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Showing 121 to 130 of 130 entries
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A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment.

Medicine

Pavone P, Praticò AD, Rizzo R, Corsello G, Ruggieri M, Parano E, Falsaperla R.
PMID: 28658095
Medicine (Baltimore). 2017 Jun;96(26):e6814. doi: 10.1097/MD.0000000000006814.

Megalencephaly and macrocephaly present with a head circumference measurement 2 standard deviations above the age-related mean. However, even if pathologic events resulting in both megalencephaly and macrocephaly may coexist, a distinction between these two entities is appropriate, as they...

High-Q Tuneable 10-GHz Bragg Resonator for Oscillator Applications.

IEEE transactions on ultrasonics, ferroelectrics, and frequency control

Bale SJ, Deshpande PD, Hough M, Porter SJ, Everard JKA.
PMID: 29389659
IEEE Trans Ultrason Ferroelectr Freq Control. 2018 Feb;65(2):281-291. doi: 10.1109/TUFFC.2017.2782567.

This paper describes the design, simulation, and measurement of a tuneable 9.365-GHz aperiodic Bragg resonator. The resonator utilizes an aperiodic arrangement of non ( /4) low-loss alumina plates ( , loss tangent of to ) mounted in a cylindrical...

COVID-19 vaccination for children: may be necessary for the full eradication of the disease.

Pediatric research

Praticò AD, Ruggieri M.
PMID: 34253861
Pediatr Res. 2021 Jul 12; doi: 10.1038/s41390-021-01643-y. Epub 2021 Jul 12.

No abstract available.

Corrigendum to: "Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically characterised cohort"☆ (J Hepatol [2020] 505-515).

Journal of hepatology

Anstee QM, Darlay R, Cockell S, Meroni M, Govaere O, Tiniakos D, Burt AD, Bedossa P, Palmer J, Liu YL, Aithal GP, Allison M, Yki-Järvinen H, Vacca M, Dufour JF, Invernizzi P, Prati D, Ekstedt M, Kechagias S, Francque S, Petta S, Bugianesi E, Clement K, Ratziu V, Schattenberg JM, Valenti L, Day CP, Cordell HJ, Daly AK.
PMID: 33678471
J Hepatol. 2021 May;74(5):1274-1275. doi: 10.1016/j.jhep.2021.02.003. Epub 2021 Mar 05.

No abstract available.

Direct and Indirect Effects of Management Intensity and Environmental Factors on the Functional Diversity of Lichens in Central European Forests.

Microorganisms

Boch S, Saiz H, Allan E, Schall P, Prati D, Schulze ED, Hessenmöller D, Sparrius LB, Fischer M.
PMID: 33672221
Microorganisms. 2021 Feb 23;9(2). doi: 10.3390/microorganisms9020463.

Using 642 forest plots from three regions in Germany, we analyzed the direct and indirect effects of forest management intensity and of environmental variables on lichen functional diversity (FDis). Environmental stand variables were affected by management intensity and acted...

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality.

medRxiv : the preprint server for health sciences

Nakanishi T, Pigazzini S, Degenhardt F, Cordioli M, Butler-Laporte G, Maya-Miles D, Nafría-Jiménez B, Bouysran Y, Niemi M, Palom A, Ellinghaus D, Khan A, Martínez-Bueno M, Rolker S, Amitano S, Tato LR, Fava F, Spinner CD, Prati D, Bernardo D, Garcia F, Darcis G, Fernández-Cadenas I, Holter JC, Banales J, Frithiof R, Kiryluk K, Duga S, Asselta R, Pereira AC, Romero-Gómez M, Bujanda L, Hov JR, Migeotte I, Renieri A, Planas AM, Ludwig KU, Buti M, Rahmouni S, Alarcón-Riquelme ME, Schulte EC, Franke A, Karlsen TH, Valenti L, Zeberg H, Richards JB, Ganna A.
PMID: 33758887
medRxiv. 2021 Mar 12; doi: 10.1101/2021.03.07.21252875.

BACKGROUND: There is considerable variability in COVID-19 outcomes amongst younger adults-and some of this variation may be due to genetic predisposition. We characterized the clinical implications of the major genetic risk factor for COVID-19 severity, and its age-dependent effect,...

Raising Knowledge and Awareness of Fragile X Syndrome in Serbia, Georgia, and Colombia: A Model for Other Developing Countries?.

The Yale journal of biology and medicine

Protic D, Salcedo-Arellano MJ, Stojkovic M, Saldarriaga W, Ávila Vidal LA, Miller RM, Tabatadze N, Peric M, Hagerman R, Budimirovic DB.
PMID: 34970093
Yale J Biol Med. 2021 Dec 29;94(4):559-571. eCollection 2021 Dec.

Fragile X syndrome is the most common monogenetic cause of inherited intellectual disability and syndromic autism spectrum disorder. Fragile X syndrome is caused by an expansion (full mutation ≥200 CGGs repeats, normal 10-45 CGGs) of the fragile X mental...

Definition of Healthy Ranges for Alanine Aminotransferase Levels: A 2021 Update.

Hepatology communications

Valenti L, Pelusi S, Bianco C, Ceriotti F, Berzuini A, Iogna Prat L, Trotti R, Malvestiti F, D'Ambrosio R, Lampertico P, Colli A, Colombo M, Tsochatzis EA, Fraquelli M, Prati D.
PMID: 34520121
Hepatol Commun. 2021 Nov;5(11):1824-1832. doi: 10.1002/hep4.1794. Epub 2021 Sep 14.

The changing epidemiology of liver disease, and modifications in the recommended analytical methodology call for a re-evaluation of the upper reference limits (URLs) of alanine aminotransferase (ALT) levels. Using the same approach consolidated 20 years ago to define the...

ASaiM-MT: a validated and optimized ASaiM workflow for metatranscriptomics analysis within Galaxy framework.

F1000Research

Mehta S, Crane M, Leith E, Batut B, Hiltemann S, Arntzen MØ, Kunath BJ, Delogu F, Sajulga R, Kumar P, Johnson JE, Griffin TJ, Jagtap PD.
PMID: 34484688
F1000Res. 2021 Feb 11;10:103. doi: 10.12688/f1000research.28608.1. eCollection 2021.

The Human Microbiome Project (HMP) aided in understanding the role of microbial communities and the influence of collective genetic material (the 'microbiome') in human health and disease. With the evolution of new sequencing technologies, researchers can now investigate the...

Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review.

Metabolic brain disease

Falsaperla R, Sciuto L, La Spina L, Sciuto S, Praticò AD, Ruggieri M.
PMID: 34403026
Metab Brain Dis. 2021 Dec;36(8):2195-2203. doi: 10.1007/s11011-021-00798-1. Epub 2021 Aug 17.

Neonatal seizures (NS) occur in the first 28 days of life; they represent an important emergency that requires a rapid diagnostic work-up to start a prompt therapy. The most common causes of NS include: intraventricular haemorrhage, hypoxic-ischemic encephalopathy, hypoglycemia,...

Showing 121 to 130 of 130 entries