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Results:
1-8
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Results: 8
Authors:
Sieb, JP
Citation: Jp. Sieb, Recurrent ptosis - reply, J NE NE PSY, 70(6), 2001, pp. 820-820
Authors:
Sieb, JP
Kraner, S
Steinlein, OK
Bufler, J
Citation: Jp. Sieb et al., Congential myasthenic syndromes, KLIN NEUROP, 31(3), 2000, pp. 148-154
Authors:
Sieb, JP
Kraner, S
Schrank, B
Reitter, B
Goebel, THH
Tzartos, SJ
Steinlein, OK
Citation: Jp. Sieb et al., Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutation, ANN NEUROL, 48(3), 2000, pp. 379-383
Authors:
Sieb, JP
Kraner, S
Rauch, M
Steinlein, OK
Citation: Jp. Sieb et al., Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by epsilon-AChR subunit truncating mutations, HUM GENET, 107(2), 2000, pp. 160-164
Authors:
Zander, T
Schwab, S
Laufenberg, I
Sieb, JP
Citation: T. Zander et al., Immunohistochemical detection of complement factors: a reliable method forthe diagnosis of myasthenia gravis, NERVENARZT, 71(8), 2000, pp. 666-669
Authors:
Sieb, JP
Hartmann, A
Citation: Jp. Sieb et A. Hartmann, Relapsing alternating ptosis in two siblings, J NE NE PSY, 69(2), 2000, pp. 282-283
Authors:
Sieb, JP
Citation: Jp. Sieb, Diagnosis and treatment of the congenital myasthenia syndrome, DEUT MED WO, 124(1-2), 1999, pp. 24-29
Authors:
Sieb, JP
Citation: Jp. Sieb, Ofloxacin in the Lamhert-Eaton myasthenic syndrome - Reply form the authors, NEUROLOGY, 52(2), 1999, pp. 435-435
Risultati:
1-8
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