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Miracles in medicine: A narrative inquiry exploring extraordinary events in pediatrics

Health science reports, 2023-11, Vol.6 (11), p.e1623-n/a

2023

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“Please, keep resuscitating my son!” The story of Gabriel

Intensive care medicine, 2022-09, Vol.48 (9), p.1266-1267

2022

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Buried bumper syndrome

VideoGIE : an official video journal of the American Society for Gastrointestinal Endoscopy, 2020-03, Vol.5 (3), p.104-106

2020

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Mealtime Support: A Pilot Case Series study of an Effective, Cost-saving Outpatient Hunger-Based Feeding Program for Tube Dependency

JPGN reports, 2022-02, Vol.3 (1), p.e154-e154

2022

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University of Alberta Hospital Acute and Convalescent Polio Care and the Reintegration of Polio Patients into Albertan Communities, 1953-80

Canadian Bulletin of Medical History, 2019, Vol.36 (1), p.112-130

Huynh, Geraldine

2019

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Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

American journal of human genetics, 2014-12, Vol.95 (6), p.637-648

2014

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Hepatic lipidomic remodeling in severe obesity manifests with steatosis and does not evolve with non-alcoholic steatohepatitis

Journal of hepatology, 2021-09, Vol.75 (3), p.524-535

2021

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Impact of specialized oral nutritional supplement on clinical, nutritional, and functional outcomes: A randomized, placebo-controlled trial in community-dwelling older adults at risk of malnutrition

Clinical nutrition (Edinburgh, Scotland), 2021-04, Vol.40 (4), p.1879-1892

2021

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Prevalence of low muscle mass and associated factors in community-dwelling older adults in Singapore

Scientific reports, 2021-11, Vol.11 (1), p.23071-23071, Article 23071

2021

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Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome

Nature genetics, 2014-03, Vol.46 (3), p.299-304

2014

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Heterozygous deletion of the VEGFC gene in 4q34.3 is associated with Milroy‐like lymphedema: First prenatal case report

American journal of medical genetics. Part A, 2022-12, Vol.188 (12), p.3550-3554

2022

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Prevalence and associated factors of sarcopenia in community-dwelling older adults at risk of malnutrition

BMC geriatrics, 2022-12, Vol.22 (1), p.997-997, Article 997

2022

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Oral nutritional supplementation with dietary counseling improves linear catch-up growth and health outcomes in children with or at risk of undernutrition: a randomized controlled trial

Frontiers in nutrition (Lausanne), 2024-07, Vol.11, p.1341963

2024

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Factors associated with muscle mass in community-dwelling older people in Singapore: Findings from the SHIELD study

PloS one, 2019-10, Vol.14 (10), p.e0223222

2019

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Effects of Oral Nutritional Supplement with β-Hydroxy-β-methylbutyrate (HMB) on Biochemical and Hematological Indices in Community-Dwelling Older Adults at Risk of Malnutrition: Findings from the SHIELD Study

Nutrients, 2024-08, Vol.16 (15), p.2495

2024

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Assessing respiratory epidemic potential in French hospitals through collection of close contact data (April-June 2020)

Scientific reports, 2024-02, Vol.14 (1), p.3702-3702, Article 3702

2024

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Associations between socio-demographics, nutrition knowledge, nutrition competencies and attitudes in community-dwelling healthy older adults in Singapore: findings from the SHIELD study

Journal of health, population and nutrition, 2021-12, Vol.40 (1), p.52-52, Article 52

2021

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Nutritional Biomarkers and Associated Factors in Community-Dwelling Older Adults: Findings from the SHIELD Study

Nutrients, 2020-10, Vol.12 (11), p.3329

2020

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A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS

Journal of the American Society of Nephrology, 2014-11, Vol.25 (11), p.2435-2443

2014

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Diabetes-specific formula with standard of care improves glycemic control, body composition, and cardiometabolic risk factors in overweight and obese adults with type 2 diabetes: results from a randomized controlled trial

Frontiers in nutrition (Lausanne), 2024-07, Vol.11, p.1400580

2024

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INF2 Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

The New England journal of medicine, 2011-12, Vol.365 (25), p.2377-2388

2011

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NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum

Human mutation, 2014-02, Vol.35 (2), p.178-186

2014

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African‐specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer

International journal of cancer, 2021-01, Vol.148 (1), p.99-105

2021

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Accuracy of Screening Tools for Pap Smears in General Practice

Journal of innovation in health informatics, 2016-09, Vol.23 (3), p.835-559

2016

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Miracles in medicine: A narrative inquiry exploring extraordinary events in pediatrics

“Please, keep resuscitating my son!” The story of Gabriel

Buried bumper syndrome

Mealtime Support: A Pilot Case Series study of an Effective, Cost-saving Outpatient Hunger-Based Feeding Program for Tube Dependency

University of Alberta Hospital Acute and Convalescent Polio Care and the Reintegration of Polio Patients into Albertan Communities, 1953-80

Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

Hepatic lipidomic remodeling in severe obesity manifests with steatosis and does not evolve with non-alcoholic steatohepatitis

Impact of specialized oral nutritional supplement on clinical, nutritional, and functional outcomes: A randomized, placebo-controlled trial in community-dwelling older adults at risk of malnutrition

Prevalence of low muscle mass and associated factors in community-dwelling older adults in Singapore

Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome

Heterozygous deletion of the VEGFC gene in 4q34.3 is associated with Milroy‐like lymphedema: First prenatal case report

Prevalence and associated factors of sarcopenia in community-dwelling older adults at risk of malnutrition

Oral nutritional supplementation with dietary counseling improves linear catch-up growth and health outcomes in children with or at risk of undernutrition: a randomized controlled trial

Factors associated with muscle mass in community-dwelling older people in Singapore: Findings from the SHIELD study

Effects of Oral Nutritional Supplement with β-Hydroxy-β-methylbutyrate (HMB) on Biochemical and Hematological Indices in Community-Dwelling Older Adults at Risk of Malnutrition: Findings from the SHIELD Study

Assessing respiratory epidemic potential in French hospitals through collection of close contact data (April-June 2020)

Associations between socio-demographics, nutrition knowledge, nutrition competencies and attitudes in community-dwelling healthy older adults in Singapore: findings from the SHIELD study

Nutritional Biomarkers and Associated Factors in Community-Dwelling Older Adults: Findings from the SHIELD Study

A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS

Diabetes-specific formula with standard of care improves glycemic control, body composition, and cardiometabolic risk factors in overweight and obese adults with type 2 diabetes: results from a randomized controlled trial

INF2 Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum

Safety and efficacy of ozanezumab in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled, phase 2 trial

African‐specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer

Accuracy of Screening Tools for Pap Smears in General Practice

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