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

Year Number of Results
2002 2
2003 4
2004 2
2005 4
2006 3
2007 3
2008 1
2009 4
2010 4
2011 3
2012 3
2013 5
2014 3
2015 3
2016 1
2017 1
2018 1
2019 1
2020 5
2021 1
2022 1
2023 1
2024 0

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49 results

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Page 1
PRRT2 Gene Mutations in Indian Paroxysmal Kinesigenic Dyskinesia Patients.
Prabhakara S, Hanumantha Rao HM, Prashanth LK, Anbazhagan K, Jacques R, Reddy BK. Prabhakara S, et al. Among authors: jacques r. Ann Indian Acad Neurol. 2021 May-Jun;24(3):425-429. doi: 10.4103/aian.AIAN_417_20. Epub 2020 Oct 28. Ann Indian Acad Neurol. 2021. PMID: 34447013 Free PMC article. No abstract available.
HDAC6 regulates human erythroid differentiation through modulation of JAK2 signalling.
Vong P, Messaoudi K, Jankovsky N, Gomilla C, Demont Y, Caulier A, Jedraszak G, Demagny J, Djordjevic S, Boyer T, Marolleau JP, Rochette J, Ouled-Haddou H, Garçon L. Vong P, et al. Among authors: rochette j. J Cell Mol Med. 2023 Jan;27(2):174-188. doi: 10.1111/jcmm.17559. Epub 2022 Dec 28. J Cell Mol Med. 2023. PMID: 36578217 Free PMC article.
New intragenic rearrangements in non-Finnish mulibrey nanism.
Jobic F, Morin G, Vincent-Delorme C, Cadet E, Cabry R, Mathieu-Dramard M, Copin H, Rochette J, Jedraszak G. Jobic F, et al. Among authors: rochette j. Am J Med Genet A. 2017 Oct;173(10):2782-2788. doi: 10.1002/ajmg.a.38381. Epub 2017 Aug 17. Am J Med Genet A. 2017. PMID: 28815877
A new role of glutathione peroxidase 4 during human erythroblast enucleation.
Ouled-Haddou H, Messaoudi K, Demont Y, Lopes Dos Santos R, Carola C, Caulier A, Vong P, Jankovsky N, Lebon D, Willaume A, Demagny J, Boyer T, Marolleau JP, Rochette J, Garçon L. Ouled-Haddou H, et al. Among authors: rochette j. Blood Adv. 2020 Nov 24;4(22):5666-5680. doi: 10.1182/bloodadvances.2020003100. Blood Adv. 2020. PMID: 33211827 Free PMC article.
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.
Delcourt M, Riant F, Mancini J, Milh M, Navarro V, Roze E, Humbertclaude V, Korff C, Des Portes V, Szepetowski P, Doummar D, Echenne B, Quintin S, Leboucq N, Singh Amrathlal R, Rochette J, Roubertie A. Delcourt M, et al. Among authors: rochette j. J Neurol Neurosurg Psychiatry. 2015 Jul;86(7):782-5. doi: 10.1136/jnnp-2014-309025. Epub 2015 Jan 16. J Neurol Neurosurg Psychiatry. 2015. PMID: 25595153
PIEZO1 activation delays erythroid differentiation of normal and hereditary xerocytosis-derived human progenitor cells.
Caulier A, Jankovsky N, Demont Y, Ouled-Haddou H, Demagny J, Guitton C, Merlusca L, Lebon D, Vong P, Aubry A, Lahary A, Rose C, Gréaume S, Cardon E, Platon J, Ouadid-Ahidouch H, Rochette J, Marolleau JP, Picard V, Garçon L. Caulier A, et al. Among authors: rochette j. Haematologica. 2020 Mar;105(3):610-622. doi: 10.3324/haematol.2019.218503. Epub 2019 Aug 14. Haematologica. 2020. PMID: 31413092 Free PMC article.
Stormorken syndrome or York platelet syndrome: A clinician's dilemma.
Singh AR, Morin G, Rochette J. Singh AR, et al. Among authors: rochette j. Mol Genet Metab Rep. 2015 Jan 29;2:80. doi: 10.1016/j.ymgmr.2015.01.003. eCollection 2015 Mar. Mol Genet Metab Rep. 2015. PMID: 28649531 Free PMC article. No abstract available.
A severe prenatal presentation of Cat Eye Syndrome.
Jedraszak G, Receveur A, Andrieux J, Naepels P, Mathieu-Dramard M, Bremond-Gignac D, Sevestre H, Copin H, Rochette J. Jedraszak G, et al. Among authors: rochette j. Clin Dysmorphol. 2013 Oct;22(4):175-177. doi: 10.1097/MCD.0000000000000011. Clin Dysmorphol. 2013. PMID: 23982124 No abstract available.
49 results