Danesino C - Search Results

1

Guala A, Folgori G, Silvestri M, Barbaglia M, Danesino C. Guala A, et al. Among authors: danesino c. Case Rep Pediatr. 2022 Dec 6;2022:3171351. doi: 10.1155/2022/3171351. eCollection 2022. Case Rep Pediatr. 2022. PMID: 36524152 Free PMC article.

2

Familial clustering of unexplained transient respiratory distress in 12 newborns from three unrelated families suggests an autosomal-recessive inheritance.

Guala A, Carrera P, Pastore G, Somaschini M, Ancora G, Faldella G, De Filippi P, Ferrero F, Guarino R, Danesino C. Guala A, et al. Among authors: danesino c. ScientificWorldJournal. 2007 Sep 28;7:1611-6. doi: 10.1100/tsw.2007.252. ScientificWorldJournal. 2007. PMID: 17906824 Free PMC article.

3

Cutaneous metaplastic synovial cyst in Ehlers-Danlos syndrome: report of a second case.

Guala A, Viglio S, Ottinetti A, Angeli G, Canova G, Colombo E, Dardano F, Danesino C, Valli M. Guala A, et al. Among authors: danesino c. Am J Dermatopathol. 2008 Feb;30(1):59-61. doi: 10.1097/DAD.0b013e31815b9c82. Am J Dermatopathol. 2008. PMID: 18212547

4

Deletion of PAX9 and oligodontia: a third family and review of the literature.

Guala A, Falco V, Breedveld G, De Filippi P, Danesino C. Guala A, et al. Among authors: danesino c. Int J Paediatr Dent. 2008 Nov;18(6):441-5. doi: 10.1111/j.1365-263X.2008.00915.x. Epub 2008 Apr 28. Int J Paediatr Dent. 2008. PMID: 18445003 Review.

5

Duplication of the pituitary stalk in a patient with a heterozygous deletion of chromosome 14 harboring the thyroid transcription factor-1 gene.

Accornero S, Danesino C, Bastianello S, D'Errico I, Guala A, Chiovato L. Accornero S, et al. Among authors: danesino c. J Clin Endocrinol Metab. 2010 Aug;95(8):3595-6. doi: 10.1210/jc.2010-0621. J Clin Endocrinol Metab. 2010. PMID: 20685887

6

Advanced magnetic resonance imaging in benign hereditary chorea: study of two familial cases.

Maccabelli G, Pichiecchio A, Guala A, Ponzio M, Palesi F, Maranzana Rt D, Poloni GU, Bastianello S, Danesino C. Maccabelli G, et al. Among authors: danesino c. Mov Disord. 2010 Nov 15;25(15):2670-4. doi: 10.1002/mds.23281. Mov Disord. 2010. PMID: 20803509

7

Association of iniencephaly, anencephaly, and fusion of cervical vertebral bodies: a new autosomal recessive syndrome?

Guala A, Massa P, Foscolo AM, Olivero F, Van Maldergem L, Danesino C. Guala A, et al. Among authors: danesino c. Clin Dysmorphol. 2013 Jan;22(1):29-32. doi: 10.1097/MCD.0b013e3283590b04. Clin Dysmorphol. 2013. PMID: 23011585 No abstract available.

8

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. Among authors: danesino c. 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.

9

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. Among authors: danesino c. 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.

10

Psychomotor Development in Cri du Chat Syndrome: Comparison in Two Italian Cohorts with Different Rehabilitation Methods.

Guala A, Spunton M, Tognon F, Pedrinazzi M, Medolago L, Cerutti Mainardi P, Spairani S, Malacarne M, Finale E, Comelli M, Danesino C. Guala A, et al. Among authors: danesino c. ScientificWorldJournal. 2016;2016:3125283. doi: 10.1155/2016/3125283. Epub 2016 Nov 28. ScientificWorldJournal. 2016. PMID: 28004033 Free PMC article.

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