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Parental mosaicism in epilepsies due to alleged de novo variants

Epilepsia (Copenhagen), 2019-06, Vol.60 (6), p.e63-e66

2019

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Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies

Molecular syndromology, 2016-09, Vol.7 (4), p.210-219

2016

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A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene

European journal of human genetics : EJHG, 2012-01, Vol.20 (1), p.84-90

2012

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Clinical Phenotype of De Novo GNAO1 Mutation: Case Report and Review of Literature

Child neurology open, 2015-04, Vol.2 (2), p.2329048X15583717-2329048X15583717

2015

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Textbook of Work Physiology: Physiological Bases of Exercise, Fourth Edition

Physiotherapy Canada, 2004, Vol.56 (4), p.248

2004

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Effect of overexpressing GLUT-1 and GLUT-4 on insulin- and contraction-stimulated glucose transport in muscle

American journal of physiology: endocrinology and metabolism, 1996-09, Vol.271 (3), p.E547-E555

1996

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Spinkel anatomi

Tidsskrift for Den norske legeforening (trykt utg.), 2013, Vol.133 (20), p.2172-2172

Dahl, Hans A

2013

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Svakt om muskel- og skjelettsystemet

Tidsskrift for Den norske legeforening (trykt utg.), 2010, Vol.130 (10), p.1059-1059

Dahl, Hans A

2010

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Axon morphology is modulated by the local environment and impacts the noninvasive investigation of its structure–function relationship

Proceedings of the National Academy of Sciences - PNAS, 2020-12, Vol.117 (52), p.33649-33659

2020

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Etiology and audiological outcomes at 3 years for 364 children in Australia

PloS one, 2013-03, Vol.8 (3), p.e59624-e59624

2013

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Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency

Epilepsia (Copenhagen), 2012-12, Vol.53 (12), p.e204-e207

2012

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Recent advances in the molecular genetics of epilepsy

Journal of Medical Genetics, 2013-05, Vol.50 (5), p.271-279

2013

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ALKBH5 Is a Mammalian RNA Demethylase that Impacts RNA Metabolism and Mouse Fertility

Molecular cell, 2013-01, Vol.49 (1), p.18-29

2013

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Long-Term Outcomes of Imatinib Treatment for Chronic Myeloid Leukemia

The New England journal of medicine, 2017-03, Vol.376 (10), p.917-927

2017

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Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage

American journal of human genetics, 2012-06, Vol.90 (6), p.1102-1107

2012

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Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis

Human molecular genetics, 2013-04, Vol.22 (7), p.1417-1423

2013

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Glucose metabolism transporters and epilepsy: Only GLUT1 has an established role

Epilepsia (Copenhagen), 2014-02, Vol.55 (2), p.e18-e21

2014

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Fish oil supplementation during pregnancy and allergic respiratory disease in the adult offspring

Journal of allergy and clinical immunology, 2017-01, Vol.139 (1), p.104-111.e4

2017

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Evaluation of 2D super-resolution ultrasound imaging of the rat renal vasculature using ex vivo micro-computed tomography

Scientific reports, 2021-12, Vol.11 (1), p.24335-24335, Article 24335

2021

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Linear Decrease in Athletic Performance During the Human Life Span

Frontiers in physiology, 2018-08, Vol.9, p.1100-1100

2018

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Phase III Trial of Cetuximab With Continuous or Intermittent Fluorouracil, Leucovorin, and Oxaliplatin (Nordic FLOX) Versus FLOX Alone in First-Line Treatment of Metastatic Colorectal Cancer: The NORDIC-VII Study

Journal of clinical oncology, 2012-05, Vol.30 (15), p.1755-1762

2012

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InSegtCone: interactive segmentation of crystalline cones in compound eyes

BMC zoology, 2022-02, Vol.7 (1), p.10-10, Article 10

2022

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Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease

American journal of human genetics, 2008-10, Vol.83 (4), p.468-478

2008

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Basophil sensitivity reflects long‐term clinical outcome of subcutaneous immunotherapy in grass pollen‐allergic patients

Allergy (Copenhagen), 2021-05, Vol.76 (5), p.1528-1538

2021

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Cystatin C proteoforms in chronic kidney disease

PloS one, 2023-02, Vol.18 (2), p.e0269436

2023

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Parental mosaicism in epilepsies due to alleged de novo variants

Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies

A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene

Clinical Phenotype of De Novo GNAO1 Mutation: Case Report and Review of Literature

Textbook of Work Physiology: Physiological Bases of Exercise, Fourth Edition

Effect of overexpressing GLUT-1 and GLUT-4 on insulin- and contraction-stimulated glucose transport in muscle

Spinkel anatomi

Svakt om muskel- og skjelettsystemet

Axon morphology is modulated by the local environment and impacts the noninvasive investigation of its structure–function relationship

Etiology and audiological outcomes at 3 years for 364 children in Australia

Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency

Recent advances in the molecular genetics of epilepsy

ALKBH5 Is a Mammalian RNA Demethylase that Impacts RNA Metabolism and Mouse Fertility

Long-Term Outcomes of Imatinib Treatment for Chronic Myeloid Leukemia

Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage

Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis

Glucose metabolism transporters and epilepsy: Only GLUT1 has an established role

Fish oil supplementation during pregnancy and allergic respiratory disease in the adult offspring

Evaluation of 2D super-resolution ultrasound imaging of the rat renal vasculature using ex vivo micro-computed tomography

Linear Decrease in Athletic Performance During the Human Life Span

Phase III Trial of Cetuximab With Continuous or Intermittent Fluorouracil, Leucovorin, and Oxaliplatin (Nordic FLOX) Versus FLOX Alone in First-Line Treatment of Metastatic Colorectal Cancer: The NORDIC-VII Study

InSegtCone: interactive segmentation of crystalline cones in compound eyes

Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease

Basophil sensitivity reflects long‐term clinical outcome of subcutaneous immunotherapy in grass pollen‐allergic patients

Cystatin C proteoforms in chronic kidney disease

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