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Seronegative myasthenic syndrome?

Nervenarzt, 2020-02, Vol.91 (2), p.150-152

2020

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Alterations in the trapezius muscle in young patients with migraine – A pilot case series with MRI

European journal of paediatric neurology, 2015-05, Vol.19 (3), p.372-376

2015

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High-dose immunoglobulin therapy in sporadic inclusion body myositis : a double-blind, placebo-controlled study

Journal of neurology, 2000-01, Vol.247 (1), p.22-28

2000

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P541: The impact of spinal muscular atrophies with regard to patients’ quality of life: a socio-economic analysis of a German patient cohort

Clinical neurophysiology, 2014-06, Vol.125, p.S196-S196

2014

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Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P

Brain (London, England : 1878), 2007-06, Vol.130 (6), p.1485-1496

2007

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G.P.166

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.855-855

2014

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Evaluation of Cost Of Illness (COI) and health care burden in Spinal Muscular Atrophies (SMA)

Journal of the neurological sciences, 2013-10, Vol.333, p.e434-e435

2013

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Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degeneration

Journal of neurology, 2011-05, Vol.258 (5), p.946-947

2011

Volltextzugriff (PDF)

Seronegatives myasthenes Syndrom?

Nervenarzt, 2020-02, Vol.91 (2), p.150-152

2020

Volltextzugriff (PDF)

Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study

Neurology, 2000-05, Vol.54 (9), p.1848

2000

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Ten-year follow-up in a case series of integrative botulinum toxin intervention in adolescents with chronic daily headache and associated muscle pain

Neuropediatrics, 2012-12, Vol.43 (6), p.339

2012

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FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

Journal of medical genetics, 2004-04, Vol.41 (4), p.e50-e50

2004

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P75 Muscle MRI findings in LGMD2L

Neuromuscular disorders : NMD, 2011, Vol.21, p.S28-S28

2011

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P4.27 Muscle MRI findings in anoctaminopathy

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.666-666

2010

Volltextzugriff (PDF)

P.47 - Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S112-S112

2017

Volltextzugriff (PDF)

Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S112

2017

Volltextzugriff (PDF)

P64 Neutral lipid storage myopathy due to PNPLA2 mutations may respond to beta-adrenergic treatment

Neuromuscular disorders : NMD, 2011, Vol.21, p.S25-S25

2011

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Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial

Orphanet journal of rare diseases, 2013-02, Vol.8 (1), p.26-26

2013

Volltextzugriff (PDF)

Primary headache in children and adolescents: update on pharmacotherapy of migraine and tension-type headache

Neuropediatrics, 2013-02, Vol.44 (1), p.3

2013

Volltextzugriff (PDF)

De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy

Neuromuscular disorders : NMD, 2002-12, Vol.12 (10), p.947-951

2002

Volltextzugriff (PDF)

G.P.166: Comparative economic impact of therapeutic innovation on health care burden of Duchenne Muscular Dystrophy (DMD) using Becker Muscular Dystrophy (BMD) as a comparator for potential clinical outcome corridor

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.855-855

2014

Volltextzugriff (PDF)

LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filaments

Acta myologica, 2006-10, Vol.25 (2), p.73

2006

Volltextzugriff (PDF)

Muscle pathology in 57 patients with myotonic dystrophy type 2

Muscle & nerve, 2004-02, Vol.29 (2), p.275-281

2004

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Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood

Acta myologica, 2004-05, Vol.23 (1), p.1

2004

Volltextzugriff (PDF)

Facharztprüfung Neurologie

2., aktualisierte Auflage.

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Seronegative myasthenic syndrome?

Alterations in the trapezius muscle in young patients with migraine – A pilot case series with MRI

High-dose immunoglobulin therapy in sporadic inclusion body myositis : a double-blind, placebo-controlled study

P541: The impact of spinal muscular atrophies with regard to patients’ quality of life: a socio-economic analysis of a German patient cohort

Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P

G.P.166

Evaluation of Cost Of Illness (COI) and health care burden in Spinal Muscular Atrophies (SMA)

Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degeneration

Seronegatives myasthenes Syndrom?

Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study

Ten-year follow-up in a case series of integrative botulinum toxin intervention in adolescents with chronic daily headache and associated muscle pain

FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

P75 Muscle MRI findings in LGMD2L

P4.27 Muscle MRI findings in anoctaminopathy

P.47 - Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene

Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene

P64 Neutral lipid storage myopathy due to PNPLA2 mutations may respond to beta-adrenergic treatment

Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial

Primary headache in children and adolescents: update on pharmacotherapy of migraine and tension-type headache

De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy

G.P.166: Comparative economic impact of therapeutic innovation on health care burden of Duchenne Muscular Dystrophy (DMD) using Becker Muscular Dystrophy (BMD) as a comparator for potential clinical outcome corridor

LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filaments

Muscle pathology in 57 patients with myotonic dystrophy type 2

Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood

Facharztprüfung Neurologie

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