Abstract
The severe functional deficits in patients suffering from traumatic peripheral nerve damage underline the necessity of an optimal therapy. The development of microsurgical techniques in the sixties contributed significantly to the progress in nerve repair. Since then, no major clinical innovation has become established. However, with an increased understanding of cellular and molecular mechanisms underlying nerve regeneration, various tubulization concepts have been developed which yield possible alternatives to direct suturing and to autologous nerve grafting in cases of short nerve defects. The vast knowledge gathered in the field of nerve regeneration needs to be further exploited in order to develop alternative therapeutic strategies to nerve autografting, which can result in donor-site defects and often lead to inappropriate results. Considering the encouraging results from preclinical studies, innovative nerve repair strategies are likely to improve the outcome of reconstructive surgical interventions. This paper outlines, in addition to the fundamentals of nerve regeneration, the current treatment options for defects of peripheral nerves. This article also reviews the developments in the use of alternative nerve guides and demonstrates new perspectives in the field of peripheral nerve reconstruction.
Zusammenfassung
Die schweren Auswirkungen traumatischer Schädigungen peripherer Nerven auf das Befinden des Patienten unterstreichen die Notwendigkeit einer optimalen Therapie. Nach der Entwicklung mikrochirurgischer Techniken, die zu einem erheblichen Fortschritt im Bereich der Nervenchirurgie beigetragen haben, konnten sich bisher klinisch keine wesentlichen Neuerungen etablieren. Mit wachsendem Verständnis der zellulären und molekularen Mechanismen der Nervenheilung gelang es jedoch verschiedene Überbrückungstechniken für Nervendefekte zu entwickeln. Einzelne davon stellen mittlerweile eine mögliche Alternative zur direkten Naht und zum Nerventransplantat bei Überbrückung kurzer Defektstrecken dar. Die oftmals unbefriedigenden Resultate des Nerventransplantates fordern vor allem in Anbetracht eines mittlerweile umfangreichen Wissens über den Vorgang der Nervenregeneration die Weiterentwicklung neuer Nervenschienen. Auf der Basis bisheriger experimenteller Resultate ist eine weitere Verbesserung der Ergebnisse nach peripherer Nervenrekonstruktion denkbar. Ziel dieser Arbeit ist die Darstellung des aktuellen Standes der Rekonstruktion und Regeneration peripherer Nerven. Zudem werden, vor dem Hintergrund der Entwicklung alternativer Nervenschienen und dessen Modifizierungen, neue Perspektiven in diesem Gebiet aufgezeigt.
Key words
nerve regeneration - nerve reconstruction - nerve graft - nerve conduits - nerve healing - tissue engineering
Schlüsselwörter
Nervenregeneration - Nervenrekonstruktion - Nerventransplantat - Nervenschiene - Nervenheilung - Gewebezšchtung
References
1
Anand P, Terenghi G, Birch R, Wellmer A, Cedarbaum JM, Lindsay RM, Williams-Chestnut RE, Sinicropi DV.
Endogenous NGF and CNTF levels in human peripheral nerve injury.
Neuroreport.
1997;
8
1935-1938
2
Ansselin AD, Fink T, Davey DF.
Peripheral nerve regeneration through nerve guides seeded with adult Schwann cells.
Neuropathol Appl Neurobiol.
1997;
23
387-398
3
Anton ES, Weskamp G, Reichardt LF, Matthew WD.
Nerve growth factor and its low-affinity receptor promote Schwann cell migration.
Proc Natl Acad Sci USA.
1994;
91
2795-2799
4
Archibald SJ, Krarup C, Shefner J, Li ST, Madison RD.
A collagen-based nerve guide conduit for peripheral nerve repair: an electrophysiological study of nerve regeneration in rodents and nonhuman primates.
J Comp Neurol.
1991;
306
685-696
5
Archibald SJ, Shefner J, Krarup C, Madison RD.
Monkey median nerve repaired by nerve graft or collagen nerve guide tube.
J Neurosci.
1995;
15
4109-4123
6
Battiston B, Tos P, Cushway TR, Geuna S.
Nerve repair by means of vein filled with muscle grafts I. Clinical results.
Microsurgery.
2000;
20
32-36
7
Boyd JG, Gordon T.
A dose-dependent facilitation and inhibition of peripheral nerve regeneration by brain-derived neurotrophic factor.
Eur J Neurosci.
2002;
15
613-626
8
Brown CE, Dyck RH.
Rapid, experience-dependent changes in levels of synaptic zinc in primary somatosensory cortex of adult mouse.
J Neurosci.
2002;
22
2617-2625
9
Brushart TM.
Motor axons preferentially reinnervate motor pathways.
J Neurosci.
1993;
13
2730-2738
10
Bunge RP, Bunge MB.
Evidence that contact with connective tissue matrix is required for normal interaction between Schwann cells and nerve fibers.
J Cell Biol.
1978;
87
943-950
11
Büngner OV.
ber die Degenerations und Regenerations-Vorgänge am Nerven nach Verletzungen.
Beitr Pathol Anal.
1891;
10
321
12
Cai D, Shen Y, Bellard M De, Tang S, Filbin MT.
Prior exposure to neurotrophins blocks inhibition of axonal regeneration by MAG and myelin via a cAMP-dependent mechanism.
Neuron.
1999;
22
89-101
13
Chen YS, Wang-Bennett LT, Coker NJ.
Facial nerve regeneration in the silicone chamber: the influence of nerve growth factor.
Exp Neurol.
1989;
103
52-60
14
Chen ZW, Wang MS.
Effects of nerve growth factor on crushed sciatic nerve regeneration in rats.
Microsurgery.
1995;
16
547-551
15
Chiu DT.
Autogenous venous nerve conduits. A review.
Hand Clin.
1999;
15
667-671
16
Chiu DT, Strauch B.
A prospective clinical evaluation of autogenous vein grafts used as a nerve conduit for distal sensory nerve defects of 3 cm or less.
Plast Reconstr Surg.
1990;
86
928-934
17 Coggeshall RE. Improvements in peripheral nerve regeneration with permeable tubes and preliminary data indicating that the improvements are associated with cells of the general connective tissue. In: Pubols, L. M., Sessle, B. J. Effect of Injury on Trigeminal and Spinal Somatosensory Systems Less. New York 1987: 69-76
18
Couturier CA, Dauge MC, Henin D, Alnot JY, Masmejean EH.
Nerve repair using a composite graft of vein and denatured skeletal muscle: morphologic analysis.
J Reconstr Microsurg.
2002;
18
681-688
19
Dahlin LB, Danielsen N, Ochi M, Lundborg G.
Axonal growth in mesothelial chambers: effects of a proximal preconditioning lesion and/or predegeneration of the distal nerve stump.
Exp Neurol.
1988;
99
655-663
20
Dahlin LB, Lundborg G.
Use of tubes in peripheral nerve repair.
Neurosurg Clin N Am.
2001;
12
341-352
21
De Bellard ME, Filbin MT.
Myelin-associated glycoprotein, MAG, selectively binds several neuronal proteins.
J Neurosci Res.
1999;
56
213-218
22
DeFranzo AJ, Morykwas MJ, LaRosse JR, Jennings DA, Challa V, Argenta LC.
Autologous denatured muscle as a nerve graft.
J Reconstr Microsurg.
1994;
10
145-149
, discussion 149-151
23
Dellon AL, Mackinnon SE.
Basic scientific and clinical applications of peripheral nerve regeneration.
Surg Annu.
1988;
20
59-100
24
den Dunnen WF, Robinson PH, Wessel R van, Pennings AJ, Leeuwen MB van, Schakenraad JM.
Long-term evaluation of degradation and foreign-body reaction of subcutaneously implanted poly (DL-lactide-epsilon-caprolactone).
J Biomed Mater Res.
1997;
36
337-346
25
Dezawa M, Takahashi I, Esaki M, Takano M, Sawada H.
Sciatic nerve regeneration in rats induced by transplantation of in vitro differentiated bone-marrow stromal cells.
Eur J Neurosci.
2001;
14
1771-1776
26
Donzelli R, Benvenuti D, Schonauer C, Mariniello G, Divitiis E De.
Microsurgical nervous reconstruction using autografts: a two-year follow-up.
J Neurosurg Sci.
1998;
42
79-83
27
Ducker TB, Kempe LG, Hayes GJ.
The metabolic background for peripheral nerve surgery.
J Neurosurg.
1969;
30
270-280
28
Eppley BL, Delfino JJ.
Collagen tube repair of the mandibular nerve: a preliminary investigation in the rat.
J Oral Maxillofac Surg.
1988;
46
41-47
29
Ernfors P, Henschen A, Olson L, Persson H.
Expression of nerve growth factor receptor mRNA is developmentally regulated and increased after axotomy in rat spinal cord motoneurons.
Neuron.
1989;
2
1605-1613
30
Fansa H, Keilhoff G, Forster G, Seidel B, Wolf G, Schneider W.
Acellular muscle with Schwann-cell implantation: an alternative biologic nerve conduit.
J Reconstr Microsurg.
1999;
15
531-537
31
Ferrari F, Castro Rodrigues A De, Malvezzi CK, Dal Pai Silva M, Padovani CR.
Inside-out vs. standard vein graft to repair a sensory nerve in rats.
Anat Rec.
1999;
256
227-232
32
Fugleholm K, Sorensen J, Schmalbruch H, Krarup C.
Axonal elongation through acellular nerve segments of the cat tibial nerve: importance of the near-nerve environment.
Brain Res.
1998;
792
309-318
33
Geuna S, Raimondo S, Nicolino S, Boux E, Fornaro M, Tos P, Battiston B, Perroteau I.
Schwann-cell proliferation in muscle-vein combined conduits for bridging rat sciatic nerve defects.
J Reconstr Microsurg.
2003;
19
119-123
, discussion 124
34
Glück T.
ber Neuroplastik. Auf dem Wege der Transplantation.
Arch Klin Chir.
1880;
25
606-616
35
Gravvanis AI, Lykoudis EG, Tagaris GA, Patralexis CG, Papalois AE, Panayotou PN, Stamatopoulos CN, Ioannovich JD.
Microchirurgical repair of nerve lesions with nerve grafts: the effect of nerve growth factor 7S.
Eur J Plast Surg.
2002;
25
187-192
36
Hanemann CO, Rosenbaum C, Kupfer S, Wosch S, Stoegbauer F, Muller HW.
Improved culture methods to expand Schwann cells with altered growth behaviour from CMT1A patients.
Glia.
1998;
23
89-98
37 Haymaker W, Woodhall B. Peripheral Nerve Injuries; Principles of Diagnosis. 2nd ed Saunders, Philadelphia 1959
38
He C, Chen Z, Chen Z.
Enhancement of motor nerve regeneration by nerve growth factor.
Microsurgery.
1992;
13
151-154
39
Heumann R, Korsching S, Bandtlow C, Thoenen H.
Changes of nerve growth factor synthesis in nonneuronal cells in response to sciatic nerve transection.
J Cell Biol.
1987;
104
1623-1631
40
His W.
Die Entwicklung der ersten Nervenbahnen beim menschlichen Embryo. bersichtliche Darstellung.
Arch Anat Physiol Lpz.
1887;
368-378
41
Ide C.
Peripheral nerve regeneration.
Neurosci Res.
1996;
25
101-121
42
IJkema-Paassen J, Jansen K, Gramsbergen A, Meek MF.
Transection of peripheral nerves, bridging strategies and effect evaluation.
Biomaterials.
2004;
25
1583-1592
43
Kanje M, Skottner A, Sjoberg J, Lundborg G.
Insulin-like growth factor I (IGF-I) stimulates regeneration of the rat sciatic nerve.
Brain Res.
1989;
486
396-398
44
Karacaoglu E, Yuksel F, Peker F, Guler MM.
Nerve regeneration through an epineurial sheath: its functional aspect compared with nerve and vein grafts.
Microsurgery.
2001;
21
196-201
45
Keskin M, Akbas H, Uysal OA, Canan S, Ayyldz M, Agar E, Kaplan S.
Enhancement of nerve regeneration and orientation across a gap with a nerve graft within a vein conduit graft: a functional, stereological, and electrophysiological study.
Plast Reconstr Surg.
2004;
113
1372-1379
46
Kilgard MP, Merzenich MM.
Cortical map reorganization enabled by nucleus basalis activity.
Science.
1998;
279
1714-1718
47
Kiyotani T, Teramachi M, Takimoto Y, Nakamura T, Shimizu Y, Endo K.
Nerve regeneration across a 25-mm gap bridged by a polyglycolic acid-collagen tube: a histological and electrophysiological evaluation of regenerated nerves.
Brain Res.
1996;
740
66-74
48
Krarup C, Archibald SJ, Madison RD.
Factors that influence peripheral nerve regeneration: an electrophysiological study of the monkey median nerve.
Ann Neurol.
2002;
51
69-81
49
Lanzetta M, Perani D, Anchisi D, Rosen B, Danna M, Scifo P, Fazio F, Lundborg G.
Early use of artificial sensibility in hand transplantation.
Scand J Plast Reconstr Surg Hand Surg.
2004;
38
106-111
50
Letourneau PC.
Cell-to-substratum adhesion and guidance of axonal elongation.
Dev Biol.
1975;
44
92-101
51
Levi R, Hamburger V.
A diffusable agent of mouse sarcoma producing hyperplasia of sympathetic ganglia and hyper-neurolization of the chick embryo.
J Exp Zool.
1951;
123
233-287
52
Li ST, Archibald SJ, Krarup C, Madison RD.
Peripheral nerve repair with collagen conduits.
Clin Mater.
1992;
9
195-200
53
Lopez TJ, Vries GH De.
Isolation and serum-free culture of primary Schwann cells from human fetal peripheral nerve.
Exp Neurol.
1999;
158
1-8
54
Lundborg G.
Brain plasticity and hand surgery: An overview.
J Hand Surg [Am].
2000;
25
2422-2252
55 Lundborg G. Nerve Injury and Repair . Churchill Livingstone, Edinburgh 1988: 1-222
56
Lundborg G.
A 25-Year Perspective of peripheral nerve surgery: evolving neuroscientific concepts and clinical significance.
J Hand Surg [Am].
2000;
25A
391-414
57
Lundborg G.
Enhancing posttraumatic nerve regeneration.
J Peripher Nerv Syst.
2002;
7
139-140
58 Lundborg G. Bridging nerve defects: the role of tissue interpositioning. In: Masquelet, A.C., Ferreira, A.C. Severe Traumatic Defects of the Upper Limb. Martin Dunitz, London 2003: 153-167
59
Lundborg G, Dahlin L, Danielsen N, Zhao Q.
Trophism, tropism, and specificity in nerve regeneration.
J Reconstr Microsurg.
1994;
10
345-354
60
Lundborg G, Hansson HA.
Regeneration of peripheral nerve through a preformed tissue space. Preliminary observations on the reorganization of regenerating nerve fibres and perineurium.
Brain Res.
1979;
178
573-576
61
Lundborg G, Richard P.
Bunge memorial lecture Nerve injury and repair - a challenge to the plastic brain.
J Peripher Nerv Syst.
2003;
8
209-226
62
Lundborg G, Rosen B.
Enhanced sensory recovery after median nerve repair: effects of early postoperative artificial sensibility using the Sensor Glove System.
J Hand Surg [Am].
2003;
28B
((Suppl 1))
38-39
63
Lundborg G, Rosen B, Abrahamson SO, Dahlin L, Danielsen N.
Tubular repair of the median nerve in the human forearm. Preliminary findings.
J Hand Surg [Br].
1994;
19
273-276
64
Lundborg G, Rosen B, Dahlin L, Danielsen N, Holmberg J.
Tubular versus conventional repair of median and ulnar nerves in the human forearm: early results from a prospective, randomized, clinical study.
J Hand Surg [Am].
1997;
22
99-106
65
Lundborg G, Rosen B, Dahlin L, Holmberg J, Rosen I.
Tubular repair of the median or ulnar nerve in the human forearm: a 5-year follow-up.
J Hand Surg [Br].
2004;
29
100-107
66 Mackinnon SE, Dellon AL. Surgery of the Peripheral Nerve: Nerve Repair and Nerve Grafting . Thieme, New York 1988: 89-129
67
Madison RD, Archibald SJ, Brushart TM.
Reinnervation accuracy of the rat femoral nerve by motor and sensory neurons.
J Neurosci.
1996;
16
5698-5703
68
Malizos KN, Dailiana ZH, Anastasiou EA, Sarmas I, Soucacos PN.
Neuromas and gaps of sensory nerves of the hand: management using vein conduits.
Am J Orthop.
1997;
26
481-485
69
Martini R, Schachner M, Brushart TM.
The L2/HNK-1 carbohydrate is preferentially expressed by previously motor axon-associated Schwann cells in reinnervated peripheral nerves.
J Neurosci.
1994;
14
7180-7191
70
Matsumoto K, Ohnishi K, Kiyotani T, Sekine T, Ueda H, Nakamura T, Endo K, Shimizu Y.
Peripheral nerve regeneration across an 80-mm gap bridged by a polyglycolic acid (PGA)-collagen tube filled with laminin-coated collagen fibers: a histological and electrophysiological evaluation of regenerated nerves.
Brain Res.
2000;
868
315-328
71
Meek MF.
Peripheral nerve regeneration and functional nerve recovery after reconstruction with a thin-walled biodegradable poly (DL-lactide-epsilon-caprolactone) nerve guide.
Cells Mater.
1997;
7
53-62
72
Meek MF, Coert JH.
Clinical use of nerve conduits in peripheral-nerve repair: review of the literature.
J Reconstr Microsurg.
2002;
18
97-109
74
Meek MF, Dijkstra JR, Dunnen WF Den, Ijkema-Paassen J, Schakenraad JM, Gramsbergen A, Robinson PH.
Functional assessment of sciatic nerve reconstruction: biodegradable poly (DLLA-epsilon-CL) nerve guides versus autologous nerve grafts.
Microsurgery.
1999;
19
381-388
73
Meek MF, Dunnen WF Den, Schakenraad JM, Robinson PH.
Evaluation of functional nerve recovery after reconstruction with a poly (DL-lactide-epsilon-caprolactone) nerve guide, filled with modified denatured muscle tissue.
Microsurgery.
1996;
17
555-561
75
Meek MF, Robinson PH, Stokroos I, Blaauw EH, Kors G, Dunnen WF den.
Electronmicroscopical evaluation of short-term nerve regeneration through a thin-walled biodegradable poly (DLLA-epsilon-CL) nerve guide filled with modified denatured muscle tissue.
Biomaterials.
2001;
22
1177-1185
76
Merle M, Dellon AL, Campbell JN, Chang PS.
Complications from silicon-polymer intubulation of nerves.
Microsurgery.
1989;
10
130-133
77
Millesi H.
Interfascicular nerve grafting.
Orthop Clin North Am.
1970;
2
419-435
78 Millesi H. Nerve grafts: indications, techniques and prognosis. In: Omer, G., Spinner, M. Management of Peripheral Nerve Problems. 1980: 410-430
79 Millesi H. Consequences of tension at the suture site. In: Posttraumatic Peripheral Nerve Regeneration. Raven, New York 1981: 277-279
80
Millesi H.
Reappraisal of nerve repair.
Surg Clin North Am.
1981;
61
321-340
81 Millesi H. Chirurgie der peripheren Nerven . Urban & Schwarzenberg, München Wien Baltimore 1992: 14-15
82
Millesi H, Meissl G, Berger A.
The interfascicular nervegrafting of the median and ulnar nerve.
J Bone Joint Surg Am.
1972;
54A
727-750
83
Miyauchi A, Kanje M, Danielson N, Dahlin LB.
Role of macrophages in the stimulation and regeneration of sensory nerves by transposed granulation tissue and temporal aspects of the response.
Scand J Plast Reconstr Surg Hand Surg.
1997;
31
17-23
84
Mosahebi A, Fuller P, Wiberg M, Terenghi G.
Effect of allogeneic Schwann cell transplantation on peripheral nerve regeneration.
Exp Neurol.
2002;
173
213-223
85
Mosahebi A, Woodward B, Wiberg M, Martin R, Terenghi G.
Retroviral labeling of Schwann cells: in vitro characterization and in vivo transplantation to improve peripheral nerve regeneration.
Glia.
2001;
34
8-17
86
Novikov L, Novikova L, Kellerth JO.
Brain-derived neurotrophic factor promotes axonal regeneration and long-term survival of adult rat spinal motoneurons in vivo.
Neuroscience.
1997;
79
765-774
87
Payr E.
Beiträge zur Technik der Blutgefäss und Nervennaht nebst Mitteilungen über die Verwendung eines resorbierbaren Metalles in der Chirurgie.
Arch Klin Chir.
1900;
62
67-111
88
Pu LL, Syed SA, Reid M, Patwa H, Goldstein JM, Forman DL, Thomson JG.
Effects of nerve growth factor on nerve regeneration through a vein graft across a gap.
Plast Reconstr Surg.
1999;
104
1379-1385
89
Ramon y Cajal S.
Degeneration and Regeneration of the Nerval System.
Oxford University Press, New York.
1928;
369-769
90
Rich KM, Luszczynski JR, Osborne PA, Johnson Jr EM.
Nerve growth factor protects adult sensory neurons from cell death and atrophy caused by nerve injury.
J Neurocytol.
1987;
16
261-268
91
Risitano G, Cavallaro G, Merrino T, Coppolino S, Ruggeri F.
Clinical results and thoughts on sensory nerve repair by autologous vein graft in emergency hand reconstruction.
Chir Main.
2002;
21
194-197
92
Rodriguez FJ, Verdu E, Ceballos D, Navarro X.
Nerve guides seeded with autologous Schwann cells improve nerve regeneration.
Exp Neurol.
2000;
161
571-584
93
Rosen B, Lundborg G.
Sensory re-education after nerve repair: aspects of timing.
Handchir Mikrochir Plast Chir.
2004;
36
8-12
94
Sahenk Z, Seharaseyon J, Mendell JR.
CNTF potentiates peripheral nerve regeneration.
Brain Res.
1994;
655
246-250
95
Scott JA.
The functional recovery of mucle proprioceptors after peripheral nerve lesions.
J Periph Nerv Syst.
1996;
1
19-27
96
Seddon HJ.
Three types of nerve injury.
Brain.
1943;
66
237-288
97
Son YJ, Thompson WJ.
Schwann cell processes guide regeneration of peripheral axons.
Neuron.
1995;
14
125-132
98
Sondell M, Sundler F, Kanje M.
Vascular endothelial growth factor is a neurotrophic factor which stimulates axonal outgrowth through the flk-1 receptor.
Eur J Neurosci.
2000;
12
4243-4254
99
Sorensen J, Fugleholm K, Moldovan M, Schmalbruch H, Krarup C.
Axonal elongation through long acellular nerve segments depends on recruitment of phagocytic cells from the near-nerve environment. Electrophysiological and morphological studies in the cat.
Brain Res.
2001;
903
185-197
100
Stanec S, Stanec Z.
Reconstruction of upper-extremity peripheral-nerve injuries with ePTFE conduits.
J Reconstr Microsurg.
1998;
14
227-232
101
Stolz B, Erulkar SD, Kuffler DP.
Macrophages direct process elongation from adult frog motoneurons in culture.
Proc R Soc Lond B Biol Sci.
1991;
244
227-231
102
Strauch B, Rodriguez DM, Diaz J, Yu HL, Kaplan G, Weinstein DE.
Autologous Schwann cells drive regeneration through a 6-cm autogenous venous nerve conduit.
J Reconstr Microsurg.
2001;
17
589-595
, discussion 596-587
103 Sunderland S. Nerves and Nerve Injuries. 2nd ed Churchill Livingstone, New York.
104
Sunderland S.
A classification of peripheral nerve injuries producing loss of function.
Brain.
1951;
74
491-516
105
Tanaka H, Tomura M, Kondo J, Teranishi Y, Buisson B, Xie FK, Henderson CE.
Low-affinity nerve growth factor receptor is associated with motoneuron axonal pathways.
Neurosci Res.
1997;
27
21-27
106
Tang JB.
Vein conduits with interposition of nerve tissue for peripheral nerve defects.
J Reconstr Microsurg.
1995;
11
21-26
107
Terzis J, Faibisoff B, Williams B.
The nerve gap: suture under tension vs graft.
Plast Reconstr Surg.
1975;
56
166-170
108
Thoenen H.
Neurotrophins and neuronal plasticity.
Science.
1995;
270
593-598
109
Tohill M, Terenghi G.
Stem-cell plasticity and therapy for injuries of the peripheral nervous system.
Biotechnol Appl Biochem.
2004;
40
17-24
110
Torigoe K.
The role of migratory Schwann cells in nerve regeneration as studied by the film model.
J Peripher Nerv Syst.
1997;
2
227-231
111
Tos P, Battiston B, Geuna S, Giacobini-Robecchi MG, Hill MA, Lanzetta M, Owen ER.
Tissue specificity in rat peripheral nerve regeneration through combined skeletal muscle and vein conduit grafts.
Microsurgery.
2000;
20
65-71
112
Vroemen M, Weidner N.
Purification of Schwann cells by selection of p75 low affinity nerve growth factor receptor expressing cells from adult peripheral nerve.
J Neurosci Methods.
2003;
124
135-143
113
Walton RL, Brown RE, Matory Jr WE, Borah GL, Dolph JL.
Autogenous vein graft repair of digital nerve defects in the finger: a retrospective clinical study.
Plast Reconstr Surg.
1989;
84
944-949
, discussion 950-942
114
Wang KK, Costas PD, Bryan DJ, Eby PL, Seckel BR.
Inside-out vein graft repair compared with nerve grafting for nerve regeneration in rats.
Microsurgery.
1995;
16
65-70
115
Weber RA, Breidenbach WC, Brown RE, Jabaley ME, Mass DP.
A randomized prospective study of polyglycolic acid conduits for digital nerve reconstruction in humans.
Plast Reconstr Surg.
2000;
106
1036-1045
, discussion 1046-1038
116
Williams HB.
The painful stump neuroma and its treatment.
Clin Plast Surg.
1984;
11
79-84
117
Wrede L.
berbrückung eines Nervendefektes mittels Seidennaht und lebenden Venenstückes.
Dtsch Med Wochenschr.
1909;
1125-1160
118
Yin Q, Kemp GJ, Frostick SP.
Neurotrophins, neurones and peripheral nerve regeneration.
J Hand Surg [Br].
1998;
23
433-437
119
Yoshii S, Oka M.
Collagen filaments as a scaffold for nerve regeneration.
J Biomed Mater Res.
2001;
56
400-405
120
Yoshii S, Oka M, Ikeda N, Akagi M, Matsusue Y, Nakamura T.
Bridging a peripheral nerve defect using collagen filaments.
J Hand Surg [Am].
2001;
26
52-59
121
Yoshii S, Oka M, Shima M, Taniguchi A, Akagi M.
30 mm regeneration of rat sciatic nerve along collagen filaments.
Brain Res.
2002;
949
202-208
122
Zhang F, Blain B, Beck J, Zhang J, Chen Z, Chen ZW, Lineaweaver WC.
Autogenous venous graft with one-stage prepared Schwann cells as a conduit for repair of long segmental nerve defects.
J Reconstr Microsurg.
2002;
18
295-300
123
Zhang Y, Campbell G, Anderson PN, Martini R, Schachner M, Lieberman AR.
Molecular basis of interactions between regenerating adult rat thalamic axons and Schwann cells in peripheral nerve grafts. II. Tenascin-C.
J Comp Neurol.
1995;
361
210-224
Correspondence
Priv. -Doz. Dr. med. N. A. Papadopulos
Department of Plastic and Reconstructive Surgery
Klinikum rechts der Isar of the Technical University of Munich
Ismaningerstr. 22
81675 Munich
Germany
Phone: +49/89/4140 21 71
Fax: +49/89/4140 48 69
Email: n.papadopulos@lrz.tum.de
Email: n_papadopulos@yahoo.com