Degeneration and Regeneration of Nerves in a Dorsal Skin Flap in the Rat

References

• Adenymo O., Wyburn G. M. Innervation of skin grafts. Transplantation 1957; 4: 152
   Google Scholar
• Burnstock C., Costa M. Adrenergic neurons, the organization, function and development in the peripheral nervous system. Chapman and Hall, London. 1975
   Google Scholar
• Chamley J. H., Dowel J. Specificity of nerve fibre attraction to autonomic effector organs in tissue culture. Exp Cell Res 1975; 90: 1
   PubMed Web of Science ®Google Scholar
• Chamley J. H., Goller J., Burnstock G. Selective growth of sympathetic nerve fibers to explants of normally densely innervated autonomic effector organs in tissue culture. Dev Biol 1973; 31: 362
   PubMed Web of Science ®Google Scholar
• Conway H. Sweating function of transplanted skin. Surg Gynecol Obstet 1939; 69: 756
   Google Scholar
• Davis L. The return of sensation to transplanted skin. Surg Gynecol Obstet 1934; 59: 533
   Google Scholar
• Davis J. S., Kitlowski E. A. Regeneration of nerves in skin grafts and skin flaps. Am J Surg 1934; 24: 501
   Google Scholar
• Eränkö O. Distribution of fluorescing islets, adrenalin and noradrenalin in the adrenal medulla of the hamster. Acta Endocrinol (Kbh) 1955; 18: 174
   PubMedGoogle Scholar
• Eränkö O. The practical histochemical demonstration of catecholamines by formaldehyde-induced fluorescence. J R Micr Soc 1967; 87: 259
   PubMedGoogle Scholar
• Eränkö O., Teräväinen H. Cholinesterases and eserine resistant carboxylic esterases in degenerating and regenerating motor end plates of the rat. J Neurochem 1967; 14: 947
   PubMedGoogle Scholar
• Falck B., Hillarp N.-Å., Thieme G., Torp A. Fluorescence of catecholamines and related compounds condensed with formaldehyde. J Histochem Cytochem 1962; 10: 348
   Web of Science ®Google Scholar
• Fitzgerald M. J. T., Martin F., Paletta F. X. Innervation of skin graft. Surg Gynecol Obstet 1967; 124: 808
   PubMedGoogle Scholar
• Gomori G. Enzymes. Microscopic histochemistry principles and practice. Univ. of Chicago Press, Chicago. 1952; 137–221
   Google Scholar
• Huhtala A., Tervo T., Huikuri K. T., Palkama A. Effects of denervations on the acetylcholinesterase-containing and fluorescent nerves of the rat iris. Acta Oftalmol 1976; 54: 85
   PubMedGoogle Scholar
• Juntunen J. Morphological studies on the induction of postsynaptic membrane of the myoneural junction. Acta Inst Anatomici Univ Helsinkiensis 1974, Suppl. 7
   Google Scholar
• Karnovsky M. J., Roots L. A “direct-coloring” thiocholine method for cholinesterases. J Histochem Cytochem 1964; 12: 219
   PubMed Web of Science ®Google Scholar
• Kernwein G. A. Recovery of sensation in split thickness skin grafts. Arch Surg 1948; 56: 459
   Google Scholar
• Kredel F. E., Evans J. P. Recovery of sensation in denervated pedicle and free skin grafts. Arch Neurol Psychiat 1933; 29: 1203
   Google Scholar
• Kredel F. E., Phemister D. B. Recovery of sympathetic nerve function in skin transplants. Arch Neurol Psychiat 1939; 42: 403
   Google Scholar
• Levi-Montalcini R., Angeletti P. U. Nerve growth factor. Physiol Rev 1968; 48: 534
   PubMed Web of Science ®Google Scholar
• Lindvall O., Björklund A. The glyoxylic acid fluorescence histochemical method: a detailed account of the methodology for the visualization of central catacholamine neurons. Histochemistry 1974; 39: 97
   PubMedGoogle Scholar
• Löfgren L. Recovery of nervous functions in skin transplants with special reference to the sympathetic functions. Acta Chir Scand 1952; 102: 229
   Google Scholar
• Malmfors T., Furness J. B., Cambell G. R., Burnstock G. Reinnervation of smooth muscle of the vas deferens transplanted into the anterior chamber of the eye. J Neurobiol 1971; 2: 193
   PubMedGoogle Scholar
• Mannerfelt L. Evaluation of functional sensation of skin grafts in the hand area. Br J Plast Surg 1962; 15: 136
   PubMedGoogle Scholar
• Mariš F. Evaluation of functional adaption of skin grafts to the hand by tactile discrimination. Acta Chir Plast (Praha) 1964; 6: 313
   PubMedGoogle Scholar
• Mariš F., Jurkovič I., Kohút P., Suchánek A. Re-innervation of free and flap skin grafts. Acta Chir Plast (Praha) 1963; 5: 54
   Google Scholar
• McCarrol H. R. The regeneration of sensation in transplanted skin. Ann Surg 1938; 108: 309
   PubMedGoogle Scholar
• Montagna W., Parakkal P. F. Cutaneous innervation. The structure and function of skin, 3rd ed. Academic Press, New York and London. 1974; 157–171
   Google Scholar
• Napier J. R. The return of pain sensibility in full thickness skin grafts. Brain 1952; 75: 147
   PubMedGoogle Scholar
• Olson L., Malmfors T. Growth characteristics of adrenergic nerves in the adult rat. Acta Physiol Scand 1970, Suppl. 348: i
   PubMedGoogle Scholar
• Orfanos C. E., Mahrle G. Ultrastructure and cytochemistry of human cutaneous nerves, with special reference to the ultrastructural localization of specific and nonspecific cholinesterases in human skin. J Invest Dermatol 1973; 61: 108
   PubMedGoogle Scholar
• Palmer B. Sympathetic denervation and reinnervation of cutaneous blood vessels following surgery. Scand J Plast Reconstr Surg 1970; 4: 93
   PubMedGoogle Scholar
• Pontén B. Grafted skin. Observations on innervation and other qualities. Acta Chir Scand 1960, Suppl. 257
   Google Scholar
• Porter R. W. Functional assessment of transplanted skin in volar defects of the digits. A comparison between free grafts and flaps. J Bone Joint Surg 1968; 50A: 955
   Google Scholar
• Rintala A. Palmar skin grafts. Acta Chir Scand 1963; 126: 474
   PubMedGoogle Scholar
• Romeis B. Mikroskopische Technik. R. Oldenburg, München. 1948
   Google Scholar
• Santoni-Rugiu P. An experimental study on the innervation of free skin grafts and pedicle flaps. Plast Reconstr Surg 1966; 38: 98
   PubMedGoogle Scholar
• Sinclair D. Cutaneous sensation. Oxford Univ. Press, London, New York and Toronto. 1967
   Google Scholar
• Sturman M. J., Duran R. J. Late results of finger-tip injuries. J Bone Joint Surg 1963; 45A: 289
   Google Scholar
• Teich-Alasia S., Garelli R., Ambroggio G. Etude du retour de la sensibilité dans les lambeaux transplantes. Ann Chir Plast 1965; 10: 35
   PubMedGoogle Scholar
• Tervo T. Histochemical demonstration of cholinesterase activity in the cornea of the rat and the effect of various denervations on the corneal nerves. Histochemistry 1976; 47: 133
   PubMedGoogle Scholar
• Thomas P. K., King H. M. The degeneration of unmyelinated axons following nerve section: an ultrastructural study. J Neurocytol 1974; 3: 497
   PubMedGoogle Scholar
• Waris T. Reinnervation of free skin autografts in the rat. Scand J Plast Reconstr Surg 1978; 12: 85
   PubMed Web of Science ®Google Scholar
• Waris T., Partanen S. Demonstration of catecholamines in peripheral adrenergic nerves in stretch preparations with fluorescence induced by aqueous solution of glyoxylic acid. Histochemistry 1975; 41: 369
   PubMedGoogle Scholar
• Waris T., Rechardt L. Histochemically demonstrable catecholamines and cholinesterases in nerve fibres of rat dorsal skin. Histochemistry 1977; 53: 203
   PubMedGoogle Scholar
• Weddell G., Zandler E. A critical evaluation of methods used to demonstrate tissue neural elements, illustrated by reference to the cornea. J Anat 1950; 84: 168
   PubMed Web of Science ®Google Scholar
• Weiss P., Taylor P. Further experimental evidence against “neurotropism” in nerve regeneration. J Exp Zool 1944; 95: 233
   Google Scholar