Concepedia

Author

Luís Negrão

Hospitais da Universidade de Coimbra

Also Known As

L Negrao, L Negrão, L. Negrao, L. Negrão, L.J. Negrão, L.J.M. Negrão, Luis Negrao, Luis Negrão, Luís Negrão, Negrao, L

73

Publications

668

Citations

14

H-Index

45

Concepts

All Affiliations

Hospitais da Universidade de CoimbraCentro Hospitalar do PortoUniversidade do PortoCentro de Genética ClínicaUniversity of Coimbra
LN

About

Luís Negrão is an author at Hospitais da Universidade de Coimbra specializing in medicine, pathogenesis, and rehabilitation.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

6

6

144

2

Health Sciences

2

2

37

3

Public Health

1

1

10

4

Epidemiology

1

1

19

5

Global Health

1

1

10

Luís Negrão

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14

Publications

471

Citations

13

H-Index

YearCitations

Atypical phenotypes in titinopathies explained by second titin mutations

Anni Evilä, Anna Vihola, J. Sarparanta,

Annals of Neurology

2014

91

Deposition and passage of transthyretin through the blood-nerve barrier in recipients of familial amyloid polyneuropathy livers

Mónica Mendes Sousa, José Ferrão, Rui Fernandes,

Laboratory Investigation

2004

64

Effect of the Combination of Uridine Nucleotides, Folic Acid and Vitamin B12 on the Clinical Expression of Peripheral Neuropathies

Luís Negrão, Pedro Almeida, Sérgio Alcino,

Pain Management

2014

47

Epidemiology of myasthenia gravis in Northern Portugal: Frequency estimates and clinical epidemiological distribution of cases

Ernestina Santos, Estér Coutinho, Isabel Moreira,

Muscle & Nerve

2016

45

New splicing mutation in the choline kinase beta (CHKB) gene causing a muscular dystrophy detected by whole-exome sequencing

Jorge Oliveira, Luís Negrão, Isabel Fineza,

Journal of Human Genetics

2015

43

Macrophagic myofasciitis and vaccination: Consequence or coincidence?

Tânia Santiago, Olinda Rebelo, Luís Negrão,

Rheumatology International

2014

30

Uridine Monophosphate, Folic Acid and Vitamin B <sub>12</sub> in Patients with Symptomatic Peripheral Entrapment Neuropathies

Luís Negrão

Pain Management

2015

25

Autosomal Recessive Axonal Neuropathy With Neuromyotonia: A Rare Entity

Joana Serra Caetano, Cármen Costa, Jonathan Baets,

Pediatric Neurology

2013

24

<i>SIGMAR1</i> gene mutation causing Distal Hereditary Motor Neuropathy in a Portuguese family.

Luciano Almendra, Francisco Laranjeira, Ana Fernández‐Marmiesse,

PubMed

2018

22

Tremor Frequency Assessment by iPhone® Applications: Correlation with EMG Analysis

Rui Araújo, Miguel Tábuas‐Pereira, Luciano Almendra,

Journal of Parkinson s Disease

2016

19

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