Search details
1.
Healthy preterm newborns: Altered innate immunity and impaired monocyte function.
Eur J Immunol
; 53(5): e2250224, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36929362
2.
Cranial ultrasound in preterm infants ≤ 32 weeks gestation-novel insights from the use of very high-frequency (18-5 MHz) transducers: a case series.
Eur J Pediatr
; 2024 Jun 03.
Article
in English
| MEDLINE | ID: mdl-38831135
3.
Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes.
Am J Hum Genet
; 102(2): 309-320, 2018 02 01.
Article
in English
| MEDLINE | ID: mdl-29394990
4.
Disorder of sex development associated with a novel homozygous nonsense mutation in COG6 expands the phenotypic spectrum of COG6-CDG.
Am J Med Genet A
; 185(4): 1187-1194, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33394555
5.
YIF1B mutations cause a post-natal neurodevelopmental syndrome associated with Golgi and primary cilium alterations.
Brain
; 143(10): 2911-2928, 2020 10 01.
Article
in English
| MEDLINE | ID: mdl-33103737
6.
Overwhelming sepsis in a neonate affected by Zellweger syndrome due to a compound heterozygosis in PEX 6 gene: a case report.
BMC Med Genet
; 21(1): 229, 2020 11 19.
Article
in English
| MEDLINE | ID: mdl-33213396
7.
Endocrine-Disrupting Chemicals and Their Effects during Female Puberty: A Review of Current Evidence.
Int J Mol Sci
; 21(6)2020 Mar 18.
Article
in English
| MEDLINE | ID: mdl-32197344
8.
Monitoring the effectiveness of hypothermia in perinatal asphyxia infants by urinary S100B levels.
Clin Chem Lab Med
; 57(7): 1017-1025, 2019 06 26.
Article
in English
| MEDLINE | ID: mdl-30753152
9.
Assessing risks of leaving the umbilical cord uncut: A case-control study.
Acta Paediatr
; 112(11): 2378-2380, 2023 11.
Article
in English
| MEDLINE | ID: mdl-37340574
10.
Correspondence on "Disorder of sex development associated with a novel homozygous nonsense mutation in COG6 expands the phenotypic spectrum of COG6-CDG".
Am J Med Genet A
; 188(1): 382-383, 2022 01.
Article
in English
| MEDLINE | ID: mdl-34562059
11.
Twelve Novel Mutations in the SLC26A3 Gene in 17 Sporadic Cases of Congenital Chloride Diarrhea.
J Pediatr Gastroenterol Nutr
; 65(1): 26-30, 2017 07.
Article
in English
| MEDLINE | ID: mdl-28644346
12.
Maternal Carriage in Late-Onset Group B Streptococcus Disease, Italy.
Emerg Infect Dis
; 27(9): 2279-2287, 2021.
Article
in English
| MEDLINE | ID: mdl-34423765
13.
Correspondence on "Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities," by Carmignac et al.
Genet Med
; 23(11): 2223-2224, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34234302
14.
Hypothermia reduces seizure burden and improves neurological outcome in severe hypoxic-ischemic encephalopathy: an observational study.
Dev Med Child Neurol
; 58(12): 1235-1241, 2016 Dec.
Article
in English
| MEDLINE | ID: mdl-27444888
15.
Pain management during therapeutic hypothermia in newborn infants with hypoxic-ischaemic encephalopathy.
Acta Paediatr
; 109(3): 628-629, 2020 03.
Article
in English
| MEDLINE | ID: mdl-31637755
16.
Prenatal diagnosis and follow-up of a case of branchio-oto-renal syndrome displays renal growth impairment after the second trimester.
J Obstet Gynaecol Res
; 41(11): 1831-4, 2015 Nov.
Article
in English
| MEDLINE | ID: mdl-26227013
17.
Prognostic value of diffusion-weighted imaging summation scores or apparent diffusion coefficient maps in newborns with hypoxic-ischemic encephalopathy.
Pediatr Radiol
; 44(9): 1141-54, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24715056
18.
Minipuberty in Male Full-term Neonates Appropriate and Small for Gestational Age and in Preterm Babies: Data from a Single Centre
J Clin Res Pediatr Endocrinol
; 16(1): 50-59, 2024 03 11.
Article
in English
| MEDLINE | ID: mdl-37750394
19.
Ultrasound-Guided Centrally Inserted Central Catheter (CICC) Placement in Newborns: A Safe Clinical Training Program in a Neonatal Intensive Care Unit.
Children (Basel)
; 11(4)2024 Mar 26.
Article
in English
| MEDLINE | ID: mdl-38671612
20.
Fetal hepatic calcification in severe KAT6A (Arboleda-Tham) syndrome.
Eur J Med Genet
; 67: 104906, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38143025