I. Conceição

发表

A new method for reproducible coil positioning in transcranial magnetic stimulation mapping.

M. de Carvalho, P. Miranda, M. Luís, 1997, Electroencephalography and clinical neurophysiology.

A peripheral pathway to restless legs syndrome? Clues from familial amyloid polyneuropathy.

J. Ferreira, T. Teodoro, P. Viana, 2015, Parkinsonism & related disorders.

Motor neuropathies mimicking amyotrophic lateral sclerosis/motor neuron disease

M. Carvalho, M. Luís, A. Pinto, 1996, Journal of the Neurological Sciences.

Motor neuron disease in three asymptomatic pVal50Met TTR gene carriers

M. de Carvalho, M. Gromicho, A. Pronto-Laborinho, 2022, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Dominant and recessive RYR1 mutations in adults with core lesions and mild muscle symptoms

Jorge Oliveira, S. Duarte, T. Evangelista, 2011, Muscle & nerve.

Abrupt onset of progressive muscular atrophy

M. Carvalho, A. Pinto, T. Evangelista, 2004, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.

Peripheral nerve involvement in classic homocystinuria: an unusual association

R. Geraldes, I. Conceição, Miguel Oliveira Santos, 2016, BMJ Case Reports.

Clinical variability in type I familial amyloid polyneuropathy (Val30Met): Comparison between late‐ and early‐onset cases in Portugal

M. de Carvalho, I. Conceição, 2007, Muscle & nerve.

Neurophysiological techniques to detect early small‐fiber dysfunction in transthyretin amyloid polyneuropathy

M. Carvalho, João Costa, I. Conceição, 2014, Muscle & nerve.

Recovery after copper-deficiency myeloneuropathy in Wilson’s disease

J. Ferreira, T. Teodoro, M. Rosa, 2013, Journal of Neurology.

The diagnostic accuracy of Sudoscan in transthyretin familial amyloid polyneuropathy

M. Carvalho, B. Miranda, I. Conceição, 2016, Clinical Neurophysiology.

Neurophysiological markers in familial amyloid polyneuropathy patients: Early changes

M. Carvalho, M. Scotto, I. Conceição, 2008, Clinical Neurophysiology.

Repetitive nerve stimulation in myasthenia gravis—relative sensitivity of different muscles

M. Carvalho, T. Evangelista, João Costa, 2004, Clinical Neurophysiology.

Novel RNA-targeted therapies for hereditary ATTR amyloidosis and their impact on the autonomic nervous system

I. Conceição, 2019, Clinical Autonomic Research.

Acquired amyloid neuropathy in a Portuguese patient after domino liver transplantation

M. de Carvalho, T. Evangelista, P. Pereira, 2010, Muscle & nerve.

Severe limb-girdle muscular dystrophy 2A in two young siblings from Guinea-Bissau associated with a novel null homozygous mutation in CAPN3 gene

P. Ninitas, I. Conceição, M. O. Santos, 2018, Neuromuscular Disorders.

A Family With 2 Different Hereditary Diseases Leading to Early Cardiac Involvement

T. Evangelista, Rosário Santos, H. Nzwalo, 2013, Journal of clinical neuromuscular disease.

Very late-onset limb-girdle muscular dystrophy type 2D: A milder form with a normal muscle biopsy

Pedro Coelho, R. Roque, I. Conceição, 2019, Journal of Clinical Neuroscience.

Epileptic seizures as a presentation of central nervous system involvement in TTR Val30Met-FAP

M. Carvalho, J. Pimentel, C. Bentes, 2016, Journal of Neurology.

Mitochondrial Neurogastrointestinal Encephalomyopathy: Novel Pathogenic Mutation in Thymidine Phosphorylase Gene in a Patient from Cape Verde Islands

M. de Carvalho, R. Roque, I. Conceição, 2019, Case reports in neurological medicine.

Quantitative sensory testing: a good tool to identify subclinical neuropathy in ATTRV30M amyloidosis patients?

A. Diaz, I. Conceição, J. Castro, 2022, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Enzyme replacement therapy with alglucosidase alfa in a late-onset Pompe disease patient during pregnancy

T. Evangelista, I. Conceição, M. O. Santos, 2018, Neuromuscular Disorders.

Clinical and therapeutic implications of presymptomatic gene testing for familial amyloidotic polyneuropathy (FAP)

M. de Carvalho, I. Conceição, Maria de Lourdes Sales-Luís, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Clinical features of TTR-FAP in Portugal

I. Conceição, 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Correlation between Sudoscan and COMPASS 31: assessment of autonomic dysfunction on hATTR V30M patients

I. Conceição, J. Castro, Isabel de Castro, 2019, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Motor excitability measurements in early stage familial amyloid polyneuropathy: The influence of tafamidis treatment

M. Carvalho, A. Caetano, I. Conceição, 2020, Neurophysiologie clinique.

Changes in nerve conduction studies predate clinical symptoms onset in early onset Val30Met hereditary ATTR amyloidosis

I. Conceição, J. Castro, Isabel de Castro, 2021, European journal of neurology.

A peripheral pathway to restless legs syndrome? Clues from familial amyloid polyneuropathy.

J. Ferreira, T. Teodoro, P. Viana, 2015, Parkinsonism & related disorders.

Evidence for central abnormality in respiratory control in primary lateral sclerosis

M. de Carvalho, A. Atalaia, A. Pinto, 2006, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.