J. Sieb

发表

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

M. Rüegg, U. Wewer, S. Tzartos, 1998, Neurology.

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

H. Reichmann, W. Poewe, A. Ceballos-Baumann, 2008, Der Nervenarzt.

The European LEMS Registry: Baseline Demographics and Treatment Approaches

R. Mantegazza, C. Desnuelle, A. Meisel, 2015, Neurology and Therapy.

Myasthenia gravis: emerging new therapy options.

J. Sieb, 2005, Current opinion in pharmacology.

Iatrogenic and toxic myopathies

T. Gillessen, J. Sieb, 2003, Muscle & nerve.

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

O. Steinlein, J. Sieb, S. Kraner, 2000, Human genetics.

Fluoroquinolone antibiotics block neuromuscular transmission

J. Sieb, 1998, Neurology.

Alopecia induced by dopamine agonists.

M. Grauer, J. Sieb, 2002, Neurology.

Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine

K. Ohno, B. Banwell, A. Engel, 2004, Neuromuscular Disorders.

Congenital myasthenic syndromes.

O. Steinlein, J. Sieb, S. Kraner, 2002, Seminars in pediatric neurology.

Myasthenia gravis: an update for the clinician

J. Sieb, 2014, Clinical and experimental immunology.

New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.

K. Ohno, S. Sine, C. Bouzat, 1996, Human molecular genetics.

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

O. Steinlein, B. Schrank, S. Tzartos, 2000, Annals of Neurology.

Periodic limb movements during REM sleep in multiple sclerosis: a previously undescribed entity

F. Paul, K. Wernecke, H. Radbruch, 2015, Neuropsychiatric disease and treatment.

Congenital myasthenic syndrome with episodic apnea in patients homozygous for a CHAT missense mutation.

O. Steinlein, H. Strassburg, I. Laufenberg, 2003, Archives of neurology.

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

D. Pongratz, P. Fischer, J. Sieb, 2005, Zeitschrift fur Rheumatologie.

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

O. Steinlein, B. Schrank, S. Tzartos, 2000 .

Congenital Myasthenic Syndrome in Cattle due to Homozygosity for a Truncating Mutation in the Acetylcholine Receptor (AChR) Epsilon‐Subunit Gene

O. Steinlein, P. Thompson, J. Sieb, 2003, Annals of the New York Academy of Sciences.

[Acute spinal epidural abscess].

H. Mattle, M. Forsting, J. Sieb, 1986, Deutsche medizinische Wochenschrift.