Detalhe da pesquisa
1.
Divergent neurodevelopmental profiles of very-low-birth-weight infants.
Pediatr Res
; 95(1): 233-240, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37626120
2.
Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome.
J Med Genet
; 58(6): 427-432, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32576657
3.
Trends in Bronchopulmonary Dysplasia Among Extremely Preterm Infants in Japan, 2003-2016.
J Pediatr
; 230: 119-125.e7, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33246013
4.
Increased incidence of retroperitoneal teratomas and decreased incidence of sacrococcygeal teratomas in infants with Down syndrome.
Pediatr Blood Cancer
; 61(2): 363-5, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23904199
5.
Effectiveness of umbilical culture for surveillance of methicillin-resistant Staphylococcus aureus among neonates admitted to neonatal intensive care units.
Infect Control Hosp Epidemiol
; 44(6): 988-990, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35770388
6.
Low placental weight may be involved in the etiology of congenital cryptorchidism in neonatal boys.
Eur J Obstet Gynecol Reprod Biol
; 289: 136-139, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37660508
7.
Changing risk factors for postpartum depression in mothers admitted to a perinatal center.
Pediatr Neonatol
; 64(3): 319-326, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36470709
8.
Abnormal placental cord insertion, hypertensive disorders of pregnancy and birth length may be involved in development of hypospadias in male fetuses.
Birth Defects Res
; 114(8): 271-276, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35218598
9.
Impacts of surgical interventions on the long-term outcomes in individuals with trisomy 18.
J Pediatr Surg
; 55(11): 2466-2470, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31954556
10.
Vitamin D deficiency presenting in an infant with neonatal lupus erythematosus.
Pediatr Int
; 53(2): 255-8, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21501313
11.
Congenital portosystemic shunt in a child with Wolf-Hirschhorn syndrome.
Am J Med Genet A
; 152A(9): 2387-9, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20683994
12.
Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly.
DNA Repair (Amst)
; 10(3): 314-21, 2011 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21227757