| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies
|
Siciliano, G.
|
|
2000
|
21 |
3 |
p. S985-S987
|
artikel
|
| 2 |
A case of Cogan's syndrome
|
Maalikjy Akkawi, N.
|
|
2000
|
21 |
3 |
p. 183-184
|
artikel
|
| 3 |
Age-dependent neurologic manifestations of HIV infection in childhood
|
Angelini, L.
|
|
2000
|
21 |
3 |
p. 135-142
|
artikel
|
| 4 |
Another case of reversibility of visual-field defect induced by vigabatrin monotherapy: is young age a favorable factor?
|
Giordano, L.
|
|
2000
|
21 |
3 |
p. 185-186
|
artikel
|
| 5 |
A novel mtDNA mutation in the ATPase6 gene studied by E. coli modeling
|
Carrozzo, R.
|
|
2000
|
21 |
3 |
p. S983-S984
|
artikel
|
| 6 |
Cavernous angiomas of the nervous system in Italy: clinical and genetic study
|
Squitieri, F.
|
|
2000
|
21 |
3 |
p. 129-134
|
artikel
|
| 7 |
Clinical and neuroradiological aspects of Sneddon's syndrome and primary antiphospholipid antibody syndrome. A follow-up study
|
Fetoni, V.
|
|
2000
|
21 |
3 |
p. 157-164
|
artikel
|
| 8 |
Correlation of clinical function and muscle CT scan images in limb-girdle muscular dystrophy
|
Vlak, M.
|
|
2000
|
21 |
3 |
p. S975-S977
|
artikel
|
| 9 |
Cytogenetic damage in peripheral lymphocytes of mitochondrial disease patients
|
Naccarati, A.
|
|
2000
|
21 |
3 |
p. S963-S965
|
artikel
|
| 10 |
Familial paroxysmal exercise-induced dyskinesia and benign epilepsy: a clinical and neurophysiological study of an uncommon disorder
|
Margari, L.
|
|
2000
|
21 |
3 |
p. 165-172
|
artikel
|
| 11 |
Gene transfer in skeletal muscle by systemic injection of DODAC lipopolyplexes
|
Pampinella, F.
|
|
2000
|
21 |
3 |
p. S967-S969
|
artikel
|
| 12 |
Long-term treatment with idebenone and riboflavin in a patient with MELAS
|
Napolitano, A.
|
|
2000
|
21 |
3 |
p. S981
|
artikel
|
| 13 |
Mitochondrial encephalomyopathies: therapeutic approaches
|
DiMauro, S.
|
|
2000
|
21 |
3 |
p. S901-S908
|
artikel
|
| 14 |
Molecular basis for treatment in motor neurone disease
|
Anneser, J.
|
|
2000
|
21 |
3 |
p. S913-S918
|
artikel
|
| 15 |
Molecular basis for treatment of mitochondrial myopathies
|
Taylor, R.W.
|
|
2000
|
21 |
3 |
p. S909-S912
|
artikel
|
| 16 |
New therapies in muscular dystrophies
|
Angelini, C.
|
|
2000
|
21 |
3 |
p. S919-S924
|
artikel
|
| 17 |
Parkinsonism in a patient with AIDS and cerebral opportunistic granulomatous lesions
|
Maggi, P.
|
|
2000
|
21 |
3 |
p. 173-176
|
artikel
|
| 18 |
Potential involvement of ubiquinone in myotonic dystrophy pathophysiology: new diagnostic approaches for new rationale therapeutics
|
Tedeschi, D.
|
|
2000
|
21 |
3 |
p. S979-S980
|
artikel
|
| 19 |
Quantitative myotonia assessment: an experimental protocol
|
Sansone, V.
|
|
2000
|
21 |
3 |
p. S971-S974
|
artikel
|
| 20 |
Regenerative capacity of human satellite cells: the mitotic clock in cell transplantation
|
Di Donna, S.
|
|
2000
|
21 |
3 |
p. S943-S951
|
artikel
|
| 21 |
Respiratory weakness in neuralgic amyotrophy: report of two cases with phrenic nerve involvement
|
Nardone, R.
|
|
2000
|
21 |
3 |
p. 177-181
|
artikel
|
| 22 |
Retroviral vectors for gene therapy of Duchenne muscular dystrophy
|
Fassati, A.
|
|
2000
|
21 |
3 |
p. S925-S927
|
artikel
|
| 23 |
Structural comparison of actin binding in utrophin and dystrophin
|
Keep, N. H.
|
|
2000
|
21 |
3 |
p. S929-S937
|
artikel
|
| 24 |
The current status of myoblast transfer
|
Patridge, T.
|
|
2000
|
21 |
3 |
p. S939-S942
|
artikel
|
| 25 |
The natural course of acalculia in left-brain-damaged patients
|
Caporali, A.
|
|
2000
|
21 |
3 |
p. 143-149
|
artikel
|
| 26 |
Therapy in myotonic disorders and in muscle channelopathies
|
Meola, G.
|
|
2000
|
21 |
3 |
p. S953-S961
|
artikel
|
| 27 |
Venous angiomas and epilepsy
|
Striano, S.
|
|
2000
|
21 |
3 |
p. 151-155
|
artikel
|
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