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Results by year

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

Year Number of Results
1972 1
1982 1
1983 2
1984 2
1985 2
1986 2
1987 3
1988 2
1989 2
1990 1
1991 3
1992 3
1993 6
1994 6
1995 1
1996 3
1997 7
1998 5
1999 3
2000 4
2001 3
2002 3
2003 1
2004 3
2005 2
2006 1
2007 1
2008 2
2009 3
2010 1
2011 1
2012 2
2013 3
2017 1
2018 2
2019 4
2020 2
2021 3
2022 4
2023 2
2024 3

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102 results

Results by year

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Page 1
DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity.
Boussard C, Delage L, Gajardo T, Kauskot A, Batignes M, Goudin N, Stolzenberg MC, Brunaud C, Panikulam P, Riller Q, Moya-Nilges M, Solarz J, Repérant C, Durel B, Bordet JC, Pellé O, Lebreton C, Magérus A, Pirabakaran V, Vargas P, Dupichaud S, Jeanpierre M, Vinit A, Zarhrate M, Masson C, Aladjidi N, Arkwright PD, Bader-Meunier B, Baron Joly S, Benadiba J, Bernard E, Berrebi D, Bodemer C, Castelle M, Charbit-Henrion F, Chbihi M, Debray A, Drabent P, Fraitag S, Hié M, Landman-Parker J, Lhermitte L, Moshous D, Rohrlich P, Ruemmele F, Welfringer-Morin A, Tusseau M, Belot A, Cerf-Bensussan N, Roelens M, Picard C, Neven B, Fischer A, Callebaut I, Ménager M, Sepulveda FE, Adam F, Rieux-Laucat F. Boussard C, et al. Among authors: jeanpierre m. Blood. 2023 Jun 1;141(22):2713-2726. doi: 10.1182/blood.2022018486. Blood. 2023. PMID: 36952639
From adhalinopathies to alpha-sarcoglycanopathies: an overview.
Jeanpierre M, Carrié A, Piccolo F, Leturcq F, Azibi K, De Toma C, Beldjord C, Merlini L, Voit T, Romero N, Sunada Y, Tomé FM, Fardeau M, Campbell KP, Kaplan JC. Jeanpierre M, et al. Neuromuscul Disord. 1996 Dec;6(6):463-5. doi: 10.1016/s0960-8966(96)00394-x. Neuromuscul Disord. 1996. PMID: 9027856 Review. No abstract available.
FSHD1 and FSHD2 form a disease continuum.
Sacconi S, Briand-Suleau A, Gros M, Baudoin C, Lemmers RJLF, Rondeau S, Lagha N, Nigumann P, Cambieri C, Puma A, Chapon F, Stojkovic T, Vial C, Bouhour F, Cao M, Pegoraro E, Petiot P, Behin A, Marc B, Eymard B, Echaniz-Laguna A, Laforet P, Salviati L, Jeanpierre M, Cristofari G, van der Maarel SM. Sacconi S, et al. Among authors: jeanpierre m. Neurology. 2019 May 7;92(19):e2273-e2285. doi: 10.1212/WNL.0000000000007456. Epub 2019 Apr 12. Neurology. 2019. PMID: 30979860 Free PMC article.
The Rise of Obesity among Total Knee Arthroplasty Patients.
Mohamed NS, Wilkie WA, Remily EA, Dávila Castrodad IM, Jean-Pierre M, Jean-Pierre N, Gbadamosi WA, Halik AK, Delanois RE. Mohamed NS, et al. J Knee Surg. 2022 Jan;35(1):1-6. doi: 10.1055/s-0040-1710566. Epub 2020 May 22. J Knee Surg. 2022. PMID: 32443160
[Genes and intra-uterine growth retardation].
Jeanpierre M. Jeanpierre M. Arch Pediatr. 1998;5 Suppl 4:332S-337S. doi: 10.1016/s0929-693x(99)80186-9. Arch Pediatr. 1998. PMID: 9853079 Review. French.
Adhalin gene polymorphism.
Allamand V, Leturcq F, Piccolo F, Jeanpierre M, Azibi K, Roberds SL, Lim LE, Campbell KP, Beckmann JS, Kaplan JC. Allamand V, et al. Among authors: jeanpierre m. Hum Mol Genet. 1994 Dec;3(12):2269. doi: 10.1093/hmg/3.12.2269. Hum Mol Genet. 1994. PMID: 7881446 No abstract available.
[L9, a novel and promising monoclonal antibody against Malaria].
Cools T, Jeanpierre M, Soulard V. Cools T, et al. Among authors: jeanpierre m. Med Sci (Paris). 2021 Aug-Sep;37(8-9):807-811. doi: 10.1051/medsci/2021125. Epub 2021 Sep 7. Med Sci (Paris). 2021. PMID: 34491193 Free article. French.
102 results