Authors:
Monani, UR
Sendtner, M
Coovert, DD
Parsons, DW
Andreassi, C
Le, TT
Jablonka, S
Schrank, B
Rossol, W
Prior, TW
Morris, GE
Burghes, AHM
Citation: Ur. Monani et al., The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy, HUM MOL GEN, 9(3), 2000, pp. 333-339
Authors:
Jablonka, S
Schrank, B
Kralewski, M
Rossoll, W
Sendtner, M
Citation: S. Jablonka et al., Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III, HUM MOL GEN, 9(3), 2000, pp. 341-346
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
Citation: Wh. Jost et B. Schrank, Repeat botulin toxin injections in anal fissure - In patients with relapseand after insufficient effect of first treatment, DIG DIS SCI, 44(8), 1999, pp. 1588-1589
Citation: Wh. Jost et al., Functional outlet obstruction: Anismus, spastic pelvic floor syndrome, anddyscoordination of the voluntary sphincter muscles - Definition, diagnosis, and treatment from the neurologic point of view, SC J GASTR, 34(5), 1999, pp. 449-453