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The Journal of Biological Chemistry
|
May 24, 1996
Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein
R B Petersen, P Parchi, S L Richardson, et al.
Journal of Biological Regulators and Homeostatic Agents
|
March 19, 2021
Giant cell tumor of extremities, surgical treatment and local adjuvants: which is the most effective?
S Colangeli, A Del Chiaro, L Andreani, et al.
Annals of Neurology
|
June 9, 1999
A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
J A Hainfellner, P Parchi, T Kitamoto, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
June 1, 1992
Isolated failure of noradrenergic transmission in a case with orthostatic hypotension and hyperactivity of gastro-colic reflex
P Cortelli, P Parchi, M Contin, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
April 1, 1994
Cardiovascular autonomic dysfunction in normotensive awake subjects with obstructive sleep apnoea syndrome
P Cortelli, P Parchi, E Sforza, et al.
Journal of Biological Regulators and Homeostatic Agents
|
January 16, 2019
Polymethylmethacrylate-augmented fenestreted pedicle-screw fixation in low bone quality patients: a case series and literature review
R Ghermandi, V Pipola, S Colangeli, et al.
Journal of Biological Regulators and Homeostatic Agents
|
December 1, 2017
Bone cement implantation syndrome: a thromboelastographic study of the effect of bone cement on coagulation
M Mordà, S Pini, F Celli, et al.
Acta Neurologica Scandinavica
|
July 22, 2008
Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease
M Ragno, M G Scarcella, G Cacchiò, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 16, 1999
Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease
B B Worrall, S T Herman, S Capellari, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 18, 2009
Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology
C Jansen, J C van Swieten, S Capellari, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 74) with videos related to
Sort By:
Page
of 8
The Journal of Biological Chemistry
|
May 24, 1996
Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein
R B Petersen, P Parchi, S L Richardson, et al.
Journal of Biological Regulators and Homeostatic Agents
|
March 19, 2021
Giant cell tumor of extremities, surgical treatment and local adjuvants: which is the most effective?
S Colangeli, A Del Chiaro, L Andreani, et al.
Annals of Neurology
|
June 9, 1999
A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
J A Hainfellner, P Parchi, T Kitamoto, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
June 1, 1992
Isolated failure of noradrenergic transmission in a case with orthostatic hypotension and hyperactivity of gastro-colic reflex
P Cortelli, P Parchi, M Contin, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
April 1, 1994
Cardiovascular autonomic dysfunction in normotensive awake subjects with obstructive sleep apnoea syndrome
P Cortelli, P Parchi, E Sforza, et al.
Journal of Biological Regulators and Homeostatic Agents
|
January 16, 2019
Polymethylmethacrylate-augmented fenestreted pedicle-screw fixation in low bone quality patients: a case series and literature review
R Ghermandi, V Pipola, S Colangeli, et al.
Journal of Biological Regulators and Homeostatic Agents
|
December 1, 2017
Bone cement implantation syndrome: a thromboelastographic study of the effect of bone cement on coagulation
M Mordà, S Pini, F Celli, et al.
Acta Neurologica Scandinavica
|
July 22, 2008
Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease
M Ragno, M G Scarcella, G Cacchiò, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 16, 1999
Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease
B B Worrall, S T Herman, S Capellari, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 18, 2009
Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology
C Jansen, J C van Swieten, S Capellari, et al.
Page
of 8