UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Guillain-Barré syndrome

Lancet, 2005-11, Vol.366 (9497), p.1653-1666

2005

Link zum Volltext

A framework for diagnosing and classifying intensive care unit-acquired weakness

Critical care medicine, 2009-10, Vol.37 (10 Suppl, ICU-Acquired Weakness: Proceedings of a Round Table Conference in Brussels, Belgium, March 2009), p.S299-S308

2009

Link zum Volltext

Verfügbarkeit prüfen

DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

American journal of human genetics, 2004-06, Vol.74 (6), p.1128-1135

2004

Link zum Volltext

Verfügbarkeit prüfen

The Safety Profile of Dalfampridine Extended Release in Multiple Sclerosis Clinical Trials

Clinical therapeutics, 2012-05, Vol.34 (5), p.1056-1069

2012

Link zum Volltext

Verfügbarkeit prüfen

Small-fiber sensory neuropathies: Clinical course and neuropathology of idiopathic cases

Annals of neurology, 1998-07, Vol.44 (1), p.47-59

1998

Link zum Volltext

Verfügbarkeit prüfen

Acute motor axonal neuropathy: An antibody-mediated attack on axolemma

Annals of neurology, 1996-10, Vol.40 (4), p.635-644

1996

Link zum Volltext

Verfügbarkeit prüfen

Neuropathological alterations in diabetic truncal neuropathy: evaluation by skin biopsy

Journal of neurology, neurosurgery and psychiatry, 1998-11, Vol.65 (5), p.762-766

1998

Link zum Volltext

Verfügbarkeit prüfen

Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34

American journal of human genetics, 1998-03, Vol.62 (3), p.633-640

1998

Link zum Volltext

Verfügbarkeit prüfen

Peripheral neuropathy from taxol and cisplatin combination chemotherapy: Clinical and electrophysiological studies

Annals of neurology, 1994-03, Vol.35 (3), p.304-311

1994

Link zum Volltext

Verfügbarkeit prüfen

The effect of systemically administered recombinant human nerve growth factor in healthy human subjects

Annals of neurology, 1994-08, Vol.36 (2), p.244-246

1994

Link zum Volltext

Verfügbarkeit prüfen

Supportive care for patients with Guillain-Barré syndrome

Archives of neurology (Chicago), 2005-08, Vol.62 (8), p.1194

2005

Link zum Volltext

Verfügbarkeit prüfen

Perioperative bilateral median neuropathy

Anesthesiology (Philadelphia), 2002-12, Vol.97 (6), p.1632-1634

2002

Link zum Volltext

Verfügbarkeit prüfen

Autonomic and peripheral (sensorimotor) neuropathy in chronic liver disease: A clinical and electrophysiologic study

Hepatology (Baltimore, Md.), 1999-06, Vol.29 (6), p.1698-1703

1999

Link zum Volltext

Verfügbarkeit prüfen

Worsening of multifocal motor neuropathy during pregnancy

Neurology, 2002-07, Vol.59 (1), p.139

2002

Link zum Volltext

Verfügbarkeit prüfen

Congenital End-Plate Acetylcholinesterase Deficiency Caused by a Nonsense Mutation and an A→G Splice-Donor–Site Mutation at Position +3 of the Collagenlike-Tail–Subunit Gene ( COLQ): How Does G at Position +3 Result in Aberrant Splicing?

American journal of human genetics, 1999-09, Vol.65 (3), p.635-644

1999

Link zum Volltext

Verfügbarkeit prüfen

Abnormal excitatory amino acid metabolism in amyotrophic lateral sclerosis

Annals of neurology, 1990-07, Vol.28 (1), p.18-25

1990

Link zum Volltext

Verfügbarkeit prüfen

Multifocal motor neuropathy: Response to human immune globulin

Annals of neurology, 1993-03, Vol.33 (3), p.237-242

1993

Link zum Volltext

Verfügbarkeit prüfen

Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembrane MPZ mutation

Muscle & nerve, 2004-06, Vol.29 (6), p.867-869

2004

Link zum Volltext

Verfügbarkeit prüfen

Sensory nerve pathology in multifocal motor neuropathy

Annals of neurology, 1996-03, Vol.39 (3), p.319-325

1996

Link zum Volltext

Verfügbarkeit prüfen

Assessment of current diagnostic criteria for Guillain-Barré syndrome

Annals of neurology, 1990, Vol.27 (S1), p.S21-S24

1990

Link zum Volltext

Verfügbarkeit prüfen

Epidermal innervation: changes with aging, topographic location, and in sensory neuropathy

Journal of the neurological sciences, 1999-04, Vol.164 (2), p.172-178

1999

Link zum Volltext

Verfügbarkeit prüfen

Intensive management and treatment of severe Guillain-Barré syndrome

Critical care medicine, , Vol.21 (3), p.433-446

Link zum Volltext

Verfügbarkeit prüfen

Nerve conduction studies in amyotrophic lateral sclerosis

Muscle & nerve, 1992-10, Vol.15 (10), p.1111-1115

1992

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 68

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieAnn Neurol

ThemaMedical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(62)
Mit Volltextzugriff
(55)

Publikationsform

Artikel
(68)

Sprache

Englisch
(68)
Japanisch
(23)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Guillain-Barré syndrome

A framework for diagnosing and classifying intensive care unit-acquired weakness

DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

The Safety Profile of Dalfampridine Extended Release in Multiple Sclerosis Clinical Trials

Small-fiber sensory neuropathies: Clinical course and neuropathology of idiopathic cases

Acute motor axonal neuropathy: An antibody-mediated attack on axolemma

Neuropathological alterations in diabetic truncal neuropathy: evaluation by skin biopsy

Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34

Peripheral neuropathy from taxol and cisplatin combination chemotherapy: Clinical and electrophysiological studies

The effect of systemically administered recombinant human nerve growth factor in healthy human subjects

Supportive care for patients with Guillain-Barré syndrome

Changing outcome in inflammatory neuropathies: Rasch-comparative responsiveness

Perioperative bilateral median neuropathy

Autonomic and peripheral (sensorimotor) neuropathy in chronic liver disease: A clinical and electrophysiologic study

Modifying the Medical Research Council grading system through Rasch analyses

Worsening of multifocal motor neuropathy during pregnancy

Congenital End-Plate Acetylcholinesterase Deficiency Caused by a Nonsense Mutation and an A→G Splice-Donor–Site Mutation at Position +3 of the Collagenlike-Tail–Subunit Gene ( COLQ): How Does G at Position +3 Result in Aberrant Splicing?

Abnormal excitatory amino acid metabolism in amyotrophic lateral sclerosis

Multifocal motor neuropathy: Response to human immune globulin

Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembrane MPZ mutation

Sensory nerve pathology in multifocal motor neuropathy

Assessment of current diagnostic criteria for Guillain-Barré syndrome

Epidermal innervation: changes with aging, topographic location, and in sensory neuropathy

Intensive management and treatment of severe Guillain-Barré syndrome

Nerve conduction studies in amyotrophic lateral sclerosis

Aktive Filter

Suchergebnisse filtern