UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Overloaded Endoplasmic Reticulum-Golgi Compartments, a Possible Pathomechanism of Peripheral Neuropathies Caused by Mutations of the Peripheral Myelin Protein PMP22

The Journal of neuroscience, 1998-01, Vol.18 (2), p.731-740

1998

Volltextzugriff (PDF)

Mutation-dependent alteration in cellular distribution of peripheral myelin protein 22 in nerve biopsies from Charcot–Marie–Tooth type 1A

Brain (London, England : 1878), 2000-05, Vol.123 (5), p.1001-1006

2000

Volltextzugriff (PDF)

Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A) : normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule expression in onion bulbs

Acta neuropathologica, 1997-10, Vol.94 (4), p.310-315

1997

Volltextzugriff (PDF)

Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies

Annals of neurology, 1996-10, Vol.40 (4), p.672-675

1996

Volltextzugriff (PDF)

Conduction velocity distributions compared to fiber size distributions in normal human sural nerve

Muscle & nerve, 1995-10, Vol.18 (10), p.1121-1127

1995

Volltextzugriff (PDF)

Peripheral Nerve Elongation by Laser Doppler Flowmetry-Monitored Expansion: An Experimental Basis for Future Application in the Management of Peripheral Nerve Defects

Plastic and reconstructive surgery (1963), 1996-03, Vol.97 (3), p.568-576

1996

Volltextzugriff (PDF)

Secondary axon atrophy and neurological dysfunction in demyelinating neuropathies

Current opinion in neurology, 2002-10, Vol.15 (5), p.611-615

2002

Volltextzugriff (PDF)

Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages

Brain (London, England : 1878), 1996-10, Vol.119 (5), p.1461-1469

1996

Volltextzugriff (PDF)

Chronic inflammatory demyelinating polyneuropathy as a complication of cat scratch disease

Journal of neurology, neurosurgery and psychiatry, 2000-06, Vol.68 (6), p.797-798

2000

Volltextzugriff (PDF)

Sensory potentials and sural nerve biopsy: A Model evaluation

Muscle & nerve, 1987-03, Vol.10 (3), p.246-262

1987

Volltextzugriff (PDF)

Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1

Human genetics, 1993-08, Vol.92 (1), p.87-90

1993

Volltextzugriff (PDF)

Low affinity NGF receptor expression in CMT1 A nerve biopsies of different disease stages

Brain (London, England : 1878), 1996-10, Vol.119 (5), p.1461-1469

1996

Volltextzugriff (PDF)

Intermediate CAG repeat lengths (53,54) for MJD/SCA3 are associated with an abnormal phenotype

Annals of neurology, 2001-06, Vol.49 (6), p.805-808

2001

Volltextzugriff (PDF)

Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion

Journal of the peripheral nervous system, 2012-06, Vol.17 (2), p.223-225

2012

Volltextzugriff (PDF)

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A

Nature genetics, 1992-12, Vol.2 (4), p.288-291

1992

Volltextzugriff (PDF)

Major histocompatibility complex class II expression and macrophage responses in genetically proven Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies

Muscle & nerve, 1998-11, Vol.21 (11), p.1419-1427

1998

Volltextzugriff (PDF)

Peripheral nerve elongation by laser Doppler flowmetry controlled expansion: Functional and neurophysiological aspects

Journal of the neurological sciences, 1994-07, Vol.124 (2), p.149-155

1994

Volltextzugriff (PDF)

1 – 17 von 17

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(17)
Mit Volltextzugriff
(16)

Publikationsform

Artikel
(17)

Sprache

Englisch
(17)
Japanisch
(4)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(16)
Science & Technology
(16)
Humans
(14)
Neurosciences & Neurology
(13)
Clinical Neurology
(12)
Neurosciences
(12)
Biological And Medical Sciences
(11)
Medical Sciences
(10)
Neurology
(9)
Adult
(6)
Female
(6)
Sural Nerve - Pathology
(6)
Animals
(5)
Charcot-Marie-Tooth Disease - Genetics
(5)
Child
(5)
Child, Preschool
(5)
Male
(5)
Myelin Proteins - Genetics
(5)
Point Mutation
(5)
Adolescent
(4)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Overloaded Endoplasmic Reticulum-Golgi Compartments, a Possible Pathomechanism of Peripheral Neuropathies Caused by Mutations of the Peripheral Myelin Protein PMP22

Mutation-dependent alteration in cellular distribution of peripheral myelin protein 22 in nerve biopsies from Charcot–Marie–Tooth type 1A

Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A) : normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule expression in onion bulbs

Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies

Conduction velocity distributions compared to fiber size distributions in normal human sural nerve

Peripheral Nerve Elongation by Laser Doppler Flowmetry-Monitored Expansion: An Experimental Basis for Future Application in the Management of Peripheral Nerve Defects

Secondary axon atrophy and neurological dysfunction in demyelinating neuropathies

Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages

Chronic inflammatory demyelinating polyneuropathy as a complication of cat scratch disease

Sensory potentials and sural nerve biopsy: A Model evaluation

Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1

Low affinity NGF receptor expression in CMT1 A nerve biopsies of different disease stages

Intermediate CAG repeat lengths (53,54) for MJD/SCA3 are associated with an abnormal phenotype

Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A

Major histocompatibility complex class II expression and macrophage responses in genetically proven Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies

Peripheral nerve elongation by laser Doppler flowmetry controlled expansion: Functional and neurophysiological aspects

Suchergebnisse filtern