases with challenging parathyroid tumor diagnoses". Endocrine
Pathology 22 1 (2011): 44-52. http://www.scopus.com/inward/record.url?eid=2-s2.0-79953284330&partnerID=MN8TOARS.
10.1007/s12022-011-9151-1
- Moura, M.M.; Cavaco, B.M.; Pinto, A.E.; Leite, V.. "High prevalence of RAS mutations in RET-negative sporadic medullary thyroid
carcinomas". Journal of Clinical Endocrinology and Metabolism 96 5 (2011): http://www.scopus.com/inward/record.url?eid=2-s2.0-79955669404&partnerID=MN8TOARS.
10.1210/jc.2010-1921
- Tomaz, R.A.; Cavaco, B.M.; Leite, V.. "Differential methylation as a cause of allele dropout at the imprinted GNAS locus".
Genetic Testing and Molecular Biomarkers 14 4 (2010): 455-460. http://www.scopus.com/inward/record.url?eid=2-s2.0-77955881209&partnerID=MN8TOARS.
10.1089/gtmb.2010.0029
- Cavaco, B.M.; Tomaz, R.A.; Fonseca, F.; Mascarenhas, M.R.; Leite, V.; Sobrinho, L.G.. "Clinical and genetic characterization
of Portuguese patients with pseudohypoparathyroidism type Ib". Endocrine 37 3 (2010): 408-414. http://www.scopus.com/inward/record.url?eid=2-s2.0-77952092694&partnerID=MN8TOARS.
10.1007/s12020-010-9321-9
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RET somatic mutations with clinicopathological features in sporadic medullary thyroid carcinomas". British Journal of Cancer
100 11 (2009): 1777-1783. http://www.scopus.com/inward/record.url?eid=2-s2.0-67349168712&partnerID=MN8TOARS.
10.1038/sj.bjc.6605056
- Pita, J.M.; Banito, A.; Cavaco, B.M.; Leite, V.. "Gene expression profiling associated with the progression to poorly differentiated
thyroid carcinomas". British Journal of Cancer 101 10 (2009): 1782-1791. http://www.scopus.com/inward/record.url?eid=2-s2.0-70449519393&partnerID=MN8TOARS.
10.1038/sj.bjc.6605340
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of differentiated thyroid carcinoma: A survey | Encuesta sobre el tratamiento del carcinoma diferenciado de tiroides". Endocrinologia
y Nutricion 55 7 (2008): 283-288. http://www.scopus.com/inward/record.url?eid=2-s2.0-51849141365&partnerID=MN8TOARS.
10.1016/S1575-0922(08)72182-X
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thyroid carcinoma (FNMTC): Analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF
and RAS mutations". Endocrine-Related Cancer 15 1 (2008): 207-215. http://www.scopus.com/inward/record.url?eid=2-s2.0-41349093968&partnerID=MN8TOARS.
10.1677/ERC-07-0214
- Cavaco, B.M.; Batista, P.F.; Sobrinho, L.G.; Leite, V.. "Mapping a new familial thyroid epithelial neoplasia susceptibility
locus to chromosome 8p23.1-p22 by high-density single-nucleotide polymorphism genome-wide linkage analysis". Journal of
Clinical Endocrinology and Metabolism 93 11 (2008): 4426-4430. http://www.scopus.com/inward/record.url?eid=2-s2.0-57349123714&partnerID=MN8TOARS.
10.1210/jc.2008-0449
- Machado, P.M.; Cavaco, B.M.; Brandão, R.; Eugénio, J.; Santos, S.; Opinião, A.; Vaz, F.. "In reply [2]". Journal of Clinical
Oncology 25 31 (2007): 5036-5038. http://www.scopus.com/inward/record.url?eid=2-s2.0-36849059259&partnerID=MN8TOARS.
10.1200/JCO.2007.13.5442
- Espadinha, C.; Cavaco, B.M.; Leite, V.. "PAX8PPAR¿ stimulates cell viability and modulates expression of thyroid-specific
genes in a human thyroid cell line". Thyroid 17 6 (2007): 497-509. http://www.scopus.com/inward/record.url?eid=2-s2.0-34447532041&partnerID=MN8TOARS.
10.1089/thy.2006.0263
- Machado, P.M.; Brandão, R.D.; Cavaco, B.M.; Eugénio, J.; Bento, S.; Nave, M.; Rodrigues, P.; Fernandes, A.; Vaz, F.. "Screening
for a BRCA2 rearrangement in high-risk breast/ovarian cancer families: Evidence for a founder effect and analysis of the associated
phenotypes". Journal of Clinical Oncology 25 15 (2007): 2027-2034. http://www.scopus.com/inward/record.url?eid=2-s2.0-34249932412&partnerID=MN8TOARS.
10.1200/JCO.2006.06.9443
- Bradley, K.J.; Cavaco, B.M.; Bowl, M.R.; Harding, B.; Cranston, T.; Fratter, C.; Besser, G.M.; et al. "Parafibromin mutations
in hereditary hyperparathyroidism syndromes and parathyroid tumours". Clinical Endocrinology 64 3 (2006): 299-306.
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10.1111/j.1365-2265.2006.02460.x
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of the chemokine receptor CCR7 in thyroid carcinomas". Journal of Endocrinology 191 1 (2006): 229-238. http://www.scopus.com/inward/record.url?eid=2-s2.0-33751047440&partnerID=MN8TOARS.
10.1677/joe.1.06688
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splice site of the gene encoding PARAFIBROMIN is associated with familial isolated primary hyperparathyroidism.". Journal
of medical genetics. 42 8 (2005): http://www.scopus.com/inward/record.url?eid=2-s2.0-33644937809&partnerID=MN8TOARS.
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a phenotypic manifestation of the hyperparathyroidism- jaw tumour syndrome". Journal of Internal Medicine 257 1 (2005):
18-26. http://www.scopus.com/inward/record.url?eid=2-s2.0-19944434120&partnerID=MN8TOARS.
10.1111/j.1365-2796.2004.01421.x
- Vieira, J.M.; Rosa Santos, S.C.; Espadinha, C.; Correia, I.; Vag, T.; Casalou, C.; Cavaco, B.M.; et al. "Expression of vascular
endothelial growth factor (VEGF) and its receptors in thyroid carcinomas of follicular origin: A potential autocrine loop".
European Journal of Endocrinology 153 5 (2005): 701-709. http://www.scopus.com/inward/record.url?eid=2-s2.0-27944499811&partnerID=MN8TOARS.
10.1530/eje.1.02009
- Martins, C.; Cavaco, B.; Tonon, G.; Kaye, F.J.; Soares, J.; Fonseca, I.. "A study of MECT1-MAML2 in mucoepidermoid carcinoma
and Warthin's tumor of salivary glands". Journal of Molecular Diagnostics 6 3 (2004): 205-210. http://www.scopus.com/inward/record.url?eid=2-s2.0-4344671950&partnerID=MN8TOARS.
10.1016/S1525-1578(10)60511-9
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tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene". Journal of Clinical Endocrinology
and Metabolism 89 4 (2004): 1747-1752. http://www.scopus.com/inward/record.url?eid=2-s2.0-11144355570&partnerID=MN8TOARS.
10.1210/jc.2003-031016
- Cavaco, B.M.; Torrinha, F.; Mendonça, E.; Pratas, S.; Boavida, J.; Sobrinho, L.G.; Leite, V.. "Preoperative diagnosis of suspicious
parathyroid adenomas by RT-PCR using mRNA extracted from left-over cells in a needle used for ultrasonically guided fine needle
aspiration cytology". Acta Cytologica 47 1 (2003): 5-12. http://www.scopus.com/inward/record.url?eid=2-s2.0-0037267594&partnerID=MN8TOARS.
10.1159/000326468
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endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism". Clinical Endocrinology
58 5 (2003): 639-646. http://www.scopus.com/inward/record.url?eid=2-s2.0-0038332150&partnerID=MN8TOARS.
10.1046/j.1365-2265.2003.01765.x
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