Detalhe da pesquisa
1.
Role of Frailty on Risk Stratification in Cardiac Surgery and Procedures.
Adv Exp Med Biol
; 1216: 99-113, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31894551
2.
Cardiac surgery in the elderly: What goals of care?
Monaldi Arch Chest Dis
; 87(2): 852, 2017 07 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28967719
3.
Cytogenetic follow-up of chromosomal mosaicism detected in first-trimester prenatal diagnosis.
Prenat Diagn
; 34(8): 739-47, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24633594
4.
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.
PLoS Genet
; 7(7): e1002173, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21779178
5.
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA gene.
Am J Hum Genet
; 87(1): 146-53, 2010 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-20598277
6.
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria.
Am J Med Genet A
; 155A(7): 1536-45, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21671391
7.
Pre-operative physical performance as a predictor of in-hospital outcomes in older patients undergoing elective cardiac surgery.
Eur J Intern Med
; 84: 80-87, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33144037
8.
Acute heart failure in the elderly: setting related differences in clinical features and management.
J Geriatr Cardiol
; 18(6): 407-415, 2021 Jun 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34220970
9.
Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1).
Eur J Hum Genet
; 16(8): 897-905, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18301446
10.
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype.
Eur J Med Genet
; 48(4): 388-96, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16378923
11.
8q12 microduplication including CHD7: clinical report on a new patient with Duane retraction syndrome type 3.
Mol Cytogenet
; 6(1): 49, 2013 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24206642
12.
Nasal abnormalities in the 9p deletion syndrome.
Arch Otolaryngol Head Neck Surg
; 133(10): 1054-6, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17938332
13.
Evolutionary descent of a human chromosome 6 neocentromere: a jump back to 17 million years ago.
Genome Res
; 19(5): 778-84, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19411601
14.
Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion.
Eur J Hum Genet
; 17(4): 426-33, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18854866
15.
Terminal osseous dysplasia with pigmentary defects: clinical description of a new family.
Am J Med Genet A
; 143A(1): 51-7, 2007 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17152064
16.
Quality assessment in cytogenetic and molecular genetic testing: the experience of the Italian Project on Standardisation and Quality Assurance.
Clin Chem Lab Med
; 42(8): 915-21, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15387442