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 NCBI Filters

Results by year

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

Year Number of Results
1966 2
1967 2
1969 1
1970 1
1976 1
1985 1
1986 1
1988 1
1989 1
1990 1
1991 3
1992 5
1993 3
1994 6
1995 5
1996 4
1997 8
1998 3
1999 6
2000 3
2001 1
2003 3
2004 5
2005 6
2006 8
2007 12
2008 10
2009 12
2010 16
2011 13
2012 11
2013 5
2015 9
2016 13
2017 10
2018 8
2019 8
2020 8
2021 12
2022 7
2023 4

Text availability

Article attribute

Article type

Publication date

Search Results

215 results

Results by year

Filters applied: . Clear all
Page 1
Blood biomarkers for assessment of mitochondrial dysfunction: An expert review.
Hubens WHG, Vallbona-Garcia A, de Coo IFM, van Tienen FHJ, Webers CAB, Smeets HJM, Gorgels TGMF. Hubens WHG, et al. Among authors: smeets hjm. Mitochondrion. 2022 Jan;62:187-204. doi: 10.1016/j.mito.2021.10.008. Epub 2021 Nov 2. Mitochondrion. 2022. PMID: 34740866 Free article. Review.
Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic Neuropathy.
Ślęczkowska M, Almomani R, Marchi M, de Greef BTA, Sopacua M, Hoeijmakers JGJ, Lindsey P, Salvi E, Bönhof GJ, Ziegler D, Malik RA, Waxman SG, Lauria G, Faber CG, Smeets HJM, Gerrits MM. Ślęczkowska M, et al. Among authors: smeets hjm. Int J Mol Sci. 2022 Jun 28;23(13):7190. doi: 10.3390/ijms23137190. Int J Mol Sci. 2022. PMID: 35806193 Free PMC article.
Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans.
Le TL, Galmiche L, Levy J, Suwannarat P, Hellebrekers DM, Morarach K, Boismoreau F, Theunissen TE, Lefebvre M, Pelet A, Martinovic J, Gelot A, Guimiot F, Calleroz A, Gitiaux C, Hully M, Goulet O, Chardot C, Drunat S, Capri Y, Bole-Feysot C, Nitschké P, Whalen S, Mouthon L, Babcock HE, Hofstra R, de Coo IF, Tabet AC, Molina TJ, Keren B, Brooks A, Smeets HJ, Marklund U, Gordon CT, Lyonnet S, Amiel J, Bondurand N. Le TL, et al. Among authors: smeets hj. J Clin Invest. 2021 Mar 15;131(6):e145837. doi: 10.1172/JCI145837. J Clin Invest. 2021. PMID: 33497358 Free PMC article.
Reproductive options in mitochondrial disease.
Smeets HJM, Sallevelt SCEH, Herbert M. Smeets HJM, et al. Handb Clin Neurol. 2023;194:207-228. doi: 10.1016/B978-0-12-821751-1.00004-X. Handb Clin Neurol. 2023. PMID: 36813314 Review.
Hydropathicity-based prediction of pain-causing NaV1.7 variants.
Xenakis MN, Kapetis D, Yang Y, Gerrits MM, Heijman J, Waxman SG, Lauria G, Faber CG, Westra RL, Lindsey PJ, Smeets HJ. Xenakis MN, et al. Among authors: smeets hj. BMC Bioinformatics. 2021 Apr 23;22(1):212. doi: 10.1186/s12859-021-04119-2. BMC Bioinformatics. 2021. PMID: 33892629 Free PMC article.
Methods in molecular cardiology: microarray technology.
van den Bosch B, Doevendans PA, Lips D, Smeets HJ. van den Bosch B, et al. Among authors: smeets hj. Neth Heart J. 2003 May;11(5):213-220. Neth Heart J. 2003. PMID: 25696214 Free PMC article. Review.
The clinical spectrum of type IV collagen mutations.
Lemmink HH, Schröder CH, Monnens LA, Smeets HJ. Lemmink HH, et al. Among authors: smeets hj. Hum Mutat. 1997;9(6):477-99. doi: 10.1002/(SICI)1098-1004(1997)9:6<477::AID-HUMU1>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9195222 Review.
215 results