Detalhe da pesquisa
1.
Pulmonary hypertension with bronchopulmonary dysplasia: Aichi cohort study.
Pediatr Int
; 64(1): e15271, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-35972055
2.
A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome.
J Pediatr Hematol Oncol
; 43(2): e250-e254, 2021 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32287101
3.
Prognostic factors of hydrops fetalis with pleural effusion.
Pediatr Int
; 59(10): 1053-1057, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28672054
4.
Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants.
Pediatr Int
; 58(6): 461-6, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26615960
5.
Risk factors for early death in transient myeloproliferative disorder without phenotypic features of Down syndrome: a case report and literature review.
J Pediatr Hematol Oncol
; 34(6): 475-9, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22510770
6.
Effects of exchange transfusion on cytokine profiles in necrotizing enterocolitis.
Pediatr Int
; 54(6): 931-3, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23279025
7.
A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondyly.
Am J Med Genet A
; 167A(11): 2851-4, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26126848
8.
Cytokine profiles before and after exchange transfusion in a neonate with transient myeloproliferative disorder and hepatic fibrosis.
J Pediatr Hematol Oncol
; 32(4): e164-6, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20445414
9.
Neonatal MRI in preterm infants with periventricular leukomalacia and mild disability.
Pediatr Int
; 51(6): 780-5, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19419519
10.
Echovirus Type 7 Virus-Associated Hemophagocytic Syndrome in a Neonate Successfully Treated With Intravenous Immunoglobulin Therapy: A Case Report.
Front Pediatr
; 7: 469, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31799224
11.
Natural histories of patients with Wolf-Hirschhorn syndrome derived from variable chromosomal abnormalities.
Congenit Anom (Kyoto)
; 59(5): 169-173, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30378700
12.
Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g.
Pediatr Neonatol
; 59(3): 274-280, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29030024
13.
Hypoxic ischemic encephalopathy in a case of intranuclear rod myopathy without any prenatal sentinel event.
Brain Dev
; 37(2): 265-9, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24787270
14.
Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state.
Brain Dev
; 37(9): 887-90, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25721947
15.
Spontaneous movements in the supine position of preterm infants with intellectual disability.
Brain Dev
; 36(7): 572-7, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24055340
16.
Spontaneous movements in the supine position of healthy term infants and preterm infants with or without periventricular leukomalacia.
Brain Dev
; 35(4): 340-8, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22656321
17.
Magnetic resonance imaging in neonates with total asphyxia.
Brain Dev
; 35(1): 53-60, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22583740
18.
Neurodevelopmental outcomes at 18 months' corrected age of infants born at 22 weeks of gestation.
Neonatology
; 100(3): 228-32, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21701211
19.
A case of systemic aplasia cutis congenita: a newly recognized syndrome?
Eur J Pediatr
; 167(4): 409-13, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17520283