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

Year Number of Results
1970 4
1972 1
1975 1
1977 3
1978 1
1979 1
1981 2
1982 1
1983 1
1984 1
1990 1
1993 1
1995 1
1996 4
1997 2
1998 3
1999 1
2001 3
2002 2
2005 2
2006 2
2010 1
2011 1
2012 1
2020 2
2022 2
2023 1

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44 results

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Page 1
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, Balousha G, Benedicenti F, Birch D, Bitoun P, Blain D, Bocquet B, Branham K, Català-Mora J, De Baere E, Dollfus H, Falana M, Giorda R, Golovleva I, Gottlob I, Heckenlively JR, Jacobson SG, Jones K, Jägle H, Janecke AR, Kellner U, Liskova P, Lorenz B, Martorell-Sampol L, Messias A, Meunier I, Belga Ottoni Porto F, Papageorgiou E, Plomp AS, de Ravel TJL, Reiff CM, Renner AB, Rosenberg T, Rudolph G, Salati R, Sener EC, Sieving PA, Stanzial F, Traboulsi EI, Tsang SH, Varsanyi B, Weleber RG, Zobor D, Stingl K, Wissinger B, Kohl S. Solaki M, et al. Among authors: salati r. Hum Mutat. 2022 Jul;43(7):832-858. doi: 10.1002/humu.24371. Epub 2022 Apr 14. Hum Mutat. 2022. PMID: 35332618 Review.
Safety and efficacy of interferon γ in friedreich's ataxia.
Vavla M, D'Angelo MG, Arrigoni F, Toschi N, Peruzzo D, Gandossini S, Russo A, Diella E, Tirelli S, Salati R, Scarpazza P, Luffarelli R, Fortuni S, Rufini A, Condò I, Testi R, Martinuzzi A. Vavla M, et al. Among authors: salati r. Mov Disord. 2020 Feb;35(2):370-371. doi: 10.1002/mds.27979. Epub 2020 Jan 13. Mov Disord. 2020. PMID: 31930551 No abstract available.
[Metabolic problems in total parenteral feeding].
Salvioli G, Salati R, Lugli R, Fratalocchi A. Salvioli G, et al. Among authors: salati r. Recenti Prog Med. 1977 Oct;63(4):329-53. Recenti Prog Med. 1977. PMID: 413175 Review. Italian. No abstract available.
Cerebral visual impairment in periventricular leukomalacia.
Lanzi G, Fazzi E, Uggetti C, Cavallini A, Danova S, Egitto MG, Ginevra OF, Salati R, Bianchi PE. Lanzi G, et al. Among authors: salati r. Neuropediatrics. 1998 Jun;29(3):145-50. doi: 10.1055/s-2007-973551. Neuropediatrics. 1998. PMID: 9706625
CNGA3 mutations in hereditary cone photoreceptor disorders.
Wissinger B, Gamer D, Jägle H, Giorda R, Marx T, Mayer S, Tippmann S, Broghammer M, Jurklies B, Rosenberg T, Jacobson SG, Sener EC, Tatlipinar S, Hoyng CB, Castellan C, Bitoun P, Andreasson S, Rudolph G, Kellner U, Lorenz B, Wolff G, Verellen-Dumoulin C, Schwartz M, Cremers FP, Apfelstedt-Sylla E, Zrenner E, Salati R, Sharpe LT, Kohl S. Wissinger B, et al. Among authors: salati r. Am J Hum Genet. 2001 Oct;69(4):722-37. doi: 10.1086/323613. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11536077 Free PMC article.
44 results