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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 16

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187 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.
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.
Salpietro V, Maroofian R, Zaki MS, Wangen J, Ciolfi A, Barresi S, Efthymiou S, Lamaze A, Aughey GN, Al Mutairi F, Rad A, Rocca C, Calì E, Accogli A, Zara F, Striano P, Mojarrad M, Tariq H, Giacopuzzi E, Taylor JC, Oprea G, Skrahina V, Rehman KU, Abd Elmaksoud M, Bassiony M, El Said HG, Abdel-Hamid MS, Al Shalan M, Seo G, Kim S, Lee H, Khang R, Issa MY, Elbendary HM, Rafat K, Marinakis NM, Traeger-Synodinos J, Ververi A, Sourmpi M, Eslahi A, Khadivi Zand F, Beiraghi Toosi M, Babaei M, Jackson A; SYNAPS Study Group; Bertoli-Avella A, Pagnamenta AT, Niceta M, Battini R, Corsello A, Leoni C, Chiarelli F, Dallapiccola B, Faqeih EA, Tallur KK, Alfadhel M, Alobeid E, Maddirevula S, Mankad K, Banka S, Ghayoor-Karimiani E, Tartaglia M, Chung WK, Green R, Alkuraya FS, Jepson JEC, Houlden H. Salpietro V, et al. Am J Hum Genet. 2024 Jan 4;111(1):200-210. doi: 10.1016/j.ajhg.2023.11.012. Epub 2023 Dec 20. Am J Hum Genet. 2024. PMID: 38118446 Free PMC article.
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.
Early IGF-1 receptor inhibition in mice mimics preterm human brain disorders and reveals a therapeutic target.
Potenzieri A, Uccella S, Preiti D, Pisoni M, Rosati S, Lavarello C, Bartolucci M, Debellis D, Catalano F, Petretto A, Nobili L, Fellin T, Tucci V, Ramenghi LA, Savardi A, Cancedda L. Potenzieri A, et al. Among authors: ramenghi la. Sci Adv. 2024 Mar;10(9):eadk8123. doi: 10.1126/sciadv.adk8123. Epub 2024 Mar 1. Sci Adv. 2024. PMID: 38427732 Free PMC article.
187 results