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Science (New York, N.Y.)
|
October 30, 1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism
L G Goldfarb, R B Petersen, M Tabaton, et al.
AJR. American Journal of Roentgenology
|
December 1, 1986
MR imaging of pulmonary emboli: an experimental study in dogs
M G Stein, J V Crues, W G Bradley, et al.
Brain Pathology (Zurich, Switzerland)
|
July 21, 1998
Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene
P Montagna, P Cortelli, P Avoni, et al.
JTO Clinical and Research Reports
|
February 27, 2023
Safety and Efficacy Outcomes From a Single-Center Study of Image-Guided Percutaneous Microwave Ablation for Primary and Metastatic Lung Malignancy
Stephen M Chan, Peter J Julien, Peter Kaganjo, et al.
Annals of Neurology
|
April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features
A Dürr, G Stevanin, G Cancel, et al.
Nature Medicine
|
September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseases
S G Chen, P Parchi, P Brown, et al.
Acta Neuropathologica
|
July 27, 2000
Chronic inflammatory demyelinating polyneuropathy associated with dysglobulinemia: a peripheral nerve biopsy study in 18 cases
A Vital, A Lagueny, J Julien, et al.
Ultrastructural Pathology
|
February 24, 2001
Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 cases
C Vital, A Vital, A Lagueny, et al.
Annals of Neurology
|
August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
P Parchi, A Giese, S Capellari, et al.
American Journal of Human Genetics
|
January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
A Ducros, C Denier, A Joutel, et al.
Page
of 23
Search research articles
Search
Showing results (211-220 of 222) with videos related to
Sort By:
Page
of 23
Science (New York, N.Y.)
|
October 30, 1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism
L G Goldfarb, R B Petersen, M Tabaton, et al.
AJR. American Journal of Roentgenology
|
December 1, 1986
MR imaging of pulmonary emboli: an experimental study in dogs
M G Stein, J V Crues, W G Bradley, et al.
Brain Pathology (Zurich, Switzerland)
|
July 21, 1998
Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene
P Montagna, P Cortelli, P Avoni, et al.
JTO Clinical and Research Reports
|
February 27, 2023
Safety and Efficacy Outcomes From a Single-Center Study of Image-Guided Percutaneous Microwave Ablation for Primary and Metastatic Lung Malignancy
Stephen M Chan, Peter J Julien, Peter Kaganjo, et al.
Annals of Neurology
|
April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features
A Dürr, G Stevanin, G Cancel, et al.
Nature Medicine
|
September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseases
S G Chen, P Parchi, P Brown, et al.
Acta Neuropathologica
|
July 27, 2000
Chronic inflammatory demyelinating polyneuropathy associated with dysglobulinemia: a peripheral nerve biopsy study in 18 cases
A Vital, A Lagueny, J Julien, et al.
Ultrastructural Pathology
|
February 24, 2001
Chronic inflammatory demyelinating polyneuropathy: immunopathological and ultrastructural study of peripheral nerve biopsy in 42 cases
C Vital, A Vital, A Lagueny, et al.
Annals of Neurology
|
August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
P Parchi, A Giese, S Capellari, et al.
American Journal of Human Genetics
|
January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
A Ducros, C Denier, A Joutel, et al.
Page
of 23