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M Marolda

Showing results (1-10 of 21) with videos related to

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Acta Neurologica|August 1, 1992
Congenital fiber type disproportion in two sisters. A clinical and histopathological studyM Marolda
Acta Neurologica|October 1, 1987
Quadriceps myopathy. Study of a case with autosomic dominant transmissionM Marolda, F S Camporeale
Rivista Di Neurologia|May 1, 1986
[Genetic, histochemical and ultrastructural study of a family with peculiar clinical expression of spinal muscular atrophy. Importance of biopsy examination in the detection of heterozygotes]M Marolda, F S Camporeale, M Sparaco
European Neurology|January 1, 1978
Clinical evaluation of (-)eburnamonine in comparison with nicergoline in patients suffering from chronic brain ischemiaM Marolda, N Fragassi, G A Buscaino
Acta Neurologica|February 1, 1981
[The problem of Duchenne's muscular dystrophy in young girls. Apropos of a case]G A Buscaino, M Marolda, L Cafiero, et al.
Acta Neurologica. Quaderni|January 1, 1981
[The problem of Duchenne's muscular dystrophy in young girls. Apropos of a clinical case]G A Buscaino, M Marolda, L Cafiero, et al.
Plant Physiology|April 1, 1995
Nucleotide sequence of a cDNA encoding mitochondrial malate dehydrogenase from EucalyptusO Poeydomenge, M Marolda, A M Boudet, et al.
Acta Neurologica|June 1, 1984
Schwartz-Jampel syndrome. Report of a caseL Santoro, M Marolda, R Nucciotti, et al.
Acta Neurologica|February 1, 1982
"Lipid storage myopathy" with muscle carnitine deficiency onlyG A Buscaino, M Marolda, A Borgia, et al.
Gene|April 17, 1996
Isolation and sequence analysis of Clpg1, a gene coding for an endopolygalacturonase of the phytopathogenic fungus Colletotrichum lindemuthianumS Centis, B Dumas, J Fournier, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Acta Neurologica|August 1, 1992
Congenital fiber type disproportion in two sisters. A clinical and histopathological studyM Marolda
Acta Neurologica|October 1, 1987
Quadriceps myopathy. Study of a case with autosomic dominant transmissionM Marolda, F S Camporeale
Rivista Di Neurologia|May 1, 1986
[Genetic, histochemical and ultrastructural study of a family with peculiar clinical expression of spinal muscular atrophy. Importance of biopsy examination in the detection of heterozygotes]M Marolda, F S Camporeale, M Sparaco
European Neurology|January 1, 1978
Clinical evaluation of (-)eburnamonine in comparison with nicergoline in patients suffering from chronic brain ischemiaM Marolda, N Fragassi, G A Buscaino
Acta Neurologica|February 1, 1981
[The problem of Duchenne's muscular dystrophy in young girls. Apropos of a case]G A Buscaino, M Marolda, L Cafiero, et al.
Acta Neurologica. Quaderni|January 1, 1981
[The problem of Duchenne's muscular dystrophy in young girls. Apropos of a clinical case]G A Buscaino, M Marolda, L Cafiero, et al.
Plant Physiology|April 1, 1995
Nucleotide sequence of a cDNA encoding mitochondrial malate dehydrogenase from EucalyptusO Poeydomenge, M Marolda, A M Boudet, et al.
Acta Neurologica|June 1, 1984
Schwartz-Jampel syndrome. Report of a caseL Santoro, M Marolda, R Nucciotti, et al.
Acta Neurologica|February 1, 1982
"Lipid storage myopathy" with muscle carnitine deficiency onlyG A Buscaino, M Marolda, A Borgia, et al.
Gene|April 17, 1996
Isolation and sequence analysis of Clpg1, a gene coding for an endopolygalacturonase of the phytopathogenic fungus Colletotrichum lindemuthianumS Centis, B Dumas, J Fournier, et al.
Pageof 3