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Shoffner, John M
~ 100  Ergebnisse:
Personensuche X
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1

Concerning "Triheptanoin vs trioctanoin for long‐chain fatt..:

Shoffner, John M.
Journal of Inherited Metabolic Disease.  42 (2019)  3 - p. 394-395 , 2019
Link: https://doi.org/10.1002/..
 
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2

MERRF Classification: Implications for Diagnosis and Clinic..:

Finsterer, Josef ; Zarrouk-Mahjoub, Sinda ; Shoffner, John M.
Pediatric Neurology.  80 (2018)  - p. 8-23 , 2018
Link: https://doi.org/10.1016/..
 
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3

Response to ''The Appalling Poling Saga'':

Shoffner, John M.
Journal of Child Neurology.  25 (2010)  4 - p. 529-529 , 2010
Link: https://doi.org/10.1177/..
 
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4

Rolandic Mitochondrial Encephalomyelopathy and MT-ND3 Mutat..:

Werner, Klaus G.E. ; Morel, Chantal F. ; Kirton, Adam...
Pediatric Neurology.  41 (2009)  1 - p. 27-33 , 2009
Link: https://doi.org/10.1016/..
 
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5

Conflict of Interest Statement Concerning "Developmental Re..:

Frye, Richard E. ; Zimmerman, Andrew W. ; Shoffner, John M.
Journal of Child Neurology.  23 (2008)  9 - p. 1089-1090 , 2008
Link: https://doi.org/10.1177/..
 
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6

Oxidative Phosphorylation Disease Diagnosis:

SHOFFNER, JOHN M.
Annals of the New York Academy of Sciences.  893 (1999)  1 - p. 42-42 , 1999
Link: https://doi.org/10.1111/..
 
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7

Tau Pathology in a Family with Dementia and a P301L Mutatio..:

Mirra, Suzanne S. ; Murrell, Jill R. ; Gearing, Marla...
Journal of Neuropathology and Experimental Neurology.  58 (1999)  4 - p. 335-345 , 1999
Link: https://doi.org/10.1097/..
 
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8

Strabismus and Mitochondrial Defects in Chronic Progressive..:

SORKIN, JEFFREY A. ; SHOFFNER, JOHN M. ; GROSSNIKLAUS, HANS E...
American Journal of Ophthalmology.  123 (1997)  2 - p. 235-242 , 1997
Link: https://doi.org/10.1016/..
 
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9

Molecular Analysis of Oxidative Phosphorylation Diseases fo..:

Shoffner, John M.
Current Protocols in Human Genetics.  13 (1997)  1 - p. , 1997
Link: https://doi.org/10.1002/..
 
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10

Oxidative phosphorylation defects and Alzheimer's disease:

Shoffner, John M.
neurogenetics.  1 (1997)  1 - p. 13-19 , 1997
Link: https://doi.org/10.1007/..
 
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11

Insulin resistance associated with maternally inherited dia..:

Gebhart, Suzanne S.P. ; Shoffner, John M. ; Koontz, Deborah..
Metabolism.  45 (1996)  4 - p. 526-531 , 1996
Link: https://doi.org/10.1016/..
 
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12

Oxidative phosphorylation defect associated with primary ad..:

North, Kathryn ; Korson, Mark S. ; Krawiecki, Nicolas..
The Journal of Pediatrics.  128 (1996)  5 - p. 688-692 , 1996
Link: https://doi.org/10.1016/..
 
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13

Mitochondrial defects in basal ganglia diseases:

Shoffner, John M.
Current Opinion in Neurology.  8 (1995)  6 - p. 474-479 , 1995
Link: https://doi.org/10.1097/..
 
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14

Mitochondrial DNA mutations in human degenerative diseases ..:

Wallace, Douglas C. ; Shoffner, John M. ; Trounce, Ian...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.  1271 (1995)  1 - p. 141-151 , 1995
Link: https://doi.org/10.1016/..
 
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15

Leber's hereditary optic neuropathy plus dystonia is caused..:

Shoffner, John M. ; Brown, Michael D. ; Stugard, Carol...
Annals of Neurology.  38 (1995)  2 - p. 163-169 , 1995
Link: https://doi.org/10.1002/..
 
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