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Physical fatigability and muscle pain in patients with Hashimoto thyroiditis

Journal of neurology, 2021-07, Vol.268 (7), p.2441-2449

2021

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Manifesting heterozygotes in carnitine palmitoyltransferase (CPT) II deficiency

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S199-S199

2016

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S45-3 Diagnostic value of muscle biopsy versus molecular genetics in myopathies

Clinical neurophysiology, 2010, Vol.121, p.S64-S65

Zierz, S

2010

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The significance of pathological spontaneous activity in various myopathies

Clinical neurophysiology, 2014-07, Vol.125 (7), p.1485-1490

2014

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EP 42. Smooth muscle involvement in Glycogenosis Type II: Thalamus hemorrhage, increased blood flow and dolichoectasia in a late-onset Pompe patient

Clinical neurophysiology, 2016-09, Vol.127 (9), p.e256-e257

2016

Volltextzugriff (PDF)

EP 89. Experimental provocation of “ice-cream headache” by ice cubes and ice water

Clinical neurophysiology, 2016-09, Vol.127 (9), p.e279-e280

2016

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Treatment of adult idiopathic inflammatory myopathies with conventional immunosuppressive drugs: Results of a retrospective study

Zeitschrift für Rheumatologie, 2019-03, Vol.78 (2), p.183-189

2019

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C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis

Journal of neurology, 2012-11, Vol.259 (11), p.2434-2439

2012

Volltextzugriff (PDF)

Polyglucosan myopathy and functional characterization of a novel GYG1 mutation

Acta neurologica Scandinavica, 2018-03, Vol.137 (3), p.308-315

2018

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Use of Complementary and Alternative Medicine in Patients Suffering from Primary Headache Disorders

Cephalalgia, 2009-10, Vol.29 (10), p.1069-1078

2009

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P.17.14 Myohistological mitochondrial changes in patients with mtDNA singular deletions, multiple deletions and A3243G point mutation

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.830-830

2013

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P 56. Myotonia congenita Thomsen and Adolph Seeligmüller from Halle a.d. Saale

Clinical neurophysiology, 2021-08, Vol.132 (8), p.e26-e27

2021

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T.P.29

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.873-873

2014

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High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study

Journal of Neural Transmission, 2005-05, Vol.112 (5), p.649-660

2005

Volltextzugriff (PDF)

MELAS associated with mutations in the POLG1 gene

Neurology, 2007-05, Vol.68 (20), p.1741

2007

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P39. Assigning pathogenicity to three novel mt-tRNA mutations associated with different mitochondrial disease presentations

Clinical neurophysiology, 2015-08, Vol.126 (8), p.e115-e115

2015

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Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations

Journal of neurology, 2011-06, Vol.258 (6), p.1085-1090

2011

Volltextzugriff (PDF)

Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism

Neurology, 2005-01, Vol.64 (2), p.371

2005

Volltextzugriff (PDF)

Unusual manifestations in two cases of necrotizing myopathy associated with SRP-antibodies

Clinical neurology and neurosurgery, 2012-09, Vol.114 (7), p.1104-1106

2012

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MuSK-antibody positive pure ocular myasthenia gravis

Journal of neurology, 2006-05, Vol.253 (5), p.659-660

2006

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Cerebrovascular reactivity is impaired in patients with cardiac failure

European heart journal, 2000-03, Vol.21 (5), p.407-413

2000

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Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2)

Neurology, 2006-07, Vol.67 (2), p.350

2006

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The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

Clinical genetics, 2010-03, Vol.77 (3), p.302-303

2010

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Unusual manifestations in two cases of necrotizing myopathy associated with SRP antibodies

Rheumatology international, 2013-05, Vol.33 (5), p.1371-1372

2013

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AMP deaminase deficiency in skeletal muscle is unlikely to be of clinical relevance

Journal of neurology, 2008-03, Vol.255 (3), p.318-322

2008

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Physical fatigability and muscle pain in patients with Hashimoto thyroiditis

Manifesting heterozygotes in carnitine palmitoyltransferase (CPT) II deficiency

S45-3 Diagnostic value of muscle biopsy versus molecular genetics in myopathies

The significance of pathological spontaneous activity in various myopathies

EP 42. Smooth muscle involvement in Glycogenosis Type II: Thalamus hemorrhage, increased blood flow and dolichoectasia in a late-onset Pompe patient

EP 89. Experimental provocation of “ice-cream headache” by ice cubes and ice water

Treatment of adult idiopathic inflammatory myopathies with conventional immunosuppressive drugs: Results of a retrospective study

C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis

Polyglucosan myopathy and functional characterization of a novel GYG1 mutation

Use of Complementary and Alternative Medicine in Patients Suffering from Primary Headache Disorders

P.17.14 Myohistological mitochondrial changes in patients with mtDNA singular deletions, multiple deletions and A3243G point mutation

P 56. Myotonia congenita Thomsen and Adolph Seeligmüller from Halle a.d. Saale

T.P.29

High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study

MELAS associated with mutations in the POLG1 gene

P39. Assigning pathogenicity to three novel mt-tRNA mutations associated with different mitochondrial disease presentations

Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations

Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism

Unusual manifestations in two cases of necrotizing myopathy associated with SRP-antibodies

MuSK-antibody positive pure ocular myasthenia gravis

Cerebrovascular reactivity is impaired in patients with cardiac failure

Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2)

The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

Unusual manifestations in two cases of necrotizing myopathy associated with SRP antibodies

AMP deaminase deficiency in skeletal muscle is unlikely to be of clinical relevance

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