Uscentcom 091923Z Apr 20 Mod Fifteen to Uscentcom Individual Protection and Individual-Unit Deployment Policy
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Part - Partie 1 of - de 2 1 1 See Part 2 for Clauses and Conditions Voir Partie 2 pour Clauses et Conditions RETURN BIDS TO: Title - Sujet RETOURNER LES SOUMISSIONS À: OCIR: SERVICE OPTIQUE Travaux publics et Services gouvernementaux Solicitation No. - N° de l'invitation Date Canada W3380-14K029/B 2015-12-09 Place Bonaventure, portail Sud-Est Client Reference No. - N° de référence du client Amendment No. - N° modif. 800, rue de La Gauchetière Ouest W3380-14-K029 004 7 ième étage Montréal File No. - N° de dossier CCC No./N° CCC - FMS No./N° VME Québec MTA-4-37394 (309) H5A 1L6 GETS Reference No. - N° de référence de SEAG FAX pour soumissions: (514) 496-3822 PW-$MTA-309-13550 Date of Original Request for Standing Offer 2015-11-06 Revision to a Request for a Standing Offer Date de la demande de l'offre à commandes originale Révision à une demande d'offre à commandes Solicitation Closes - L'invitation prend fin Time Zone Fuseau horaire Regional Individual Standing Offer (RISO) at - à 02:00 PM on - le 2015-12-11 Heure Normale du Offre à commandes individuelle régionale (OCIR) l'Est HNE Address Enquiries to: - Adresser toutes questions à: Buyer Id - Id de l'acheteur Paradis, Mary mta309 The referenced document is hereby revised; unless Telephone No. - N° de téléphone FAX No. - N° de FAX otherwise indicated, all other terms and conditions of the Offer remain the same. (514) 496-3874 ( ) (514) 496-3822 Delivery Required - Livraison exigée Ce document est par la présente révisé; sauf indication contraire, les modalités de l'offre demeurent les mêmes. -
Fusion of Multiple Heterogeneous Networks for Predicting Circrna
www.nature.com/scientificreports OPEN Fusion of multiple heterogeneous networks for predicting circRNA- disease associations Received: 22 January 2019 Lei Deng1, Wei Zhang1, Yechuan Shi1 & Yongjun Tang2 Accepted: 18 June 2019 Circular RNAs (circRNAs) are a newly identifed type of non-coding RNA (ncRNA) that plays crucial roles Published: xx xx xxxx in many cellular processes and human diseases, and are potential disease biomarkers and therapeutic targets in human diseases. However, experimentally verifed circRNA-disease associations are very rare. Hence, developing an accurate and efcient method to predict the association between circRNA and disease may be benefcial to disease prevention, diagnosis, and treatment. Here, we propose a computational method named KATZCPDA, which is based on the KATZ method and the integrations among circRNAs, proteins, and diseases to predict circRNA-disease associations. KATZCPDA not only verifes existing circRNA-disease associations but also predicts unknown associations. As demonstrated by leave-one-out and 10-fold cross-validation, KATZCPDA achieves AUC values of 0.959 and 0.958, respectively. The performance of KATZCPDA was substantially higher than those of previously developed network-based methods. To further demonstrate the efectiveness of KATZCPDA, we apply KATZCPDA to predict the associated circRNAs of Colorectal cancer, glioma, breast cancer, and Tuberculosis. The results illustrated that the predicted circRNA-disease associations could rank the top 10 of the experimentally verifed associations. Circular RNA (circRNA) is a class of non-coding RNA recently discovered. Unlike linear RNA, circRNA forms a continuous cycle of covalent closures and is highly represented in the eukaryotic transcriptome. Previous research has found thousands of prototype circRNAs in human, mouse and nematode cells1–4. -
International Requisition Form
PleasePlease place place collection collection kit kit INTERNATIONAL barcode here. REQUISITION FORM barcode here. REQUISITION FORM 123456-2-X PLEASE COMPLETE ALL FIELDS. REQUISITION FORMS SUBMITTED WITH MISSING INFORMATION MAY CAUSE A DELAY IN TURNAROUND TIME OF THE TEST. PLEASE COMPLETE ALL FIELDS. REQUISITION FORMS SUBMITTED WITH MISSING INFORMATION MAY CAUSE A DELAY IN TURNAROUND TIME OF THE TEST. PATIENT INFORMATION ORDERING CLINICIAN INFORMATION PATIENT NAME (LAST, FIRST) NAME OF ORGANIZATION 1 PatIENT INFORmatION (Must be completed in English) 2 ORDERING CLINICIAN (Must be completed in English) DATE OF BIRTH (MM/DD/YYYY) Organization (Clinic, Hospital, or Lab): Patient Name (Last, First): ADDRESS TELEPHONE CITYPatient DOB (DD/MM/YYYY): STATE ZIP CODE ORDERINGLIMS-ID: CLINICIAN TELEPHONE EMAIL Patient Street Address: Telephone: I would like to receive emails about my test from Natera Y N City: Country: Ordering Clinician: PATIENT MALE OR FEMALE? M-V26.34 F-V26.31 PATIENT PREGNANT? Y-V22.1 N DATE OF SAMPLE COLLECTION (MM/DD/YY):_____________________________ Telephone: Email: PAYMENT PLEASEPatient CHECK male orONE: female: M F BILL INSURANCE BILL CLINIC BILL CLINIC/CA Prenatal SELF-PAY Patient pregnant? Program YPDC N INSURANCE COMPANY (Please enclose a photocopy (front and CLINICIAN INFORMED CONSENT MEMBERDate of ID sample collectionSUBSCRIBER (DD/MM/YYYY): NAME (if different than patient) back) or all relevant insurance cards) If you would like the results of this case to be sent to an additional FAX fax number other than what is indicated on your setup form, please IF SELF-PAY, CHECK CARD TYPE: VISA MASTER CARD AMEX DISCOVER provide the fax number. -
LIST of OCCUPATIONAL DISEASES (Revised 2010)
LIST OF OCCUPATIONAL DISEASES (revised 2010) Identification and recognition of occupational diseases: Criteria for incorporating diseases in the ILO list of occupational diseases Occupational Safety and Health Series, No. 74 List of occupational diseases (revised 2010) Identification and recognition of occupational diseases: Criteria for incorporating diseases in the ILO list of occupational diseases INTERNATIONAL LABOUR OFFICE • GENEVA Copyright © International Labour Organization 2010 First published 2010 Publications of the International Labour Office enjoy copyright under Protocol 2 of the Universal Copyright Convention. Nevertheless, short excerpts from them may be reproduced without authorization, on condition that the source is indicated. For rights of reproduction or translation, application should be made to ILO Publications (Rights and Permissions), International Labour Office, CH-1211 Geneva 22, Switzerland, or by email: pubdroit@ ilo.org. The International Labour Office welcomes such applications. Libraries, institutions and other users registered with reproduction rights organizations may make copies in accordance with the licences issued to them for this purpose. Visit www.ifrro.org to find the reproduction rights organization in your country. ILO List of occupational diseases (revised 2010). Identification and recognition of occupational diseases: Criteria for incorporating diseases in the ILO list of occupational diseases Geneva, International Labour Office, 2010 (Occupational Safety and Health Series, No. 74) occupational disease / definition. 13.04.3 ISBN 978-92-2-123795-2 ISSN 0078-3129 Also available in French: Liste des maladies professionnelles (révisée en 2010): Identification et reconnaissance des maladies professionnelles: critères pour incorporer des maladies dans la liste des maladies professionnelles de l’OIT (ISBN 978-92-2-223795-1, ISSN 0250-412x), Geneva, 2010, and in Spanish: Lista de enfermedades profesionales (revisada en 2010). -
ICD-10 International Statistical Classification of Diseases and Related Health Problems
ICD-10 International Statistical Classification of Diseases and Related Health Problems 10th Revision Volume 2 Instruction manual 2010 Edition WHO Library Cataloguing-in-Publication Data International statistical classification of diseases and related health problems. - 10th revision, edition 2010. 3 v. Contents: v. 1. Tabular list – v. 2. Instruction manual – v. 3. Alphabetical index. 1.Diseases - classification. 2.Classification. 3.Manuals. I.World Health Organization. II.ICD-10. ISBN 978 92 4 154834 2 (NLM classification: WB 15) © World Health Organization 2011 All rights reserved. Publications of the World Health Organization are available on the WHO web site (www.who.int) or can be purchased from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for noncommercial distribution – should be addressed to WHO Press through the WHO web site (http://www.who.int/about/licensing/copyright_form). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. -
FAQ REGARDING DISEASE REPORTING in MONTANA | Rev
Disease Reporting in Montana: Frequently Asked Questions Title 50 Section 1-202 of the Montana Code Annotated (MCA) outlines the general powers and duties of the Montana Department of Public Health & Human Services (DPHHS). The three primary duties that serve as the foundation for disease reporting in Montana state that DPHHS shall: • Study conditions affecting the citizens of the state by making use of birth, death, and sickness records; • Make investigations, disseminate information, and make recommendations for control of diseases and improvement of public health to persons, groups, or the public; and • Adopt and enforce rules regarding the reporting and control of communicable diseases. In order to meet these obligations, DPHHS works closely with local health jurisdictions to collect and analyze disease reports. Although anyone may report a case of communicable disease, such reports are submitted primarily by health care providers and laboratories. The Administrative Rules of Montana (ARM), Title 37, Chapter 114, Communicable Disease Control, outline the rules for communicable disease control, including disease reporting. Communicable disease surveillance is defined as the ongoing collection, analysis, interpretation, and dissemination of disease data. Accurate and timely disease reporting is the foundation of an effective surveillance program, which is key to applying effective public health interventions to mitigate the impact of disease. What diseases are reportable? A list of reportable diseases is maintained in ARM 37.114.203. The list continues to evolve and is consistent with the Council of State and Territorial Epidemiologists (CSTE) list of Nationally Notifiable Diseases maintained by the Centers for Disease Control and Prevention (CDC). In addition to the named conditions on the list, any occurrence of a case/cases of communicable disease in the 20th edition of the Control of Communicable Diseases Manual with a frequency in excess of normal expectancy or any unusual incident of unexplained illness or death in a human or animal should be reported. -
Summary of Notifiable Diseases — United States, 2010
Morbidity and Mortality Weekly Report Weekly / Vol. 59 / No. 53 June 1, 2012 Summary of Notifiable Diseases — United States, 2010 U.S. Department of Health and Human Services Centers for Disease Control and Prevention Morbidity and Mortality Weekly Report CONTENTS Preface .......................................................................................................................2 TABLE 5. Reported cases and incidence* of notifiable diseases,† by Background .............................................................................................................2 race — United States, 2010 .......................................................................... 43 Infectious Diseases Designated as Notifiable at the National Level TABLE 6. Reported cases and incidence* of notifiable diseases,† by during 2010* .........................................................................................................3 ethnicity — United States, 2010 ................................................................. 45 Data Sources ...........................................................................................................4 PART 2: Graphs and Maps for Selected Notifiable Diseases Interpreting Data ...................................................................................................4 in the United States, 2010 ............................................................................. 47 Transition in NNDSS Data Collection and Reporting ................................5 PART 3: Historical Summaries -
National Policy for Rare Diseases, 2021
NATIONAL POLICY FOR RARE DISEASES, 2021 Table of Contents 1. BACKGROUND 2. RARE DISEASES – ISSUES & CHALLENGES 3. THE INDIAN SCENARIO 4. EXPERIENCES FROM OTHER COUNTRIES 5. NEED TO BALANCE COMPETING PRIORITIES 6. DEFINITION & DISEASES COVERED 7. POLICY DIRECTION 8. PREVENTION AND CONTROL 9. CENTRES OF EXCELLENCE AND NIDAN KENDRA 10. GOVERNMENT OF INDIA SUPPORT IN TREATMENT 11. DEVELOPMENT OF MANPOWER 12. CONSTITUTION OF CONSORTIUM 13. INCREASING AFFORDABILITY OF DRUG RELATED TO RARE DISEASES 14. IMPLEMENTATION STRATEGY 2 1. Background Ministry of Health and family Welfare, Government of India formulated a National Policy for Treatment of Rare Diseases (NPTRD) in July, 2017. Implementation of the policy, however, faced certain challenges. A limiting factor in its implementation was bringing States on board and lack of clarity on how much Government could support in terms of tertiary care. Public Health and Hospitals is primarily a State subject. Stakeholder consultation with the State Governments at the draft stage of formulation of the policy could not be done in an elaborate manner. When the policy was shared with State Governments, issues such as cost effectiveness of interventions for rare disease vis- a-vis other health priorities, the sharing of expenditure between Central and State Governments, flexibility to State Governments to accept the policy or change it according to their situation, were raised by some of the State Governments. In the circumstances, though framed with best intent, the policy had implementation challenges and gaps, including the issue of cost effectiveness of supporting such health interventions for limited resource situation, which made it not feasible to implement. -
BRAIN DISORDERS “Forebrain” Disorders
The Animal Neurology & Imaging Center 5 Camino Karsten Algodones, New Mexico 87001 Phone: 505- Fax: 505- Email: [email protected] Website: www.theanic.com BRAIN DISORDERS Seizures, circling, a head turn or tilt, a change in personality and/or level of awareness, sensation deficits, visual problems, weakness and in coordination are the most common clinical signs resulting from problems affecting your pets brain. Before we can determine the exact cause of the signs (ie the diagnosis), we must perform a neurological exam in order to establish what is referred to as the “neurological localization”. On the basis of the neurological examination your dog or cat brain disorder may “localize” to one of three major areas: the “forebrain” comprised of the cerebrum and thalamus, the “brainstem” comprised of the midbrain, ponds, and Medulla, and the cerebellum Based on where the problem localizes in the brain, a list of diseases (the so-called "differential diagnosis") is then generated which includes the most likely disease conditions that could be affecting your pet’s brain. The “differential diagnoses” for any given brain problem can be narrowed down based on some specific information: the patient’s age and breed, whether the condition has come on suddenly or slowly, whether the condition is progressing or static, where the problem localizes. Below, the three primary brain localizations are considered individually because specific diseases will affect each region. “Forebrain” Disorders The most common clinical signs seen in pets with forebrain problems include seizures, visual problems, facial sensation abnormalities, circling, and changes in personality or level of consciousness. And mature dogs, epilepsy (seizures due to spontaneous, chaotic electrical activity in 2 the brain), autoimmune inflammation, tumors and strokes are the most common conditions affecting the forebrain. -
History of the Statistical Classification of Diseases and Causes of Death
Copyright information All material appearing in this report is in the public domain and may be reproduced or copied without permission; citation as to source, however, is appreciated. Suggested citation Moriyama IM, Loy RM, Robb-Smith AHT. History of the statistical classification of diseases and causes of death. Rosenberg HM, Hoyert DL, eds. Hyattsville, MD: National Center for Health Statistics. 2011. Library of Congress Cataloging-in-Publication Data Moriyama, Iwao M. (Iwao Milton), 1909-2006, author. History of the statistical classification of diseases and causes of death / by Iwao M. Moriyama, Ph.D., Ruth M. Loy, MBE, A.H.T. Robb-Smith, M.D. ; edited and updated by Harry M. Rosenberg, Ph.D., Donna L. Hoyert, Ph.D. p. ; cm. -- (DHHS publication ; no. (PHS) 2011-1125) “March 2011.” Includes bibliographical references. ISBN-13: 978-0-8406-0644-0 ISBN-10: 0-8406-0644-3 1. International statistical classification of diseases and related health problems. 10th revision. 2. International statistical classification of diseases and related health problems. 11th revision. 3. Nosology--History. 4. Death- -Causes--Classification--History. I. Loy, Ruth M., author. II. Robb-Smith, A. H. T. (Alastair Hamish Tearloch), author. III. Rosenberg, Harry M. (Harry Michael), editor. IV. Hoyert, Donna L., editor. V. National Center for Health Statistics (U.S.) VI. Title. VII. Series: DHHS publication ; no. (PHS) 2011- 1125. [DNLM: 1. International classification of diseases. 2. Disease-- classification. 3. International Classification of Diseases--history. 4. Cause of Death. 5. History, 20th Century. WB 15] RB115.M72 2011 616.07’8012--dc22 2010044437 For sale by the U.S. -
Elite 2016 Premium Protection Sunglasses Eyeshields Pg
Elite 2016 Premium Protection Sunglasses Eyeshields Pg. 6 Pg. 12 Pg. 18 Goggles Boogie Integration Pg. 24 Pg. 25 Safety Rx Lens Matrix NSN Products Pg. 32 Pg. 34 Pg. 39 Focus on the advantage seeker. Smith Elite begins our developmental process by listening to the world’s top tier special operators. This group of advantage seekers require innovative and functional solutions to very specific problems. We optimize technology for those elite maximizers seeking an advantage through cutting-edge innovation, and calibrate product to deliver peak performance for taking on competition and adversity. This dialogue between the development team and the user is what allows Smith to continually protect the eyes of those that demand MilSpec level protection. The results of this collaborative effort is a higher level of quality in products for all Smith advantage seekers. 2016 Elite Collection 3 Model Overview Drop Elite Gray Man Elite Frontman Elite Pg. 16 Pg. 16 Pg. 17 Hudson Elite Hideout Elite Prospect Elite Pg. 17 Pg. 18 Pg. 18 Director Elite Chamber Elite Aegis Echo II Pg. 19 Pg. 19 Pg. 22 © Smith Sport Optics Inc. 2015 © Smith Sport Optics Inc. Aegis Arc PivLock™ Echo Elite PivLock™ V2 Elite Pg. 23 Pg. 24 Pg. 25 Boogie SOEP Boogie Sport Boogie Regulator Pg. 28 Pg. 29 Pg. 29 OTW Turbo Fan OTW LoPro Pg. 30 Pg. 31 Pg. 32 660% COMMON MISCONCEPTION Not all ballistic eyewear is the same. Many users are being misled when they are sold “ballistic” eyewear. Truth be told, eyewear can be labeled “ballistic” if it can stop a .25 inch diameter steel ball at 150 feet per second (FPS), which is the ANSI Z87.1 standard. -
Detecting and Diagnosing Brain Diseases with Medical Imaging Table of Contents 3 Brainwatch Table of Contents
BRAINWATCH DETECTING AND diaGNOSING braiN diSEASES with MEdicaL IMAGING tabLE OF CONTENTS 3 brainwatch tabLE OF CONTENTS INTRODUCTIOn: What IS A NEUROradiOLOGIST? .................. 4 1 Imaging brain tumours: The neuroradiologist as the central chair on the brain tumour board .............................................................................9 2 Advanced imaging techniques in the diagnosis of dementia: from structure to function and back again ....................................................................................................................................17 3 Magnetic resonance imaging in the diagnosis of multiple sclerosis ...............................................................................................23 4 Magnetic resonance imaging in the diagnosis and treatment of Parkinson’s disease ......................................31 5 Radiotherapy of brain malignancies ...........................................39 6 Neuroimaging research ..................................................................................... 47 7 The patient’s view on brain imaging: European Federation of Neurological Associations .......................57 8 The Patient’s view on brain imaging: Austrian Self-Help Association ...........................................................................................65 9 Authors ..........................................................................................................................................71 photocredits .............................................................................................................................