Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 4
1978 2
1980 3
1981 2
1988 1
1989 1
1990 1
1991 1
1992 2
1993 1
1995 2
1996 1
1998 2
2000 2
2001 2
2002 1
2003 1
2005 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

30 results

Results by year

Filters applied: . Clear all
Page 1
Neurological presentations of mitochondrial diseases.
Zeviani M, Bertagnolio B, Uziel G. Zeviani M, et al. Among authors: bertagnolio b. J Inherit Metab Dis. 1996;19(4):504-20. doi: 10.1007/BF01799111. J Inherit Metab Dis. 1996. PMID: 8884574 Review.
Renal pathological changes in Fabry disease.
Sessa A, Meroni M, Battini G, Maglio A, Brambilla PL, Bertella M, Nebuloni M, Pallotti F, Giordano F, Bertagnolio B, Tosoni A. Sessa A, et al. Among authors: bertagnolio b. J Inherit Metab Dis. 2001;24 Suppl 2:66-70; discussion 65. doi: 10.1023/a:1012423924648. J Inherit Metab Dis. 2001. PMID: 11758681 Review.
[Metabolic myopathies].
Finocchiaro G, Zeviani M, Garavaglia B, Gellera C, Bertagnolio B, Rimoldi M, Di Donato S. Finocchiaro G, et al. Among authors: bertagnolio b. Minerva Pediatr. 1991 Mar;43(3):81-9. Minerva Pediatr. 1991. PMID: 1870530 Italian. No abstract available.
Heterogeneity of carnitine-palmitoyltransferase deficiency.
Di Donato S, Castiglione A, Rimoldi M, Cornelio F, Vendemia F, Cardace G, Bertagnolio B. Di Donato S, et al. Among authors: bertagnolio b. J Neurol Sci. 1981 May;50(2):207-15. doi: 10.1016/0022-510x(81)90167-2. J Neurol Sci. 1981. PMID: 7229666
'Atypical' clinical variants of Anderson-Fabry disease.
Sessa A, Meroni M, Battini G, Amato M, Righetti M, Bertella M, Brambilla P, Bertagnolio B. Sessa A, et al. Among authors: bertagnolio b. Nephron. 2001 Dec;89(4):469-70. doi: 10.1159/000046124. Nephron. 2001. PMID: 11721170 No abstract available.
Renal transplantation in patients with Fabry disease.
Sessa A, Meroni M, Battini G, Maglio A, Nebuloni M, Tosoni A, Panichi V, Bertagnolio B. Sessa A, et al. Among authors: bertagnolio b. Nephron. 2002 Jun;91(2):348-51. doi: 10.1159/000058419. Nephron. 2002. PMID: 12053080
Reconstitution of lymphocyte subpopulations in children with inherited metabolic storage diseases after haematopoietic cell transplantation.
Corti P, Peters C, Balduzzi A, Bertagnolio B, Biondi A, Bugarin C, Dassi M, Furlan F, Gaipa G, Longoni D, Maglia O, Parini R, Perseghin P, Uderzo C, Uziel G, Masera G, Rovelli A. Corti P, et al. Among authors: bertagnolio b. Br J Haematol. 2005 Jul;130(2):249-55. doi: 10.1111/j.1365-2141.2005.05585.x. Br J Haematol. 2005. PMID: 16029453 Free article.
MR imaging and proton MR spectroscopy in adult Krabbe disease.
Farina L, Bizzi A, Finocchiaro G, Pareyson D, Sghirlanzoni A, Bertagnolio B, Savoiardo M, Naidu S, Singhal BS, Wenger DA. Farina L, et al. Among authors: bertagnolio b. AJNR Am J Neuroradiol. 2000 Sep;21(8):1478-82. AJNR Am J Neuroradiol. 2000. PMID: 11003282 Free PMC article.
30 results