User profiles for Nathan Hambly
Nathan HamblyDepartment of Medicine, McMaster University Verified email at medportal.ca Cited by 1154 |
Macitentan reduces progression of TGF-β1-induced pulmonary fibrosis and pulmonary hypertension
Idiopathic pulmonary fibrosis (IPF) is a progressive disease with an unknown cause. Two
drugs, nintedanib and pirfenidone, have been shown to slow, but not stop, disease progression…
drugs, nintedanib and pirfenidone, have been shown to slow, but not stop, disease progression…
[HTML][HTML] Pulmonary hypertension: diagnostic approach and optimal management
N Hambly, F Alawfi, S Mehta - CMAJ, 2016 - Can Med Assoc
… Contributors: Nathan Hambly was involved in conception and design of the review, …
Competing interests: Nathan Hambly has received consultancy honoraria from Actelion …
Competing interests: Nathan Hambly has received consultancy honoraria from Actelion …
Monoclonal antibodies for the treatment of refractory asthma
In severe refractory asthma, both an understanding of the underlying pathophysiologic
mechanisms driving airway inflammation and the identification of appropriate biomarkers in …
mechanisms driving airway inflammation and the identification of appropriate biomarkers in …
[HTML][HTML] The Canadian Registry for Pulmonary Fibrosis: design and rationale of a national pulmonary fibrosis registry
Background. The relative rarity and diversity of fibrotic interstitial lung disease (ILD) have
made it challenging to study these diseases in single-centre cohorts. Here we describe …
made it challenging to study these diseases in single-centre cohorts. Here we describe …
Antacid therapy in idiopathic pulmonary fibrosis: more questions than answers?
Idiopathic pulmonary fibrosis (IPF) is a progressive parenchymal lung disease of complex
cause. Gastro-oesophageal reflux (GER) and microaspiration have been proposed as risk …
cause. Gastro-oesophageal reflux (GER) and microaspiration have been proposed as risk …
Prevalence and characteristics of progressive fibrosing interstitial lung disease in a prospective registry
N Hambly, MM Farooqi… - European …, 2022 - Eur Respiratory Soc
Background Progressive fibrosing interstitial lung disease (PF-ILD) is characterised by
progressive physiological, symptomatic and/or radiographic worsening. The real-world …
progressive physiological, symptomatic and/or radiographic worsening. The real-world …
Inhalational exposures in patients with fibrotic interstitial lung disease: presentation, pulmonary function and survival in the Canadian Registry for Pulmonary Fibrosis
Background and objective Inhalational exposures are a known cause of interstitial lung
disease (ILD), but little is understood about their prevalence across ILD subtypes and their …
disease (ILD), but little is understood about their prevalence across ILD subtypes and their …
Practical considerations for the diagnosis and treatment of fibrotic interstitial lung disease during the coronavirus disease 2019 pandemic
… Fisher MD g , Nathan Hambly MD h , Martin Kolb MD h , Julie Morisset MD i , Shane
Shapera MD g , Christopher J. Ryerson MD a b … SD Nathan, U. Costabel, C. Albera, et al. …
Shapera MD g , Christopher J. Ryerson MD a b … SD Nathan, U. Costabel, C. Albera, et al. …
Travel distance to subspecialty clinic and outcomes in patients with fibrotic interstitial lung disease
Rationale: Early access to subspecialty care is associated with improved outcomes for patients
with fibrotic interstitial lung disease (ILD). Access to ILD care may be limited for patients …
with fibrotic interstitial lung disease (ILD). Access to ILD care may be limited for patients …
[HTML][HTML] Infliximab therapy in refractory sarcoidosis: a multicenter real-world analysis
Background Infliximab is a monoclonal antibody that binds and neutralizes circulating tumor
necrosis factor-alpha, a key inflammatory cytokine in the pathophysiology of sarcoidosis. …
necrosis factor-alpha, a key inflammatory cytokine in the pathophysiology of sarcoidosis. …