Hereditary Peripheral NeuropathiesG. Kuhlenbäumer "Hereditary Peripheral Neuropathies" deals with the Charcot-Marie-Tooth group of neuropathies and related primary hereditary neuropathies. The knowledge in this field has grown exponentially during the last ten years. The book is divided into two sections. The first section deals with the clinical presentation, electrophysiological features and differential diagnosis of these disorders as well as with the general biology of the peripheral nerve. The second section gives a detailed account of the known disease entities. The book will be interesting for both the clinician with a special interest in PNS diseases as well as for the researcher. |
Contents
I | 3 |
II | 5 |
III | 6 |
IV | 8 |
VI | 9 |
VIII | 10 |
IX | 15 |
XI | 16 |
XCIII | 134 |
XCV | 135 |
XCVII | 136 |
XCVIII | 137 |
XCIX | 138 |
C | 139 |
CII | 146 |
CIV | 148 |
XII | 18 |
XIII | 20 |
XIV | 21 |
XVI | 22 |
XVII | 23 |
XVIII | 24 |
XXI | 25 |
XXII | 26 |
XXIV | 27 |
XXVII | 29 |
XXVIII | 32 |
XXX | 33 |
XXXI | 34 |
XXXIV | 35 |
XXXVII | 37 |
XXXIX | 38 |
XLI | 41 |
XLII | 44 |
XLIV | 46 |
XLV | 48 |
XLVIII | 49 |
XLIX | 50 |
L | 52 |
LII | 53 |
LIII | 55 |
LV | 56 |
LVIII | 58 |
LIX | 59 |
LXI | 60 |
LXII | 61 |
LXIV | 62 |
LXVI | 63 |
LXVIII | 73 |
LXXI | 74 |
LXXII | 75 |
LXXIV | 83 |
LXXV | 85 |
LXXVI | 86 |
LXXVII | 87 |
LXXIX | 88 |
LXXXI | 92 |
LXXXII | 94 |
LXXXIII | 95 |
LXXXIV | 96 |
LXXXV | 103 |
LXXXVI | 104 |
LXXXVIII | 105 |
LXXXIX | 109 |
XC | 121 |
XCI | 131 |
XCII | 133 |
CV | 149 |
CVI | 150 |
CVIII | 151 |
CIX | 152 |
CXI | 153 |
CXIII | 154 |
CXV | 157 |
CXVI | 160 |
CXIX | 161 |
CXX | 163 |
CXXII | 165 |
CXXIII | 166 |
CXXIV | 167 |
CXXV | 170 |
CXXVI | 172 |
CXXVII | 174 |
CXXIX | 175 |
CXXXI | 176 |
CXXXIII | 179 |
CXXXIV | 185 |
CXXXV | 189 |
CXXXVI | 191 |
CXXXVII | 193 |
CXXXVIII | 194 |
CXXXIX | 195 |
CXLI | 196 |
CXLII | 197 |
CXLV | 199 |
CXLVII | 200 |
CXLVIII | 201 |
CXLIX | 203 |
CL | 204 |
CLI | 206 |
CLII | 207 |
CLIII | 209 |
CLV | 210 |
CLVII | 211 |
CLVIII | 213 |
CLIX | 215 |
CLX | 223 |
CLXII | 227 |
CLXIII | 228 |
CLXV | 229 |
CLXVII | 231 |
CLXVIII | 232 |
CLXIX | 233 |
CLXX | 234 |
CLXXII | 237 |
255 | |
Other editions - View all
Hereditary Peripheral Neuropathies G. Kuhlenbäumer,F. Stögbauer,E. B. Ringelstein,P. Young Limited preview - 2006 |
Hereditary Peripheral Neuropathies G. Kuhlenbäumer,F. Stögbauer,E. B. Ringelstein,P. Young No preview available - 2014 |
Common terms and phrases
affected Ann Neurol autosomal dominant autosomal recessive Broeckhoven Charcot-Marie-Tooth disease type chromosome Clinical features CMAPS CMT1 CMT1B CMT2 CMT4A CMTX congenital decade demyelinating detected dHMN diagnosis disease type 1A disorders E-mail EGR2 electrophysiological foot deformities GDAP1 genetic testing genetics and pathomechanism Giant axonal neuropathy GJB1 hereditary motor hereditary neuropathies hereditary sensory HMSN HNPP HSAN HSAN1 Hum Genet IKBKAP involvement Jonghe locus loss Lupski JR mice mNCVs molecular genetic motor and sensory muscles muscular atrophy myelin sheath myelinated fibers Nat Genet NCVs NEFL Nelis nerve biopsy nerve conduction neurofilament Neurology neuropa neuropathy type neuropathy with liability normal OMIM onion bulbs onset pain paranodal Pathology patients peripheral myelin peripheral nerve peripheral neuropathy pes cavus phenotype Phone point mutations pressure palsies rare Schwann cell sensory neuropathy severe sural nerve sural nerve biopsy Suter symptoms syndrome Thomas PK Timmerman tion typical unmyelinated Website X-linked