Perri A - Search Results

1

Response to long-term growth hormone therapy in patients affected by RASopathies and growth hormone deficiency: Patterns of growth, puberty and final height data.

Tamburrino F, Gibertoni D, Rossi C, Scarano E, Perri A, Montanari F, Fantini MP, Pession A, Tartaglia M, Mazzanti L. Tamburrino F, et al. Among authors: perri a. Am J Med Genet A. 2015 Nov;167A(11):2786-94. doi: 10.1002/ajmg.a.37260. Epub 2015 Jul 31. Am J Med Genet A. 2015. PMID: 26227443

2

Pelvic ultrasonography in patients with Turner syndrome: age-related findings in different karyotypes.

Mazzanti L, Cacciari E, Bergamaschi R, Tassinari D, Magnani C, Perri A, Scarano E, Pluchinotta V. Mazzanti L, et al. Among authors: perri a. J Pediatr. 1997 Jul;131(1 Pt 1):135-40. doi: 10.1016/s0022-3476(97)70137-9. J Pediatr. 1997. PMID: 9255205

3

Barber-Say Syndrome: report of a new case.

Mazzanti L, Bergamaschi R, Neri I, Perri A, Patrizi A, Cacciari E, Forabosco A. Mazzanti L, et al. Among authors: perri a. Am J Med Genet. 1998 Jun 30;78(2):188-91. Am J Med Genet. 1998. PMID: 9674915

4

Turner's syndrome: cardiologic profile according to the different chromosomal patterns and long-term clinical follow-Up of 136 nonpreselected patients.

Prandstraller D, Mazzanti L, Picchio FM, Magnani C, Bergamaschi R, Perri A, Tsingos E, Cacciari E. Prandstraller D, et al. Among authors: perri a. Pediatr Cardiol. 1999 Mar-Apr;20(2):108-12. doi: 10.1007/s002469900416. Pediatr Cardiol. 1999. PMID: 9986886

5

Reduced spontaneous growth hormone secretion in patients with Turner's syndrome.

Pirazzoli P, Mazzanti L, Bergamaschi R, Perri A, Scarano E, Nanni S, Zucchini S, Gualandi S, Cicognani A, Cacciari E. Pirazzoli P, et al. Among authors: perri a. Acta Paediatr. 1999 Jun;88(6):610-3. doi: 10.1080/08035259950169242. Acta Paediatr. 1999. PMID: 10419243

6

Turner syndrome strategies to improve care outcomes--cardiac evaluation using new imaging techniques.

Mazzanti L, Lovato L, Prandstraller D, Scarano E, Tamburrino F, Montanari F, Mineo GG, Perri A, Vestrucci B, Giardini A. Mazzanti L, et al. Among authors: perri a. Pediatr Endocrinol Rev. 2012 May;9 Suppl 2:701-9. Pediatr Endocrinol Rev. 2012. PMID: 22946280

7

GH Therapy and first final height data in Noonan-like syndrome with loose anagen hair (Mazzanti syndrome).

Mazzanti L, Tamburrino F, Scarano E, Perri A, Vestrucci B, Guidetti M, Rossi C, Tartaglia M. Mazzanti L, et al. Among authors: perri a. Am J Med Genet A. 2013 Nov;161A(11):2756-61. doi: 10.1002/ajmg.a.36255. Epub 2013 Oct 3. Am J Med Genet A. 2013. PMID: 24124081

8

New insights on diabetes in Turner syndrome: results from an observational study in adulthood.

Ibarra-Gasparini D, Altieri P, Scarano E, Perri A, Morselli-Labate AM, Pagotto U, Mazzanti L, Pasquali R, Gambineri A. Ibarra-Gasparini D, et al. Among authors: perri a. Endocrine. 2018 Mar;59(3):651-660. doi: 10.1007/s12020-017-1336-z. Epub 2017 Jun 7. Endocrine. 2018. PMID: 28593616

9

HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype.

Severi G, Bonora E, Perri A, Scarano E, Mazzanti L, Isidori F, Zuntini R, Menabò S, Graziano C. Severi G, et al. Among authors: perri a. Cytogenet Genome Res. 2019;157(3):135-140. doi: 10.1159/000499174. Epub 2018 Mar 26. Cytogenet Genome Res. 2019. PMID: 30933954

10

Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disorders.

Magini P, Scarano E, Donati I, Sensi A, Mazzanti L, Perri A, Tamburrino F, Mongelli P, Percesepe A, Visconti P, Parmeggiani A, Seri M, Graziano C. Magini P, et al. Among authors: perri a. Gene. 2019 Jul 20;706:162-171. doi: 10.1016/j.gene.2019.05.007. Epub 2019 May 11. Gene. 2019. PMID: 31085274

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