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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1957 | 1 |
2005 | 1 |
2011 | 1 |
2015 | 1 |
2017 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
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7 results
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Page 1
Immune responses to alglucosidase in infantile Pompe disease: recommendations from an Italian pediatric expert panel.
Ital J Pediatr. 2022 Mar 5;48(1):41. doi: 10.1186/s13052-022-01219-4.
Ital J Pediatr. 2022.
PMID: 35248118
Free PMC article.
Review.
Nationwide survey on the management of pediatric pharyngitis in Italian emergency units.
Milani GP, Rosa C, Tuzger N, Alberti I, Ghizzi C, Zampogna S, Amigoni A, Agostoni C, Peroni D, Marchisio P, Chiappini E; IPSE study group.
Milani GP, et al.
Ital J Pediatr. 2023 Sep 5;49(1):114. doi: 10.1186/s13052-023-01514-8.
Ital J Pediatr. 2023.
PMID: 37670391
Free PMC article.
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Muscle MRI of classic infantile pompe patients: Fatty substitution and edema-like changes.
Pichiecchio A, Rossi M, Cinnante C, Colafati GS, De Icco R, Parini R, Menni F, Furlan F, Burlina A, Sacchini M, Donati MA, Fecarotta S, Casa RD, Deodato F, Taurisano R, Di Rocco M.
Pichiecchio A, et al. Among authors: casa rd.
Muscle Nerve. 2017 Jun;55(6):841-848. doi: 10.1002/mus.25417. Epub 2017 Feb 9.
Muscle Nerve. 2017.
PMID: 27668838
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Glycogen storage disease type Ia (GSDIa) but not Glycogen storage disease type Ib (GSDIb) is associated to an increased risk of metabolic syndrome: possible role of microsomal glucose 6-phosphate accumulation.
Melis D, Rossi A, Pivonello R, Salerno M, Balivo F, Spadarella S, Muscogiuri G, Casa RD, Formisano P, Andria G, Colao A, Parenti G.
Melis D, et al. Among authors: casa rd.
Orphanet J Rare Dis. 2015 Jul 29;10:91. doi: 10.1186/s13023-015-0301-2.
Orphanet J Rare Dis. 2015.
PMID: 26219379
Free PMC article.
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Efficacy of ACE-inhibitor therapy on renal disease in glycogen storage disease type 1: a multicentre retrospective study.
Melis D, Parenti G, Gatti R, Casa RD, Parini R, Riva E, Burlina AB, Dionisi Vici C, Di Rocco M, Furlan F, Torcoletti M, Papadia F, Donati A, Benigno V, Andria G.
Melis D, et al. Among authors: casa rd.
Clin Endocrinol (Oxf). 2005 Jul;63(1):19-25. doi: 10.1111/j.1365-2265.2005.02292.x.
Clin Endocrinol (Oxf). 2005.
PMID: 15963056
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Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22.
Melis D, Genesio R, Cappuccio G, MariaGinocchio V, Casa RD, Menna G, Buffardi S, Poggi V, Leszle A, Imperati F, Carella M, Izzo A, Del Giudice E, Nitsch L, Andria G.
Melis D, et al. Among authors: casa rd.
Am J Med Genet A. 2011 Jul;155A(7):1697-705. doi: 10.1002/ajmg.a.33976. Epub 2011 Jun 10.
Am J Med Genet A. 2011.
PMID: 21671372
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[Muscular & hepatic biopsies in the diagnosis of visceral glycogenosis].
CASA RD.
CASA RD.
Arch Ital Pediatr Pueric. 1957;18(5):335-41.
Arch Ital Pediatr Pueric. 1957.
PMID: 13479233
Italian.
No abstract available.
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