Gary S Johnson (G S Johnson)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 9

Top Topics

Subarachnoid Hemorrhage

Electron Microscopy

Top Venues

Journal of veterinary internal medicine

Animal genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Stefan H Keller, Gary S Johnson, Garrett Bullock, Tendai Mhlanga-Mutangadura, Malte Schwartz, Savannah G Pattridge, Juyuan Guo, Gregg D Kortz, Martin L Katz
Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions. Genes 15 (2) (2024)
Stefan H Keller, Gary S Johnson, Garrett Bullock, Tendai Mhlanga-Mutangadura, Malte Schwartz, Savannah G Pattridge, Juyuan Guo, Gregg D Kortz, Martin L Katz
Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions. Genes 15 (2) (2024)
Stefan H Keller, Gary S Johnson, Garrett Bullock, Tendai Mhlanga-Mutangadura, Malte Schwartz, Savannah G Pattridge, Juyuan Guo, Gregg D Kortz, Martin L Katz
Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions. Genes 15 (2) (2024)
Stefan H Keller, Gary S Johnson, Garrett Bullock, Tendai Mhlanga-Mutangadura, Malte Schwartz, Savannah G Pattridge, Juyuan Guo, Gregg D Kortz, Martin L Katz
Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions. Genes 15 (2) (2024)
Stefan H Keller, Gary S Johnson, Garrett Bullock, Tendai Mhlanga-Mutangadura, Malte Schwartz, Savannah G Pattridge, Juyuan Guo, Gregg D Kortz, Martin L Katz
Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions. Genes 15 (2) (2024)
Garrett Bullock, Gary S Johnson, Savannah G Pattridge, Tendai Mhlanga-Mutangadura, Juyuan Guo, James Cook, Rebecca S Campbell, Charles H Vite, Martin L Katz
A Homozygous MAN2B1 Missense Mutation in a Doberman Pinscher Dog with Neurodegeneration, Cytoplasmic Vacuoles, Autofluorescent Storage Granules, and an α-Mannosidase Deficiency. Genes 14 (9) (2023)
J A Jaffey, G Bullock, E Teplin, J Guo, N A Villani, T Mhlanga-Mutangadura, R D Schnabel, L A Cohn, Gary S Johnson
A homozygous ADAMTS2 nonsense mutation in a Doberman Pinscher dog with Ehlers Danlos syndrome and extreme skin fragility. Animal genetics 50 (5) (2019)
A Kolicheski, Gary S Johnson, N A Villani, D P O'Brien, T Mhlanga-Mutangadura, D A Wenger, K Mikoloski, J S Eagleson, J F Taylor, R D Schnabel, M L Katz
GM2 Gangliosidosis in Shiba Inu Dogs with an In-Frame Deletion in HEXB. Journal of veterinary internal medicine 31 (5) (2017)
Jared A Jaffey, M R Harmon, N A Villani, E K Creighton, Gary S Johnson, U Giger, J R Dodam
Long-term Treatment with Methylene Blue in a Dog with Hereditary Methemoglobinemia Caused by Cytochrome b5 Reductase Deficiency. Journal of veterinary internal medicine 31 (6) (2017)