Peripheral Nerve Disorders
Pathology and Genetics
Published on 1. August 2014
320 pages
978-1-118-61841-7 (ISBN)
Description
Peripheral Nerve Disorders: Pathology and Genetics is adefinitive, clinically-oriented guide to the pathology ofperipheral nerve disorders.
These commonly seen neurological challenges have many causes andaccurate diagnosis is often necessary via pathological analysis.New techniques exploiting molecular biological knowledge haveopened up new vistas to understanding the pathogenesis of thesedisorders, and hence their effective management.
This new title takes a disease-oriented approach to understandingthe pathology of these conditions. It combines classical andcontemporary techniques to enable practitioners in neurology andneuropathology to better understanding of the disease processesunderlying patients' presentations and to formulateappropriate management plans.
Peripheral Nerve Disorders: Pathology and Genetics is avaluable resource for neurologists, neuropathologists,pathologists, neurobiologists and geneticists.
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Book
10/2014
Wiley
€204.50
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Software
08/2014
Wiley
€229.96
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Persons
Jean-Michel Vallat, Neurology Laboratory, National Referral Center for Rare Peripheral Neuropathies, University Hospital, Limoges, France
Joachim Weis, Director, Institute of Neuropathology, RWTH Aachen University Hospital, JARA Brain Translational Medicine, Germany
Content
Contributor list vii
Foreword x
Preface xi
Abbreviations xiii
1 Clinical assessment and classification of peripheral nervediseases 1
Pierre Bouche
2 Combined muscle and nerve biopsy 12
Anne Vital
3 Cutaneous nerve biopsy 15
Claudia Sommer and Maria Nolano
4 Methods for examination of peripheral nerve 24
Juan M. Bilbao Douglas C. Anthony and Umberto De Girolami
5 Complications from nerve biopsy 30
Richard A.C. Hughes
6 Anatomy of the peripheral nerve 32
Rosalind King
7 Basic pathology of the peripheral nervous system 38
J. Michael Schröder and Joachim Weis
8 Introduction to the hereditary neuropathies 59
Joachim Weis and Jan Senderek
9 Autosomal dominant demyelinatingCharcot-Marie-Tooth (CMT1) neuropathies 62
Jean-Michel Vallat and Stéphane Mathis
10 Autosomal dominant neuropathy of the axonalCharcot-Marie-Tooth type 2 72
J. Michael Schröder Joachim Weis and Jan Senderek
11 Autosomal recessive demyelinating or axonalCharcot-Marie-Tooth neuropathy 85
Kristl G. Claeys Martin Lammens Jan Senderek and Joachim Weis
12 Dominant and recessive intermediate CMT (CMTDI and CMTRI)102
Joachim Weis Andreas Roos Istvan Katona Kristl G. Claeys and JanSenderek
13 X-linked neuropathy of the Charcot-Marie-Toothtype 111
J. Michael Schröder and Jan Senderek
14 Hereditary sensory and autonomic neuropathy 119
Rosalind King
15 Hereditary neuropathy with liability to pressure palsy126
Benjamin Ellezam
16 Familial amyloid polyneuropathy 131
Manuel Melo Pires Ricardo Taipa and António Guimarães
17 Peripheral neuropathies in mitochondrial disorders 138
Benoît Funalot
18 Giant axonal neuropathy 142
Robert Ouvrier and Manoj Menezes
19 Neuroaxonal dystrophy 146
Robert Ouvrier and Manoj Menezes
20 Peripheral nerve involvement in neurolipidoses 149
Robert Ouvrier and Manoj Menezes
21 Other hereditary neuropathies 158
Stéphane Mathis Meriem Tazir and Jean-Michel Vallat
22 Adult polyglucosan body disease 167
Alexander Lossos Or Kakhlon and Dov Soffer
23 Polyneuropathies associated with neurofibromatosis 172
Joachim Weis
24 Vasculitides 175
Michael P. Collins and P. James B. Dyck
25 Infectious and tropical neuropathies 196
Leila Chimelli and Jean-Michel Vallat
26 Sarcoid neuropathy 210
Anne Vital
27 Guillain-Barré syndromes and chronic inflammatorydemyelinating polyradiculoneuropathy 214
Laurent Magy
28 Diabetic neuropathies 224
Robert E. Schmidt
29 Neuropathies in metabolic diseases other than diabetesmellitus 233
Martin Lammens
30 Toxic neuropathies 238
Sebastian Brandner
31 Polyneuropathy associated with a monoclonal gammopathy247
Yuichi Kawagashira Haruki Koike Jean-Michel Vallat and GenSobue
32 Paraneoplastic peripheral neuropathies 259
Jean-Christophe Antoine
33 Neuropathies in malnutrition and alcoholism 267
Martin Lammens
34 Critical illness polyneuropathy 273
Douglas C. Anthony and David Lacomis
35 Non-vasculitic ischemic neuropathies 276
Robert E. Schmidt
36 Traumatic and compressive lesions of peripheral nerves280
Carlos Ortiz-Hidalgo and Roy O. Weller
37 Localized hypertrophic neuropathy intraneural perineuriomapolyneuropathy with perineurial cell hyperplasia and minifascicularneuropathy 287
Joachim Weis
38 Neurolymphomatosis and rare focal or multifocal lesions291
Joachim Weis
Index 294
Abbreviations
(genes are written in italics)
- α-Gal
- Alpha-Galactosidase
- α -NAGA
- α -N-Acetylgalactosaminidase
- AARS
- Alanyl-tRNA-synthetase
- AAV
- ANCA-Associated Vasculitides
- ABCA1
- ATP-Binding Cassette Transporter A1
- ACA
- Acrodermatitis chronica atrophicans
- ACE
- Angiotensin-Converting Enzyme
- ACR
- American College of Rheumatology
- AD
- Autosomal Dominant
- ADCA
- Autosomal dominant spinocerebellar atrophies
- AFB
- Acid Fast Bacilli
- AFLP
- Amplified Fragment Length Polymorphism
- AIDP
- Acute Inflammatory Demyelinating Polyneuropathy
- ALN
- Alcohol Related Neuropathy
- ALS
- Amyotrophic Lateral Sclerosis
- ALS11
- Amyotrophic Lateral Sclerosis of Type 11
- AMAN
- Acute Motor Axonal Neuropathy
- AMP
- Adenosine Monophosphate
- AMSAN
- Acute Motor and Sensory Axonal Neuropathy
- ANA
- Antinuclear Antibody
- ANCA
- Anti-Neutrophil Cytoplasmic Antibody
- ANS
- Ataxia Neuropathy Spectrum
- APBD
- Adult Polyglucosan Body Disease
- APC
- antigen-Presenting Cell
- Apo
- Apolipoproteins
- ApoA-I
- Apolipoprotein A-I
- ApoB
- Apolipoprotein B
- AR
- Autosomal Recessive
- AR CMT
- Autosomal Recessive Charcot–Marie–Tooth Neuropathy
- AR CMT1
- Autosomal Recessive Charcot–Marie–Tooth Neuropathy, of Demyelinating Type
- AR CMT2
- Autosomal Recessive Charcot–Marie–Tooth Neuropathy, of Axonal Type
- ARHGEF10
- Rho Guanine-Nucleotide Exchange [GEF] Factor 10
- ARSA
- Arylsulfatase A
- ATL1
- Atlastin 1
- B.b
- Borrelia burgdorferi
- BBW rats
- Biobreeding Wor rats
- BDNF
- Brain Derived Neurotrophic Factor
- BEAR
- Brain Stem Evoked Auditory Responses
- CAN
- Congenital Amyelinating Neuropathy
- CANOMAD
- Chronic Ataxic Neuropathy, Ophthalmoplegia, IgM paraprotein, cold Agglutinins and Disialosyl antibodies
- CCT
- Cytosolic Chaparonin-Containing T-complex peptide
- CD4
- Cluster of Differentiation 4
- CES
- Cholesterol Emboli Syndrome
- CETP
- Cholesteryl Ester Transfer Protein
- CG
- Cryoglobulinemia
- CHCC
- Chapel Hill Consensus Conference
- CHIKV
- Chikungunya Virus
- CHN
- Congenital Hypomyelination Neuropathy
- CHS
- Chediak–Higashi Syndrome
- CIDP
- Chronic Inflammatory Demyelinating Polyneuropathy/Polyradiculoneuropathy
- CIM
- Critical Illness Myopathy
- CIP
- Critical Illness Polyneuropathy
- CIPA
- Congenital Insensitivity to Pain with Anhydrosis
- CIPN
- Chemotherapy-Induced Toxic Peripheral Neuropathies
- CMAP
- Compound Muscle Action Potential(s)
- CMT
- Charcot–Marie–Tooth
- CMT DI
- Charcot–Marie–Tooth Neuropathy, Autosomal Dominant, of Intermediate type
- CMT RIA
- Charcot–Marie–Tooth Neuropathy, Autosomal Recessive, of Intermediate type A
- CMT X
- X-linked Charcot–Marie–Tooth Neuropathy
- CMT
- Charcot–Marie–Tooth disease/neuropathy
- CMT1
- Charcot–Marie–Tooth neuropathy, autosomal dominant, of demyelinating type
- CMT2
- Charcot–Marie–Tooth neuropathy, autosomal dominant, of axonal type/type 2
- CMT4
- Charcot–Marie–Tooth neuropathy, autosomal recessive, of demyelinating type
- CMTID
- Intermediate Charcot–Marie–Tooth
- CMTX
- X-linked Charcot–Marie–Tooth
- CMV
- Cytomegalovirus
- CNM
- Centronuclear Myopathy
- CNS
- Central Nervous System
- CNTF
- Ciliary Neuron Trophic Factor
- COPD
- Chronic Obstructive Pulmonary Disease
- COX
- Cytochrome c OXidase
- CRMP5
- Collapsin Response Mediator Protein 5
- CSAP
- Compound Sensory Action Potential
- CSF
- Cerebrospinal Fluid
- CSNAP
- Compound Sensory Nerve Action Potential
- CTD
- Connective Tissue Disease
- CTL
- Cytotoxic T Lymphocyte
- CTX
- Cerebrotendinous Xanthomatosis
- Cx31
- Connexin 31 (= GJB3)
- Cx32
- Connexin 32
- DANP
- Diabetic Autonomic Neuropathy
- DCBU
- Dorsal Cutaneous Branch of the Ulnar nerve
- DCCT
- Diabetes Control and Complications Trial
- DCRPN
- Diabetic Cervical Radiculoplexus Neuropathy
- DDT
- Dichloro-Diphenyl-Trichloroethane
- DHH
- Desert Hedgehog Homolog (Drosophila)
- dHMN
- Distal Hereditary Motor Neuropathy
- DIC
- Disseminated Intravascular Coagulation
- DILS
- Diffuse Infiltrative Lymphocytic Syndrome
- DLRPN
- Diabetic Lumbosacral Radiculoplexus Neuropathy
- DNA
- DeoxyRiboNucleic Acid
- DNM
- Dynamin
- DNM2
- Dynamin 2
- DNMT
- DNA Methyl Transferase
- DNP
- Diabetic Neuropathy
- DRG
- Dorsal Root Ganglia
- DSD
- Déjérine–Sottas Disease
- DSS
- Déjérine–Sottas Syndrome
- dSMA
- Distal SMA
- DSP
- Distal Sensory Polyneuropathy
- DβH
- Dopamine β-hydroxylase
- EAN
- Experimental Allergic Neuritis
- EBV
- Epstein–Barr virus
- EEG
- Electroencephalogram
- EGPA
- Eosinophilic Granulomatosis with PolyAngiitis
- EGR
- Early Growth Response Gene
- EGR2
- Early Growth Response 2 encoding gene
- ELISA
- Enzyme-Linked Immunosorbent Assay
- EM
- Electron Microscopy
- EMA
- Epithelial Membrane Antigen
- EMG
- Electromyography
- ENF
- Epidermal Nerve Fibres
- ENMG
- ElectroNeuroMyoGraphy
- ER
- Endoplasmic Reticulum
- ERK/MAPK
- Extracellular Signal-Regulated Kinases/Mitogen-Activated Protein Kinases
- ERT
- Enzyme Replacement Therapy
- ESR
- Erythrocyte Sedimentation Rate
- FAM134B
- FAMily with sequence similarity 134, member B
- FAP
- Familial Amyloid Neuropathy
- FBLN5
- Fibulin 5
- FFM
- Focally Folded Myelin
- FGD4
- FYVE, RhoGEF and PH Domain-containing protein 4 encoding gene
- FIG4
- Polyphosphoinositide phosphatase encoding gene
- FLAIR
- Fluid-Attenuated Inversion-Recovery
- FLC
- Fibrous Long-spacing Collagen
- Frabin
- FGD1-related F-actin binding protein
- FSGS
- Focal Segmental GlomeruloSclerosis
- GAN
- Giant Axonal Neuropathy (GAN1)
- GAP-43
- Growth Associated Protein-43
- GARS
- Glycyl-tRNA...
