172 results on '"Sousa, Alda"'
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2. PSICOPEDAGOGIA CLÍNICA: A LUDICIDADE COMO ESTRATÉGIA PARA O DESENVOLVIMENTO INFANTIL
3. A review of migraine genetics: gathering genomic and transcriptomic factors
4. A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
5. A Trans-acting Factor May Modify Age at Onset in Familial Amyloid Polyneuropathy ATTRV30M in Portugal
6. Functional characterization of a novelPRRT2variant found in a Portuguese patient with hemiplegic migraine
7. O custo do leito UTI do paciente COVID-19 em unidades hospitalares de Minas Gerais: referências para avaliação do modelo de financiamento durante a Pandemia/ The cost of the ITU bed for the COVID-19 pacient in hospital units of Minas Gerais: references for assessing the financing model during the Pandemic
8. Functional characterization of a novel PRRT2 variant found in a Portuguese patient with hemiplegic migraine.
9. Les répercussions craniofaciales dans l’agénésie des incisives latérales maxillaires
10. Craniofacial repercussions in maxillary lateral incisors agenesis
11. A High Methylation Level of a Novel −284 bp CpG Island in the RAMP1 Gene Promoter Is Potentially Associated with Migraine in Women
12. A review of migraine genetics: gathering genomic and transcriptomic factors
13. 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
14. Overcoming artefact: anticipation in 284 Portuguese kindreds with familial amyloid polyneuropathy (FAP) ATTRV30M
15. Additional file 2 of A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
16. Additional file 1 of A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
17. Additional file 3 of A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
18. Psychological Follow-up of Presymptomatic Genetic Testing for Spinocerebellar Ataxia Type 2 (SCA2) in Cuba
19. The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutation
20. Cerebellar Ataxia, Hemiplegic Migraine, and Related Phenotypes Due to a CACNA1A Missense Mutation: 12-Year Follow-up of a Large Portuguese Family
21. Beyond Val30Met transthyretin (TTR): variants associated with age-at-onset in hereditary ATTRv amyloidosis
22. Genetic anticipation in Portuguese kindreds with familial amyloidotic polyneuropathy is unlikely to be caused by triplet repeat expansions
23. Going Deep into Synaptic Vesicle Machinery Genes and Migraine Susceptibility – A Case‐Control Association Study
24. Evidence of Syntaxin 1A Involvement in Migraine Susceptibility: A Portuguese Study
25. Familial Clustering of Migraine: Further Evidence From a Portuguese Study
26. Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease
27. Familial ATTR amyloidosis: microalbuminuria as a predictor of symptomatic disease and clinical nephropathy
28. Inherited and acquired risk factors and their combined effects in pediatric stroke
29. C1 QAandC1 QCmodify age‐at‐onset in familial amyloid polyneuropathy patients
30. Diferenças morfológicas no plexo pampiniforme e no mediastino testicular em touros Nelore e Canchim pré-púberes identificadas por ultrassonografia modo B.
31. Differences in testicular biometrics of prepubertal Nelore and Canchim bulls.
32. Large normal alleles of ATXN2 decrease age at onset in transthyretin familial amyloid polyneuropathy Val30Met patients
33. Genetic Study of Late-Onset in Hereditary Amyloid Neuropathy (HAN) — Type I (Portuguese, Andrade)
34. Is the Homozygous State for Hereditary Amyloid Neuropathy (HAN) — Type I (Portuguese, Andrade) Incompatible with Early Intrauterine Life?
35. mtDNA copy number associated with age of onset in familial amyloid polyneuropathy
36. A Trans-acting Factor May Modify Age at Onset in Familial Amyloid Polyneuropathy ATTRV30M in Portugal
37. C1QA and C1QC modify age‐at‐onset in familial amyloid polyneuropathy patients.
38. Familial amyloid polyneuropathy in Portugal: New genes modulating age‐at‐onset
39. mtDNA copy number associated with age of onset in familial amyloid polyneuropathy.
40. Soroepidemiologia da hepatite C em pacientes HIV/AIDS do serviço ambulatorial especializado do Programa DST/AIDS de Imperatriz-Maranhão
41. Variants in RBP4 and AR genes modulate age at onset in familial amyloid polyneuropathy (FAP ATTRV30M)
42. Desenvolvimento de estimação de estados em tempo-real para a rede de distribuição
43. Familial amyloid polyneuropathy in Portugal: New genes modulating age-at-onset.
44. Population genetics of wild-type CAG repeats in the Machado-Joseph disease gene in Portugal
45. The hidden story behind gender differences in familial amyloid polyneuropathy (FAP) ATTRV30M
46. Unravelling the epidemiology of late-onset and asymptomatic carriers of FAP ATTR V30M in a Portuguese population
47. Insucesso escolar e auto-avaliação na adolescência
48. Consumo de drogas ilícitas e factores de risco em adolescentes em meio escolar
49. Interaction between γ-Aminobutyric Acid A Receptor Genes: New Evidence in Migraine Susceptibility
50. Assessing Risk Factors for Migraine: Differences in Gender Transmission
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