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Favorable outcome of COVID‐19 in pediatric patients with primary immunodeficiency

Pediatric allergy and immunology, 2023-03, Vol.34 (3), p.e13928-n/a

2023

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Imaging in trauma in limited-resource settings: A literature review

African Journal of Emergency Medicine, 2019-01, Vol.9 (Suppl), p.S21-S27

Willett, Jessica K

2019

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DNA‐Binding domain mutations confer severe outcome at an early age among STAT1 gain‐of‐function patients

Pediatric allergy and immunology, 2022-01, Vol.33 (1), p.e13694-n/a

2022

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A Unique Comprehensive Model to Screen Newborns for Severe Combined Immunodeficiency-An Ontario Single-Centre Experience Spanning 2013-2023

Genes, 2024-07, Vol.15 (7), p.920

2024

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Homozygous duplication identified by whole genome sequencing causes LRBA deficiency

Npj genomic medicine, 2021-11, Vol.6 (1), p.96-96, Article 96

2021

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The impact of COVID-19 infection in pediatric and adult patients with primary immunodeficiency: a single center analysis

LymphoSign journal, 2024-01, p.1-6

2024

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A novel variant in RUNX1 in a patient with refractory eosinophilic gastrointestinal disease and long-term clinical response to ketotifen

LymphoSign journal, 2022-09, Vol.9 (3), p.72-76

2022

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Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant

Frontiers in immunology, 2022-01, Vol.13, p.801832

2022

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CTLA4 haploinsufficiency caused by a novel heterozygous splice site mutation

LymphoSign journal, 2022-06, Vol.9 (2), p.40-44

2022

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An unusual presentation of DiGeorge syndrome

LymphoSign journal, 2022-06, Vol.9 (2), p.52-56

2022

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A novel mutation in TRAC in a patient with abnormal newborn screening for severe combined immunodeficiency

LymphoSign journal, 2022-03, Vol.9 (1), p.5-10

2022

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Novel heterozygous FOXN1 mutation identified following newborn screening for severe combined immunodeficiency is associated with improving immune parameters

LymphoSign journal, 2022-06, Vol.9 (2), p.45-51

2022

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Utilization of next-generation sequencing to define the role of heterozygous FOXN1 variants in immunodeficiency

The journal of allergy and clinical immunology. Global, 2024-08, Vol.3 (3), p.100267-100267, Article 100267

2024

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Utilization of Next Generation Sequencing to Define the Role of Heterozygous FOXN1 Mutations in Immune Disorders

Journal of allergy and clinical immunology, 2024-02, Vol.153 (2), p.AB108

2024

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Perspectives of women in science: data sharing in primary immunodeficiency

LymphoSign journal, 2023-06, Vol.10 (2), p.27-29

Willett-Pachul, Jessica

2023

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Case series of COVID-19 outcomes in adult patients with inborn errors of immunity

LymphoSign journal, 2022-09, Vol.9 (3), p.62-66

2022

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A relaxation response training for women undergoing breast biopsy: Exploring integrated care

Breast (Edinburgh), 2013-10, Vol.22 (5), p.799-805

2013

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Mind-body group treatment for women coping with infertility: a pilot study

Journal of psychosomatic obstetrics and gynaecology, 2015-06, Vol.36 (2), p.75-83

2015

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Corrigendum: A novel variant in RUNX1 in a patient with refractory eosinophilic gastrointestinal disease and long-term clinical response to ketotifen

LymphoSign journal, 2023-12, Vol.10 (4), p.77-77

2023

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A novel splice site variant in FOXN1 in a patient with abnormal newborn screening for severe combined immunodeficiency and congenital lymphopenia

LymphoSign journal, 2021-03, Vol.8 (1), p.1-4

2021

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Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant

Frontiers in immunology, 2022, Vol.13, p.801832-801832

2022

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Evaluation of Dose and Safety of AAV7m8 and AAV8BP2 in the Non-Human Primate Retina

Human gene therapy, 2017-02, Vol.28 (2), p.154-167

2017

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A Comparison of Different Methods for Evaluating Diet, Physical Activity, and Long-Term Weight Gain in 3 Prospective Cohort Studies

The Journal of nutrition, 2015-11, Vol.145 (11), p.2527-2534

2015

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Privacy Attitudes and Data Valuation Among Fitness Tracker Users

Transforming Digital Worlds, p.229-239

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Learned Motor Patterns Are Replayed in Human Motor Cortex during Sleep

The Journal of neuroscience, 2022-06, Vol.42 (25), p.5007-5020

2022

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Favorable outcome of COVID‐19 in pediatric patients with primary immunodeficiency

Imaging in trauma in limited-resource settings: A literature review

DNA‐Binding domain mutations confer severe outcome at an early age among STAT1 gain‐of‐function patients

A Unique Comprehensive Model to Screen Newborns for Severe Combined Immunodeficiency-An Ontario Single-Centre Experience Spanning 2013-2023

Homozygous duplication identified by whole genome sequencing causes LRBA deficiency

The impact of COVID-19 infection in pediatric and adult patients with primary immunodeficiency: a single center analysis

A novel variant in RUNX1 in a patient with refractory eosinophilic gastrointestinal disease and long-term clinical response to ketotifen

Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant

CTLA4 haploinsufficiency caused by a novel heterozygous splice site mutation

An unusual presentation of DiGeorge syndrome

A novel mutation in TRAC in a patient with abnormal newborn screening for severe combined immunodeficiency

Novel heterozygous FOXN1 mutation identified following newborn screening for severe combined immunodeficiency is associated with improving immune parameters

Utilization of next-generation sequencing to define the role of heterozygous FOXN1 variants in immunodeficiency

Utilization of Next Generation Sequencing to Define the Role of Heterozygous FOXN1 Mutations in Immune Disorders

Perspectives of women in science: data sharing in primary immunodeficiency

Case series of COVID-19 outcomes in adult patients with inborn errors of immunity

A relaxation response training for women undergoing breast biopsy: Exploring integrated care

Mind-body group treatment for women coping with infertility: a pilot study

Corrigendum: A novel variant in RUNX1 in a patient with refractory eosinophilic gastrointestinal disease and long-term clinical response to ketotifen

A novel splice site variant in FOXN1 in a patient with abnormal newborn screening for severe combined immunodeficiency and congenital lymphopenia

Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant

Evaluation of Dose and Safety of AAV7m8 and AAV8BP2 in the Non-Human Primate Retina

A Comparison of Different Methods for Evaluating Diet, Physical Activity, and Long-Term Weight Gain in 3 Prospective Cohort Studies

Privacy Attitudes and Data Valuation Among Fitness Tracker Users

Learned Motor Patterns Are Replayed in Human Motor Cortex during Sleep

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