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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 1 |
2010 | 3 |
2011 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
Search Results
6 results
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Page 1
New insights into CC2D2A-related Joubert syndrome.
J Med Genet. 2023 Jun;60(6):578-586. doi: 10.1136/jmg-2022-108754. Epub 2022 Nov 1.
J Med Genet. 2023.
PMID: 36319078
Low prevalence of coagulation F2 and F5 polymorphisms in mothers and children in a large cohort of patients with neonatal arterial ischemic stroke.
Renaud C, Tardy-Poncet B, Presles E, Chabrier S; AVCnn group.
Renaud C, et al.
Br J Haematol. 2010 Sep;150(6):709-12. doi: 10.1111/j.1365-2141.2010.08259.x.
Br J Haematol. 2010.
PMID: 20528875
Free article.
Review.
No abstract available.
Item in Clipboard
Lipoprotein (a), birth weight and neonatal stroke.
Renaud C, Bonneau C, Presles E, Laporte S, Depeyre A, Varlet MN, Chabrier S; AVCnn Group.
Renaud C, et al.
Neonatology. 2010;98(3):225-8. doi: 10.1159/000281015. Epub 2010 Apr 13.
Neonatology. 2010.
PMID: 20428016
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Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype.
Micol R, Ben Slama L, Suarez F, Le Mignot L, Beauté J, Mahlaoui N, Dubois d'Enghien C, Laugé A, Hall J, Couturier J, Vallée L, Delobel B, Rivier F, Nguyen K, Billette de Villemeur T, Stephan JL, Bordigoni P, Bertrand Y, Aladjidi N, Pedespan JM, Thomas C, Pellier I, Koenig M, Hermine O, Picard C, Moshous D, Neven B, Lanternier F, Blanche S, Tardieu M, Debré M, Fischer A, Stoppa-Lyonnet D; CEREDIH Network Investigators.
Micol R, et al.
J Allergy Clin Immunol. 2011 Aug;128(2):382-9.e1. doi: 10.1016/j.jaci.2011.03.052. Epub 2011 Jun 12.
J Allergy Clin Immunol. 2011.
PMID: 21665257
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Motor outcomes after neonatal arterial ischemic stroke related to early MRI data in a prospective study.
Husson B, Hertz-Pannier L, Renaud C, Allard D, Presles E, Landrieu P, Chabrier S; AVCnn Group.
Husson B, et al.
Pediatrics. 2010 Oct;126(4):912-8. doi: 10.1542/peds.2009-3611. Epub 2010 Sep 20.
Pediatrics. 2010.
PMID: 20855393
Free article.
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[GEFS + syndrome: phenotypic variations from the newborn to the adult in a large French pedigree].
Audic-Gerard F, Szepetowski P, Genton P.
Audic-Gerard F, et al.
Rev Neurol (Paris). 2003 Feb;159(2):189-95.
Rev Neurol (Paris). 2003.
PMID: 12660571
French.
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