Battaglia A - Search Results

1

Del 1p36 syndrome: a newly emerging clinical entity.

Battaglia A. Battaglia A. Brain Dev. 2005 Aug;27(5):358-61. doi: 10.1016/j.braindev.2004.03.011. Brain Dev. 2005. PMID: 16023552 Review.

2

Natural history of Wolf-Hirschhorn syndrome: experience with 15 cases.

Battaglia A, Carey JC, Cederholm P, Viskochil DH, Brothman AR, Galasso C. Battaglia A, et al. Pediatrics. 1999 Apr;103(4 Pt 1):830-6. doi: 10.1542/peds.103.4.830. Pediatrics. 1999. PMID: 10103318

3

Wolf-Hirschhorn syndrome (WHS): a history in pictures.

Battaglia A, Carey JC, Viskochil DH, Cederholm P, Opitz JM. Battaglia A, et al. Clin Dysmorphol. 2000 Jan;9(1):25-30. doi: 10.1097/00019605-200009010-00005. Clin Dysmorphol. 2000. PMID: 10649793

4

del (9p) syndrome: proposed behavior phenotype.

Chilosi A, Battaglia A, Brizzolara D, Cipriani P, Pfanner L, Carey JC. Chilosi A, et al. Among authors: battaglia a. Am J Med Genet. 2001 Apr 22;100(2):138-44. doi: 10.1002/ajmg.1230. Am J Med Genet. 2001. PMID: 11298375

5

Wolf-Hirschhorn (4p-) syndrome.

Battaglia A, Carey JC, Wright TJ. Battaglia A, et al. Adv Pediatr. 2001;48:75-113. Adv Pediatr. 2001. PMID: 11480768 Review.

6

Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.

Battaglia A, Brothman AR, Carey JC. Battaglia A, et al. Am J Med Genet. 2002 Sep 15;112(1):103-6. doi: 10.1002/ajmg.10640. Am J Med Genet. 2002. PMID: 12239731

7

Characterization of the phenotype and definition of the deletion in a new patient with ring chromosome 22.

Battini R, Battaglia A, Bertini V, Cioni G, Parrini B, Rapalini E, Simi P, Tinelli F, Valetto A. Battini R, et al. Among authors: battaglia a. Am J Med Genet A. 2004 Oct 1;130A(2):196-9. doi: 10.1002/ajmg.a.30276. Am J Med Genet A. 2004. PMID: 15372517

8

Seizure and EEG patterns in Wolf-Hirschhorn (4p-) syndrome.

Battaglia A, Carey JC. Battaglia A, et al. Brain Dev. 2005 Aug;27(5):362-4. doi: 10.1016/j.braindev.2004.02.017. Epub 2005 Apr 22. Brain Dev. 2005. PMID: 16023553 Review.

9

The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.

Battaglia A. Battaglia A. Brain Dev. 2005 Aug;27(5):365-9. doi: 10.1016/j.braindev.2004.08.006. Epub 2005 Apr 22. Brain Dev. 2005. PMID: 16023554 Review.

10

Familial complex 3q;10q rearrangement unraveled by subtelomeric FISH analysis.

Battaglia A, Novelli A, Ceccarini C, Carey JC. Battaglia A, et al. Am J Med Genet A. 2006 Jan 15;140(2):144-50. doi: 10.1002/ajmg.a.31042. Am J Med Genet A. 2006. PMID: 16353244

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