Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
N. Bresolin

Veröffentlichungen von N. Bresolin zu Bresolin, N. ->
weitere Veröffentlichungen von N. Bresolin:
Retroviral vectors for gene therapy of Duchenne muscular dystrophy (2000)
Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and platelets (1987)
Normal muscle mitochondrial function in Ramsay-Hunt syndrome (1989)
McArdle's disease: two clinical expressions in the same pedigree (1990)
CK-MM PGAM-MM G6PD and am biochemical markers of functional innervated cultured human muscle fibers (1991)
Clonal analysis and differentiative properties of adult human muscle cells (1986)
Clonal analysis and differentiative properties of adult human muscle cells (1986)
Muscle glucose-6-phosphate dehydrogenase deficiency (1989)
Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and31P-MR spectroscopy (1994)
Multiple sclerosis and mitochondrial myopathy: An unusual combination of diseases (1994)
A case of mitochondrial myopathy, lactic acidosis and complex I deficiency (1990)
Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency (1993)
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C (1995)
An atypical case of partial merosin deficiency congenital muscular dystrophy (1997)
A novel mitochondrial tRNAIle point mutation in chronic progressive external ophthalmoplegia (1998)
Veröffentlichungen zu Bresolin, N.
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Fassati, A., Bresolin, N. Retroviral vectors for gene therapy of Duchenne muscular dystrophy
in: Neurological sciences , ISSN 1590-3478, Vol. 21 (3. 2000), p. S925
Zugang: zum Volltext
ähnliche Vorschläge
2000
zeige Details
2
Meola, G., Bresolin, N., ... Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and platelets
in: Journal of neurology , ISSN 1432-1459, Vol. 235 (2. 1987), p. 74-79
Zugang: zum Volltext
ähnliche Vorschläge
1987
zeige Details
3
Sacquegna, T., Montagna, P., ... Normal muscle mitochondrial function in Ramsay-Hunt syndrome
in: Neurological sciences , ISSN 1590-3478, Vol. 10 (1. 1989), p. 73-75
Zugang: zum Volltext
ähnliche Vorschläge
1989
zeige Details
4
Papadimitriou, A., Manta, P., ... McArdle's disease: two clinical expressions in the same pedigree
in: Journal of neurology , ISSN 1432-1459, Vol. 237 (4. 1990), p. 267-270
Zugang: zum Volltext
ähnliche Vorschläge
1990
zeige Details
5
Meola, G, Velicogna, M, ... CK-MM PGAM-MM G6PD and am biochemical markers of functional innervated cultured human muscle fibers
in: Cytotechnology , ISSN 1573-0778, Vol. 5 (1. 1991), p. 176-177
Zugang: zum Volltext
ähnliche Vorschläge
1991
zeige Details
6
Meola, G., Velicogna, M., ... Clonal analysis and differentiative properties of adult human muscle cells
in: Cell Biology International Reports, in: Cell Biology International Reports . - Amsterdam : Elsevier, ISSN 0309-1651, ZDB-ID 2197149-3 Vol. 10, No. 3 (1986), p. 211
Zugang: zum Volltext
ähnliche Vorschläge
1986
zeige Details
7
Meola, G., Velicogna, M., ... Clonal analysis and differentiative properties of adult human muscle cells
in: Cell Biology International Reports, in: Cell Biology International Reports . - Amsterdam : Elsevier, ISSN 0309-1651, ZDB-ID 2197149-3 Vol. 10, No. 3 (1986), p. 211
Zugang: zum Volltext
ähnliche Vorschläge
1986
zeige Details
8
Bresolin, N., Bet, L., ... Muscle glucose-6-phosphate dehydrogenase deficiency
in: Journal of neurology , ISSN 1432-1459, Vol. 236 (4. 1989), p. 193-198
Zugang: zum Volltext
ähnliche Vorschläge
1989
zeige Details
9
Vita, G., Toscano, A., ... Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and31P-MR spectroscopy
in: Journal of neurology , ISSN 1432-1459, Vol. 241 (5. 1994), p. 289-294
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
10
Bet, L., Moggio, M., ... Multiple sclerosis and mitochondrial myopathy: An unusual combination of diseases
in: Journal of neurology , ISSN 1432-1459, Vol. 241 (8. 1994), p. 511-516
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
11
Bet, L., Bresolin, N., ... A case of mitochondrial myopathy, lactic acidosis and complex I deficiency
in: Journal of neurology , ISSN 1432-1459, Vol. 237 (7. 1990), p. 399-404
Zugang: zum Volltext
ähnliche Vorschläge
1990
zeige Details
12
Bresolin, N., Comi, G. P., ... Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency
in: Journal of neurology , ISSN 1432-1459, Vol. 240 (5. 1993), p. 272-277
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
13
Toscano, A., Fazio, M. C., ... Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C
in: Journal of neurology , ISSN 1432-1459, Vol. 242 (4. 1995), p. 203-209
Zugang: zum Volltext
ähnliche Vorschläge
1995
zeige Details
14
Prelle, A., Comi, G. P., ... An atypical case of partial merosin deficiency congenital muscular dystrophy
in: Journal of neurology , ISSN 1432-1459, Vol. 244 (6. 1997), p. 391-395
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
15
Franceschina, L., Salani, S., ... A novel mitochondrial tRNAIle point mutation in chronic progressive external ophthalmoplegia
in: Journal of neurology , ISSN 1432-1459, Vol. 245 (11. 1998), p. 755-758
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
16
Hadjigeorgiou, G. M., Comi, G. P., ... Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 22 (6. 1999), p. 762-763
Zugang: zum Volltext
ähnliche Vorschläge
1999
zeige Details
17
Harms, L., Bock, A., ... Fourth metting of the European Neurological Society 25–29 June 1994 Barcelona, Spain
in: Journal of neurology , ISSN 1432-1459, Vol. 241 (1. 1994), p. 1-164
Zugang: zum Volltext
ähnliche Vorschläge
1994