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A Map of Toll-like Receptor Expression in the Intestinal Epithelium Reveals Distinct Spatial, Cell Type-Specific, and Temporal Patterns

Immunity (Cambridge, Mass.), 2018-09, Vol.49 (3), p.560-575.e6

2018

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Systemically dispersed innate IL-13—expressing cells in type 2 immunity

Proceedings of the National Academy of Sciences - PNAS, 2010-06, Vol.107 (25), p.11489-11494

2010

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Marking and quantifying IL-17A-producing cells in vivo

PloS one, 2012-06, Vol.7 (6), p.e39750-e39750

2012

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A novel model for IFN-γ-mediated autoinflammatory syndromes

The Journal of immunology (1950), 2015-03, Vol.194 (5), p.2358-2368

2015

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Autosomal Recessive Agammaglobulinemia Due to a Homozygous Mutation in PIK3R1

Journal of clinical immunology, 2018, Vol.38 (1), p.88-95

2018

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Immunoreactive trypsinogen levels in newborn screened infants with an inconclusive diagnosis of cystic fibrosis

BMC pediatrics, 2019-10, Vol.19 (1), p.369-369, Article 369

2019

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Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis

The Journal of pediatrics, 2017-05, Vol.184, p.165-171.e1

2017

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Estimation of GFR in Patients With Cystic Fibrosis: A Cross-Sectional Study

Canadian journal of kidney health and disease, 2020-01, Vol.7, p.2054358119899312

2020

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Conservative management of an acquired tracheoesophageal fistula caused by a swallowed button battery: A case report

Journal of pediatric surgery case reports, 2024-02, Vol.101, p.102761, Article 102761

2024

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DELAYED URTICARIAL-LIKE ERUPTION TO CYSTIC FIBROSIS DRUG TRIKAFTA IN A PEDIATRIC FEMALE PATIENT

Chest, 2023-10, Vol.164 (4), p.A3964-A3965

2023

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Effect of Placental Malaria and HIV Infection on the Antibody Responses to Plasmodium falciparum in Infants

The Journal of infectious diseases, 2008-12, Vol.198 (11), p.1609-1619

2008

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Pulmonary sequestration causing severe cardiac failure requiring lobectomy in an extreme preterm infant

Journal of pediatric surgery case reports, 2015-10, Vol.3 (10), p.415-418

2015

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RECURRENT CROUP AND ITS MANAGEMENT ACROSS CANADA: A NATIONWIDE SURVEY OF CLINICAL DECISION-MAKING AND DIAGNOSTICS

Chest, 2023-10, Vol.164 (4), p.A5177-A5178

2023

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Section 6: Home ventilation in children with chronic lung diseases

Canadian journal of respiratory, critical care, and sleep medicine, 2018-08, Vol.2 (sup1), p.41-52

2018

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Outcomes of Cystic Fibrosis Screening-Positive Infants With Inconclusive Diagnosis at School Age

Pediatrics (Evanston), 2021-12, Vol.148 (6), p.1

2021

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Inconclusive diagnosis of cystic fibrosis after newborn screening

Pediatrics (Evanston), 2015-06, Vol.135 (6), p.e1377

2015

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Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics

Human molecular genetics, 2016-10, Vol.25 (20), p.4590-4600

2016

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A randomized trial of oral prednisone for cystic fibrosis pulmonary exacerbation treatment

The European respiratory journal, 2024-06, Vol.63 (6), p.2302278

2024

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Complementary and alternative medicine use in children with asthma

Complementary therapies in clinical practice, 2019-05, Vol.35, p.272-277

2019

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Phosphorus Retention and Remobilization along Hydrological Pathways in Karst Terrain

Environmental science & technology, 2014-05, Vol.48 (9), p.4860-4868

2014

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Clinical Translation of SC-DARIC33: A Pharmacologically Controlled CD33-Targeted Anti-AML CAR T Cell Product Regulated By Low Nanomolar Concentrations of Rapamycin

Blood, 2021-11, Vol.138 (Supplement 1), p.905-905

2021

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A Map of Toll-like Receptor Expression in the Intestinal Epithelium Reveals Distinct Spatial, Cell Type-Specific, and Temporal Patterns

Systemically dispersed innate IL-13—expressing cells in type 2 immunity

Marking and quantifying IL-17A-producing cells in vivo

A novel model for IFN-γ-mediated autoinflammatory syndromes

Drug-regulated CD33-targeted CAR T cells control AML using clinically optimized rapamycin dosing

Autosomal Recessive Agammaglobulinemia Due to a Homozygous Mutation in PIK3R1

Immunoreactive trypsinogen levels in newborn screened infants with an inconclusive diagnosis of cystic fibrosis

Psychosocial Response to Uncertain Newborn Screening Results for Cystic Fibrosis

Estimation of GFR in Patients With Cystic Fibrosis: A Cross-Sectional Study

High-quality read-based phasing of cystic fibrosis cohort informs genetic understanding of disease modification

Conservative management of an acquired tracheoesophageal fistula caused by a swallowed button battery: A case report

Genetic evidence supports the development of SLC26A9 targeting therapies for the treatment of lung disease

DELAYED URTICARIAL-LIKE ERUPTION TO CYSTIC FIBROSIS DRUG TRIKAFTA IN A PEDIATRIC FEMALE PATIENT

Effect of Placental Malaria and HIV Infection on the Antibody Responses to Plasmodium falciparum in Infants

Pulmonary sequestration causing severe cardiac failure requiring lobectomy in an extreme preterm infant

RECURRENT CROUP AND ITS MANAGEMENT ACROSS CANADA: A NATIONWIDE SURVEY OF CLINICAL DECISION-MAKING AND DIAGNOSTICS

Section 6: Home ventilation in children with chronic lung diseases

Outcomes of Cystic Fibrosis Screening-Positive Infants With Inconclusive Diagnosis at School Age

Inconclusive diagnosis of cystic fibrosis after newborn screening

Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics

A randomized trial of oral prednisone for cystic fibrosis pulmonary exacerbation treatment

Complementary and alternative medicine use in children with asthma

Unsupervised home spirometry is not equivalent to supervised clinic spirometry in children and young people with cystic fibrosis: Results from the CLIMB‐CF study

Phosphorus Retention and Remobilization along Hydrological Pathways in Karst Terrain

Clinical Translation of SC-DARIC33: A Pharmacologically Controlled CD33-Targeted Anti-AML CAR T Cell Product Regulated By Low Nanomolar Concentrations of Rapamycin

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