| human | Q5 |
| P7893 | CIÊNCIAVITAE ID | 2010-F622-BB71 |
| P496 | ORCID iD | 0000-0001-9803-9584 |
| P3829 | Publons author ID | 1185465 |
| P1053 | ResearcherID | J-4967-2013 |
| P1153 | Scopus author ID | 14021726700 |
| P69 | educated at | Faculty of Sciences of the University of Porto | Q10279390 |
| Instituto de Ciências Biomédicas Abel Salazar | Q62080174 | ||
| P108 | employer | Institute for Molecular and Cell Biology | Q10302765 |
| Instituto de Ciências Biomédicas Abel Salazar | Q62080174 | ||
| P734 | family name | Lemos | Q37232183 |
| Lemos | Q37232183 | ||
| Lemos | Q37232183 | ||
| P735 | given name | Carolina | Q5044762 |
| Carolina | Q5044762 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q48119093 | A Trans-acting Factor May Modify Age at Onset in Familial Amyloid Polyneuropathy ATTRV30M in Portugal. |
| Q54405607 | A role for endothelin receptor type A in migraine without aura susceptibility? A study in Portuguese patients. |
| Q34491551 | Assessing risk factors for migraine: differences in gender transmission |
| Q44354952 | BDNF and CGRP interaction: implications in migraine susceptibility. |
| Q63989031 | CD44v6 expression is a novel predictive marker of therapy response and poor prognosis in gastric cancer patients: |
| Q49955161 | Comparison between the Visual Analog Scale and the Numerical Rating Scale in the perception of esthetics and pain |
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| Q63436753 | Dental repercussions of maxillary lateral incisor agenesis |
| Q57949822 | Familial Clustering of Migraine: Further Evidence From a Portuguese Study |
| Q53097233 | Familial aggregation of cluster headache. |
| Q45066359 | Familial aggregation of maxillary lateral incisor agenesis |
| Q37620178 | Familial amyloid polyneuropathy in Portugal: New genes modulating age-at-onset |
| Q57949541 | Familial hemiplegic migraine due to L263V SCN1A mutation: Discordance for epilepsy between two kindreds from Douro Valley |
| Q51819010 | First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy. |
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| Q57949553 | Identification of Genetic Risk Factors for Maxillary Lateral Incisor Agenesis |
| Q44407986 | Impact of liver transplantation on the natural history of oculopathy in Portuguese patients with transthyretin (V30M) amyloidosis |
| Q34989746 | Interaction between γ-aminobutyric acid A receptor genes: new evidence in migraine susceptibility |
| Q45305559 | Intergenerational instability in Huntington disease: extreme repeat changes among 134 transmissions |
| Q36357240 | Ophthalmological manifestations in hereditary transthyretin (ATTR V30M) carriers: a review of 513 cases |
| Q43595662 | Overcoming artefact: anticipation in 284 Portuguese kindreds with familial amyloid polyneuropathy (FAP) ATTRV30M. |
| Q48412678 | Psychological follow-up of presymptomatic genetic testing for spinocerebellar ataxia type 2 (SCA2) in Cuba. |
| Q57949967 | Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine |
| Q57949853 | Role of the Disease in the Psychological Impact of Pre-Symptomatic Testing for SCA2 and FAP ATTRV30M: Experience with the Disease, Kinship and Gender of the Transmitting Parent |
| Q37307905 | The C677T polymorphism in MTHFR is not associated with migraine in Portugal. |
| Q51897049 | Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes. |
| Q37058522 | Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M) |
| Q64119031 | and modify age-at-onset in familial amyloid polyneuropathy patients |
| Q50091454 | mtDNA copy number associated with age of onset in familial amyloid polyneuropathy |
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