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Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large Portuguese family

JAMA neurology, 2013-02, Vol.70 (2), p.235

2013

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BDNF and CGRP interaction: Implications in migraine susceptibility

Cephalalgia, 2010-11, Vol.30 (11), p.1375-1382

2010

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Familial Aggregation of Maxillary Lateral Incisor Agenesis

Journal of dental research, 2010-06, Vol.89 (6), p.621-625

2010

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The hidden story behind gender differences in familial amyloid polyneuropathy (FAP) ATTRV30M

Orphanet journal of rare diseases, 2015-11, Vol.10 (73), p.O4-O4

2015

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Familial amyloidotic polyneuropathy in Sweden: geographical distribution, age of onset, and prevalence

Human heredity, 1993-09, Vol.43 (5), p.288-294

1993

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C1 QA and C1 QC modify age‐at‐onset in familial amyloid polyneuropathy patients

Annals of clinical and translational neurology, 2019-04, Vol.6 (4), p.748-754

2019

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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

Journal of genetic counseling, 2009-10, Vol.18 (5), p.483-493

2009

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Insucesso escolar e auto-avaliação na adolescência

Psicologia (Lisbon, Portugal), 2014-08, Vol.5 (3), p.289

2014

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Familial amyloid polyneuropathy in Portugal: New genes modulating age‐at‐onset

Annals of clinical and translational neurology, 2017-02, Vol.4 (2), p.98-105

2017

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Familial Clustering of Migraine: Further Evidence From a Portuguese Study

Headache, 2009-03, Vol.49 (3), p.404-411

2009

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Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study

Clinical genetics, 1991-12, Vol.40 (6), p.452-460

1991

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Craniofacial repercussions in maxillary lateral incisors agenesis

International orthodontics, 2011-09, Vol.9 (3), p.274-285

2011

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Familial ATTR amyloidosis: microalbuminuria as a predictor of symptomatic disease and clinical nephropathy

Nephrology, dialysis, transplantation, 2003-03, Vol.18 (3), p.532-538

2003

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Interaction between gamma -Aminobutyric Acid A Receptor Genes: New Evidence in Migraine Susceptibility: e74087

PloS one, 2013-09, Vol.8 (9)

2013

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Inherited and acquired risk factors and their combined effects in pediatric stroke

Pediatric neurology, 2003-02, Vol.28 (2), p.134-138

2003

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Les répercussions craniofaciales dans l’agénésie des incisives latérales maxillaires

International orthodontics, 2011-09, Vol.9 (3), p.274-285

2011

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Population Genetics of Wild-Type CAG Repeats in the Machado-Joseph Disease Gene in Portugal

Human heredity, 2005-01, Vol.60 (3), p.156-163

2005

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The C677T polymorphism in MTHFR is not associated with migraine in Portugal

Disease markers, 2008, Vol.25 (2), p.107-113

2008

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End-stage renal disease and dialysis in hereditary amyloidosis TTR V30M: presentation, survival and prognostic factors

Amyloid, 2004-03, Vol.11 (1), p.27-37

2004

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Genetic models for variation of age at onset in familial amyloid polyneuropathy

Neuromuscular disorders : NMD, 1996-02, Vol.6, p.S41-S41

Sousa, Alda

1996

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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

Brazilian Journal of Health Review, 2022-04, Vol.5 (2), p.5661-5686

2022

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Synthesis, characterization, and structure of a new N-nitrosamine of cyclam (1,4,8,11-tetraazacyclotetradecane)

Tetrahedron letters, 2005-03, Vol.46 (11), p.1889-1891

2005

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Desenvolvimento de estimação de estados em tempo-real para a rede de distribuição

de Sousa, Alda Cristina Rodrigues

2011

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A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected

Journal of medical genetics, 1994-04, Vol.31 (4), p.293-299

1994

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Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice

European journal of human genetics : EJHG, 2003-11, Vol.11 (11), p.872-878

2003

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Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large Portuguese family

BDNF and CGRP interaction: Implications in migraine susceptibility

Familial Aggregation of Maxillary Lateral Incisor Agenesis

The hidden story behind gender differences in familial amyloid polyneuropathy (FAP) ATTRV30M

Familial amyloidotic polyneuropathy in Sweden: geographical distribution, age of onset, and prevalence

C1 QA and C1 QC modify age‐at‐onset in familial amyloid polyneuropathy patients

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

Insucesso escolar e auto-avaliação na adolescência

Familial amyloid polyneuropathy in Portugal: New genes modulating age‐at‐onset

Familial Clustering of Migraine: Further Evidence From a Portuguese Study

Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study

Craniofacial repercussions in maxillary lateral incisors agenesis

Familial ATTR amyloidosis: microalbuminuria as a predictor of symptomatic disease and clinical nephropathy

Interaction between gamma -Aminobutyric Acid A Receptor Genes: New Evidence in Migraine Susceptibility: e74087

Inherited and acquired risk factors and their combined effects in pediatric stroke

Les répercussions craniofaciales dans l’agénésie des incisives latérales maxillaires

Population Genetics of Wild-Type CAG Repeats in the Machado-Joseph Disease Gene in Portugal

The C677T polymorphism in MTHFR is not associated with migraine in Portugal

End-stage renal disease and dialysis in hereditary amyloidosis TTR V30M: presentation, survival and prognostic factors

Genetic models for variation of age at onset in familial amyloid polyneuropathy

Synthesis, characterization, and structure of a new N-nitrosamine of cyclam (1,4,8,11-tetraazacyclotetradecane)

Desenvolvimento de estimação de estados em tempo-real para a rede de distribuição

A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected

Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice

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