User profiles for T. Maher
Toby Michael MaherKeck Medicine of University of Southern California Verified email at rbht.nhs.uk Cited by 32911 |
Acute exacerbation of idiopathic pulmonary fibrosis. An international working group report
…, Y Kondoh, DJ Lederer, JS Lee, TM Maher… - American journal of …, 2016 - atsjournals.org
Acute exacerbation of idiopathic pulmonary fibrosis has been defined as an acute, clinically
significant, respiratory deterioration of unidentifiable cause. The objective of this …
significant, respiratory deterioration of unidentifiable cause. The objective of this …
[HTML][HTML] Global incidence and prevalence of idiopathic pulmonary fibrosis
TM Maher, E Bendstrup, L Dron, J Langley, G Smith… - Respiratory …, 2021 - Springer
Background Idiopathic pulmonary fibrosis (IPF) is a progressive debilitating lung disease
with considerable morbidity. Heterogeneity in epidemiologic studies means the full impact of …
with considerable morbidity. Heterogeneity in epidemiologic studies means the full impact of …
Idiopathic pulmonary fibrosis: Disease mechanisms and drug development
… Maher has received grants and personal fees from GlaxoSmithKline R&D and AstraZeneca,
and personal fees from Boehringer Ingelheim, Roche, Bayer, Samumed, Galapagos, …
and personal fees from Boehringer Ingelheim, Roche, Bayer, Samumed, Galapagos, …
Idiopathic pulmonary fibrosis (an update) and progressive pulmonary fibrosis in adults: an official ATS/ERS/JRS/ALAT clinical practice guideline
Background: This American Thoracic Society, European Respiratory Society, Japanese
Respiratory Society, and Asociación Latinoamericana de Tórax guideline updates prior …
Respiratory Society, and Asociación Latinoamericana de Tórax guideline updates prior …
Interstitial lung disease in systemic sclerosis: a simple staging system
…, DM Hansell, SJ Copley, TM Maher… - American journal of …, 2008 - atsjournals.org
… Group comparisons were made using Student's t test, Wilcoxon rank sum, χ 2 statistics and
Fisher's exact test, as appropriate. A P value of less than 0.05 was considered significant. …
Fisher's exact test, as appropriate. A P value of less than 0.05 was considered significant. …
[HTML][HTML] Nintedanib for systemic sclerosis–associated interstitial lung disease
…, K Tetzlaff, M Kuwana, TM Maher - … England Journal of …, 2019 - Mass Medical Soc
Background Interstitial lung disease (ILD) is a common manifestation of systemic sclerosis
and a leading cause of systemic sclerosis–related death. Nintedanib, a tyrosine kinase …
and a leading cause of systemic sclerosis–related death. Nintedanib, a tyrosine kinase …
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
We performed a genome-wide association study of non-Hispanic, white individuals with fibrotic
idiopathic interstitial pneumonias (IIPs; n = 1,616) and controls (n = 4,683), with follow-up …
idiopathic interstitial pneumonias (IIPs; n = 1,616) and controls (n = 4,683), with follow-up …
Risk of QT interval prolongation associated with use of hydroxychloroquine with or without concomitant azithromycin among hospitalized patients testing positive for …
NJ Mercuro, CF Yen, DJ Shim, TR Maher… - JAMA …, 2020 - jamanetwork.com
Importance Administration of hydroxychloroquine with or without azithromycin for the treatment
of coronavirus disease 2019 (COVID-19)–associated pneumonia carries increased risk of …
of coronavirus disease 2019 (COVID-19)–associated pneumonia carries increased risk of …
[HTML][HTML] Pulmonary fibrosis secondary to COVID-19: a call to arms?
…, G Della Casa, N Sverzellati, TM Maher - The Lancet …, 2020 - thelancet.com
As of May 6, 2020, nearly 3· 7 million people have been infected and around 260 000 people
have died from coronavirus disease 2019 (COVID-19) worldwide. 1 Almost all COVID-19-…
have died from coronavirus disease 2019 (COVID-19) worldwide. 1 Almost all COVID-19-…
Congenital bilateral absence of the vas deferens: a primarily genital form of cystic fibrosis
…, JA Amos, M Dean, B Gerrard, C Stewart, TA Maher… - Jama, 1992 - jamanetwork.com
Objective. —Almost all males with cystic fibrosis (CF) have absent vasa deferentia. It has
been suggested that otherwise healthy males with congenital bilateral absence of the vas …
been suggested that otherwise healthy males with congenital bilateral absence of the vas …