Hans Tritschler - Publications

Columbia University, New York, NY 

8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
1996 Barbiroli B, Medori R, Tritschler HJ, Iotti S, Lodi R, Zaniol P. Thioctic acid stimulates muscle ATP production in patients with type 2-diabetes and diabetic polyneuropathy. An in vivo phosphorus magnetic resonance spectroscopy study Diabetes Und Stoffwechsel. 5: 71-76.  0.514
1995 Barbiroli B, Medori R, Tritschler HJ, Klopstock T, Seibel P, Reichmann H, Iotti S, Lodi R, Zaniol P. Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathy. Journal of Neurology. 242: 472-7. PMID 7595680 DOI: 10.1007/BF00873552  0.539
1994 Tritschler HJ, Packer L, Medori R. Oxidative stress and mitochondrial dysfunction in neurodegeneration. Biochemistry and Molecular Biology International. 34: 169-81. PMID 7849618  0.568
1993 Tritschler HJ, Medori R. Mitochondrial DNA alterations as a source of human disorders. Neurology. 43: 280-8. PMID 8437690 DOI: 10.1212/Wnl.43.2.280  0.588
1993 Medori R, Tritschler HJ. Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism. American Journal of Human Genetics. 53: 822-7. PMID 8105681  0.713
1992 Medori R, Tritschler HJ, Gambetti P. Production of single-stranded DNA for sequencing: an alternative approach. Biotechniques. 12: 346-50. PMID 1349213  0.533
1992 Medori R, Montagna P, Tritschler HJ, LeBlanc A, Cortelli P, Tinuper P, Lugaresi E, Gambetti P. Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178. Neurology. 42: 669-70. PMID 1347910 DOI: 10.1212/Wnl.42.3.669  0.736
1992 Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. The New England Journal of Medicine. 326: 444-9. PMID 1346338 DOI: 10.1056/Nejm199202133260704  0.433
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