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Petillo, Roberta
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1

Comprehensive Molecular Analysis of Disease-Related Genes a..:

Fioretti, Tiziana ; Martora, Fabrizio ; De Maggio, Ilaria...
Biomedicines.  12 (2024)  5 - p. 1112 , 2024
Link: https://doi.org/10.3390/..
 
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2

Interatrial block as a first clinical presentation of atria..:

Iavarone, Michele ; Covino, Simona ; Petillo, Roberta...
European Heart Journal - Case Reports.  7 (2023)  12 - p. , 2023
Link: https://doi.org/10.1093/..
 
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3

De Novo Mutation in KMT2C Manifesting as Kleefstra Syndrome..:

Siano, Maria Anna ; De Maggio, Ilaria ; Petillo, Roberta...
Pediatric Reports.  14 (2022)  1 - p. 131-139 , 2022
Link: https://doi.org/10.3390/..
 
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4

The Role of TRPM4 Gene Mutations in Causing Familial Progre..:

Palladino, Alberto ; Papa, Andrea Antonio ; Petillo, Roberta...
Genes.  13 (2022)  2 - p. 258 , 2022
Link: https://doi.org/10.3390/..
 
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5

CLCN1 Molecular Characterization in 19 South-Italian Patien..:

Orsini, Chiara ; Petillo, Roberta ; D'Ambrosio, Paola...
Frontiers in Neurology.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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6

Digenic Inheritance of Shortened Repeat Units of the D4Z4 R..:

Cascella, Raffaella ; Strafella, Claudia ; Caputo, Valerio...
Frontiers in Neurology.  9 (2018)  - p. , 2018
Link: https://doi.org/10.3389/..
 
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7

Upper limb function in Duchenne muscular dystrophy: 24 mont..:

Pane, Marika ; Coratti, Giorgia ; Brogna, Claudia...
PLOS ONE.  13 (2018)  6 - p. e0199223 , 2018
Link: https://doi.org/10.1371/..
 
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8

Heart transplantation in patients with dystrophinopathic ca..:

Papa, Andrea Antonio ; D'Ambrosio, Paola ; Petillo, Roberta..
Intractable & Rare Diseases Research.  6 (2017)  2 - p. 95-101 , 2017
Link: https://doi.org/10.5582/..
 
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9

Brachydactyly type E in an Italian family with 6p25 trisomy:

Fontana, Paolo ; Tortora, Cristina ; Petillo, Roberta...
European Journal of Medical Genetics.  60 (2017)  3 - p. 195-199 , 2017
Link: https://doi.org/10.1016/..
 
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10

Diagnosis of Duchenne Muscular Dystrophy in Italy in the la..:

D'Amico, Adele ; Catteruccia, Michela ; Baranello, Giovanni...
Neuromuscular Disorders.  27 (2017)  5 - p. 447-451 , 2017
Link: https://doi.org/10.1016/..
 
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11

A novel 5q11.2 microdeletion in a child with mild developme..:

Fontana, Paolo ; Tortora, Cristina ; Petillo, Roberta...
American Journal of Medical Genetics Part A.  170 (2016)  9 - p. 2445-2448 , 2016
Link: https://doi.org/10.1002/..
 
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12

The genetic basis of undiagnosed muscular dystrophies and m..:

Savarese, Marco ; Di Fruscio, Giuseppina ; Torella, Annalaura...
Neurology.  87 (2016)  1 - p. 71-76 , 2016
Link: https://doi.org/10.1212/..
 
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13

Timed Rise from Floor as a Predictor of Disease Progression..:

Mazzone, Elena S. ; Coratti, Giorgia ; Sormani, Maria Pia...
PLOS ONE.  11 (2016)  3 - p. e0151445 , 2016
Link: https://doi.org/10.1371/..
 
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14

Prevalence of congenital muscular dystrophy in Italy: A pop..:

Graziano, Alessandra ; Bianco, Flaviana ; D'Amico, Adele...
Neurology.  84 (2015)  9 - p. 904-911 , 2015
Link: https://doi.org/10.1212/..
 
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15

Benefits of glucocorticoids in non-ambulant boys/men with D..:

Pane, Marika ; Fanelli, Lavinia ; Mazzone, Elena Stacy...
Neuromuscular Disorders.  25 (2015)  10 - p. 749-753 , 2015
Link: https://doi.org/10.1016/..
 
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