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Books on the topic 'Ganglionic'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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1

Clinical handbook of mindfulness. Springer, 2009.

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2

Wightman, Wayne. Ganglion & other stories. Tachyon Publication, 1995.

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3

Nozdrachev, A. D. Zvezdchatyĭ gangliĭ: Struktura i funkt͡s︡ii. "Nauka", 2002.

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4

Parker, Philip M., and James N. Parker. Ganglions: A medical dictionary, bibliography, and annotated research guide to Internet references. ICON Health Publications, 2004.

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5

Cheng-Pei, Choh-Vivian. Organisation of centromeric domains in nuclei of murine dorsal root ganglion neurons in vitro. National Library of Canada, 1996.

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6

Moore, Matthew R. Central nervous system regeneration: Survival of retinal ganglion cells and optic nerve in mouse following axotomy and grafting. s.n.], 1986.

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7

McTeague, Jennifer Ann. Morphological changes in the first thoracis ganglion following limb loss and regeneration in the snapping shrimp, Alpheus heterochelis. National Library of Canada, 1992.

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8

Billia, Filio. Localization of chromatin domains in dorsal root ganglion neurons, in vitro, and in hippocampal neurons exhibiting long-term potentiation. National Library of Canada, 1991.

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9

Hodaie, Mojgan. The effect of patterns of electrical stimulation on the expression of the preprotachykinin gene in rat superior cervical ganglion neurons. National Library of Canada, 1994.

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10

Gerber, Albert Benjamin. Miracles on Park Avenue. L. Stuart, 1986.

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11

Probabilistic similarity networks. MIT Press, 1991.

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12

Brain biochemistry and brain disorders. Oxford University Press, 1992.

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13

Kharkevich, Dimitry A. Pharmacology of Ganglionic Transmission. Brand: Springer, 2011.

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14

Rita, Moretti, ed. Corticobasal ganglionic degeneration: Cognitive and functional aspects. Nova Science Publishers, 2005.

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15

(Editor), Rita Moretti, Paola Torre (Editor), and Rodolfo M. Antonello (Editor), eds. Corticobasal Ganglionic Degeneration: Cognitive And Functional Aspects. Nova Biomedical Books, 2005.

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16

1918-, Karczmar A. G., Kōketsu Kyōzō 1922-, and Nishi Syogoro, eds. Autonomic and enteric ganglia: Transmission and its pharmacology. Plenum Press, 1985.

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17

1918-, Karczmar A. G., Kōketsu Kyōzō 1922-, and Nishi Syogoro, eds. Autonomic and enteric ganglia: Transmission and its pharmacology. Plenum Press, 1986.

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18

Kim, Lincoln. Role of sympathetic post-ganglionic neurons in cutaneous wound healing in Rattus norvegicus. 2004.

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19

Gilden, Don, Randall J. Cohrs, Ravi Mahalingam, and Maria A. Nagel. Varicella Zoster Virus Infection of the Nervous System. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0149.

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Varicella zoster virus (VZV) is a human herpesvirus that causes varicella (chickenpox), after which virus becomes latent in ganglionic neurons along the entire neuraxis. Reactivation of VZV due to a decline in the cell-mediated immune response to VZV in elderly or immunocompromised individuals causes zoster (shingles), frequently complicated by chronic pain (postherpetic neuralgia) and serious neurological disease (meningoencephalitis, myelitis and VZV vasculopathy due to retrograde spread of virus after zoster. Here, we describe clinical, laboratory and pathological features of neurological complications of VZV reactivation, including diagnostic testing to verify VZV infection of the nervous system, since all neurological complications of zoster may occur without rash. We also discuss VZV latency, primate models to study varicella pathogenesis and immunity, and immunization of elderly individuals to prevent VZV reactivation.
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20

Clinical Handbook of Mindfulness. Springer, 2010.

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21

Edmond Ganglion & fils. Editions Du Rocher, 1999.

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22

Edmond Ganglion & fils. Gallimard, 2001.

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23

Vlastimil, Liora G. Ganglion Cells: Morphology, Functional Development and Role in Disease. Nova Science Publishers, Incorporated, 2014.

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24

Lin, Chia Shiang (Sean). Ganglion Impar Block: Fluoroscopy and Ultrasound. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199908004.003.0036.

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Blockade of the ganglion impar (also known as ganglion of Walther or sacrococcygeal ganglion) is indicated for evaluating and managing visceral or sympathetic-maintained pain in the coccygeal and perineal area. Ganglion impar neurolysis has been reported in the palliative treatment for malignancies of the pelvis with cancer pain in the perineal area. Ultrasound can be successively used to locate the sacrococcygeal joint (SCJ) and facilitate the performance of ganglion impar block. However, ultrasound can also complement fluoroscopy, as lateral fluoroscopy is still needed to establish safe depth and monitor the spread of the injectate, especially with neurolytic injections.
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25

Egloff, Joel. Edmond Ganglion E Hijo (Otras Lenguas). Grupo Oceano, 2001.

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26

Greenberg, Brian Scott. Neurotrophin regulation of sensory neurons in the trigeminal ganglion: Effect of NGF infusion on neuronal survival. 2002.

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27

Kastler, Adrian, and Bruno Kastler. Cervical Sympathetic Block and Neurolysis: Computed Tomography. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199908004.003.0029.

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The stellate ganglion blockade technique is used to treat complex regional pain syndrome (CRPS). It is now well established that stellate blockades should be performed under imaging guidance. It has been suggested that alcohol may bring longer lasting relief in cases of severe intractable cancer-related pain arising from regional neoplasms invading the stellate ganglion, but frequent onset of Horner’s syndrome can outweigh the technique’s efficacy. Radiofrequency neurolysis (RFN) has become a common procedure in the management of chronic neuropathic pain. This chapter reviews indications of stellate ganglion procedures and describes the basic anatomical background, as knowledge of the anatomical surroundings of the stellate ganglion is a necessary prerequisite to a safe and successful procedure. Then it demonstrates how CT-guidance allows a step-by-step control of positioning the needle tip at target for either alcohol or radiofrequency thermal ablation, and discusses the results, advantages, and disadvantages of each approach.
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28

McLachlan, A. J. Autonomic Ganglia (Autonomic Nervous System). Informa Healthcare, 1995.

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29

Kerr, Bradley J. The link between an Nav1.7 mutation and erythromelalgia. Edited by Paul Farquhar-Smith, Pierre Beaulieu, and Sian Jagger. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198834359.003.0081.

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The landmark paper discussed in this chapter is ‘Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons’, published by Dib-Hajj et al. in 2005. The voltage-dependent sodium channels Nav1.7, Nav1.8, and Nav1.9 have a restricted pattern of expression in sensory neurons in the periphery and are concentrated in small nociceptive neurons of the dorsal root ganglion, the trigeminal ganglion, and the nodose ganglion. In this paper, Dib-Hajj and colleagues studied a family with erythromelalgia (Weir Mitchell disease), an autosomal-dominant, inherited pain disorder in which burning pain in the extremities can be triggered by warming of the skin or moderate exertion. By identifying a novel mutation in SCN9A, which encodes Nav1.7, they established the critical role of this specific ion channel in this patient population. These findings represent an important first step towards developing isoform-specific channel blockers for the treatment of an inherited chronic pain condition.
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30

Shoemaker, Sarah Elizabeth. Neurotransmitter plasticity in the trigeminal ganglion following nerve growth factor infusion. 2000.

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31

Publications, ICON Health. Ganglions - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References. ICON Health Publications, 2004.

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32

Sri-Ram, Kesavan, Anthony Mcgrath, Eric Yeung, et al. Benign tumours of soft tissues. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.002003.

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♦ Ganglion cyst♦ Intramuscular myxoma♦ Myositis ossificans♦ Nodular fasciitis♦ Haemangioma♦ Lipoma♦ Cavernous lymphangioma♦ Glomus tumour♦ Neurofibroma♦ Desmoid tumour♦ Elastofibroma♦ Schwannoma♦ Synovial chondromatosis.
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33

Kleef, Maarten van. Radiofrequency Lesions of the Dorsal Root Ganglion in the Treatment of Spinal Pain. Universitaire Pers Maasstricht, 1996.

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34

Wong, Stacy N., and Line G. Jacques. Neuropathic Groin Pain. Edited by Meghan E. Lark, Nasa Fujihara, and Kevin C. Chung. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190617127.003.0017.

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Chronic neuropathic groin pain may be iatrogenic or posttraumatic and can be disabling or even crippling in some individuals. Patients may have significant sleep disturbances and may experience psychosocial effects along with significant physical limitations. A combination of pharmacologic treatments with physical therapy and local infiltrations may be useful. Neurostimulation techniques, including spinal cord stimulation, peripheral nerve stimulation, and dorsal root ganglion stimulation, have shown promising results in the treatment of chronic neuropathic pain. In certain cases, surgical approaches, including selective neurectomy, can be effective; in other cases, the pain will remain chronic and intractable despite all interventional measures. In summary, patients with neuropathic groin pain can be treated after a thorough pretreatment investigation. Dorsal root ganglion stimulation is a viable option and should be considered when treating this challenging patient population.
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35

M, Shapley R., and Lam Dominic Man-Kit, eds. Contrast sensitivity. MIT Press, 1993.

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36

DiMuro, John M., and Mehul J. Desai. Sympathetic Blockade of the Spine. Edited by Mehul J. Desai. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199350940.003.0030.

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This chapter focuses on the typical pain complaints and their appropriateness for sympathetic blockade and neurolysis. Anatomic considerations, block technique, associated risks, and evidence of a successful block are covered for the stellate ganglion block, T2 sympathetic block, thoracic splanchnic block, celiac plexus block, superior hypogastric plexus block, and ganglion of impar block. Sympathetic blockade is commonly used for visceral pain syndromes. Visceral pain syndromes typically are not responsive to neuraxial blocks as well as conventional rehabilitative and pharmacologic treatments. Spinal sympathetic techniques involve careful prevertebral needle placement, typically using fluoroscopic guidance. The proximity of major vessels near the target injection area is the primary risk of these techniques. In general, sympathetic blocks are non-diagnostic, but they can still help determine whether a sympathetically mediated pain condition may be present and if sympatholysis may be an effective treatment option.
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37

McClenahan, Maureen F., and William Beckman. Pain Management Techniques. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190217518.003.0011.

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This chapter provides a broad review of various interventional pain management procedures with a focus on indications, anatomy, and complications. Specific techniques reviewed include transforaminal epidural steroid injection, lumbar sympathetic block, stellate ganglion block, cervical and lumbar radiofrequency ablation, gasserian ganglion block, sacroiliac joint injection, celiac plexus block, lateral femoral cutaneous nerve block, ilioinguinal block, lumbar medial branch block, obturator nerve block, ankle block, occipital nerve block, superior hypogastric plexus block, spinal cord stimulation, and intrathecal drug delivery systems. The chapter reviews contrast agents, neurolytic agents, botulinum toxin use, corticosteroids, and ziconotide pharmacology and side effects in addition to diagnosis and management of local anesthetic toxicity syndrome. It also discusses indications for neurosurgical techniques including dorsal root entry zone lesioning. In addition, information on radiation safety and the use of anticoagulants with neuraxial blocks is covered.
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38

Lamyman, Michael, and Roderick Dunn. Tumours. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757689.003.0017.

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Hand tumours occur in a spectrum from common benign conditions (such as ganglions) and rare, aggressive metastatic sarcoma. We present a clear account of benign and malignant soft tissue and bone tumours affecting the hand and upper limb, including diagnostic features, useful investigations, and classifications. Treatment plans are discussed, with some operative details for the different types of ganglia.
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39

Narouze, Samer N. Cervical Sympathetic Block: Fluoroscopy. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199908004.003.0027.

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In those patients with significant sympathetically maintained pain, repeated blocks may provide a therapeutic value and help facilitate physical therapy and rehabilitation. Cervical sympathetic blocks have been traditionally performed by using surface landmarks, however imaging-guided blocks are strongly recommended to avoid potential serious complications. Most preganglionic sympathetic efferents innervating the head, neck, and upper extremity either pass through or synapse at the stellate ganglion. This provides an ideal target for blockade of sympathetic innervation to the head, neck, and upper limbs. The stellate ganglion block can be performed at the C6 and C7 transverse processes. Fluoroscopy is a reliable method for identifying bony surfaces, which facilitates identifying the C6 and C7 transverse processes; however, this is only a surrogate marker, because the location of the cervical sympathetic trunk is defined by the fascial plane of the prevertebral fascia, which cannot be visualized with fluoroscopy.
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40

Perney, Teresa M. Substance P release, calcium homeostasis and phospholipid metabolism in dorsal root ganglion neurons in vitro. 1989.

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41

Beattie, R. Mark, Anil Dhawan, and John W.L. Puntis. Hirschsprung's disease. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569862.003.0039.

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Hirschprung's disease 280Neuronal intestinal dysplasia 281Intestinal pseudo-obstruction 281Hirschsprung's disease is the absence of ganglion cells in the myenteric plexus of the most distal bowel. Presentation is with constipation. Incidence is 1 in 5000. Long-segment Hirschsprung's disease is familial, with equal sex incidence. The gene is on chromosome 10. It is associated with Down's syndrome and there is a high frequency of other congenital abnormalities....
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42

Schwenk, Karen L. The role of afferent input to the Superior Cervical Ganglion in the plasticity of cerebrovascular axons. 1995.

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43

Völgyi, Béla, Garrett T. Kenyon, David W. Marshak, and Botir Sagdullaev, eds. Encoding Visual Features by Parallel Ganglion Cell Initiated Pathways in the Healthy, Diseased and Artificial Retina. Frontiers Media SA, 2019. http://dx.doi.org/10.3389/978-2-88963-105-6.

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44

Bunting, Timothy Andrew *. Effects of aging and ethanol on the electric membrane properties of mouse dorsal root ganglion neurons. 1988.

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45

Efectividad de la punción aspiración con aguja fina frente a biopsia ganglionar en el diagnóstico de neoplasias linfoides. Instituto de Salud Carlos III, 2017. http://dx.doi.org/10.4321/repisalud.5779.

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46

Jenkins, Liberty. Neuropathy. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0234.

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Neuropathy is disease of the peripheral nerves. The pathological process may affect the nerve at the root (radiculopathy), the dorsal root ganglion (ganglionopathy), the plexus (plexopathy), or anywhere along the terminal pathway, typically at sites of entrapment or in a length-dependent pattern. The cranial nerves may also be affected. The process may affect a single nerve (a mononeuropathy) or multiple discrete nerves (mononeuritis multiplex) or form a confluent, typically distal, and symmetrical pattern (polyneuropathy).
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47

Narouze, Samer N. Cervical Sympathetic Block: Ultrasound. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199908004.003.0028.

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To improve the safety of the stellate ganglion block (SGB), the techniques for SGB have evolved over time from the standard blind technique to fluoroscopy and more recently to ultrasound-guided technique. Ultrasound-guided SGB may also improve the safety of the procedure by direct visualization of vascular structures and soft-tissue structures. Accordingly, the risk of vascular and soft-tissue injury may be minimized. Ultrasound guidance will allow direct monitoring of the spread of the injectate and hence may minimize complications such as recurrent laryngeal nerve (RLN) palsy and intrathecal, epidural, or intravascular spread.
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48

Filler, Aaron G. Piriformis Syndrome and Other Nerve Entrapments of the Posterior Pelvis. Edited by Meghan E. Lark, Nasa Fujihara, and Kevin C. Chung. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190617127.003.0011.

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Not every case of neurologically based pelvic/genital numbness/incontinence is due to cauda equina syndrome. Pelvic pain, incontinence, and sexual dysfunction can result from treatable peripheral nerve injury or entrapment affecting the pudendal nerves or impar ganglion. Learning the signs, physical exam findings, tests, and surgical options greatly expands a neurosurgeon’s range. The pudendal nerve and nerve to the obturator internus muscle arise after S2, S3, and S4 spinal nerves traverse the piriformis muscle. They exit the sciatic notch with the sciatic nerve but then re-enter the pelvis, where the pudendal nerve then gives off bladder, rectal, and genital branches.
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49

Shafer, Andrew J. Plasticity of calcitonin gene-related peptide immunoreactive axons in the rat superior cervical ganglion following infusion of nerve growth factor. 1998.

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50

Parallel Processing in the Visual System: The Classification of Retinal Ganglion Cells and its Impact on the Neurobiology of Vision. Springer, 2012.

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