Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

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

Year Number of Results
1906 1
1908 1
1954 1
1959 1
1962 1
1963 1
1964 1
1965 1
1967 1
1968 2
1969 2
1970 5
1971 4
1972 3
1973 2
1974 5
1975 4
1976 1
1977 5
1978 4
1979 3
1980 8
1981 4
1982 5
1983 9
1984 13
1985 21
1986 8
1987 14
1988 20
1989 17
1990 15
1991 11
1992 24
1993 22
1994 32
1995 32
1996 27
1997 35
1998 23
1999 18
2000 20
2001 22
2002 15
2003 22
2004 30
2005 23
2006 24
2007 22
2008 26
2009 21
2010 33
2011 33
2012 27
2013 32
2014 45
2015 30
2016 33
2017 29
2018 32
2019 42
2020 34
2021 28
2022 32
2023 25
2024 28
2025 2

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

1,054 results

Results by year

Filters applied: . Clear all
Page 1
Pulmonary Hypertension.
Poch D, Mandel J. Poch D, et al. Among authors: mandel j. Ann Intern Med. 2021 Apr;174(4):ITC49-ITC64. doi: 10.7326/AITC202104200. Epub 2021 Apr 13. Ann Intern Med. 2021. PMID: 33844574 Review.
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M. Campuzano V, et al. Among authors: mandel jl. Science. 1996 Mar 8;271(5254):1423-7. doi: 10.1126/science.271.5254.1423. Science. 1996. PMID: 8596916
Immunosequencing applications in cutaneous T-cell lymphoma.
Mandel J, Gleason L, Joffe D, Bhatti S, Nikbakht N. Mandel J, et al. Front Immunol. 2023 Dec 21;14:1300061. doi: 10.3389/fimmu.2023.1300061. eCollection 2023. Front Immunol. 2023. PMID: 38213330 Free PMC article. Review.
Pulmonary veno-occlusive disease.
Mandel J, Mark EJ, Hales CA. Mandel J, et al. Am J Respir Crit Care Med. 2000 Nov;162(5):1964-73. doi: 10.1164/ajrccm.162.5.9912045. Am J Respir Crit Care Med. 2000. PMID: 11069841 Review. No abstract available.
Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease.
Muller J, Stoetzel C, Vincent MC, Leitch CC, Laurier V, Danse JM, Hellé S, Marion V, Bennouna-Greene V, Vicaire S, Megarbane A, Kaplan J, Drouin-Garraud V, Hamdani M, Sigaudy S, Francannet C, Roume J, Bitoun P, Goldenberg A, Philip N, Odent S, Green J, Cossée M, Davis EE, Katsanis N, Bonneau D, Verloes A, Poch O, Mandel JL, Dollfus H. Muller J, et al. Among authors: mandel jl. Hum Genet. 2010 Mar;127(5):583-93. doi: 10.1007/s00439-010-0804-9. Epub 2010 Feb 23. Hum Genet. 2010. PMID: 20177705 Free PMC article.
Frataxin fracas.
Cossée M, Campuzano V, Koutnikova H, Fischbeck K, Mandel JL, Koenig M, Bidichandani SI, Patel PI, Moltè MD, Cañizares J, De Frutos R, Pianese L, Cavalcanti F, Monticelli A, Cocozza S, Montermini L, Pandolfo M. Cossée M, et al. Among authors: mandel jl. Nat Genet. 1997 Apr;15(4):337-8. doi: 10.1038/ng0497-337. Nat Genet. 1997. PMID: 9090376 No abstract available.
Lessons from two series by physicians and caregivers' self-reported data in DDX3X-related disorders.
Ruault V, Burger P, Gradels-Hauguel J, Ruiz N; Xtraordinaire; Jamra RA, Afenjar A, Alembik Y, Alessandri JL, Arpin S, Barcia G, Bendová Š, Bruel AL, Charles P, Chatron N, Chopra M, Conrad S, Daire VC, Cospain A, Coubes C, Coursimault J, Delahaye-Duriez A, Doco M, Dufour W, Durand B, Engel C, Faivre L, Ferroul F, Fradin M, Frenkiel H, Fusco C, Garavelli L, Garde A, Gerard B, Germanaud D, Goujon L, Gouronc A, Ginglinger E, Goldenberg A, Hancarova M, Havlovicová M, Heron D, Isidor B, Marçais NJ, Keren B, Koch-Hogrebe M, Kuentz P, Lamure V, Lebre AS, Lecoquierre F, Lehman N, Lesca G, Lyonnet S, Martin D, Mignot C, Neuhann TM, Nicolas G, Nizon M, Petit F, Philippe C, Piton A, Pollazzon M, Prchalová D, Putoux A, Rio M, Rondeau S, Rossi M, Sabbagh Q, Saugier-Veber P, Schmetz A, Steffann J, Thauvin-Robinet C, Toutain A, Them FTM, Trimarchi G, Vincent M, Vlčková M, Wieczorek D, Willems M, Yauy K, Zelinová M, Ziegler A; GENIDA Project; Chaumette B, Sadikovic B, Mandel JL, Geneviève D. Ruault V, et al. Among authors: mandel jl. Mol Genet Genomic Med. 2024 Jan;12(1):e2363. doi: 10.1002/mgg3.2363. Mol Genet Genomic Med. 2024. PMID: 38284452 Free PMC article.
X-linked adrenoleukodystrophy.
Aubourg P, Mandel JL. Aubourg P, et al. Among authors: mandel jl. Ann N Y Acad Sci. 1996 Dec 27;804:461-76. doi: 10.1111/j.1749-6632.1996.tb18637.x. Ann N Y Acad Sci. 1996. PMID: 8993565 Review. No abstract available.
Premotor potentials.
Mandel JD. Mandel JD. Phys Med Rehabil Clin N Am. 1998 Nov;9(4):765-76, vi. Phys Med Rehabil Clin N Am. 1998. PMID: 9894094 Review.
1,054 results