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Printz family -- See Prince family


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Prinz Albrecht Strasse (Berlin, Germany) -- See Niederkirchnerstrasse (Berlin, Germany)


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Prinz-Edward-Insel -- See Prince Edward Island


  1
 

Prinz family -- See Prince family


  1
Prinz, Joachim, 1902-1988. : Joachim Prinz, rebellious rabbi : an autobiography : the German and early American years / edited and introduced by Michael A. Meyer  2007 1
Prinz, Yvonne. : Something about the author. Volume 175 / Lisa Kumar, project editor  2007 1
Bloch, Ernst, 1885-1977. Prinzip Hoffnung. : Religion without redemption : social contradictions and awakened dreams in Latin America / Luis Martínez Andrade ; translated by Antonio Carmona Báez ; foreword by Michael Löwy  2015 1
Hertz, Heinrich, 1857-1894. Prinzipien der Mechanik : Mechanistic images in geometric form : Heinrich Hertz's 'Principles of mechanics' / Jesper Lützen  2005 1
Medical Informatics -- Priodicals : Computers, informatics, nursing (Online)  2002- 1
 

Prion-Associated Disorders -- See Prion Diseases


A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
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Prion Disease -- See Prion Diseases


A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
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  Prion diseases -- 2 Related Subjects   2
Prion diseases.   31
Prion Diseases -- complications. : Neurodegeneration and prion disease / edited by David R. Brown  2005 1
Prion diseases -- Congresses. : Infectious diseases from nature : mechanisms of viral emergence and persistence / C.J. Peters and C.H. Calisher (eds.)  2005 1
Prion Diseases -- diagnosis.   3
Prion diseases -- Diagnosis -- United States. : Advancing prion science : guidance for the National Prion Research Program, interim report / Rick Erdtmann and Laura Sivitz, editors ; Committee on Transmissible Spongiform Encephalopathies: Assessment of Relevant Science, Medical Follow-Up Agency, Institute of Medicine of the National Academies  2003 1
Prion Diseases -- drug therapy. : Novel approaches to treating symptoms and slowing the progress of neurodegenerative diseases / Andrew B. Tobin  2019 1
Prion Diseases -- etiology.   2
Prion Diseases -- genetics. : Prion-like propagation of Parkinson's disease / Patrik Brundin  2014 1
Prion diseases -- Government policy -- United States. : Advancing prion science : guidance for the national prion research program / Committee on Transmissible Spongiform Encephalopathies: Assessment of Relevant Science ; Rick Erdtmann and Laura B. Sivitz, editors  2004 1
Prion Diseases -- history.   4
  Prion diseases in animals -- 2 Related Subjects   2
Prion diseases in animals.   2
Prion diseases in animals -- History. : How the Cows Turned Mad : Unlocking the Mysteries of Mad Cow Disease  2014 1
Prion diseases -- Juvenile literature. : Mad cow disease / by Barbara Sheen  2005 1
Prion Diseases -- metabolism. : Prion-like propagation of Parkinson's disease / Patrik Brundin  2014 1
Prion diseases -- Pathogenesis. : Prions and diseases. Volume 2, Animals, humans and the environment / Wen-Quan Zou, Pierluigi Gambetti, editors  2013 1
Prion Diseases -- pathology. : Prions and diseases. Volume 1, Physiology and pathophysiology / edited by Wen-Quan Zou and Pierluigi Gambetti  2013 1
Prion diseases -- Pathophysiology. : Prions and diseases. Volume 1, Physiology and pathophysiology / edited by Wen-Quan Zou and Pierluigi Gambetti  2013 1
Prion Diseases -- physiopathology.   6
Prion diseases -- Popular works. : Deadly feasts : tracking the secrets of a terrifying new plague / Richard Rhodes  1997 1
Prion Diseases -- prevention & control.   2
Prion diseases -- Research -- United States. : Advancing prion science : guidance for the National Prion Research Program, interim report / Rick Erdtmann and Laura Sivitz, editors ; Committee on Transmissible Spongiform Encephalopathies: Assessment of Relevant Science, Medical Follow-Up Agency, Institute of Medicine of the National Academies  2003 1
 

Prion-Induced Disorder -- See Prion Diseases


A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
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Prion-Induced Disorders -- See Prion Diseases


A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
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Prion infections -- See Prion diseases


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Prion Protein Disease -- See Prion Diseases


A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
  1
 

Prion Protein Diseases -- See Prion Diseases


A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
  1
 

Prion proteins -- See Prions


  1
 

Prionotemmus -- See Macropus


  1
Prions.   43
Prions -- Congresses. : Self-perpetuating structural states in biology, disease, and genetics / edited by Susan Lindquist, Steve Henikoff  2002 1
Prions -- genetics.   3
Prions -- history.   2
Prions -- immunology. : Prions and mad cow disease / edited by Brian K. Nunnally, Ira S. Krull  2004 1
Prions -- pathogenicity.   4
Prions -- pathology : Prions and diseases. Volume 2, Animals, humans and the environment / Wen-Quan Zou, Pierluigi Gambetti, editors  2013 1
Prions -- Periodicals : Prion (Online)    1
Prions -- physiology.   2
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