Di Battista E - Search Results

1

Gigantism with pituitary macroadenoma: an unusual variant of McCune-Albright syndrome.

Queirolo S, Gallarotti F, Capuano E, Garrè ML, Spaziante R, Di Battista E. Queirolo S, et al. Among authors: di battista e. J Pediatr Endocrinol Metab. 2009 Feb;22(2):177-9. doi: 10.1515/jpem.2009.22.2.177. J Pediatr Endocrinol Metab. 2009. PMID: 19449675 No abstract available.

2

Endocrine and growth features in childhood craniopharyngioma: a mono-institutional study.

Di Battista E, Naselli A, Queirolo S, Gallarotti F, Garré ML, Milanaccio C, Cama A. Di Battista E, et al. J Pediatr Endocrinol Metab. 2006 Apr;19 Suppl 1:431-7. J Pediatr Endocrinol Metab. 2006. PMID: 16700321

3

Genetic abnormalities and CNS tumors: report of two cases of ependymoma associated with Klinefelter's Syndrome (KS).

Garrè ML, Capra V, Di Battista E, Giampietri L, Nozza P, Raso A, Pezzolo A, Rossi A, Milanaccio C, Pavanello M, Naselli A. Garrè ML, et al. Among authors: di battista e. Childs Nerv Syst. 2007 Feb;23(2):219-23. doi: 10.1007/s00381-006-0179-3. Epub 2006 Oct 13. Childs Nerv Syst. 2007. PMID: 17058088

4

Parental origin of Gsalpha mutations in the McCune-Albright syndrome and in isolated endocrine tumors.

Mantovani G, Bondioni S, Lania AG, Corbetta S, de Sanctis L, Cappa M, Di Battista E, Chanson P, Beck-Peccoz P, Spada A. Mantovani G, et al. Among authors: di battista e. J Clin Endocrinol Metab. 2004 Jun;89(6):3007-9. doi: 10.1210/jc.2004-0194. J Clin Endocrinol Metab. 2004. PMID: 15181091

5

Unresolved problems in optimal therapy of pubertal disorders in oncological and bone marrow transplanted patients.

Bozzola M, Albanese A, Butler GE, Cherubini V, Cicognani A, Caruso-Nicoletti M, Crowne E, De Sanctis V, Di Battista E, Hokken-Koelega AC, Severi F, Wonke B, Cavallo L; International Workshop on Management of Puberty for Optimum Auxological Results. Bozzola M, et al. Among authors: di battista e. J Pediatr Endocrinol Metab. 2001 Jul;14 Suppl 2:997-1002. doi: 10.1515/jpem-2001-s212. J Pediatr Endocrinol Metab. 2001. PMID: 11529406 Review.

6

Long-term follow-up of skeletal dysplasia in thalassaemia major.

Naselli A, Vignolo M, Di Battista E, Garzia P, Forni GL, Traverso T, Aicardi G. Naselli A, et al. Among authors: di battista e. J Pediatr Endocrinol Metab. 1998;11 Suppl 3:817-25. J Pediatr Endocrinol Metab. 1998. PMID: 10091152

7

Turner's syndrome.

Guarneri MP, Abusrewil SA, Bernasconi S, Bona G, Cavallo L, Cicognani A, Di Battista E, Salvatoni A; International Workshop on Management of Puberty for Optimum Auxological Results. Guarneri MP, et al. Among authors: di battista e. J Pediatr Endocrinol Metab. 2001 Jul;14 Suppl 2:959-65. J Pediatr Endocrinol Metab. 2001. PMID: 11529402 Review.

8

Trichorhinophalangeal syndrome type I in monozygotic twins discordant for hip pathology. Report on the morphological evolution of cone-shaped epiphyses and the unusual pattern of skeletal maturation.

Naselli A, Vignolo M, Di Battista E, Papale V, Aicardi G, Becchetti S, Tomà P. Naselli A, et al. Among authors: di battista e. Pediatr Radiol. 1998 Nov;28(11):851-5. doi: 10.1007/s002470050481. Pediatr Radiol. 1998. PMID: 9799317 Review.

9

Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1.

Capra V, Severino M, Rossi A, Nozza P, Doneda C, Perri K, Pavanello M, Fiorio P, Gimelli G, Tassano E, Di Battista E. Capra V, et al. Among authors: di battista e. Am J Med Genet A. 2014 Feb;164A(2):495-9. doi: 10.1002/ajmg.a.36283. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311370

10

Blood cell mitochondrial DNA content and premature ovarian aging.

Bonomi M, Somigliana E, Cacciatore C, Busnelli M, Rossetti R, Bonetti S, Paffoni A, Mari D, Ragni G, Persani L; Italian Network for the study of Ovarian Dysfunctions. Bonomi M, et al. PLoS One. 2012;7(8):e42423. doi: 10.1371/journal.pone.0042423. Epub 2012 Aug 3. PLoS One. 2012. PMID: 22879975 Free PMC article.

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