Introduction to general feedback theory of human behavior

per McFarland, Robert L.
Publicat 1962

Suggestions to a Psychiatric Investigator on the Use of Bibliographical Resources

per Johnson, Barbara Coe, McFarland, Robert L.
Publicat 1955

Teaching NeuroImages: Neuroradiologic evolution of Leigh disease

per Ng, Yi Shiau, Lim, Ming, Thomas, Gareth, McFarland, Robert
Publicat a Neurology (2016)

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

per McFarland, Robert B., Abelow, Irene, Blomstrom, Darlene, Glaser, Robert J.
Publicat 1965

The genetic basis of isolated mitochondrial complex II deficiency

per Fullerton, Millie, McFarland, Robert, Taylor, Robert W., Alston, Charlotte L.
Publicat a Mol Genet Metab (2020)

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

per Yarham, John W., McFarland, Robert, Taylor, Robert W., Elson, Joanna L.
Publicat 2012

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

per Alston, Charlotte L., Blakely, Emma L., McFarland, Robert, Taylor, Robert W.
Publicat a J Neurol Sci (2020)

Current and Emerging Clinical Treatment in Mitochondrial Disease

per Tinker, Rory J., Lim, Albert Z., Stefanetti, Renae J., McFarland, Robert
Publicat a Mol Diagn Ther (2021)

Causes of Death in Adults with Mitochondrial Disease

per Barends, Marlieke, Verschuren, Lotte, Morava, Eva, Nesbitt, Victoria, Turnbull, Doug, McFarland, Robert
Publicat a JIMD Rep (2015)

Scientific and Ethical Issues in Mitochondrial Donation

per Craven, Lyndsey, Murphy, Julie, Turnbull, Doug M., Taylor, Robert W., Gorman, Grainne S., McFarland, Robert
Publicat a New Bioeth (2018)

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

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

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

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

Maternally inherited mitochondrial DNA disease in consanguineous families

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

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

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

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

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

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

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

Decreased male reproductive success in association with mitochondrial dysfunction

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

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

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

Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort Study

per Braz, Luis P., Ng, Yi Shiau, Gorman, Gráinne S., Schaefer, Andrew M., McFarland, Robert, Taylor, Robert W., Turnbull, Doug M., Whittaker, Roger G.
Publicat a 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

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