Guala A - Search Results

1

A Psychometric Tool for a Virtual Reality Rehabilitation Approach for Dyslexia.

Pedroli E, Padula P, Guala A, Meardi MT, Riva G, Albani G. Pedroli E, et al. Among authors: guala a. Comput Math Methods Med. 2017;2017:7048676. doi: 10.1155/2017/7048676. Epub 2017 Feb 13. Comput Math Methods Med. 2017. PMID: 28286543 Free PMC article.

2

¹⁸F-FDG PET Identifies Altered Brain Metabolism in Patients with Cri du Chat Syndrome.

Cistaro A, Quartuccio N, Piccardo A, Fania P, Spunton M, Liava A, Danesino C, Albani G, Guala A. Cistaro A, et al. Among authors: guala a. J Nucl Med. 2020 Aug;61(8):1195-1199. doi: 10.2967/jnumed.119.236893. Epub 2019 Dec 13. J Nucl Med. 2020. PMID: 31836684 Free article. Clinical Trial.

3

18F-FDG PET brain findings in disease-discordant monozygotic mosaic twins with Cri du Chat (5p-) syndrome.

Cistaro A, Schiera IG, Fania P, Tognon F, Liava A, Danesino C, Albani G, Guala A, Vogrig A, Quartuccio N. Cistaro A, et al. Among authors: guala a. Neurocase. 2021 Jun;27(3):319-322. doi: 10.1080/13554794.2021.1957118. Epub 2021 Aug 2. Neurocase. 2021. PMID: 34338587

4

Skin picking disorder in 97 Italian and Spanish Cri du chat patients.

Spunton M, Guala A, Liverani ME, Medolago L, Tognon F, Casado F, Del Valle M, Porras J, Larrea I, Porta G, Albani G, Nevado J, Danesino C. Spunton M, et al. Among authors: guala a. Am J Med Genet A. 2019 Aug;179(8):1525-1530. doi: 10.1002/ajmg.a.61259. Epub 2019 Jun 12. Am J Med Genet A. 2019. PMID: 31187941

5

Anesthesia in Cri du Chat syndrome: Information on 51 Italian patients.

Guala A, Spunton M, Mainardi PC, Emmig U, Acucella G, Danesino C. Guala A, et al. Am J Med Genet A. 2015 May;167A(5):1168-70. doi: 10.1002/ajmg.a.36992. Epub 2015 Mar 28. Am J Med Genet A. 2015. PMID: 25820652 No abstract available.

6

Neoplasia in Cri du Chat Syndrome from Italian and German Databases.

Guala A, Spunton M, Kalantari S, Kennerknecht I, Danesino C. Guala A, et al. Case Rep Genet. 2017;2017:5181624. doi: 10.1155/2017/5181624. Epub 2017 Apr 24. Case Rep Genet. 2017. PMID: 28523196 Free PMC article.

7

Maternal germinal mosaicism for SCN1A in sibs with a mild form of Dravet syndrome.

Guala A, Peruzzi C, Gennaro E, Pennese L, Danesino C. Guala A, et al. Am J Med Genet A. 2015 May;167A(5):1165-7. doi: 10.1002/ajmg.a.36990. Am J Med Genet A. 2015. PMID: 25885068 No abstract available.

8

Children and adults affected by Cri du Chat syndrome: Care's recommendations.

Liverani ME, Spano A, Danesino C, Malacarne M, Cavani S, Spunton M, Guala A. Liverani ME, et al. Among authors: guala a. Pediatr Rep. 2019 Feb 26;11(1):7839. doi: 10.4081/pr.2019.7839. eCollection 2019 Feb 26. Pediatr Rep. 2019. PMID: 30838120 Free PMC article.

9

[The Cri du Chat syndrome: a study on the quality of care].

Cerruti Mainardi P, Spunton M, Arcuri V, Pastore G, Pedrinazzi M, Nardi S, Castronovo C, Alessi D, Guala A. Cerruti Mainardi P, et al. Among authors: guala a. Minerva Pediatr. 2012 Aug;64(4):395-400. Minerva Pediatr. 2012. PMID: 22728611 Italian.

10

Ring chromosome 13 with loss of the region D13S317-D13S285: phenotypic overlap with XK syndrome.

Guala A, Dellavecchia C, Mannarino S, Rognone F, Giglio S, Minelli A, Danesino C. Guala A, et al. Am J Med Genet. 1997 Oct 31;72(3):319-23. Am J Med Genet. 1997. PMID: 9332662 Review.

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