Introduction to general feedback theory of human behavior

by McFarland, Robert L.
Published 1962

Suggestions to a Psychiatric Investigator on the Use of Bibliographical Resources

by Johnson, Barbara Coe, McFarland, Robert L.
Published 1955

Teaching NeuroImages: Neuroradiologic evolution of Leigh disease

by Ng, Yi Shiau, Lim, Ming, Thomas, Gareth, McFarland, Robert
Published in Neurology (2016)

An evaluation of methods for culturing group A streptococci from the pharynx

by McFarland, Robert B., Abelow, Irene, Blomstrom, Darlene, Glaser, Robert J.
Published 1965

The genetic basis of isolated mitochondrial complex II deficiency

by Fullerton, Millie, McFarland, Robert, Taylor, Robert W., Alston, Charlotte L.
Published in Mol Genet Metab (2020)

A proposed consensus panel of organisms for determining evolutionary conservation of mt-tRNA point mutations

by Yarham, John W., McFarland, Robert, Taylor, Robert W., Elson, Joanna L.
Published 2012

The m.15043G > A MT-CYB variant is not a pathogenic mtDNA variant

by Alston, Charlotte L., Blakely, Emma L., McFarland, Robert, Taylor, Robert W.
Published in J Neurol Sci (2020)

Current and Emerging Clinical Treatment in Mitochondrial Disease

by Tinker, Rory J., Lim, Albert Z., Stefanetti, Renae J., McFarland, Robert
Published in Mol Diagn Ther (2021)

Causes of Death in Adults with Mitochondrial Disease

by Barends, Marlieke, Verschuren, Lotte, Morava, Eva, Nesbitt, Victoria, Turnbull, Doug, McFarland, Robert
Published in JIMD Rep (2015)

Scientific and Ethical Issues in Mitochondrial Donation

by Craven, Lyndsey, Murphy, Julie, Turnbull, Doug M., Taylor, Robert W., Gorman, Grainne S., McFarland, Robert
Published in New Bioeth (2018)

Perceived fatigue is highly prevalent and debilitating in patients with mitochondrial disease

by Gorman, Gráinne S., Elson, Joanna L., Newman, Jane, Payne, Brendan, McFarland, Robert, Newton, Julia L., Turnbull, Douglass M.
Published in Neuromuscul Disord (2015)

MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscle

by Blakely, Emma L., Butterworth, Anna, Hadden, Robert D.M., Bodi, Istvan, He, Langping, McFarland, Robert, Taylor, Robert W.
Published 2012

Maternally inherited mitochondrial DNA disease in consanguineous families

by Alston, Charlotte L, He, Langping, Morris, Andrew A, Hughes, Imelda, Goede, Christian de, Turnbull, Douglass M, McFarland, Robert, Taylor, Robert W
Published 2011

Cerebellar Ataxia in Patients with Mitochondrial DNA Disease: A Molecular Clinicopathological Study

by Lax, Nichola Zoe, Hepplewhite, Philippa Denis, Reeve, Amy Katherine, Nesbitt, Victoria, McFarland, Robert, Jaros, Evelyn, Taylor, Robert William, Turnbull, Douglass Matthew
Published 2012

Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report

by Gupta, Asheeta, Colmenero, Isabel, Ragge, Nicola K., Blakely, Emma L., He, Langping, McFarland, Robert, Taylor, Robert W., Vogt, Julie, Milford, David V.
Published in BMC Res Notes (2016)

De novo CTBP1 variant is associated with decreased mitochondrial respiratory chain activities

by Sommerville, Ewen W., Alston, Charlotte L., Pyle, Angela, He, Langping, Falkous, Gavin, Naismith, Karen, Chinnery, Patrick F., McFarland, Robert, Taylor, Robert W.
Published in Neurol Genet (2017)

Decreased male reproductive success in association with mitochondrial dysfunction

by Martikainen, Mika H, Grady, John P, Ng, Yi Shiau, Alston, Charlotte L, Gorman, Grainne S, Taylor, Robert W, McFarland, Robert, Turnbull, Doug M
Published in Eur J Hum Genet (2017)

Measuring the effects of exercise in neuromuscular disorders: a systematic review and meta-analyses

by Stefanetti, Renae J., Blain, Alasdair, Jimenez-Moreno, Cecilia, Errington, Linda, Ng, Yi Shiau, McFarland, Robert, Turnbull, Doug M., Newman, Jane, Gorman, Gráinne S
Published in Wellcome Open Res (2020)

Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort Study

by Braz, Luis P., Ng, Yi Shiau, Gorman, Gráinne S., Schaefer, Andrew M., McFarland, Robert, Taylor, Robert W., Turnbull, Doug M., Whittaker, Roger G.
Published in Neurol Clin Pract (2021)

Loss‐of‐function mutations in ISCA2 disrupt 4Fe–4S cluster machinery and cause a fatal leukodystrophy with hyperglycinemia and mtDNA depletion

by Alaimo, Joseph T., Besse, Arnaud, Alston, Charlotte L., Pang, Ki, Appadurai, Vivek, Samanta, Monisha, Smpokou, Patroula, McFarland, Robert, Taylor, Robert W., Bonnen, Penelope E.
Published in Hum Mutat (2018)