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

Year Number of Results
1987 1
1988 2
1990 4
1991 2
1992 1
1993 4
1994 6
1995 1
1996 5
1997 6
1998 8
1999 14
2000 17
2001 30
2002 25
2003 37
2004 33
2005 53
2006 33
2007 49
2008 64
2009 60
2010 57
2011 70
2012 59
2013 70
2014 109
2015 143
2016 141
2017 134
2018 173
2019 168
2020 172
2021 206
2022 169
2023 174
2024 69

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2,040 results

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Page 1
Neurodevelopmental Outcomes in Early Childhood.
Duncan AF, Matthews MA. Duncan AF, et al. Clin Perinatol. 2018 Sep;45(3):377-392. doi: 10.1016/j.clp.2018.05.001. Clin Perinatol. 2018. PMID: 30144844 Review.
The microbiome-shaping roles of bacteriocins.
Heilbronner S, Krismer B, Brötz-Oesterhelt H, Peschel A. Heilbronner S, et al. Nat Rev Microbiol. 2021 Nov;19(11):726-739. doi: 10.1038/s41579-021-00569-w. Epub 2021 Jun 1. Nat Rev Microbiol. 2021. PMID: 34075213 Review.
Metagenome-based and activity-based screening approaches have strongly expanded our knowledge of the abundance and diversity of bacteriocin biosynthetic gene clusters and the properties of a continuously growing list of bacteriocin classes. The dynamic acquisition, diversificatio …
Metagenome-based and activity-based screening approaches have strongly expanded our knowledge of the abundance and diversity of bacteriocin …
Clinical practice. Protein-losing enteropathy in children.
Braamskamp MJ, Dolman KM, Tabbers MM. Braamskamp MJ, et al. Eur J Pediatr. 2010 Oct;169(10):1179-85. doi: 10.1007/s00431-010-1235-2. Epub 2010 Jun 23. Eur J Pediatr. 2010. PMID: 20571826 Free PMC article. Review.
While considering PLE, other causes of hypoproteinemia such as malnutrition, impaired synthesis, or protein loss through other organs like the kidney, liver, or skin, have to be excluded. The disorders causing PLE can be divided into those due to protein loss from i …
While considering PLE, other causes of hypoproteinemia such as malnutrition, impaired synthesis, or protein loss through other organs …
Insensible Losses.
Roberts AE. Roberts AE. J Gen Intern Med. 2022 Sep;37(12):3191-3192. doi: 10.1007/s11606-022-07700-4. Epub 2022 Jun 29. J Gen Intern Med. 2022. PMID: 35771401 Free PMC article. No abstract available.
Distribution of EGFR amplification, combined chromosome 7 gain and chromosome 10 loss, and TERT promoter mutation in brain tumors and their potential for the reclassification of IDHwt astrocytoma to glioblastoma.
Stichel D, Ebrahimi A, Reuss D, Schrimpf D, Ono T, Shirahata M, Reifenberger G, Weller M, Hänggi D, Wick W, Herold-Mende C, Westphal M, Brandner S, Pfister SM, Capper D, Sahm F, von Deimling A. Stichel D, et al. Acta Neuropathol. 2018 Nov;136(5):793-803. doi: 10.1007/s00401-018-1905-0. Epub 2018 Sep 5. Acta Neuropathol. 2018. PMID: 30187121 Free article.
EGFR amplification (EGFRamp), the combination of gain of chromosome 7 and loss of chromosome 10 (7+/10-), and TERT promoter mutation (pTERTmut) are alterations frequently observed in adult IDH-wild-type (IDHwt) glioblastoma (GBM). ...
EGFR amplification (EGFRamp), the combination of gain of chromosome 7 and loss of chromosome 10 (7+/10-), and TERT promoter mutation …
[Chronic intestinal failure].
Brockmann JG, Hüsing-Kabar A, Bohlen K, Höckelmann CL, Pascher A. Brockmann JG, et al. Chirurg. 2022 Feb;93(2):205-214. doi: 10.1007/s00104-021-01423-8. Epub 2021 Jul 15. Chirurg. 2022. PMID: 34264370 German.
The term intestinal failure (IF) is understood as the transient or irreversible loss of the resorptive capacity of the bowels. This includes a multitude of diseases, some of which have anatomical causes and others functional causes. ...
The term intestinal failure (IF) is understood as the transient or irreversible loss of the resorptive capacity of the bowels. This i …
Brain oscillatory dysfunctions in dystonia.
Lofredi R, Kühn AA. Lofredi R, et al. Handb Clin Neurol. 2022;184:249-257. doi: 10.1016/B978-0-12-819410-2.00026-6. Handb Clin Neurol. 2022. PMID: 35034739 Review.
Dystonia is a hyperkinetic movement disorder associated with loss of inhibition, abnormal plasticity, dysfunctional sensorimotor integration, and brain oscillatory dysfunctions at cortical and subcortical levels of the central nervous system. ...
Dystonia is a hyperkinetic movement disorder associated with loss of inhibition, abnormal plasticity, dysfunctional sensorimotor inte …
Loss of H3K27me3 in WHO grade 3 meningioma.
Maier AD, Brøchner CB, Mirian C, Haslund-Vinding J, Bartek J Jr, Ekström TJ, Poulsen FR, Scheie D, Mathiesen T. Maier AD, et al. Brain Tumor Pathol. 2022 Oct;39(4):200-209. doi: 10.1007/s10014-022-00436-3. Epub 2022 Jun 9. Brain Tumor Pathol. 2022. PMID: 35678886
Immunohistochemical quantification of H3K27me3 was reported to distinguish meningioma patients with an unfavorable prognosis but is not yet established as a prognostic biomarker within WHO grade 3 meningiomas. We studied H3K27me3 loss in a series of biopsies from primary a …
Immunohistochemical quantification of H3K27me3 was reported to distinguish meningioma patients with an unfavorable prognosis but is not yet …
Endothelial Notch1 signaling in white adipose tissue promotes cancer cachexia.
Taylor J, Uhl L, Moll I, Hasan SS, Wiedmann L, Morgenstern J, Giaimo BD, Friedrich T, Alsina-Sanchis E, De Angelis Rigotti F, Mülfarth R, Kaltenbach S, Schenk D, Nickel F, Fleming T, Sprinzak D, Mogler C, Korff T, Billeter AT, Müller-Stich BP, Berriel Diaz M, Borggrefe T, Herzig S, Rohm M, Rodriguez-Vita J, Fischer A. Taylor J, et al. Nat Cancer. 2023 Nov;4(11):1544-1560. doi: 10.1038/s43018-023-00622-y. Epub 2023 Sep 25. Nat Cancer. 2023. PMID: 37749321 Free PMC article.
Cachexia is a major cause of morbidity and mortality in individuals with cancer and is characterized by weight loss due to adipose and muscle tissue wasting. Hallmarks of white adipose tissue (WAT) remodeling, which often precedes weight loss, are impaired lipid sto …
Cachexia is a major cause of morbidity and mortality in individuals with cancer and is characterized by weight loss due to adipose an …
Rett syndrome.
Naidu SB. Naidu SB. Indian J Pediatr. 1997 Sep-Oct;64(5):651-9. doi: 10.1007/BF02726119. Indian J Pediatr. 1997. PMID: 10771898 Review.
Rett syndrome (RS) is a neurological disorder that mainly, and possibly exclusively, affects girls. After its description in 1966 by Andreas Rett in the Wiener Klinische Wochenschrift, awareness and interest in RS were enhanced by the 1983 report of Hagberg et al. in the A …
Rett syndrome (RS) is a neurological disorder that mainly, and possibly exclusively, affects girls. After its description in 1966 by Andr …
2,040 results