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Results of search for 'au:"Marolda, M"', page 1 of 2
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Authors
Balbi, R
Barbieri, F
Bassi, A
Borgia, G
Buscaino, G A
Cafiero, L
Camporeale, F
Camporeale, F S
Carandente, M
Cioffi, M
Di Lorenzo, R
Esposito, V
Filla, A
Maiuri, F
Marolda, M
Nucciotti, R
Orsini, A V
Santoro, L
Scarafile, P
Zotti, G
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Child, Preschool
Electromyography
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Muscles
Muscular Diseases
Muscular Dystrophies
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Your search returned 21 results.
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1.
Congenital fiber type disproportion in two sisters. A clinical and histopathological study.
[electronic resource]
by
Marolda, M
Producer:
19930408
In:
Acta neurologica
vol. 14
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2.
Quadriceps myopathy. Study of a case with autosomic dominant transmission.
[electronic resource]
by
Marolda, M
Camporeale, F S
Producer:
19890606
In:
Acta neurologica
vol. 9
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3.
Clinical evaluation of (-)eburnamonine in comparison with nicergoline in patients suffering from chronic brain ischemia.
[electronic resource]
by
Marolda, M
Fragassi, N
Buscaino, G A
Producer:
19791017
In:
European neurology
vol. 17 Suppl 1
Online resources:
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4.
[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].
[electronic resource]
by
Marolda, M
Camporeale, F S
Sparaco, M
Producer:
19870114
In:
Rivista di neurologia
vol. 56
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5.
[The problem of Duchenne's muscular dystrophy in young girls. Apropos of a clinical case].
[electronic resource]
by
Buscaino, G A
Marolda, M
Cafiero, L
Borgia, G
Producer:
19811014
In:
Acta neurologica. Quaderni
vol. 42
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6.
[The problem of Duchenne's muscular dystrophy in young girls. Apropos of a case].
[electronic resource]
by
Buscaino, G A
Marolda, M
Cafiero, L
Borgia, G
Producer:
19810827
In:
Acta neurologica
vol. 3
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7.
Schwartz-Jampel syndrome. Report of a case.
[electronic resource]
by
Santoro, L
Marolda, M
Nucciotti, R
Camporeale, F
Marasco, E
Producer:
19840924
In:
Acta neurologica
vol. 6
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8.
Nucleotide sequence of a cDNA encoding mitochondrial malate dehydrogenase from Eucalyptus.
[electronic resource]
by
Poeydomenge, O
Marolda, M
Boudet, A M
Grima-Pettenati, J
Producer:
19950630
In:
Plant physiology
vol. 107
Online resources:
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9.
"Lipid storage myopathy" with muscle carnitine deficiency only.
[electronic resource]
by
Buscaino, G A
Marolda, M
Borgia, A
Cocchiararo, M
Scarafile, P
Producer:
19820814
In:
Acta neurologica
vol. 4
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10.
Isolation and sequence analysis of Clpg1, a gene coding for an endopolygalacturonase of the phytopathogenic fungus Colletotrichum lindemuthianum.
[electronic resource]
by
Centis, S
Dumas, B
Fournier, J
Marolda, M
Esquerré-Tugayé, M T
Producer:
19960620
In:
Gene
vol. 170
Online resources:
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11.
"Central core" and "multicore" disease. Clinical, histochemical and ultrastructural study of two cases with unusual hereditary transmission.
[electronic resource]
by
Marolda, M
Filla, A
Pellegrini, G
Esposito, V
Maiuri, F
Zotti, G
Producer:
19860312
In:
Acta neurologica
vol. 7
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12.
Ophthalmoplegia plus with late onset. Histochemical, ultrastructural, metabolic and electrophysiopathological study of a case.
[electronic resource]
by
Marolda, M
Peretti, A
Esposito, V
Maiuri, F
Scarafile, P
Camporeale, F S
Producer:
19841115
In:
Acta neurologica
vol. 6
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13.
[Apropos of a case of myopathy with histologic and electrophysiologic findings of both a myogenic and neurogenic nature].
[electronic resource]
by
Marolda, M
Nucciotti, R
Camporeale, F S
Simeone, A
Di Lorenzo, R
Delehaye, L
Producer:
19831123
In:
Rivista di neurologia
vol. 53
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14.
Myotonic dystrophy and pilomatricomas: an unusual association.
[electronic resource]
by
Filla, A
Perretti, A
Barbieri, F
Marolda, M
Pelosi, L
Delfino, M
Corona, M
Producer:
19821021
In:
Acta neurologica
vol. 4
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15.
A case of "centronuclear myopathy" with late clinical onset. Clinical electrophysiological, histochemical study.
[electronic resource]
by
Marolda, M
Camporeale, F
Santoro, L
Signorelli, C
Di Lorenzo, R
Zotti, G
Barbieri, F
Producer:
19840424
In:
Acta neurologica
vol. 5
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16.
Steroid myopathy: clinical and immunohistochemical study of a case.
[electronic resource]
by
Marolda, M
Palma, V
Camporeale, F S
Carandente, M
Cioffi, M
Orsini, A V
Gentile, A
Producer:
19920401
In:
Italian journal of neurological sciences
vol. 12
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17.
Diagnostic significance of Pacinian corpuscle degeneration in Friedreich's ataxia.
[electronic resource]
by
Marolda, M
Filla, A
Giordano-Lanza, G
Passeretti, U
Serino, L
Campanella, G
Buscaino, G A
Producer:
19810327
In:
Acta neurologica
vol. 2
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18.
[Sanfilippo's disease: clinico-genetic and biological study of 2 families].
[electronic resource]
by
Carlomagno, S
Federico, A
Vitiello, F
Pinto, L
Vertucci, P
Marolda, M
Balbi, R
Guazzi, G C
Producer:
19750115
In:
Acta neurologica
vol. 29
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19.
A case of facio-scapulo-humero-peroneal myopathy with inflammatory changes. Preliminary data on distribution of mononuclear cells in muscle tissue.
[electronic resource]
by
Marolda, M
Camporeale, F S
Orsini, A V
Cioffi, M
Ricci, M
De Mattia, G
Buscaino, G A
Producer:
19920508
In:
Italian journal of neurological sciences
vol. 13
Online resources:
Available from publisher's website
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20.
Myopathy associated with AIDS.
[electronic resource]
by
Marolda, M
De Mercato, R
Camporeale, F S
Carandente, M
Noce, S
Cioffi, M
Orsini, A V
Cauli, M
Bassi, A
Producer:
19891107
In:
Italian journal of neurological sciences
vol. 10
Online resources:
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