Evaluation of CDC’s Hemophilia Surveillance Program — Universal Data Collection (1998–2011) and Community Counts (2011–2019), United States-Reference-Cited by-同舟云学术

Evaluation of CDC’s Hemophilia Surveillance Program — Universal Data Collection (1998–2011) and Community Counts (2011–2019), United States

Published:2020-09-04 Issue:5 Volume:69 Page:1-18
ISSN:1546-0738
Container-title:MMWR. Surveillance Summaries
language:
Short-container-title:MMWR Surveill. Summ.

Author:

Schieve Laura A.¹,Byams Vanessa R.¹,Dupervil Brandi¹,Oakley Meredith A.¹,Miller Connie H.¹,Soucie J. Michael¹,Abe Karon¹,Bean Christopher J.¹,Hooper W. Craig¹

Affiliation:

1. Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, CDC

Publisher

Centers for Disease Control MMWR Office

Subject

Health Information Management,Health, Toxicology and Mutagenesis,Health (social science),Epidemiology

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4. Population-based surveillance of haemophilia and patient outcomes in Indiana using multiple data sources.;Okolo;Haemophilia,2019

5. Men with severe hemophilia in the United States: birth cohort analysis of a large national database.;Mazepa;Blood,2016

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