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Myasthenia gravis: an update for the clinician

Clinical and experimental immunology, 2014-03, Vol.175 (3), p.408-418

Sieb, J. P.

2014

Volltextzugriff (PDF)

Fatigue in multiple sclerosis is closely related to sleep disorders: a polysomnographic cross-sectional study

Multiple sclerosis, 2011-05, Vol.17 (5), p.613-622

2011

Volltextzugriff (PDF)

New Mutations in Acetylcholine Receptor Subunit Genes Reveal Heterogeneity in the Slow-Channel Congenital Myasthenic Syndrome

Human molecular genetics, 1996-09, Vol.5 (9), p.1217-1227

1996

Volltextzugriff (PDF)

Myasthenia gravis: emerging new therapy options

Current opinion in pharmacology, 2005-06, Vol.5 (3), p.303-307

Sieb, Joern P

2005

Volltextzugriff (PDF)

Familial meningioma is not allelic to neurofibromatosis 2

Neurology, 1993-10, Vol.43 (10), p.2096

1993

Volltextzugriff (PDF)

Severe congenital myasthenic syndrome due to homozygosity of the 1293insG ε-acetylcholine receptor subunit mutation

Annals of neurology, 2000-09, Vol.48 (3), p.379-383

2000

Volltextzugriff (PDF)

Effects of the quinoline derivatives quinine, quinidine, and chloroquine on neuromuscular transmission

Brain research, 1996-03, Vol.712 (2), p.179-189

1996

Volltextzugriff (PDF)

Myasthenia gravis and myasthenic syndromes

Zeitschrift für Rheumatologie, 2009-08, Vol.68 (6), p.465

2009

Volltextzugriff (PDF)

Relapsing alternating ptosis in two siblings

Journal of neurology, neurosurgery and psychiatry, 2000-08, Vol.69 (2), p.282-283

2000

Volltextzugriff (PDF)

Congenital myasthenic syndrome of Brahman cattle in South Africa

Veterinary record, 2003-12, Vol.153 (25), p.779-781

2003

Volltextzugriff (PDF)

Nontraumatic spinal epidural and subdural hematomas

Neurology, 1987-08, Vol.37 (8), p.1351

1987

Volltextzugriff (PDF)

Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency

Neurology, 1998-01, Vol.50 (1), p.54

1998

Volltextzugriff (PDF)

Recurrent focal myositis

Muscle & nerve, 1997-09, Vol.20 (9), p.1205-1206

1997

Volltextzugriff (PDF)

Ephedrine: effects on neuromuscular transmission

Brain research, 1993-09, Vol.623 (1), p.167-171

1993

Volltextzugriff (PDF)

Congenital myasthenic syndrome due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene

European journal of neurology, 2002-11, Vol.9 (6), p.694-695

2002

Volltextzugriff (PDF)

Fluoroquinolone antibiotics block neuromuscular transmission

Neurology, 1998-03, Vol.50 (3), p.804

Sieb, J P

1998

Volltextzugriff (PDF)

Sporadic adult-onset distal myopathy with rimmed vacuoles, 15–18 nm tubulofilaments and extensive rod formation

Journal of the neurological sciences, 1997-02, Vol.146 (1), p.81-84

1997

Volltextzugriff (PDF)

Intermittent apomorphine injections as rescue therapy for advanced Parkinson's disease. Consensus statement

Nervenarzt, 2008-04, Vol.79 (4), p.475

2008

Volltextzugriff (PDF)

Endplate ultrastructure in a case of primary fibromyalgia

Clinical rheumatology, 1997-11, Vol.16 (6), p.637-638

1997

Volltextzugriff (PDF)

Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by ε-AChR subunit truncating mutations

Human genetics, 2000-08, Vol.107 (2), p.160-164

2000

Volltextzugriff (PDF)

Occurrence of chloroquine-induced myopathy after low-dose treatment of rheumatoid arthritis for seven years

Zeitschrift für Rheumatologie, 2005-05, Vol.64 (4), p.274

2005

Volltextzugriff (PDF)

Familial CNS tumors

Journal of neurology, 1992-07, Vol.239 (6), p.343-344

1992

Volltextzugriff (PDF)

Iatrogenic and toxic myopathies

Muscle & nerve, 2003-02, Vol.27 (2), p.142-156

2003

Volltextzugriff (PDF)

Immunohistochemical detection of complement factors: a reliable method for the diagnosis of myasthenia gravis

Nervenarzt, 2000-08, Vol.71 (8), p.666

2000

Volltextzugriff (PDF)

An autosomal-recessive congenital myasthenic syndrome with tubular aggregates in a libyan family

Neuromuscular disorders : NMD, 1996-03, Vol.6 (2), p.115-119

1996

Volltextzugriff (PDF)

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Myasthenia gravis: an update for the clinician

Fatigue in multiple sclerosis is closely related to sleep disorders: a polysomnographic cross-sectional study

New Mutations in Acetylcholine Receptor Subunit Genes Reveal Heterogeneity in the Slow-Channel Congenital Myasthenic Syndrome

Myasthenia gravis: emerging new therapy options

Familial meningioma is not allelic to neurofibromatosis 2

Severe congenital myasthenic syndrome due to homozygosity of the 1293insG ε-acetylcholine receptor subunit mutation

Effects of the quinoline derivatives quinine, quinidine, and chloroquine on neuromuscular transmission

Myasthenia gravis and myasthenic syndromes

Relapsing alternating ptosis in two siblings

Congenital myasthenic syndrome of Brahman cattle in South Africa

Nontraumatic spinal epidural and subdural hematomas

Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency

Recurrent focal myositis

Ephedrine: effects on neuromuscular transmission

Congenital myasthenic syndrome due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene

Fluoroquinolone antibiotics block neuromuscular transmission

Sporadic adult-onset distal myopathy with rimmed vacuoles, 15–18 nm tubulofilaments and extensive rod formation

Intermittent apomorphine injections as rescue therapy for advanced Parkinson's disease. Consensus statement

Endplate ultrastructure in a case of primary fibromyalgia

Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by ε-AChR subunit truncating mutations

Occurrence of chloroquine-induced myopathy after low-dose treatment of rheumatoid arthritis for seven years

Familial CNS tumors

Iatrogenic and toxic myopathies

Immunohistochemical detection of complement factors: a reliable method for the diagnosis of myasthenia gravis

An autosomal-recessive congenital myasthenic syndrome with tubular aggregates in a libyan family

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