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Showing 1 to 12 of 363 entries
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Fairness-aware classifier with prejudice remover regularizer

interventions

Akaho S, Asoh H, Kamishima T, Sakuma J.
GSID: OG1oDIm0SgIJ
T Kamishima, S Akaho, H Asoh, J Sakuma - Joint European conference on …, 2012 - Springer

With the spread of data mining technologies and the accumulation of social data, such technologies and data are being used for determinations that seriously affect individuals' …

A preliminary assessment of the intubating laryngeal mask airway.

Journal of anesthesia

Nakazawa K, Makita K, Nishimura K, Saitoh Y, Tanaka N, Ishikawa S, Amaha K.
PMID: 28921074
J Anesth. 1997 Dec;11(4):311-313. doi: 10.1007/BF02480752.

No abstract available.

Ventilatory effects of laparoscopic cholecystectomy under general anesthesia.

Journal of anesthesia

Ishikawa S, Makita K, Sawa T, Toyooka H, Amaha K.
PMID: 28921108
J Anesth. 1997 Sep;11(3):179-183. doi: 10.1007/BF02480034.

PURPOSE: To investigate the ventilatory effect of laparoscopic cholecystectomy in patients under general anesthesia with epidural block.METHODS: We measured arterial blood gas, pulmonary carbon dioxide elimination (0000126;RESULTS: After starting peritoneal insufflation the PaCOCONCLUSION: These results suggest that (1) transperitoneal...

Cost of Glycemic Target Achievement with Sodium Glucose Co-transporter 2 Inhibitors in Patients with Type 2 Diabetes in the UK.

Diabetes therapy : research, treatment and education of diabetes and related disorders

Evans M, Achha S, Neslusan C.
PMID: 28948541
Diabetes Ther. 2017 Oct;8(5):1175-1185. doi: 10.1007/s13300-017-0312-1. Epub 2017 Sep 25.

INTRODUCTION: Diabetes-related costs make up a large portion of healthcare expenditures in the UK. Many of these costs are related to treatment of diabetes-related complications. Reducing HbA1c to

Prevalence of Congenital Heart Disease and Pulmonary Hypertension in Down's Syndrome: An Echocardiographic Study.

Journal of cardiovascular ultrasound

Espinola-Zavaleta N, Soto ME, Romero-Gonzalez A, Gómez-Puente Ldel C, Muñoz-Castellanos L, Gopal AS, Keirns C, Lupi-Herrera E.
PMID: 26140148
J Cardiovasc Ultrasound. 2015 Jun;23(2):72-7. doi: 10.4250/jcu.2015.23.2.72. Epub 2015 Jun 26.

BACKGROUND: Down's syndrome (DS) is a genetic anomaly, which undergoes increased morbidity and mortality when associated with congenital heart disease (CHD). The aims of the study were to determine the prevalence of CHD and pulmonary hypertension (PH) in DS.METHODS:...

Quantum Dephasing in a Gated GaAs Triple Quantum Dot due to Nonergodic Noise.

Physical review letters

Delbecq MR, Nakajima T, Stano P, Otsuka T, Amaha S, Yoneda J, Takeda K, Allison G, Ludwig A, Wieck AD, Tarucha S.
PMID: 26871350
Phys Rev Lett. 2016 Jan 29;116(4):046802. doi: 10.1103/PhysRevLett.116.046802. Epub 2016 Jan 26.

We extract the phase coherence of a qubit defined by singlet and triplet electronic states in a gated GaAs triple quantum dot, measuring on time scales much shorter than the decorrelation time of the environmental noise. In this nonergodic...

Anaphylactic Shock Following Repeated Rasburicase Treatment.

The Annals of pharmacotherapy

Alaya S, Mofredj A, Darmon N, Tassaioust K, Mrabet A.
PMID: 29095045
Ann Pharmacother. 2018 Mar;52(3):295-296. doi: 10.1177/1060028017740599. Epub 2017 Nov 02.

No abstract available.

Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response.

Molecular cytogenetics

Fichera M, Barone R, Grillo L, De Grandi M, Fiore V, Morana I, Maniscalchi T, Vinci M, Amata S, Spalletta A, Sorge G, Signorelli SS.
PMID: 25540671
Mol Cytogenet. 2014 Dec 19;7(1):90. doi: 10.1186/s13039-014-0090-7. eCollection 2014.

BACKGROUND: Despite the extensive use of chromosomal microarray technologies in patients with neurodevelopmental disorders has permitted the identification of an increasing number of causative submicroscopic rearrangements throughout the genome, constitutional duplications involving chromosome 1q22 have seldom been described in...

A Case Report of Ablepharon-Macrostomia Syndrome with Amniotic Membrane Grafting.

Case reports in ophthalmology

Feinstein E, Traish AS, Aakalu V, Kassem IS.
PMID: 26600791
Case Rep Ophthalmol. 2015 Oct 30;6(3):366-72. doi: 10.1159/000441615. eCollection 2015.

We describe a rare case of an infant who was born with multiple congenital anomalies, including the absence of eyelids. This patient had many dysmorphic features consistent with a severe phenotype of ablepharon-macrostomia syndrome (AMS) including a fish-like appearance...

Local Intrinsic Dimension Estimation by Generalized Linear Modeling.

Neural computation

Hino H, Fujiki J, Akaho S, Murata N.
PMID: 28410058
Neural Comput. 2017 Jul;29(7):1838-1878. doi: 10.1162/NECO_a_00969. Epub 2017 Apr 14.

We propose a method for intrinsic dimension estimation. By fitting the power of distance from an inspection point and the number of samples included inside a ball with a radius equal to the distance, to a regression model, we...

Methodological issues for designing and conducting a multicenter, international clinical trial in Acute Stroke: Experience from ARTSS-2 trial.

Contemporary clinical trials

Rahbar MH, Dickerson AS, Cai C, Pedroza C, Hessabi M, Shen L, Pandurengan R, Jacobs ANM, Indupuru H, Sline MR, Delgado RI, Macdonald C, Ford GA, Grotta JC, Barreto AD.
PMID: 26278031
Contemp Clin Trials. 2015 Sep;44:139-148. doi: 10.1016/j.cct.2015.08.007. Epub 2015 Aug 13.

BACKGROUND: We describe innovations in the study design and the efficient data coordination of a randomized multicenter trial of Argatroban in Combination with Recombinant Tissue Plasminogen Activator for Acute Stroke (ARTSS-2).METHODS: ARTSS-2 is a 3-arm, multisite/multiregional randomized controlled trials...

Molecular Detection of Human Cytomegalovirus (HCMV) Among Infants with Congenital Anomalies in Khartoum State, Sudan.

The open virology journal

Ebrahim MG, Ali AS, Mustafa MO, Musa DF, El Hussein AR, Elkhidir IM, Enan KA.
PMID: 26862356
Open Virol J. 2015 Dec 10;9:38-41. doi: 10.2174/1874357901509010038. eCollection 2015.

Human Cytomegalovirus (HCMV) infection still represents the most common potentially serious viral complication in humans and is a major cause of congenital anomalies in infants. This study is aimed to detect HCMV in infants with congenital anomalies. Study subjects...

Showing 1 to 12 of 363 entries