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Page 1
Andersen's syndrome mutants produce a knockdown of inwardly rectifying K(+) channel in mouse skeletal muscle in vivo.
Simkin D, Robin G, Giuliano S, Vukolic A, Moceri P, Guy N, Wagner KD, Lacampagne A, Allard B, Bendahhou S. Simkin D, et al. Cell Tissue Res. 2018 Feb;371(2):309-323. doi: 10.1007/s00441-017-2696-7. Epub 2017 Oct 10. Cell Tissue Res. 2018. PMID: 29018970 Free article.
Andersen's syndrome (AS) is a rare autosomal disorder that has been defined by the triad of periodic paralysis, cardiac arrhythmia, and developmental anomalies. ...Whole-cell voltage-clamp recordings in individual skeletal muscle fibers confirmed the reduction of in
Andersen's syndrome (AS) is a rare autosomal disorder that has been defined by the triad of periodic paralysis, cardiac arrhyt
Pantoprazole in Patients at Risk for Gastrointestinal Bleeding in the ICU.
Krag M, Marker S, Perner A, Wetterslev J, Wise MP, Schefold JC, Keus F, Guttormsen AB, Bendel S, Borthwick M, Lange T, Rasmussen BS, Siegemund M, Bundgaard H, Elkmann T, Jensen JV, Nielsen RD, Liboriussen L, Bestle MH, Elkjær JM, Palmqvist DF, Bäcklund M, Laake JH, Bådstøløkken PM, Grönlund J, Breum O, Walli A, Winding R, Iversen S, Jarnvig IL, White JO, Brand B, Madsen MB, Quist L, Thornberg KJ, Møller A, Wiis J, Granholm A, Anthon CT, Meyhoff TS, Hjortrup PB, Aagaard SR, Andreasen JB, Sørensen CA, Haure P, Hauge J, Hollinger A, Scheuzger J, Tuchscherer D, Vuilliomenet T, Takala J, Jakob SM, Vang ML, Pælestik KB, Andersen KLD, van der Horst ICC, Dieperink W, Fjølner J, Kjer CKW, Sølling C, Sølling CG, Karttunen J, Morgan MPG, Sjøbø B, Engstrøm J, Agerholm-Larsen B, Møller MH; SUP-ICU trial group. Krag M, et al. N Engl J Med. 2018 Dec 6;379(23):2199-2208. doi: 10.1056/NEJMoa1714919. Epub 2018 Oct 24. N Engl J Med. 2018. PMID: 30354950 Clinical Trial.
Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.
Zagaglia S, Selch C, Nisevic JR, Mei D, Michalak Z, Hernandez-Hernandez L, Krithika S, Vezyroglou K, Varadkar SM, Pepler A, Biskup S, Leão M, Gärtner J, Merkenschlager A, Jaksch M, Møller RS, Gardella E, Kristiansen BS, Hansen LK, Vari MS, Helbig KL, Desai S, Smith-Hicks CL, Hino-Fukuyo N, Talvik T, Laugesaar R, Ilves P, Õunap K, Körber I, Hartlieb T, Kudernatsch M, Winkler P, Schimmel M, Hasse A, Knuf M, Heinemeyer J, Makowski C, Ghedia S, Subramanian GM, Striano P, Thomas RH, Micallef C, Thom M, Werring DJ, Kluger GJ, Cross JH, Guerrini R, Balestrini S, Sisodiya SM. Zagaglia S, et al. Neurology. 2018 Nov 27;91(22):e2078-e2088. doi: 10.1212/WNL.0000000000006567. Epub 2018 Nov 9. Neurology. 2018. PMID: 30413629 Free PMC article.
Prevention of Vitamin K Deficiency Bleeding in Newborn Infants: A Position Paper by the ESPGHAN Committee on Nutrition.
Mihatsch WA, Braegger C, Bronsky J, Campoy C, Domellöf M, Fewtrell M, Mis NF, Hojsak I, Hulst J, Indrio F, Lapillonne A, Mlgaard C, Embleton N, van Goudoever J; ESPGHAN Committee on Nutrition. Mihatsch WA, et al. J Pediatr Gastroenterol Nutr. 2016 Jul;63(1):123-9. doi: 10.1097/MPG.0000000000001232. J Pediatr Gastroenterol Nutr. 2016. PMID: 27050049 Free article.
Vitamin K deficiency bleeding (VKDB) due to physiologically low vitamin K plasma concentrations is a serious risk for newborn and young infants and can be largely prevented by adequate vitamin K supplementation. ...Parental refusal of vitamin K prophyl …
Vitamin K deficiency bleeding (VKDB) due to physiologically low vitamin K plasma concentrations is a serious risk for newborn …
Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes.
Sacconi S, Simkin D, Arrighi N, Chapon F, Larroque MM, Vicart S, Sternberg D, Fontaine B, Barhanin J, Desnuelle C, Bendahhou S. Sacconi S, et al. Am J Physiol Cell Physiol. 2009 Oct;297(4):C876-85. doi: 10.1152/ajpcell.00519.2008. Epub 2009 Jul 1. Am J Physiol Cell Physiol. 2009. PMID: 19570891 Free article.
Several studies have shown that Andersen's syndrome mutations lead to a loss of function of the K+ channel activity in vitro. ...Our data describe for the first time the functional consequences of Andersen's syndrome mutations ex vivo and provid …
Several studies have shown that Andersen's syndrome mutations lead to a loss of function of the K+ channel activity in …
Primary Periodic Paralyses: A Review of Etiologies and Their Pathogeneses.
Farooque U, Cheema AY, Kumar R, Saini G, Kataria S. Farooque U, et al. Cureus. 2020 Aug 29;12(8):e10112. doi: 10.7759/cureus.10112. Cureus. 2020. PMID: 33005530 Free PMC article. Review.
Some of these periodic paralyses are hyperkalemic periodic paralysis (Na-channel mutation), hypokalemic periodic paralysis (Na- or Ca-channel mutation), Andersen's syndrome (K-channel mutation), etc....
Some of these periodic paralyses are hyperkalemic periodic paralysis (Na-channel mutation), hypokalemic periodic paralysis (Na- or Ca-channe …
Climate change and respiratory health: a European Respiratory Society position statement.
Vicedo-Cabrera AM, Melén E, Forastiere F, Gehring U, Katsouyanni K, Yorgancioglu A, Ulrik CS, Hansen K, Powell P, Ward B, Hoffmann B, Andersen ZJ. Vicedo-Cabrera AM, et al. Eur Respir J. 2023 Sep 3;62(2):2201960. doi: 10.1183/13993003.01960-2022. Print 2023 Aug. Eur Respir J. 2023. PMID: 37661094 No abstract available.
A glutamate residue at the C terminus regulates activity of inward rectifier K+ channels: implication for Andersen's syndrome.
Chen L, Kawano T, Bajic S, Kaziro Y, Itoh H, Art JJ, Nakajima Y, Nakajima S. Chen L, et al. Proc Natl Acad Sci U S A. 2002 Jun 11;99(12):8430-5. doi: 10.1073/pnas.122682899. Epub 2002 May 28. Proc Natl Acad Sci U S A. 2002. PMID: 12034888 Free PMC article.
The mutated GIRK2 retained the ability to interact with G protein betagamma subunits, and it showed almost the same inwardly rectifying property as the wild type. The mutated GIRK1 and GIRK2 retained ion selectivity to K(+) ions. This glutamate residue corresponds to one o …
The mutated GIRK2 retained the ability to interact with G protein betagamma subunits, and it showed almost the same inwardly rectifying prop …
Local extracellular K(+) in cortex regulates norepinephrine levels, network state, and behavioral output.
Dietz AG, Weikop P, Hauglund N, Andersen M, Petersen NC, Rose L, Hirase H, Nedergaard M. Dietz AG, et al. Proc Natl Acad Sci U S A. 2023 Oct 3;120(40):e2305071120. doi: 10.1073/pnas.2305071120. Epub 2023 Sep 29. Proc Natl Acad Sci U S A. 2023. PMID: 37774097 Free PMC article.
Extracellular potassium concentration ([K(+)](e)) is known to increase as a function of arousal. [K(+)](e) is also a potent modulator of transmitter release. ...Imposing a [K(+)](e) increase is adequate to boost local NE levels, and conversely, lowering [K
Extracellular potassium concentration ([K(+)](e)) is known to increase as a function of arousal. [K(+)](e) is also a potent mo …
On the definition of stigma.
Andersen MM, Varga S, Folker AP. Andersen MM, et al. J Eval Clin Pract. 2022 Oct;28(5):847-853. doi: 10.1111/jep.13684. Epub 2022 Apr 23. J Eval Clin Pract. 2022. PMID: 35462457 Free PMC article.
BACKGROUND: There are thousands of papers about stigma, for instance about stigma's impact on wellbeing, mental or physical health. But the definition of stigma has received only modest attention. ...We first interpret, analyze and reconsider each of the six components in …
BACKGROUND: There are thousands of papers about stigma, for instance about stigma's impact on wellbeing, mental or physical health. B …
1,338 results