Publications by authors named "Peter Smit"

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Incessant Atrial Tachycardia From the Left Atrial Appendage Treated With Appendage Ligation.
Yonathan F Melman, Eric M Lindley, Abishek Kashyap, Rami Alharethi, Peter Smit

JACC Case Rep· July 2024

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Pulmonary gangliocytic paraganglioma: An under-recognized mimic of carcinoid tumor.
Julia R Naso, Diping Wang, Arthur O Romero, Timothy Leclair, Peter Smit

Hum Pathol· April 2024

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Robotic Thoracic Surgery: Current Practices and Emerging Technologies.
Elliot L Servais, Peter J Smit

Thorac Surg Clin· February 2023

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Inflammatory Bowel Disease in Glycogen Storage Disease Type Ia.
Nicole T Lawrence, Tayoot Chengsupanimit, Laurie M Brown, Terry G J Derks, G Peter A Smit

J Pediatr Gastroenterol Nutr· February 2017

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Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome.
Christiaan P Sentner, Irene J Hoogeveen, David A Weinstein, René Santer, Elaine Murphy, G Peter A Smit

J Inherit Metab Dis· September 2016

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Patients' Willingness to Take Multiple-Tablet Antiretroviral Therapy Regimens for Treatment of HIV.
Esther A N Engelhard, Colette Smit, Sigrid C J M Vervoort, Peter J Smit, Pythia T Nieuwkerk

Drugs Real World Outcomes· June 2016

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Muscle Ultrasound in Patients with Glycogen Storage Disease Types I and III.
Renate J Verbeek, Christiaan P Sentner, G Peter A Smit, Natasha M Maurits, Terry G J Derks

Ultrasound Med Biol· January 2016

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Erratum to: In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseases.
Tatiéle Nalin, Koen Venema, David A Weinstein, Carolina F M de Souza, Ingrid D S Perry, G Peter A Smit

J Inherit Metab Dis· September 2015

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Dietary management in glycogen storage disease type III: what is the evidence?
Terry G J Derks, G Peter A Smit

J Inherit Metab Dis· May 2015

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In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseases.
Tatiéle Nalin, Koen Venema, David A Weinstein, Carolina F M de Souza, Ingrid D S Perry, G Peter A Smit

J Inherit Metab Dis· May 2015

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Pain: a prevalent feature in patients with mucopolysaccharidosis. Results of a cross-sectional national survey.
Marion M G Brands, Deniz Güngör, Johanna M P van den Hout, Francois P J Karstens, Esmee Oussoren, G Peter A Smit

J Inherit Metab Dis· March 2015

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Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy.
Julie Clar, Blandine Gri, Julien Calderaro, Marie-Christine Birling, Yann Hérault, G Peter A Smit

Kidney Int· October 2014

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Experimental evidence for protein oxidative damage and altered antioxidant defense in patients with medium-chain acyl-CoA dehydrogenase deficiency.
Terry G J Derks, Catharina M L Touw, Graziela S Ribas, Giovana B Biancini, Camila S Vanzin, G Peter A Smit

J Inherit Metab Dis· September 2014

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Dietary advanced glycation end-products, its pulmonary receptor, and high mobility group box 1 in aspiration lung injury.
Peter J Smit, Weidun A Guo, Bruce A Davidson, Barbara A Mullan, Jadwiga D Helinski

J Surg Res· September 2014

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Liver transplantation in glycogen storage disease type I.
Susanna J B Boers, Gepke Visser, Peter G P A Smit, Sabine A Fuchs

Orphanet J Rare Dis· April 2014

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Foreign body in right side of chest.
Peter Smit, Jeffrey Brewer

JAMA· August 2013

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A new coding system for metabolic disorders demonstrates gaps in the international disease classifications ICD-10 and SNOMED-CT, which can be barriers to genotype-phenotype data sharing.
Annet Sollie, Rolf H Sijmons, Dick Lindhout, Ans T van der Ploeg, M Estela Rubio Gozalbo, G Peter A Smit

Hum Mutat· July 2013

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Dietary treatment of glycogen storage disease type Ia: uncooked cornstarch and/or continuous nocturnal gastric drip-feeding?
Terry G J Derks, Danielle H Martens, Christiaan P Sentner, Margreet van Rijn, Foekje de Boer, G Peter A Smit

Mol Genet Metab· May 2013

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In vitro and in vivo consequences of variant medium-chain acyl-CoA dehydrogenase genotypes.
Catharina M L Touw, G Peter A Smit, Klary E Niezen-Koning, Conny Bosgraaf-de Boer, Albert Gerding

Orphanet J Rare Dis· March 2013

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Molecular characterization of hepatocellular adenomas developed in patients with glycogen storage disease type I.
Julien Calderaro, Philippe Labrune, Guillaume Morcrette, Sandra Rebouissou, Dominique Franco, G Peter A Smit

J Hepatol· February 2013

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Mutation Analysis in Glycogen Storage Disease Type III Patients in the Netherlands: Novel Genotype-Phenotype Relationships and Five Novel Mutations in the AGL Gene.
Christiaan P Sentner, Yvonne J Vos, Klary N Niezen-Koning, Bart Mol, G Peter A Smit

JIMD Rep· February 2013

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Heart Failure Due to Severe Hypertrophic Cardiomyopathy Reversed by Low Calorie, High Protein Dietary Adjustments in a Glycogen Storage Disease Type IIIa Patient.
Christiaan P Sentner, Kadir Caliskan, Wim B Vletter, G Peter A Smit

JIMD Rep· February 2013

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HIV-related stigma within communities of gay men: a literature review.
Peter J Smit, Michael Brady, Michael Carter, Ricardo Fernandes, Lance Lamore

AIDS Care· January 2013

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A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene.
Merel S Ebberink, Janet Koster, Gepke Visser, Francjan van Spronsen, Irene Stolte-Dijkstra, G Peter A Smit

J Med Genet· May 2012

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Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study.
Catharina M L Touw, G Peter A Smit, Maaike de Vries, Johannis B C de Klerk, Annet M Bosch

Orphanet J Rare Dis· May 2012

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