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Cosi, Alessandra
47  results:
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1

Pediatric Moyamoya Disease and Syndrome in Italy: A Multice..:

Po', Chiara ; Nosadini, Margherita ; Zedde, Marialuisa...
Frontiers in Pediatrics.  10 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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2

Le mycophénolate mofétil en traitement d'induction et trait..:

Rosati, Anna ; Cosi, Alessandra ; Basile, Massimo...
Revue du Rhumatisme.  85 (2018)  1 - p. 90-94 , 2018
Link: https://doi.org/10.1016/..
 
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3

Mycophenolate mofetil as induction and long-term maintainin..:

Rosati, Anna ; Cosi, Alessandra ; Basile, Massimo...
Joint Bone Spine.  84 (2017)  3 - p. 353-356 , 2017
Link: https://doi.org/10.1016/..
 
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4

Optic atrophy plus phenotype due to mutations in the OPA1 g..:

Ranieri, Michela ; Del Bo, Roberto ; Bordoni, Andreina...
Journal of the Neurological Sciences.  315 (2012)  1-2 - p. 146-149 , 2012
Link: https://doi.org/10.1016/..
 
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5

Clinical and molecular features of an infant patient affect..:

Ronchi, Dario ; Cosi, Alessandra ; Tonduti, Davide...
BMC Neurology.  11 (2011)  1 - p. , 2011
Link: https://doi.org/10.1186/..
 
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6

Unusual adult-onset Leigh syndrome presentation due to the ..:

Ronchi, Dario ; Bordoni, Andreina ; Cosi, Alessandra...
Biochemical and Biophysical Research Communications.  412 (2011)  2 - p. 245-248 , 2011
Link: https://doi.org/10.1016/..
 
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7

Two novel mutations in PEO1 (Twinkle) gene associated with ..:

Ronchi, Dario ; Fassone, Elisa ; Bordoni, Andreina...
Journal of the Neurological Sciences.  308 (2011)  1-2 - p. 173-176 , 2011
Link: https://doi.org/10.1016/..
 
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8

Pediatric Moyamoya Disease and Syndrome in Italy: A Multice..:

Po', Chiara ; Nosadini, Margherita ; Zedde, Marialuisa...
info:eu-repo/semantics/altIdentifier/pmid/35601411.  , 2022
Link: https://hdl.handle.net/1..
 
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9

Optic atrophy plus phenotype due to mutations in the OPA1 g..:

Ranieri, Michela ; Del Bo, Roberto ; Bordoni, Andreina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315002.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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10

The novel mitochondrial tRNAAsn gene mutation m.5709T>C pro..:

Ronchi, Dario ; Sciacco, Monica ; Bordoni, Andreina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283170.  , 2012
Link: http://www.ncbi.nlm.nih...
 
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11

Clinical and molecular features of an infant patient affect..:

Ronchi, Dario ; Cosi, Alessandra ; Tonduti, Davide...
http://www.biomedcentral.com/1471-2377/11/85.  , 2011
Link: http://www.biomedcentral..
 
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12

Clinical and molecular features of an infant patient affect..:

Moggio Maurizio ; Capovilla Giuseppe ; Cagdas Sophie...
http://www.biomedcentral.com/1471-2377/11/85.  , 2011
Link: https://doi.org/10.1186/..
 
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13

Two novel mutations in PEO1 (Twinkle) gene associated with ..:

Ronchi, Dario ; Fassone, Elisa ; Bordoni, Andreina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158327.  , 2011
Link: http://www.ncbi.nlm.nih...
 
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14

Pediatric Moyamoya Disease and Syndrome in Italy: A Multice..:

Chiara Po' ; Margherita Nosadini ; Marialuisa Zedde...
https://www.frontiersin.org/articles/10.3389/fped.2022.892445/full.  , 2022
Link: https://doi.org/10.3389/..
 
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15

Data_Sheet_1_Pediatric Moyamoya Disease and Syndrome in Ita..:

Chiara Po' ; Margherita Nosadini ; Marialuisa Zedde...
doi:10.3389/fped.2022.892445.s001.  , 2022
Link: https://doi.org/10.3389/..
 
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