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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1994 2
1996 5
1997 3
1998 4
1999 1
2000 1
2001 3
2002 4
2003 3
2004 2
2005 2
2006 1
2007 3
2008 4
2009 4
2010 5
2011 4
2012 2
2013 7
2014 1
2015 16
2016 21
2017 15
2018 21
2019 13
2020 16
2021 19
2022 14
2023 11
2024 14

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185 results

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Page 1
Neonatal Hypoglycemia and Brain Vulnerability.
De Angelis LC, Brigati G, Polleri G, Malova M, Parodi A, Minghetti D, Rossi A, Massirio P, Traggiai C, Maghnie M, Ramenghi LA. De Angelis LC, et al. Among authors: ramenghi la. Front Endocrinol (Lausanne). 2021 Mar 16;12:634305. doi: 10.3389/fendo.2021.634305. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 33796072 Free PMC article. Review.
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.
Salpietro V, Dixon CL, Guo H, Bello OD, Vandrovcova J, Efthymiou S, Maroofian R, Heimer G, Burglen L, Valence S, Torti E, Hacke M, Rankin J, Tariq H, Colin E, Procaccio V, Striano P, Mankad K, Lieb A, Chen S, Pisani L, Bettencourt C, Männikkö R, Manole A, Brusco A, Grosso E, Ferrero GB, Armstrong-Moron J, Gueden S, Bar-Yosef O, Tzadok M, Monaghan KG, Santiago-Sim T, Person RE, Cho MT, Willaert R, Yoo Y, Chae JH, Quan Y, Wu H, Wang T, Bernier RA, Xia K, Blesson A, Jain M, Motazacker MM, Jaeger B, Schneider AL, Boysen K, Muir AM, Myers CT, Gavrilova RH, Gunderson L, Schultz-Rogers L, Klee EW, Dyment D, Osmond M, Parellada M, Llorente C, Gonzalez-Peñas J, Carracedo A, Van Haeringen A, Ruivenkamp C, Nava C, Heron D, Nardello R, Iacomino M, Minetti C, Skabar A, Fabretto A; SYNAPS Study Group; Raspall-Chaure M, Chez M, Tsai A, Fassi E, Shinawi M, Constantino JN, De Zorzi R, Fortuna S, Kok F, Keren B, Bonneau D, Choi M, Benzeev B, Zara F, Mefford HC, Scheffer IE, Clayton-Smith J, Macaya A, Rothman JE, Eichler EE, Kullmann DM, Houlden H. Salpietro V, et al. Nat Commun. 2019 Jul 12;10(1):3094. doi: 10.1038/s41467-019-10910-w. Nat Commun. 2019. PMID: 31300657 Free PMC article.
Neonatal Transportation School.
Bellini C, Ramenghi LA, Gente M. Bellini C, et al. Among authors: ramenghi la. Air Med J. 2022 Jul-Aug;41(4):334-335. doi: 10.1016/j.amj.2022.05.001. Epub 2022 May 28. Air Med J. 2022. PMID: 35750436 No abstract available.
Neonatal stroke.
Rutherford MA, Ramenghi LA, Cowan FM. Rutherford MA, et al. Among authors: ramenghi la. Arch Dis Child Fetal Neonatal Ed. 2012 Sep;97(5):F377-84. doi: 10.1136/fetalneonatal-2010-196451. Arch Dis Child Fetal Neonatal Ed. 2012. PMID: 22933099 Review.
Neonatal cerebral sinovenous thrombosis.
Ramenghi LA, Cardiello V, Rossi A. Ramenghi LA, et al. Handb Clin Neurol. 2019;162:267-280. doi: 10.1016/B978-0-444-64029-1.00012-6. Handb Clin Neurol. 2019. PMID: 31324314 Review.
Neonatal stroke.
Ramenghi LA, Bassi L, Fumagalli M, Ometto A, Groppo M, De Carli A, Pisoni S, Dessimone F, Farè P, Mosca F. Ramenghi LA, et al. Minerva Pediatr. 2010 Jun;62(3 Suppl 1):177-9. Minerva Pediatr. 2010. PMID: 21089737 Review.
Heparin for the treatment of thrombosis in neonates.
Romantsik O, Bruschettini M, Zappettini S, Ramenghi LA, Calevo MG. Romantsik O, et al. Among authors: ramenghi la. Cochrane Database Syst Rev. 2016 Nov 7;11(11):CD012185. doi: 10.1002/14651858.CD012185.pub2. Cochrane Database Syst Rev. 2016. PMID: 27820879 Free PMC article. Review.
Effective Passive Cooling During Neonatal Transport.
Bellini C, Ramenghi LA, Gente M. Bellini C, et al. Among authors: ramenghi la. Ther Hypothermia Temp Manag. 2022 Sep;12(3):168-170. doi: 10.1089/ther.2021.0021. Epub 2021 Nov 17. Ther Hypothermia Temp Manag. 2022. PMID: 34788556
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease.
Calì E, Lin SJ, Rocca C, Sahin Y, Al Shamsi A, El Chehadeh S, Chaabouni M, Mankad K, Galanaki E, Efthymiou S, Sudhakar S, Athanasiou-Fragkouli A, Çelik T, Narlı N, Bianca S, Murphy D, De Carvalho Moreira FM; SYNaPS Study Group; Andrea Accogli, Petree C, Huang K, Monastiri K, Edizadeh M, Nardello R, Ognibene M, De Marco P, Ruggieri M, Zara F, Striano P, Şahin Y, Al-Gazali L, Abi Warde MT, Gerard B, Zifarelli G, Beetz C, Fortuna S, Soler M, Valente EM, Varshney G, Maroofian R, Salpietro V, Houlden H. Calì E, et al. Genet Med. 2022 Oct;24(10):2194-2203. doi: 10.1016/j.gim.2022.07.013. Epub 2022 Aug 24. Genet Med. 2022. PMID: 36001086 Free PMC article.
185 results