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
2009 1
2010 2
2011 1
2012 1
2013 2
2014 6
2015 5
2016 11
2017 10
2018 9
2019 6
2020 7
2021 7
2022 5
2023 5
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

67 results

Results by year

Filters applied: . Clear all
Page 1
Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency.
Huemer M, Diodato D, Schwahn B, Schiff M, Bandeira A, Benoist JF, Burlina A, Cerone R, Couce ML, Garcia-Cazorla A, la Marca G, Pasquini E, Vilarinho L, Weisfeld-Adams JD, Kožich V, Blom H, Baumgartner MR, Dionisi-Vici C. Huemer M, et al. Among authors: diodato d. J Inherit Metab Dis. 2017 Jan;40(1):21-48. doi: 10.1007/s10545-016-9991-4. Epub 2016 Nov 30. J Inherit Metab Dis. 2017. PMID: 27905001 Free PMC article. Review.
The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.
Martinelli D, Diodato D, Ponzi E, Monné M, Boenzi S, Bertini E, Fiermonte G, Dionisi-Vici C. Martinelli D, et al. Among authors: diodato d. Orphanet J Rare Dis. 2015 Mar 11;10:29. doi: 10.1186/s13023-015-0242-9. Orphanet J Rare Dis. 2015. PMID: 25874378 Free PMC article. Review.
Biomarkers for mitochondrial energy metabolism diseases.
Boenzi S, Diodato D. Boenzi S, et al. Among authors: diodato d. Essays Biochem. 2018 Jul 20;62(3):443-454. doi: 10.1042/EBC20170111. Print 2018 Jul 20. Essays Biochem. 2018. PMID: 29980631 Review.
Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness.
Sinibaldi L, Garone G, Mandarino A, Iarossi G, Chioma L, Dentici ML, Merla G, Agolini E, Micalizzi A, Mancini C, Niceta M, Macchiaiolo M, Diodato D, Onesimo R, Blandino R, Delogu AB, De Rosa G, Trevisan V, Iademarco M, Zampino G, Tartaglia M, Novelli A, Bartuli A, Digilio MC, Calcagni G. Sinibaldi L, et al. Among authors: diodato d. Clin Genet. 2023 Nov;104(5):528-541. doi: 10.1111/cge.14404. Epub 2023 Jul 17. Clin Genet. 2023. PMID: 37455656
The new paradigm of economic complexity.
Balland PA, Broekel T, Diodato D, Giuliani E, Hausmann R, O'Clery N, Rigby D. Balland PA, et al. Among authors: diodato d. Res Policy. 2022 Apr;51(3):104450. doi: 10.1016/j.respol.2021.104450. Res Policy. 2022. PMID: 35370320 Free PMC article.
Vocal Cord Paralysis and Feeding Difficulties as Early Diagnostic Clues of Congenital Myasthenic Syndrome with Neonatal Onset: A Case Report and Review of Literature.
De Rose DU, Ronci S, Caoci S, Maddaloni C, Diodato D, Catteruccia M, Fattori F, Bosco L, Pro S, Savarese I, Bersani I, Randi F, Trozzi M, Meucci D, Calzolari F, Salvatori G, Solinas A, Dotta A, Campi F. De Rose DU, et al. Among authors: diodato d. J Pers Med. 2023 May 6;13(5):798. doi: 10.3390/jpm13050798. J Pers Med. 2023. PMID: 37240968 Free PMC article. Review.
The mitochondrial brain: From mitochondrial genome to neurodegeneration.
Turnbull HE, Lax NZ, Diodato D, Ansorge O, Turnbull DM. Turnbull HE, et al. Among authors: diodato d. Biochim Biophys Acta. 2010 Jan;1802(1):111-21. doi: 10.1016/j.bbadis.2009.07.010. Epub 2009 Aug 6. Biochim Biophys Acta. 2010. PMID: 19647794 Free PMC article. Review.
67 results