Detalhe da pesquisa
1.
Spectrum of Disease in Hospitalized Newborns with Congenital Micrognathia: A Cohort of 3,236 Infants at North American Tertiary-Care Intensive Care Units.
J Pediatr
; 265: 113799, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37879601
2.
Genomic Contributors to Esophageal Atresia and Tracheoesophageal Fistula: A 12 Year Retrospective Review.
J Pediatr
; 271: 114060, 2024 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38641166
3.
Expansion of the prenatal phenotype of Baraitser-Winter syndrome: Presentation of two cases of multiple congenital anomaly syndrome.
Am J Med Genet A
; : e63719, 2024 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38789278
4.
Delivery Room Resuscitation of Infants with Congenital Diaphragmatic Hernia: Lessons Learned through Video Review.
Fetal Diagn Ther
; 2024 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38531327
5.
The Delivery Room Resuscitation of Infants with Congenital Diaphragmatic Hernia Treated with Fetoscopic Endoluminal Tracheal Occlusion: Beyond the Balloon.
Fetal Diagn Ther
; 51(2): 184-190, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38198774
6.
Update on Management and Outcomes of Congenital Diaphragmatic Hernia.
J Intensive Care Med
; : 8850666231212874, 2023 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37933125
7.
The Genomics of Congenital Diaphragmatic Hernia: A 10-Year Retrospective Review.
J Pediatr
; 248: 108-113.e2, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35430246
8.
Current Practices for Genetic Testing in Neonatal Extracorporeal Membrane Oxygenation: Findings from a National survey.
Perfusion
; : 2676591221130178, 2022 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36169593
9.
Hyperinsulinism in an individual with an EP300 variant of Rubinstein-Taybi syndrome.
Am J Med Genet A
; 185(4): 1251-1255, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33442921
10.
Broadening the phenotypic spectrum of Pearson syndrome: Five new cases and a review of the literature.
Am J Med Genet A
; 182(2): 365-373, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31825167
11.
Congenital diaphragmatic hernia as a prominent feature of a SPECC1L-related syndrome.
Am J Med Genet A
; 182(12): 2919-2925, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32954677
12.
Reconsidering ECMO in Premature Neonates.
Fetal Diagn Ther
; 47(12): 927-932, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32871582
13.
Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases.
J Pediatr
; 246: 251-265.e2, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35314152
14.
50 Years Ago in TheJournalofPediatrics: Molecular Diagnostics Determine Underlying Genetic Etiologies for Well-Described Clinical Syndromes.
J Pediatr
; 239: 49, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34794643
15.
Randomized Controlled Trials of Pulmonary Vasodilator Therapy Adjunctive to Inhaled Nitric Oxide for Persistent Pulmonary Hypertension of the Newborn: A Systematic Review.
Clin Perinatol
; 51(1): 253-269, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38325945
16.
Neonatal Thrombocytopenia as a Presenting Finding in de novo Pyruvate Kinase Deficiency.
Neonatology
; 120(5): 661-665, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37473739
17.
Respiratory function after birth in infants with congenital diaphragmatic hernia.
Arch Dis Child Fetal Neonatal Ed
; 108(5): 535-539, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36400455
18.
Expanding neonatal ECMO criteria: When is the premature neonate too premature.
Semin Fetal Neonatal Med
; 27(6): 101403, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36435713
19.
Achieving adequate growth in infants with congenital diaphragmatic hernia prior to discharge.
J Pediatr Surg
; 56(12): 2200-2206, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33888352
20.
Effect of Whole-Genome Sequencing on the Clinical Management of Acutely Ill Infants With Suspected Genetic Disease: A Randomized Clinical Trial.
JAMA Pediatr
; 175(12): 1218-1226, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34570182