Books on the topic 'Genetic disorders Pathophysiology'
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Ahuja, Satpal. Usher syndrome: Pathogenesis, diagnosis, and therapy. Hauppauge, N.Y: Nova Science Publishers, 2011.
Find full textNicola, Cirillo. Techniques in epidermal biology: An integrated approach to autoimmune skin disease. Hauppauge, N.Y: Nova Science Publishers, 2011.
Find full textTranscription factors and human disease. New York: Oxford University Press, 1998.
Find full textSimmons Center International Conference on HLA-B27 Related Disorders (2nd 1991 Dallas, Tex.). HLA-B27⁺ Spondyloarthropathies: Proceedings of the second Simmons Center International Conference on HLA-B27 Related Disorders held April 10-14, 1991 in Dallas, Texas. Edited by Lipsky Peter E and Taurog Joel D. New York: Elsevier, 1991.
Find full textMagne, Ueland Per, and Rozen Rima, eds. MTHFR polymorphisms and disease. Georgetown, Tex: Landes Bioscience/ Eurekah.com, 2005.
Find full textCohen, Sidney. The chemical brain: The neurochemistry of addictive disorders. Irvine, Calif: CareInstitute, 1988.
Find full textFuchs, Jürgen, 1957 June 28-, Podda Maurizio 1965-, and Packer Lester, eds. Redox-genome interactions in health and disease. New York: M. Dekker, 2004.
Find full textSteven, Whitney, ed. The addiction solution: Unraveling the mysteries of addiction through cutting-edge brain science. New York: Rodale, 2010.
Find full textLovelace, Robert E. Charcot-Marie-Tooth disorders: Pathophysiology, molecular genetics and therapy. Chichester: Wiley, 1990.
Find full textInternational Conference on Charcot-Marie-Tooth Disease (2nd 1987 Harriman, N.Y.). Charcot-Marie-Tooth disorders: Pathophysiology, molecular genetics, and therapy. Edited by Lovelace Robert E and Shapiro Howard K. New York: Liss, 1990.
Find full textMichael, Krawczak, ed. Venous thrombosis: From genes to clinical medicine : the molecular genetics of an archetypal multigene disorder. Oxford: Bios Scientific Pub., 1997.
Find full textDavid, Isenberg, and Rademacher T. W, eds. Abnormalities of IgG glycosylation and immunological disorders. Chichester: Wiley, 1996.
Find full textE, Vance Dennis, and Vance Jean E, eds. Biochemistry of lipids, lipoproteins, and membranes. Amsterdam: Elsevier, 1991.
Find full textErnesto, Carafoli, and Brini Marisa, eds. Calcium signalling and disease: Molecular pathology of calcium. New York: Springer, 2007.
Find full textTakao, Kumazawa, Kruger Lawrence, and Mizumura Kazue, eds. The polymodal receptor: A gateway to pathological pain. Amsterdam: Elsevier, 1996.
Find full textBlanco, Ignacio. Blanco's Overview of Alpha-1 Antitrypsin Deficiency: History, Biology, Pathophysiology, Related Diseases, Diagnosis and Treatment. Elsevier Science & Technology Books, 2017.
Find full textBlanco, Ignacio. Blanco's Overview of Alpha-1 Antitrypsin Deficiency: History, Biology, Pathophysiology, Related Diseases, Diagnosis and Treatment. Elsevier Science & Technology Books, 2017.
Find full textPittenger, Christopher. The Neurobiology of Tic Disorders and Obsessive-Compulsive Disorder. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0065.
Full textYoungblood, Mark W., and Hal Blumenfeld. Biological Basis of Primary Generalized Epilepsies—Pathophysiology. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0037.
Full textSemenza, Gregg L. Transcription Factors and Human Disease (Oxford Monographs on Medical Genetics). Oxford University Press, USA, 1989.
Find full textDrouin-Ouellet, Janelle, and Roger A. Barker. Disease-Modifying Therapies in Neurodegenerative Disorders. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190233563.003.0016.
Full textTombetti, Enrico, and Justin C. Mason. Pathophysiology of vasculitis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198755777.003.0017.
Full textPurcell, Shaun M. Genetic Methodologies and Applications. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0001.
Full text(Editor), Jürgen Fuchs, Maurizio Podda (Editor), and Lester Packer (Editor), eds. Redox-Genome Interactions in Health and Disease (Oxidative Stress and Disease). CRC, 2003.
Find full textPoppe, Andrew, and Angus W. MacDonald III. Cognitive Neuroscience Approaches to Personality Disorders. Edited by Christian Schmahl, K. Luan Phan, Robert O. Friedel, and Larry J. Siever. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199362318.003.0004.
Full text1931-, Bellugi Ursula, St George Marie, and Galaburda Albert M. 1948-, eds. Journey from cognition to brain to gene: Perspectives from Williams Syndrome. Cambridge, Mass: MIT Press, 2001.
Find full textWhitney, Steven, and David Kipper. The Addiction Solution: Unraveling the Mysteries of Addiction Through Cutting-Edge Brain Science. Rodale Books, 2011.
Find full textHyman, Steven E. The Present and Future of Psychiatric Diagnosis. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0070.
Full textGraves, Tracey. Neurogenetic disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0223.
Full textJ, Weatherall D., ed. Disorders of hemoglobin: Genetics, pathophysiology, and clinical management. 2nd ed. Cambridge: Cambridge University Press, 2009.
Find full textForget, Bernard G., Douglas R. Higgs, David J. Weatherall, and Martin H. Steinberg. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2010.
Find full textForget, Bernard G., Douglas R. Higgs, David J. Weatherall, and Martin H. Steinberg. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2009.
Find full text(Foreword), H. Franklin Bunn, Martin H. Steinberg (Editor), Bernard G. Forget (Editor), Douglas R. Higgs (Editor), and Ronald L. Nagel (Editor), eds. Disorders of Hemoglobin: Genetics, Pathophysiology and Clinical Management. Cambridge University Press, 2001.
Find full textForget, Bernard G., Douglas R. Higgs, David J. Weatherall, and Martin H. Steinberg. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2009.
Find full textForget, Bernard G., Douglas R. Higgs, David J. Weatherall, and Martin H. Steinberg. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management. Cambridge University Press, 2009.
Find full textFeusner, Jamie D., and Danyale McCurdy-McKinnon. Body Dysmorphic Disorder. Edited by Christopher Pittenger. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190228163.003.0050.
Full textMcCurdy-McKinnon, Danyale, and Jamie D. Feusner. Neurobiology of Body Dysmorphic Disorder : Heritability/Genetics, Brain Circuitry, and Visual Processing. Edited by Katharine A. Phillips. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190254131.003.0020.
Full textGenesis, Pathophysiology and Management of Venous and Lymphatic Disorders. Elsevier, 2022. http://dx.doi.org/10.1016/c2020-0-03522-x.
Full textDodman, Nicholas H., and Louis Shuster. Spontaneously Occurring Animal Models of OCD. Edited by Christopher Pittenger. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190228163.003.0032.
Full textPittenger, Christopher, ed. Obsessive-compulsive Disorder. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190228163.001.0001.
Full textSousek, Alexandra, and Mehdi Tafti. The genetics of sleep. Edited by Sudhansu Chokroverty, Luigi Ferini-Strambi, and Christopher Kennard. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199682003.003.0005.
Full textPillai, Jagan A., and James B. Leverenz. Pathogenesis of Lewy Body Dementia. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0020.
Full textSonuga-Barke, Edmund J. S. Attention-Deficit/Hyperactivity Disorder. Edited by Philip David Zelazo. Oxford University Press, 2013. http://dx.doi.org/10.1093/oxfordhb/9780199958474.013.0022.
Full textCharcot-Marie-Tooth disorders: Pathophysiology, molecular genetics, and therapy (Neurology and neurobiology). Liss, 1989.
Find full textTurner, Helen E., Richard Eastell, and Ashley Grossman, eds. Endocrinology (Oxford Desk Reference). Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199672837.001.0001.
Full textLovelace, Robert, ed. Charcot-marie-tooth Disorders: PATHOPHYSIOLOGY, MOLECULAR GENETICS, AND THERAPY (DISCONTINUED (Neurology and Neurobiology)). John Wiley & Sons, 1990.
Find full textNielsen, David A., Dmitri Proudnikov, and Mary Jeanne Kreek. The Genetics of Impulsivity. Edited by Jon E. Grant and Marc N. Potenza. Oxford University Press, 2012. http://dx.doi.org/10.1093/oxfordhb/9780195389715.013.0080.
Full textSoileau, Michael J., and Kelvin L. Chou. Parkinson Disease. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0002.
Full textCharlson, Robert W., and Matthew S. Robbins. Migraine and Other Headache Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0047.
Full textTaylor, Eric. Developmental Neuropsychiatry. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198827801.001.0001.
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