Haller RG - Search Results

1

Mitochondrial encephalomyopathy with coenzyme Q10 deficiency.

Sobreira C, Hirano M, Shanske S, Keller RK, Haller RG, Davidson E, Santorelli FM, Miranda AF, Bonilla E, Mojon DS, Barreira AA, King MP, DiMauro S. Sobreira C, et al. Among authors: haller rg. Neurology. 1997 May;48(5):1238-43. doi: 10.1212/wnl.48.5.1238. Neurology. 1997. PMID: 9153450

2

Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency.

Haller RG, Lewis SF, Estabrook RW, DiMauro S, Servidei S, Foster DW. Haller RG, et al. J Clin Invest. 1989 Jul;84(1):155-61. doi: 10.1172/JCI114135. J Clin Invest. 1989. PMID: 2544623 Free PMC article.

3

Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients.

Tsujino S, Shanske S, Brownell AK, Haller RG, DiMauro S. Tsujino S, et al. Among authors: haller rg. Ann Neurol. 1994 Oct;36(4):661-5. doi: 10.1002/ana.410360418. Ann Neurol. 1994. PMID: 7944300

4

Paradoxically enhanced glucose production during exercise in humans with blocked glycolysis caused by muscle phosphofructokinase deficiency.

Vissing J, Galbo H, Haller RG. Vissing J, et al. Among authors: haller rg. Neurology. 1996 Sep;47(3):766-71. doi: 10.1212/wnl.47.3.766. Neurology. 1996. PMID: 8797477

5

Exercise fuel mobilization in mitochondrial myopathy: a metabolic dilemma.

Vissing J, Galbo H, Haller RG. Vissing J, et al. Among authors: haller rg. Ann Neurol. 1996 Oct;40(4):655-62. doi: 10.1002/ana.410400416. Ann Neurol. 1996. PMID: 8871586

6

Reduced levels of skeletal muscle Na+K+ -ATPase in McArdle disease.

Haller RG, Clausen T, Vissing J. Haller RG, et al. Neurology. 1998 Jan;50(1):37-40. doi: 10.1212/wnl.50.1.37. Neurology. 1998. PMID: 9443454

7

Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.

Karadimas CL, Greenstein P, Sue CM, Joseph JT, Tanji K, Haller RG, Taivassalo T, Davidson MM, Shanske S, Bonilla E, DiMauro S. Karadimas CL, et al. Among authors: haller rg. Neurology. 2000 Sep 12;55(5):644-9. doi: 10.1212/wnl.55.5.644. Neurology. 2000. PMID: 10980727

8

Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects.

Taivassalo T, Shoubridge EA, Chen J, Kennaway NG, DiMauro S, Arnold DL, Haller RG. Taivassalo T, et al. Among authors: haller rg. Ann Neurol. 2001 Aug;50(2):133-41. doi: 10.1002/ana.1050. Ann Neurol. 2001. PMID: 11506394

9

Venous oxygen levels during aerobic forearm exercise: An index of impaired oxidative metabolism in mitochondrial myopathy.

Taivassalo T, Abbott A, Wyrick P, Haller RG. Taivassalo T, et al. Among authors: haller rg. Ann Neurol. 2002 Jan;51(1):38-44. doi: 10.1002/ana.10027. Ann Neurol. 2002. PMID: 11782982

10

The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients.

Taivassalo T, Jensen TD, Kennaway N, DiMauro S, Vissing J, Haller RG. Taivassalo T, et al. Among authors: haller rg. Brain. 2003 Feb;126(Pt 2):413-23. doi: 10.1093/brain/awg028. Brain. 2003. PMID: 12538407

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