Search Results - "Silva, L.H.L."

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotype

    SPG76: An extremely rare hereditary spastic paraplegia with a new expanding complicated phenotype by Souza, P.V.S., Silva, L.H.L., Badia, B.M.L., Farias, I.B., Pinto, W.B.V.R., Oliveira, A.S.B.

    Published in Revue neurologique (01-10-2019)
    Get full text
    Journal Article
    Save to List
    Saved in:
  2. 2
    Motor neuron disease with leukodystrophy due to CSF1R mutation

    Motor neuron disease with leukodystrophy due to CSF1R mutation by Souza, P.V.S., Badia, B.M.L., Silva, L.H.L., Farias, I.B., Pinto, W.B.V.R., Oliveira, A.S.B.

    Published in Revue neurologique (01-03-2020)
    Get full text
    Journal Article
    Save to List
    Saved in:
  3. 3
    Rapidly progressive bulbar-onset ALS due to SS18L1 mutation

    Rapidly progressive bulbar-onset ALS due to SS18L1 mutation by Pinto, W.B.V.R., Silva, L.H.L., Badia, B.M.L., Yanagiura, M.T., Souza, P.V.S., Oliveira, A.S.B.

    Published in Revue neurologique (01-03-2020)
    Get full text
    Journal Article
    Save to List
    Saved in:
  4. 4
    VASCULITE DE ARTÉRIA CEREBRAL MÉDIA ASSOCIADA A AFASIA GLOBAL SÚBITA COMO MANIFESTAÇÃO PRECOCE DO LÚPUS ERITEMATOSO SISTÊMICO: RELATO DE CASO

    VASCULITE DE ARTÉRIA CEREBRAL MÉDIA ASSOCIADA A AFASIA GLOBAL SÚBITA COMO MANIFESTAÇÃO PRECOCE DO LÚPUS ERITEMATOSO SISTÊMICO: RELATO DE CASO by Scherer, D., Silvatti, J., Silva, L.H.L., Neto, E.T.R.

    Get full text
    Journal Article
    Save to List
    Saved in:

Search Tools: