Roberto Della Casa
Roberto Della Casa
Ricercatore di Pediatria, UniversitÓ Federico II, Napoli
Verified email at unina.it
Title
Cited by
Cited by
Year
Genotype/phenotype correlation in glycogen storage disease type 1b: a multicentre study and review of the literature
D Melis, R Fulceri, G Parenti, P Marcolongo, R Gatti, R Parini, E Riva, ...
European journal of pediatrics 164 (8), 501-508, 2005
802005
Long-term enzyme replacement therapy for pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cells
M Rossi, G Parenti, R Della Casa, A Romano, G Mansi, T Agovino, ...
Journal of child neurology 22 (5), 565-573, 2007
702007
Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C
S Fecarotta, A Romano, R Della Casa, E Del Giudice, D Bruschini, ...
Orphanet journal of rare diseases 10 (1), 1-11, 2015
552015
Brain damage in glycogen storage disease type I
D Melis, G Parenti, R Della Casa, M Sibilio, A Romano, F Di Salle, ...
The Journal of pediatrics 144 (5), 637-642, 2004
542004
A chaperone enhances blood α-glucosidase activity in Pompe disease patients treated with enzyme replacement therapy
G Parenti, S Fecarotta, G La Marca, B Rossi, S Ascione, MA Donati, ...
Molecular Therapy 22 (11), 2004-2012, 2014
502014
The videofluoroscopic swallowing study shows a sustained improvement of dysphagia in children with Niemann–Pick disease type C after therapy with miglustat
S Fecarotta, M Amitrano, A Romano, R Della Casa, D Bruschini, L Astarita, ...
American Journal of Medical Genetics Part A 155 (3), 540-547, 2011
492011
Crohn's‐like ileo‐colitis in patients affected by glycogen storage disease Ib: two years’ follow‐up of patients with a wide spectrum of gastrointestinal signs
D Melis, G Parenti, RD Casa, M Sibilio, RB Canani, G Terrin, S Cucchiara, ...
Acta Paediatrica 92 (12), 1415-1421, 2003
462003
APECED: a paradigm of complex interactions between genetic background and susceptibility factors
L De Martino, D Capalbo, N Improda, F D'Elia, R Di Mase, R D’Assante, ...
Frontiers in immunology 4, 331, 2013
452013
HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis‐like presentation
S Fecarotta, G Parenti, P Vajro, A Zuppaldi, RD Casa, MT Carbone, ...
Journal of Inherited Metabolic Disease: Official Journal of the Society forá…, 2006
452006
Multisystem involvement in congenital insensitivity to pain with anhidrosis (CIPA), a nerve growth factor receptor (Trk A)‐related disorder
E Toscano, R Della Casa, S Mardy, L Gaetaniello, F Sadile, Y Indo, ...
Journal of the Peripheral Nervous System 5 (4), 243-243, 2000
442000
Increased prevalence of thyroid autoimmunity and hypothyroidism in patients with glycogen storage disease type I
D Melis, R Pivonello, G Parenti, R Della Casa, M Salerno, G Lombardi, ...
The Journal of pediatrics 150 (3), 300-305. e1, 2007
422007
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy
R Parini, P De Lorenzo, A Dardis, A Burlina, A Cassio, P Cavarzere, ...
Orphanet journal of rare diseases 13 (1), 1-12, 2018
412018
Management of otolaryngological manifestations in mucopolysaccharidoses: our experience
M Mesolella, M Cimmino, E Cantone, A Marino, M Cozzolino, ...
Acta Otorhinolaryngologica Italica 33 (4), 267, 2013
342013
Efficacy of ACE‐inhibitor therapy on renal disease in glycogen storage disease type 1: a multicentre retrospective study
D Melis, G Parenti, R Gatti, RD Casa, R Parini, E Riva, AB Burlina, CD Vici, ...
Clinical endocrinology 63 (1), 19-25, 2005
322005
Long-term follow-up of patients with phenylketonuria treated with tetrahydrobiopterin: a seven years experience
I Scala, D Concolino, R Della Casa, A Nastasi, C Ungaro, S Paladino, ...
Orphanet journal of rare diseases 10 (1), 1-12, 2015
282015
Vitamin D status in patients affected by Smith-Lemli-Opitz syndrome
M Rossi, G Federico, G Corso, G Parenti, A Battagliese, AR Frascogna, ...
Journal of inherited metabolic disease 28 (1), 69-80, 2005
262005
Vitamin E supplementation improves neutropenia and reduces the frequency of infections in patients with glycogen storage disease type 1b
D Melis, R Della Casa, R Parini, M Rigoldi, C Cacciapuoti, P Marcolongo, ...
European journal of pediatrics 168 (9), 1069-1074, 2009
232009
Muscle MRI of classic infantile pompe patients: Fatty substitution and edema‐like changes
A Pichiecchio, M Rossi, C Cinnante, GS Colafati, R De Icco, R Parini, ...
Muscle & nerve 55 (6), 841-848, 2017
172017
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22
D Melis, R Genesio, G Cappuccio, V MariaGinocchio, RD Casa, G Menna, ...
American Journal of Medical Genetics Part A 155 (7), 1697-1705, 2011
172011
Impaired bone metabolism in glycogen storage disease type 1 is associated with poor metabolic control in type 1a and with granulocyte colony-stimulating factor therapy in type 1b
D Melis, R Pivonello, M Cozzolino, R Della Casa, F Balivo, A Del Puente, ...
Hormone research in paediatrics 81 (1), 55-62, 2014
152014
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