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Neurology
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November 30, 2000
Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia
P Hedera, S DiMauro, E Bonilla, et al.
Immunitat Und Infektion
|
June 1, 1983
[Immunomodulation by symptomaticly active antirheumatic agents]
R Dreher, K Fink, H Seidel, et al.
Neurology
|
October 11, 1991
Allele-specific sequencing confirms novel prion gene polymorphism in Creutzfeldt-Jakob disease
J K Fink, J T Warren, I Drury, et al.
British Journal of Cancer
|
January 13, 2006
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism
D Meierhofer, J A Mayr, K Fink, et al.
Medizinische Klinik, Intensivmedizin Und Notfallmedizin
|
August 27, 2017
[Preclinical use of mild therapeutic hypothermia after cardiac arrest by the emergency services in Baden-Württemberg, Germany]
R Fantin, B Schmid, C Busche, et al.
Archives of Neurology
|
September 17, 2003
The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis
Peter Hedera, Elizabeth M Petty, Melanie R Bui, et al.
Pediatric Pulmonology
|
September 24, 2019
Evaluation of hospitalization data for the CFFPR-PHIS linked data set
Jonathan D Cogen, Anna V Faino, Frankline Onchiri, et al.
American Journal of Human Genetics
|
September 26, 2003
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)
Shirley Rainier, Jing-Hua Chai, Debra Tokarz, et al.
Oncology
|
January 1, 1984
Combination chemotherapy with BCNU, vincristine, mitomycin-C and prednisone in refractory breast carcinoma. A pilot study
N J DiBella, D Garfield, K Fink, et al.
Neuropharmacology
|
November 5, 2016
The effect of sazetidine-A and other nicotinic ligands on nicotine controlled goal-tracking in female and male rats
S Charntikov, A M Falco, K Fink, et al.
Page
of 37
Search research articles
Search
Showing results (171-180 of 363) with videos related to
Sort By:
Page
of 37
Neurology
|
November 30, 2000
Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia
P Hedera, S DiMauro, E Bonilla, et al.
Immunitat Und Infektion
|
June 1, 1983
[Immunomodulation by symptomaticly active antirheumatic agents]
R Dreher, K Fink, H Seidel, et al.
Neurology
|
October 11, 1991
Allele-specific sequencing confirms novel prion gene polymorphism in Creutzfeldt-Jakob disease
J K Fink, J T Warren, I Drury, et al.
British Journal of Cancer
|
January 13, 2006
Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism
D Meierhofer, J A Mayr, K Fink, et al.
Medizinische Klinik, Intensivmedizin Und Notfallmedizin
|
August 27, 2017
[Preclinical use of mild therapeutic hypothermia after cardiac arrest by the emergency services in Baden-Württemberg, Germany]
R Fantin, B Schmid, C Busche, et al.
Archives of Neurology
|
September 17, 2003
The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis
Peter Hedera, Elizabeth M Petty, Melanie R Bui, et al.
Pediatric Pulmonology
|
September 24, 2019
Evaluation of hospitalization data for the CFFPR-PHIS linked data set
Jonathan D Cogen, Anna V Faino, Frankline Onchiri, et al.
American Journal of Human Genetics
|
September 26, 2003
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)
Shirley Rainier, Jing-Hua Chai, Debra Tokarz, et al.
Oncology
|
January 1, 1984
Combination chemotherapy with BCNU, vincristine, mitomycin-C and prednisone in refractory breast carcinoma. A pilot study
N J DiBella, D Garfield, K Fink, et al.
Neuropharmacology
|
November 5, 2016
The effect of sazetidine-A and other nicotinic ligands on nicotine controlled goal-tracking in female and male rats
S Charntikov, A M Falco, K Fink, et al.
Page
of 37