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List of works by Nanna Witting

A PET activation study of brush-evoked allodynia in patients with nerve injury pain.

scientific article published on 20 December 2005

A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy

scientific article published on 3 June 2016

Aerobic Training in Patients with Congenital Myopathy

scientific article published on 11 January 2016

Axial myopathy: an overlooked feature of muscle diseases.

scientific article

Becker muscular dystrophy with widespread muscle hypertrophy and a non-sense mutation of exon 2

scientific article published on 28 August 2012

Botulinum toxin treatment improves dysphagia in patients with oculopharyngeal muscular dystrophy and sporadic inclusion body myositis

scientific article published in 2022

Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E

scientific article published on 10 April 2015

Clinical and neurophysiological response to pharmacological treatment of DOK7 congenital myasthenia in an older patient.

scientific article

Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblasts

scientific article published on 17 January 2018

Congenital titinopathy: Comprehensive characterisation and pathogenic insights

scientific article published on 25 April 2018

Decreased variability of the 6-minute walk test by heart rate correction in patients with neuromuscular disease

scientific article

Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype.

scientific article published on December 2011

Differential effect of painful heterotopic stimulation on capsaicin-induced pain and allodynia ⬇️

scientific article published on August 10, 1998

Differential recruitment of endogenous pain inhibitory systems in neuropathic pain patients

scientific article published on 01 May 2003

Effect of sildenafil on skeletal and cardiac muscle in Becker muscular dystrophy

scientific article published on 15 July 2014

Effects of Sildenafil on Cerebrovascular Reactivity in Patients with Becker Muscular Dystrophy.

scientific article published on 2 August 2016

Endocrine function over time in patients with myotonic dystrophy type 1

scientific article published on 25 August 2014

Frequency and Phenotype of Myotubular Myopathy Amongst Danish Patients with Congenital Myopathy Older than 5 Years

scientific article published on June 2015

Frequency and phenotype of patients carrying TPM2 and TPM3 gene mutations in a cohort of 94 patients with congenital myopathy

scientific article published on 3 January 2014

Has basic research contributed to chronic pain treatment?

scientific article

High prevalence of cardiac involvement in patients with myotonic dystrophy type 1: a cross-sectional study

scientific article published on 20 March 2014

LGMD2L with bone affection: Overlapping phenotype of dominant and recessive ANO5‐induced disease ⬇️

scientific article published on November 1, 2012

Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy.

scientific article published on 22 December 2015

Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy.

scientific article

Myocardial fibrosis in patients with myotonic dystrophy type 1: a cardiovascular magnetic resonance study

scientific article published on August 2014

Ocular, bulbar, limb, and cardiopulmonary involvement in oculopharyngeal muscular dystrophy

scientific article published on 10 March 2014

Pharmacologic treatment of downstream of tyrosine kinase 7 congenital myasthenic syndrome.

scientific article published on March 2014

Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome.

scientific article published on 29 December 2017

Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark

scientific article published on 21 March 2017

Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations.

scientific article published on 14 July 2015

Progression of cardiac involvement in patients with limb-girdle type 2 and Becker muscular dystrophies: A 9-year follow-up study

scientific article published on 27 December 2014

Reliability of the 2- and 6-minute walk tests in neuromuscular diseases

scientific article published on 01 April 2017

Repetitive intradermal capsaicin: differential effect on pain and areas of allodynia and punctate hyperalgesia

scientific article published on 01 January 2000

Response

scientific article published on 26 January 2013

Severe axial myopathy in McArdle disease.

scientific article

The antimyotonic effect of lamotrigine in non-dystrophic myotonias: a double-blind randomized study.

scientific article published in September 2017

Two- and 6-minute walk tests assess walking capability equally in neuromuscular diseases.

scientific article published on 6 January 2016

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