Diplomate in Neurology, Module 1 Required Reading--Dallas, Amsterdam
Frederick R Carrick, DC, PhD, DACAN, DABCN, DACNB, DAAPM, FACCN
Professor of Neurology
Module one of the Diplomate in Neurology Program will be an interactive study of neuron theory as it applies to chiropractic practice. This module is a clinical module where the breadth of information common to all health care professionals will be used as a basis from which application based knowledge will be developed.
The following pages in Kandel , Schwartz and Jessell: IIIrd Edition : Principles of Neural Science are required reading in preparation for module 1.
Part I An Overall View
pp 2-16
Part II Cell and Molecular Biology of the Neuron
pp 34-120
Part III Elementary Interactions Between Neurons: Synaptic Transmission
pp 120-135
pp 153-225
pp 258-270
I have used the following studies in my preparation of the depth of information in my lecture for module 1. I will explore the concepts of immediate early gene responses to a variety of frequencies of integration. Specifically I will develop the concept of neuronal membrane and action potentiation in concert with fuel delivery. The disease forms of aberrations of these systems will be emphasized so that the participant will be able to associate application with the breadth and depth of the module.
We will discuss synaptogenesis and the embryologic relationships of human kind to clinical applications. A comparative anatomical review will allow the participant to understand behaviour in their patients that is more basic to lower life forms. A basic review of biochemistry may be helpful in this module. Participants must bring diagnostic equipment to each module as this round of the program is a hands on application based learning module.
There will be hands on application utilizing live patients and patient scenario to enhance the ethnographic studies of the module.
Neurophysiological summation and survivability will be contrasted to a variety of syndromes and disease states of humankind. The participant will be able to develop his/her art of application based upon a firm foundation in the basic clinical sciences.
The references that I will use in my lectures will be posted 2 weeks before each module.
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Gilchrist, J. M.; Sikirica, M.; Stopa, E.; Shanske, S. Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in strokelike episodes. Stroke. 1996 Aug; 27(8): 1420-3; ISSN: 0039-2499.
Ikonomidou, C.; Qin, Qin Y.; Labruyere, J.; Olney, J. W. Motor neuron degeneration induced by excitotoxin agonists has features in common with those seen in the SOD-1 transgenic mouse model of amyotrophic lateral sclerosis. J-Neuropathol-Exp-Neurol. 1996 Feb; 55(2): 211-24; ISSN: 0022-3069.
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Kosel, S.; Lucking, C. B.; Egensperger, R.; Mehraein, P.; Graeber, M. B. Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonism. J-Neurosci-Res. 1996 Apr 15; 44(2): 174-83; ISSN: 0360-4012.
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Love, S.; Hilton, D. A. Assessment of the distribution of mitochondrial ribosomal RNA in melas and in thrombotic cerebral infarcts by in situ hybridization. J-Pathol. 1996 Feb; 178(2): 182-9; ISSN: 0022-3417.
Majander, A.; Finel, M.; Savontaus, M. L.; Nikoskelainen, E.; Wikstrom, M. Catalytic activity of complex I in cell lines that possess replacement mutations in the ND genes in Leber's hereditary optic neuropathy. Eur-J-Biochem. 1996 Jul 1; 239(1):
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Mallard, K.; Jones, D. B.; Richmond, J.; McGill, M.; Foulis, A. K. Expression of the human heat shock protein 60 in thyroid, pancreatic, hepatic and adrenal autoimmunity. J-Autoimmun. 1996 Feb; 9(1): 89-96; ISSN: 0896-8411.
Pizzorusso, T.; Maffei, L. Plasticity in the developing visual system. Curr-Opin-Neurol. 1996 Apr; 9(2): 122-5; ISSN: 1350-7540.
Martin, M. A.; Molina, J. A.; Jimenez Jimenez, F. J.; Benito Leon, J.; Orti Pareja, M.; Campos, Y.; Arenas, J. Respiratory-chain enzyme activities in isolated mitochondria of lymphocytes from untreated Parkinson's disease patients. Grupo-Centro de Trastornos del Movimiento. Neurology. 1996 May; 46(5): 1343-6; ISSN: 0028-3878.
Matsuishi, T.; Sakai, T.; Naito, E.; Nagamitsu, S.; Kuroda, Y.; Iwashita, H.; Kato, H. Elevated cerebrospinal fluid lactate/pyruvate ratio in Machado-Joseph disease. Acta-Neurol-Scand. 1996 Jan; 93(1): 72-5; ISSN: 0001-6314.
McArdle, A.; McArdle, F.; Jackson, M. J.; Page, S. F.; Fahal, I.; Edwards, R. H. Investigation by polymerase chain reaction of enteroviral infection in patients with chronic fatigue syndrome. Clin-Sci-Colch. 1996 Apr; 90(4): 295-300; ISSN: 0143-5221.
Melberg, A.; Lundberg, P. O.; Henriksson, K. G.; Olsson, Y.; Stalberg, E. Muscle-nerve involvement in autosomal dominant progressive external ophthalmoplegia with hypogonadism. Muscle-Nerve. 1996 Jun; 19(6): 751-7; ISSN: 0148-639X.
Merril, C. R.; Zullo, S.; Ghanbari, H.; Herman, M. M.; Kleinman, J. E.; Bigelow, L. B.; Bartko, J. J.; Sabourin, D. J. Possible relationship between conditions associated with chronic hypoxia and brain mitochondrial DNA deletions. Arch-Biochem-
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Mierzewska, H. [Mitochondrial diseases. Part II -- diagnosis and detailed review]. Choroby mitochondrialne. Czesc II -- Diagnostyka oraz czesc szczegolowa. Neurol-Neurochir-Pol. 1996 Mar; 30(2): 279-92; ISSN: 0028-3843.
Mourelatos, Z.; Gonatas, N. K.; Stieber, A.; Gurney, M. E.; Dal Canto, M. C. The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease. Proc-Natl-Acad-Sci-U-S-A. 1996 May 28; 93(11): 5472-7; ISSN: 0027-8424.
Nada, M. A.; Vianey Saban, C.; Roe, C. R.; Ding, J. H.; Mathieu, M.; Wappner, R. S.; Bialer, M. G.; McGlynn, J. A.; Mandon, G. Prenatal diagnosis of mitochondrial fatty acid oxidation defects. Prenat-Diagn. 1996 Feb; 16(2): 117-24; ISSN: 0197-3851.
Pitkanen, S.; Robinson, B. H. Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase. J-Clin-Invest. 1996 Jul 15; 98(2): 345-51; ISSN: 0021-9738.
Santorelli, F. M.; Mak, S. C.; Vazquez Memije, E.; Shanske, S.; Kranz Eble, P.; Jain, K. D.; Bluestone, D. L.; De Vivo, D. C.; DiMauro, S. Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutation. Pediatr-Res. 1996 May;
39(5): 914-7; ISSN: 0031-3998.
Stefani, A.; Pisani, A.; Mercuri, N. B.; Calabresi, P. The modulation of calcium currents by the activation of mGluRs. Functional implications. Mol-Neurobiol. 1996 Aug; 13(1): 81-95; ISSN: 0893-7648.
Sasaki, S.; Iwata, M. Impairment of fast axonal transport in the proximal axons of anterior horn neurons in amyotrophic lateral sclerosis. Neurology. 1996 Aug; 47(2): 535-40; ISSN: 0028-3878.
Schaefer, J.; Jackson, S.; Dick, D. J.; Turnbull, D. M. Trifunctional enzyme deficiency: adult presentation of a usually fatal beta-oxidation defect. Ann-Neurol. 1996 Oct; 40(4): 597-602; ISSN: 0364-5134.
Shimoda Matsubayashi, S.; Matsumine, H.; Kobayashi, T.; Nakagawa Hattori, Y.; Shimizu, Y.; Mizuno, Y. Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's disease. Biochem-Biophys-Res-Commun. 1996 Sep 13; 226(2): 561-5; ISSN: 0006-291X.
Shishido, F.; Uemura, K.; Inugami, A.; Tomura, N.; Higano, S.; Fujita, H.; Sasaki, H.; Kanno, I.; Murakami, M.; Watahiki, Y.; Nagata, K. Cerebral oxygen and glucose metabolism and blood flow in mitochondrial encephalomyopathy: a PET study.
Neuroradiology. 1996 Feb; 38(2): 102-7; ISSN: 0028-3940.
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