E-LIB Suche - Ergebnisse für: Di Blasi, Claudia

1

Hemodynamic profiles in treatment-naive arterial hypertensi..:

Glinz, Delphine ; Bläsi, Claudia ; Villiger, Andrea...
Journal of Hypertension. 39 (2020) 6 - p. 1246-1253 , 2020

Link: https://doi.org/10.1097/..

2

Variable disease severity in Saudi Arabian and Sudanese fam..:

Di Blasi, Claudia ; Bellafiore, Emanuela ; Salih, Mustafa AM...
BMC Research Notes. 4 (2011) 1 - p. , 2011

Link: https://doi.org/10.1186/..

3

Osteopontin is highly expressed in severely dystrophic musc..:

Zanotti, Simona ; Gibertini, Sara ; Di Blasi, Claudia...
Histopathology. 59 (2011) 6 - p. 1215-1228 , 2011

Link: https://doi.org/10.1111/..

4

Calsequestrin and junctin immunoreactivity in hexagonally c..:

Di Blasi, Claudia ; Blasevich, Flavia ; Bellafiore, Emanuela...
Neuromuscular Disorders. 20 (2010) 5 - p. 326-329 , 2010

Link: https://doi.org/10.1016/..

5

LAMA2 stop-codon mutation: Merosin-deficient congenital mus..:

Vigliano, Piernanda ; Dassi, Patrizia ; Blasi, Claudia Di..
European Journal of Paediatric Neurology. 13 (2009) 1 - p. 72-76 , 2009

Link: https://doi.org/10.1016/..

6

Danon disease: A novel LAMP2 mutation affecting the pre-mRN..:

Di Blasi, Claudia ; Jarre, Laura ; Blasevich, Flavia..
Neuromuscular Disorders. 18 (2008) 12 - p. 962-966 , 2008

Link: https://doi.org/10.1016/..

7

Severe Congenital Muscular Dystrophy in a LAMA2-Mutated Cas:

Di Blasi, Claudia ; van Alfen, Nens ; Colleoni, Francesca..
Pediatric Neurology. 37 (2007) 3 - p. 212-214 , 2007

Link: https://doi.org/10.1016/..

8

Decorin and biglycan expression is differentially altered i..:

Zanotti, Simona ; Negri, Tiziana ; Cappelletti, Cristina...
Brain. 128 (2005) 11 - p. 2546-2555 , 2005

Link: https://doi.org/10.1093/..

9

Abnormal lysosomal and ubiquitin‐proteasome pathways in 19p..:

Di Blasi, Claudia ; Moghadaszadeh, Behzad ; Ciano, Claudia...
Annals of Neurology. 56 (2004) 1 - p. 133-138 , 2004

Link: https://doi.org/10.1002/..

10

Partial laminin ?2 chain deficiency in a patient with myopa..:

Di Blasi, Claudia ; Mora, Marina ; Pareyson, Davide...
Annals of Neurology. 47 (2000) 6 - p. 811-816 , 2000

Link: https://doi.org/10.1002/..

11

Transforming growth factor-β1 and fibrosis in congenital mu..:

Bernasconi, Pia ; Di Blasi, Claudia ; Mora, Marina...
Neuromuscular Disorders. 9 (1999) 1 - p. 28-33 , 1999

Link: https://doi.org/10.1016/..

12

Concomitant deficiency of β- and γ-sarcoglycans in 20 α-sar..:

Barresi, Rita ; Confalonieri, Valeria ; Lanfossi, Massimo...
Acta Neuropathologica. 94 (1997) 1 - p. 28-35 , 1997

Link: https://doi.org/10.1007/..

13

Developmental expression of dystrophin, dystrophin-associat..:

Mora, Marina ; Di Blasi, Claudia ; Barresi, Rita...
Developmental Brain Research. 91 (1996) 1 - p. 70-82 , 1996

Link: https://doi.org/10.1016/..

14

Mild clinical phenotype in a 12-year-old boy with partial m..:

Mora, Marina ; Moroni, Isabella ; Uziel, Graziella...
Neuromuscular Disorders. 6 (1996) 5 - p. 377-381 , 1996

Link: https://doi.org/10.1016/..

15

Clinical heterogeneity of adhalin deficiency:

Morandi, Lucia ; Barresi, Rita ; Di Blasi, Claudia...
Annals of Neurology. 39 (1996) 2 - p. 196-202 , 1996

Link: https://doi.org/10.1002/..