UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 175

Sortiert nach

Sonography of the median nerve in Charcot-Marie-Tooth disease

American journal of roentgenology (1976), 2002-06, Vol.178 (6), p.1553

2002

Volltextzugriff (PDF)

Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease

The European journal of neuroscience, 2006-03, Vol.23 (6), p.1445-1452

2006

Volltextzugriff (PDF)

Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A disease

Neurobiology of disease, 2004-06, Vol.16 (1), p.263-273

2004

Volltextzugriff (PDF)

Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease

Experimental neurology, 2004-11, Vol.190 (1), p.213-223

2004

Volltextzugriff (PDF)

Impaired Expression of Ciliary Neurotrophic Factor in Charcot-Marie-Tooth Type 1A Neuropathy

Journal of neuropathology and experimental neurology, 2009-05, Vol.68 (5), p.441-455

2009

Volltextzugriff (PDF)

Impaired Expression of Ciliary Neurotrophic Factor in Charcot-Marie-Tooth Type 1 A Neuropathy

Journal of neuropathology and experimental neurology, 2009, Vol.68 (5), p.441-455

2009

Volltextzugriff (PDF)

Experimental Charcot–Marie–Tooth type 1A: A cDNA microarrays analysis

Molecular and cellular neuroscience, 2005-04, Vol.28 (4), p.703-714

2005

Volltextzugriff (PDF)

Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type1A disease

The European journal of neuroscience, 2006-03, Vol.23 (6), p.1445-1452

2006

Volltextzugriff (PDF)

Postvibration Depression of the H-Reflex as a Result of a Dual Mechanism: An Experimental Study in Humans

Journal of clinical neurophysiology, 2001-09, Vol.18 (5), p.460-470

2001

Volltextzugriff (PDF)

PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A

Annals of neurology, 2001-07, Vol.50 (1), p.47-55

2001

Volltextzugriff (PDF)

Testing for pre-synaptic and post-synaptic changes in the soleus H reflex pathway following selective muscle vibration in humans

Neuroscience letters, 1997-08, Vol.231 (2), p.99-102

1997

Volltextzugriff (PDF)

Presynaptic and postsynaptic mechanisms underlying H-reflex changes produced by a selective voluntary contraction

Muscle & nerve, 1998-04, Vol.21 (4), p.439-453

1998

Volltextzugriff (PDF)

Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

Annals of neurology, 1997-12, Vol.42 (6), p.866-872

1997

Volltextzugriff (PDF)

Insulin treatment enhances expression of IGF-I in sural nerves of diabetic patients

Muscle & nerve, 2001-05, Vol.24 (5), p.622-629

2001

Volltextzugriff (PDF)

New subcortical components of the cerebral somatosensory evoked potential in man

Acta neurologica Scandinavica, 1978-12, Vol.58 (6), p.325-332

1978

Volltextzugriff (PDF)

Minocycline for Symptomatic Neurosyphilis in Patients Allergic to Penicillin: Letter

The New England journal of medicine, 1997-10, Vol.337 (18), p.1322

1997

Volltextzugriff (PDF)

A study of lactoferrin and antibodies against lactoferrin in neurological diseases

Advances in experimental medicine and biology, 1998, Vol.443, p.301

1998

Volltextzugriff (PDF)

Handbook of spinal cord monitoring

Electroencephalography and clinical neurophysiology, 1995-09, Vol.95 (3), p.217

Abbruzzese, Michele

1995

Volltextzugriff (PDF)

Correlation between PMP-22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

Annals of neurology, 1997-12, Vol.42 (6), p.866-872

1997

Volltextzugriff (PDF)

Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: A reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients

Neuroscience letters, 1996-07, Vol.213 (1), p.71-73

1996

Volltextzugriff (PDF)

Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding

Neuroscience letters, 1995-07, Vol.194 (1), p.136-138

1995

Volltextzugriff (PDF)

Interindividual variability of central delay changes in the soleus H reflex pathway

Muscle & nerve, 1992-01, Vol.15 (1), p.21-26

1992

Volltextzugriff (PDF)

Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients

Journal of neurology, 1995-05, Vol.242 (5), p.295-298

1995

Volltextzugriff (PDF)

Surface recording of the spinal ventral root discharge in man: an experimental study

Brain (London, England : 1878), 1983-12, Vol.106 (4), p.897-909

1983

Volltextzugriff (PDF)

Assessment of motor neuron excitability in Parkinsonian rigidity by the F wave

Journal of neurology, 1985-01, Vol.232 (4), p.246-249

1985

Volltextzugriff (PDF)

1 – 25 von 175

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(165)
Mit Volltextzugriff
(153)

Publikationsform

Artikel
(173)
Berichte
(1)
Reviews
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Sonography of the median nerve in Charcot-Marie-Tooth disease

Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease

Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A disease

Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease

Impaired Expression of Ciliary Neurotrophic Factor in Charcot-Marie-Tooth Type 1A Neuropathy

Impaired Expression of Ciliary Neurotrophic Factor in Charcot-Marie-Tooth Type 1 A Neuropathy

Experimental Charcot–Marie–Tooth type 1A: A cDNA microarrays analysis

Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type1A disease

Postvibration Depression of the H-Reflex as a Result of a Dual Mechanism: An Experimental Study in Humans

PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A

Testing for pre-synaptic and post-synaptic changes in the soleus H reflex pathway following selective muscle vibration in humans

Presynaptic and postsynaptic mechanisms underlying H-reflex changes produced by a selective voluntary contraction

Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

Insulin treatment enhances expression of IGF-I in sural nerves of diabetic patients

New subcortical components of the cerebral somatosensory evoked potential in man

Minocycline for Symptomatic Neurosyphilis in Patients Allergic to Penicillin: Letter

A study of lactoferrin and antibodies against lactoferrin in neurological diseases

Handbook of spinal cord monitoring

Correlation between PMP-22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: A reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients

Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding

Interindividual variability of central delay changes in the soleus H reflex pathway

Molecular diagnosis of hereditary neuropathy with liability to pressure palsies (HNPP) by detection of 17p11.2 deletion in Italian patients

Surface recording of the spinal ventral root discharge in man: an experimental study

Assessment of motor neuron excitability in Parkinsonian rigidity by the F wave

Suchergebnisse filtern