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Risk factors for subclinical and clinical ketosis and association with production parameters in dairy cows in the Netherlands

Journal of dairy science, 2015-02, Vol.98 (2), p.880-888

2015

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Efficacy and tolerability of perampanel in ten patients with Lafora disease

Epilepsy & behavior, 2016-09, Vol.62, p.132-135

2016

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Brain Dopamine–Serotonin Vesicular Transport Disease and Its Treatment

The New England journal of medicine, 2013-02, Vol.368 (6), p.543-550

2013

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Lafora disease - from pathogenesis to treatment strategies

Nature reviews. Neurology, 2018-10, Vol.14 (10), p.606-617

2018

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Raw milk producers with high levels of hygiene and safety

Epidemiology and infection, 2020-01, Vol.148, p.e14, Article e14

2020

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Neuronal ceroid lipofuscinoses

Epileptic disorders, 2016-09, Vol.18 (s2), p.S73-S88

2016

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Pathogenesis of Lafora Disease: Transition of Soluble Glycogen to Insoluble Polyglucosan

International journal of molecular sciences, 2017-08, Vol.18 (8), p.1743

2017

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Diagnostic yield of genetic testing in epileptic encephalopathy in childhood

Epilepsia (Copenhagen), 2015-05, Vol.56 (5), p.707-716

2015

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Amylopectinosis of the fatal epilepsy Lafora disease resists autophagic glycogen catabolism

EMBO molecular medicine, 2024-05, Vol.16 (5), p.1047-1050

2024

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Lafora disease in miniature Wirehaired Dachshunds

PloS one, 2017-08, Vol.12 (8), p.e0182024-e0182024

2017

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A retrospective cohort study comparing dairy calf treatment decisions by farm personnel with veterinary observations of clinical signs

Journal of dairy science, 2019-07, Vol.102 (7), p.6391-6403

2019

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Natural History of SURF1 Deficiency: A Retrospective Chart Review

Pediatric neurology, 2023-03, Vol.140, p.40-46

2023

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Global characterization of copy number variants in epilepsy patients from whole genome sequencing

PLoS genetics, 2018-04, Vol.14 (4), p.e1007285-e1007285

2018

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Sensitive quantification of α-glucans in mouse tissues, cell cultures, and human cerebrospinal fluid

The Journal of biological chemistry, 2020-10, Vol.295 (43), p.14698-14709

2020

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Raw milk producers with high levels of hygiene and safety - CORRIGENDUM

Epidemiology and infection, 2020-04, Vol.148, p.e77-e77, Article e77

2020

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Evaluation of the effects of oral colostrum supplementation during the first fourteen days on the health and performance of preweaned calves

Journal of dairy science, 2009-01, Vol.92 (1), p.286-295

2009

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Lafora disease offers a unique window into neuronal glycogen metabolism

The Journal of biological chemistry, 2018-05, Vol.293 (19), p.7117-7125

2018

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Ppp1r3d deficiency preferentially inhibits neuronal and cardiac Lafora body formation in a mouse model of the fatal epilepsy Lafora disease

Journal of neurochemistry, 2021-06, Vol.157 (6), p.1897-1910

2021

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Lafora disease

Epileptic disorders, 2016-09, Vol.18 (s2), p.S38-S62

2016

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The best evidence for progressive myoclonic epilepsy: A pathway to precision therapy

Seizure (London, England), 2019-10, Vol.71, p.247-257

2019

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Gys1 antisense therapy rescues neuropathological bases of murine Lafora disease

Brain (London, England : 1878), 2021-11, Vol.144 (10), p.2985-2993

2021

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Exposure to benzene and other hydrocarbons and risk of bladder cancer among male offshore petroleum workers

British journal of cancer, 2023-09, Vol.129 (5), p.838-851

2023

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Relationship between hypertension and non-obstructive coronary artery disease in chronic coronary syndrome (the NORIC registry)

PloS one, 2022-01, Vol.17 (1), p.e0262290-e0262290

2022

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Targeting therapy to minimize antimicrobial use in preweaned calves: Effects on health, growth, and treatment costs

Journal of dairy science, 2009-09, Vol.92 (9), p.4707-4714

2009

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Both gain‐of‐function and loss‐of‐function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome

Epilepsia (Copenhagen), 2019-09, Vol.60 (9), p.1881-1894

2019

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Risk factors for subclinical and clinical ketosis and association with production parameters in dairy cows in the Netherlands

Efficacy and tolerability of perampanel in ten patients with Lafora disease

Brain Dopamine–Serotonin Vesicular Transport Disease and Its Treatment

Lafora disease - from pathogenesis to treatment strategies

Raw milk producers with high levels of hygiene and safety

Neuronal ceroid lipofuscinoses

Pathogenesis of Lafora Disease: Transition of Soluble Glycogen to Insoluble Polyglucosan

Diagnostic yield of genetic testing in epileptic encephalopathy in childhood

Amylopectinosis of the fatal epilepsy Lafora disease resists autophagic glycogen catabolism

Lafora disease in miniature Wirehaired Dachshunds

A retrospective cohort study comparing dairy calf treatment decisions by farm personnel with veterinary observations of clinical signs

Natural History of SURF1 Deficiency: A Retrospective Chart Review

Global characterization of copy number variants in epilepsy patients from whole genome sequencing

Sensitive quantification of α-glucans in mouse tissues, cell cultures, and human cerebrospinal fluid

Raw milk producers with high levels of hygiene and safety - CORRIGENDUM

Evaluation of the effects of oral colostrum supplementation during the first fourteen days on the health and performance of preweaned calves

Lafora disease offers a unique window into neuronal glycogen metabolism

Ppp1r3d deficiency preferentially inhibits neuronal and cardiac Lafora body formation in a mouse model of the fatal epilepsy Lafora disease

Lafora disease

The best evidence for progressive myoclonic epilepsy: A pathway to precision therapy

Gys1 antisense therapy rescues neuropathological bases of murine Lafora disease

Exposure to benzene and other hydrocarbons and risk of bladder cancer among male offshore petroleum workers

Relationship between hypertension and non-obstructive coronary artery disease in chronic coronary syndrome (the NORIC registry)

Targeting therapy to minimize antimicrobial use in preweaned calves: Effects on health, growth, and treatment costs

Both gain‐of‐function and loss‐of‐function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome

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