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E Neuen-Jacob

Showing results (41-50 of 53) with videos related to

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Fortschritte Der Neurologie-Psychiatrie|April 9, 2010
[Myosin storage myopathy: a rare subtype of protein aggregate myopathies]I C Kiphuth, E Neuen-Jacob, T Struffert, et al.
Neuropediatrics|September 26, 2001
Reducing body myopathy with cytoplasmic bodies and rigid spine syndrome: a mixed congenital myopathyH H Goebel, L E Halbig, L Goldfarb, et al.
Neuropediatrics|May 8, 2008
Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H)A Koy, B Ilkovski, N Laing, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1994
Multisystem triglyceride storage disorder without ichthyosis in two siblingsR Wessalowski, H Schroten, E Neuen-Jacob, et al.
Journal of Neurovirology|June 19, 2004
Dopamine deficits and regulation of the cAMP second messenger system in brains of simian immunodeficiency virus-infected rhesus monkeysM Jenuwein, C Scheller, E Neuen-Jacob, et al.
Neuropediatrics|May 1, 1988
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosisT Voit, O Krogmann, H G Lenard, et al.
Journal of Alzheimer'S Disease : JAD|March 16, 2007
Alterations in expression of glutamatergic transporters and receptors in sporadic Alzheimer's diseaseC P Jacob, E Koutsilieri, J Bartl, et al.
Journal of Neurosurgery|August 10, 2000
Multiple intracranial juvenile xanthogranulomas. Case reportJ Boström, G Janssen, M Messing-Jünger, et al.
Cancer Gene Therapy|January 5, 2002
Local inflammation and devascularization--in vivo mechanisms of the "bystander effect" in VPC-mediated HSV-Tk/GCV gene therapy for human malignant gliomaF W Floeth, N Shand, H Bojar, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Novel TPM3 mutation in a family with cap myopathy and review of the literatureT Schreckenbach, J M Schröder, T Voit, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Fortschritte Der Neurologie-Psychiatrie|April 9, 2010
[Myosin storage myopathy: a rare subtype of protein aggregate myopathies]I C Kiphuth, E Neuen-Jacob, T Struffert, et al.
Neuropediatrics|September 26, 2001
Reducing body myopathy with cytoplasmic bodies and rigid spine syndrome: a mixed congenital myopathyH H Goebel, L E Halbig, L Goldfarb, et al.
Neuropediatrics|May 8, 2008
Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H)A Koy, B Ilkovski, N Laing, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1994
Multisystem triglyceride storage disorder without ichthyosis in two siblingsR Wessalowski, H Schroten, E Neuen-Jacob, et al.
Journal of Neurovirology|June 19, 2004
Dopamine deficits and regulation of the cAMP second messenger system in brains of simian immunodeficiency virus-infected rhesus monkeysM Jenuwein, C Scheller, E Neuen-Jacob, et al.
Neuropediatrics|May 1, 1988
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosisT Voit, O Krogmann, H G Lenard, et al.
Journal of Alzheimer'S Disease : JAD|March 16, 2007
Alterations in expression of glutamatergic transporters and receptors in sporadic Alzheimer's diseaseC P Jacob, E Koutsilieri, J Bartl, et al.
Journal of Neurosurgery|August 10, 2000
Multiple intracranial juvenile xanthogranulomas. Case reportJ Boström, G Janssen, M Messing-Jünger, et al.
Cancer Gene Therapy|January 5, 2002
Local inflammation and devascularization--in vivo mechanisms of the "bystander effect" in VPC-mediated HSV-Tk/GCV gene therapy for human malignant gliomaF W Floeth, N Shand, H Bojar, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Novel TPM3 mutation in a family with cap myopathy and review of the literatureT Schreckenbach, J M Schröder, T Voit, et al.
Pageof 6