Nadine Romain

发表

Reproducibility and Absolute Quantification of Muscle Glycogen in Patients with Glycogen Storage Disease by 13C NMR Spectroscopy at 7 Tesla

R. Haller, C. Malloy, S. Cheshkov, 2014, PloS one.

timearea and proton transverse relaxation Effect of acute head-down tilt on skeletal muscle

D. Felsenberg, G. Dudley, B. Levine, 2015 .

Progressive Exercise Training Improves Maximal Aerobic Capacity in Individuals with Well-Healed Burn Injuries.

C. Crandall, R. Haller, S. Romero, 2019, American journal of physiology. Regulatory, integrative and comparative physiology.

The effect of rowing ergometry and resistive exercise on skeletal muscle structure and function during bed rest.

B. Levine, R. Haller, P. Snell, 2014, Journal of applied physiology.

Isolated Cytochrome c Oxidase Deficiency in G93A SOD1 Mice Overexpressing CCS Protein*

D. Winge, R. Haller, F. Pierrel, 2008, Journal of Biological Chemistry.

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

Katrien Stouffs, Melanie Bahlo, Holger Prokisch, 2016, American journal of human genetics.

TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies

Robert W. Taylor, Aaron R D'Souza, M. Minczuk, 2015, American journal of human genetics.

Failure to up-regulate transcription of genes necessary for muscle adaptation underlies limb girdle muscular dystrophy 2A (calpainopathy).

S. Nelson, A. Hevener, R. Haller, 2016, Human molecular genetics.

Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle.

R. Haller, K. Vandenborne, E. Kudryashova, 2009, Human molecular genetics.

Failure to upregulate transcription of genes necessary for muscle adaptation underlies limb girdle muscular dystrophy 2 A ( calpainopathy )

S. Nelson, A. Hevener, R. Haller, 2016 .

Pathological mechanisms underlying single large‐scale mitochondrial DNA deletions

Robert W. Taylor, D. Turnbull, R. Haller, 2018, Annals of neurology.

Immunocytochemical Detection of Ornithine Decarboxylase

R. Schipper, W. Lange, A. Otten, 1999, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency.

Jonathan C. Cohen, Sun Young Park, R. Haller, 2017, Molecular genetics and metabolism.

unloading plus resistance exercise expression in human skeletal muscle: effect of limb Pretranslational markers of contractile protein

B. Levine, P. Tesch, H. Sweeney, 2015 .

Review: Microgravity and skeletal muscle Invited Physiology of a Microgravity Environment

J. West, B. Levine, J. Widrick, 2015 .

hindlimb development. II. Expression of MHC isoforms Effects of spaceflight and thyroid deficiency on rat

B. Levine, C. Reggiani, C. Pandorf, 2015 .