Cystic Fibrosis Genotype and Assessing Rates of Decline in Pulmonary Status

Journal article

Peer reviewed

Robert H CLEVELAND, David ZURAKOWSKI, Dubhfeasa SLATTERY and Andrew A COLIN

Radiology, Vol.253(3), pp.813-821

2009

PMID: 19952026

Abstract

Errors of metabolism

Biological and medical sciences

Metabolic diseases

Investigative techniques, diagnostic techniques (general aspects)

Medical sciences

Miscellaneous hereditary metabolic disorders

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These are selected metrics from InCites Benchmarking & Analytics tool, related to this output

Citation topics: 1 Clinical & Life Sciences; 1.285 Cystic Fibrosis; 1.285.529 Cystic Fibrosis
Web Of Science research areas: Radiology, Nuclear Medicine & Medical Imaging
ESI research areas: Clinical Medicine

This output has contributed to the advancement of the following goals:

Source: InCites

Title: Cystic Fibrosis Genotype and Assessing Rates of Decline in Pulmonary Status
Creators: Robert H CLEVELAND - Department of Radiology, Children's Hospital Boston, Harvard Medical School, 300 Longwood Ave, Boston, MA 02115, United States
David ZURAKOWSKI - Departments of Anesthesiology and Surgery, Children's Hospital Boston, Harvard Medical School, 300 Longwood Ave, Boston, MA 02115, United States
Dubhfeasa SLATTERY - Division of Respiratory Diseases, Children's Hospital Boston, Harvard Medical School, 300 Longwood Ave, Boston, MA 02115, United States
Andrew A COLIN - Division of Respiratory Diseases, Children's Hospital Boston, Harvard Medical School, 300 Longwood Ave, Boston, MA 02115, United States
Publication Details: Radiology, Vol.253(3), pp.813-821
Publisher: Radiological Society of North America; Oak Brook, IL
Academic Unit: Miller School of Medicine; UMMG Department of Pediatrics; UMMG Dept of Pediatrics - Pulmonary Disease
Language: English
Resource Type: Journal article
PMID: 19952026
Record Identifier: 991031560791202976