UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 63

Sortiert nach

Th2-M2 immunity in lesions of muscular sarcoidosis and macrophagic myofasciitis

Neuropathology and applied neurobiology, 2015-12, Vol.41 (7), p.952-963

2015

Volltextzugriff (PDF)

The Curse of Apneic Spells

Seminars in pediatric neurology, 2018-07, Vol.26, p.56-58

2018

Volltextzugriff (PDF)

Myofibrillar disorganization characterizes myopathy of camptocormia in Parkinson’s disease

Acta neuropathologica, 2012-03, Vol.123 (3), p.419-432

2012

Volltextzugriff (PDF)

SIL1 mutations and clinical spectrum in patients with Marinesco-Sjögren syndrome

Brain (London, England : 1878), 2013-12, Vol.136 (Pt 12), p.3634-3644

2013

Volltextzugriff (PDF)

GNE myopathy in Roma patients homozygous for the p.I618T founder mutation

Neuromuscular disorders : NMD, 2015-09, Vol.25 (9), p.713-718

2015

Volltextzugriff (PDF)

Apoptosis-related Proteins in Skeletal Muscle Fibers of Spinal Muscular Atrophy

Journal of neuropathology and experimental neurology, 1997-02, Vol.56 (2), p.150-156

1997

Volltextzugriff (PDF)

Desmin-related myopathy with mallory body-like inclusions is caused by mutations of the selenoprotein N gene

Annals of neurology, 2004-05, Vol.55 (5), p.676-686

2004

Volltextzugriff (PDF)

Mutations in the β-tropomyosin ( TPM2) gene – a rare cause of nemaline myopathy

Neuromuscular disorders : NMD, 2002-02, Vol.12 (2), p.151-158

2002

Volltextzugriff (PDF)

Genotype–phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle α-actin

Neuromuscular disorders : NMD, 2004-09, Vol.14 (8), p.461-470

2004

Volltextzugriff (PDF)

Novel slow-skeletal myosin ( MYH7) mutation in the original myosin storage myopathy kindred

Neuromuscular disorders : NMD, 2006-06, Vol.16 (6), p.357-360

2006

Volltextzugriff (PDF)

Frontotemporal dementia: the post-tau era

Neurology, 2006-08, Vol.67 (4), p.560

2006

Volltextzugriff (PDF)

Immune-mediated rippling muscle disease with myasthenia gravis: A report of seven patients with long-term follow-up in two

Neuromuscular disorders : NMD, 2009-03, Vol.19 (3), p.223-228

2009

Volltextzugriff (PDF)

Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene ( ACTA1 ) mutation

Neuromuscular disorders : NMD, 2010-08, Vol.20 (8), p.531-533

2010

Volltextzugriff (PDF)

Delayed or late-onset type II glycogenosis with globular inclusions

Acta neuropathologica, 2005-08, Vol.110 (2), p.151-157

2005

Volltextzugriff (PDF)

The Eighth Meryon Society Lecture read at Worcester College, Oxford on 2 July, 2004

Neuromuscular disorders : NMD, 2004-12, Vol.14 (12), p.822-828

Goebel, Hans H

2004

Volltextzugriff (PDF)

Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity

Neuromuscular disorders : NMD, 2010-11, Vol.20 (11), p.701-708

2010

Volltextzugriff (PDF)

A series of west European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin

Journal of neurology, 2004-02, Vol.251 (2), p.143-149

2004

Volltextzugriff (PDF)

Expression of Different Isoforms of Nitric Oxide Synthase in Experimentally Denervated and Reinnervated Skeletal Muscle

Journal of neuropathology and experimental neurology, 1997-12, Vol.56 (12), p.1283-1289

1997

Volltextzugriff (PDF)

Infantile Intranuclear Rod Myopathy

Journal of child neurology, 1997-01, Vol.12 (1), p.22-30

1997

Volltextzugriff (PDF)

Expression Profile of Stress Proteins, Intermediate Filaments, and Adhesion Molecules in Experimentally Denervated and Reinnervated Rat Facial Muscle

Experimental neurology, 1997-07, Vol.146 (1), p.125-134

1997

Volltextzugriff (PDF)

Immunolocalization of tenascin-C in human type II fiber atrophy

Journal of molecular neuroscience, 1999-08, Vol.13 (1-2), p.167-176

1999

Volltextzugriff (PDF)

Hamartoma of the triceps surae muscle

Acta neuropathologica, 1997-07, Vol.94 (1), p.91-94

1997

Volltextzugriff (PDF)

Ultrastructural Pathology of Eccrine Sweat Gland Epithelial Cells in Globoid Cell Leukodystrophy

Journal of child neurology, 1993-04, Vol.8 (2), p.171-174

1993

Volltextzugriff (PDF)

Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approach

Brain & development (Tokyo. 1979), 1995-03, Vol.17 (2), p.83-88

1995

Volltextzugriff (PDF)

Alcohol-related acute axonal polyneuropathy: a differential diagnosis of Guillain-Barré syndrome

Archives of neurology (Chicago), 1998-10, Vol.55 (10), p.1329

1998

Volltextzugriff (PDF)

1 – 25 von 63

Suche als RSS-Feed

Aktive Filter

ThemaFemale

ThemaNeurosciences & Neurology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

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

Publikationsform

Artikel
(63)

Sprache

Englisch
(63)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

13 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Th2-M2 immunity in lesions of muscular sarcoidosis and macrophagic myofasciitis

The Curse of Apneic Spells

Myofibrillar disorganization characterizes myopathy of camptocormia in Parkinson’s disease

SIL1 mutations and clinical spectrum in patients with Marinesco-Sjögren syndrome

GNE myopathy in Roma patients homozygous for the p.I618T founder mutation

Apoptosis-related Proteins in Skeletal Muscle Fibers of Spinal Muscular Atrophy

Desmin-related myopathy with mallory body-like inclusions is caused by mutations of the selenoprotein N gene

Mutations in the β-tropomyosin ( TPM2) gene – a rare cause of nemaline myopathy

Genotype–phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle α-actin

Novel slow-skeletal myosin ( MYH7) mutation in the original myosin storage myopathy kindred

Frontotemporal dementia: the post-tau era

Immune-mediated rippling muscle disease with myasthenia gravis: A report of seven patients with long-term follow-up in two

Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene ( ACTA1 ) mutation

Delayed or late-onset type II glycogenosis with globular inclusions

The Eighth Meryon Society Lecture read at Worcester College, Oxford on 2 July, 2004

Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity

A series of west European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin

Expression of Different Isoforms of Nitric Oxide Synthase in Experimentally Denervated and Reinnervated Skeletal Muscle

Infantile Intranuclear Rod Myopathy

Expression Profile of Stress Proteins, Intermediate Filaments, and Adhesion Molecules in Experimentally Denervated and Reinnervated Rat Facial Muscle

Immunolocalization of tenascin-C in human type II fiber atrophy

Hamartoma of the triceps surae muscle

Ultrastructural Pathology of Eccrine Sweat Gland Epithelial Cells in Globoid Cell Leukodystrophy

Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approach

Alcohol-related acute axonal polyneuropathy: a differential diagnosis of Guillain-Barré syndrome

Aktive Filter

Suchergebnisse filtern