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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 2 |
2012 | 1 |
2018 | 1 |
2020 | 2 |
2022 | 1 |
2024 | 0 |
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Page 1
Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National Experience.
Int J Neonatal Screen. 2022 Aug 9;8(3):47. doi: 10.3390/ijns8030047.
Int J Neonatal Screen. 2022.
PMID: 35997437
Free PMC article.
Mutations in the GLA Gene and LysoGb3: Is It Really Anderson-Fabry Disease?
Duro G, Zizzo C, Cammarata G, Burlina A, Burlina A, Polo G, Scalia S, Oliveri R, Sciarrino S, Francofonte D, Alessandro R, Pisani A, Palladino G, Napoletano R, Tenuta M, Masarone D, Limongelli G, Riccio E, Frustaci A, Chimenti C, Ferri C, Pieruzzi F, Pieroni M, Spada M, Castana C, Caserta M, Monte I, Rodolico MS, Feriozzi S, Battaglia Y, Amico L, Losi MA, Autore C, Lombardi M, Zoccali C, Testa A, Postorino M, Mignani R, Zachara E, Giordano A, Colomba P.
Duro G, et al. Among authors: castana c.
Int J Mol Sci. 2018 Nov 23;19(12):3726. doi: 10.3390/ijms19123726.
Int J Mol Sci. 2018.
PMID: 30477121
Free PMC article.
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Next generation sequencing panel in undifferentiated autoinflammatory diseases identifies patients with colchicine-responder recurrent fevers.
Papa R, Rusmini M, Volpi S, Caorsi R, Picco P, Grossi A, Caroli F, Bovis F, Musso V, Obici L, Castana C, Ravelli A, Van Gijn ME, Ceccherini I, Gattorno M.
Papa R, et al. Among authors: castana c.
Rheumatology (Oxford). 2020 Feb 1;59(2):344-360. doi: 10.1093/rheumatology/kez270.
Rheumatology (Oxford). 2020.
PMID: 31325311
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Next generation sequencing panel in undifferentiated autoinflammatory diseases identifies patients with colchicine-responder recurrent fevers.
Papa R, Rusmini M, Volpi S, Caorsi R, Picco P, Grossi A, Caroli F, Bovis F, Musso V, Obici L, Castana C, Ravelli A, Van Gijn ME, Ceccherini I, Gattorno M.
Papa R, et al. Among authors: castana c.
Rheumatology (Oxford). 2020 Feb 1;59(2):458. doi: 10.1093/rheumatology/kez376.
Rheumatology (Oxford). 2020.
PMID: 31410474
No abstract available.
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Ketogenic diet in early myoclonic encephalopathy due to non ketotic hyperglycinemia.
Cusmai R, Martinelli D, Moavero R, Dionisi Vici C, Vigevano F, Castana C, Elia M, Bernabei S, Bevivino E.
Cusmai R, et al. Among authors: castana c.
Eur J Paediatr Neurol. 2012 Sep;16(5):509-13. doi: 10.1016/j.ejpn.2011.12.015. Epub 2012 Jan 18.
Eur J Paediatr Neurol. 2012.
PMID: 22261077
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Clinical manifestations and management of four children with Pearson syndrome.
Tumino M, Meli C, Farruggia P, La Spina M, Faraci M, Castana C, Di Raimondo V, Alfano M, Pittalà A, Lo Nigro L, Russo G, Di Cataldo A.
Tumino M, et al. Among authors: castana c.
Am J Med Genet A. 2011 Dec;155A(12):3063-6. doi: 10.1002/ajmg.a.34288. Epub 2011 Oct 19.
Am J Med Genet A. 2011.
PMID: 22012855
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Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1.
Ferreira M, Torraco A, Rizza T, Fattori F, Meschini MC, Castana C, Go NE, Nargang FE, Duarte M, Piemonte F, Dionisi-Vici C, Videira A, Vilarinho L, Santorelli FM, Carrozzo R, Bertini E.
Ferreira M, et al. Among authors: castana c.
Neurogenetics. 2011 Feb;12(1):9-17. doi: 10.1007/s10048-010-0265-2. Epub 2011 Jan 4.
Neurogenetics. 2011.
PMID: 21203893
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