Introduction to general feedback theory of human behavior

por McFarland, Robert L.
Publicado 1962

Suggestions to a Psychiatric Investigator on the Use of Bibliographical Resources

por Johnson, Barbara Coe, McFarland, Robert L.
Publicado 1955

Teaching NeuroImages: Neuroradiologic evolution of Leigh disease

por Ng, Yi Shiau, Lim, Ming, Thomas, Gareth, McFarland, Robert
Publicado en Neurology (2016)

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

por McFarland, Robert B., Abelow, Irene, Blomstrom, Darlene, Glaser, Robert J.
Publicado 1965

The genetic basis of isolated mitochondrial complex II deficiency

por Fullerton, Millie, McFarland, Robert, Taylor, Robert W., Alston, Charlotte L.
Publicado en Mol Genet Metab (2020)

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

por Yarham, John W., McFarland, Robert, Taylor, Robert W., Elson, Joanna L.
Publicado 2012

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

por Alston, Charlotte L., Blakely, Emma L., McFarland, Robert, Taylor, Robert W.
Publicado en J Neurol Sci (2020)

Current and Emerging Clinical Treatment in Mitochondrial Disease

por Tinker, Rory J., Lim, Albert Z., Stefanetti, Renae J., McFarland, Robert
Publicado en Mol Diagn Ther (2021)

Causes of Death in Adults with Mitochondrial Disease

por Barends, Marlieke, Verschuren, Lotte, Morava, Eva, Nesbitt, Victoria, Turnbull, Doug, McFarland, Robert
Publicado en JIMD Rep (2015)

Scientific and Ethical Issues in Mitochondrial Donation

por Craven, Lyndsey, Murphy, Julie, Turnbull, Doug M., Taylor, Robert W., Gorman, Grainne S., McFarland, Robert
Publicado en New Bioeth (2018)

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

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

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

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

Maternally inherited mitochondrial DNA disease in consanguineous families

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

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

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

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

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

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

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

Decreased male reproductive success in association with mitochondrial dysfunction

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

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

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

Neuromuscular Junction Abnormalities in Mitochondrial Disease: An Observational Cohort Study

por Braz, Luis P., Ng, Yi Shiau, Gorman, Gráinne S., Schaefer, Andrew M., McFarland, Robert, Taylor, Robert W., Turnbull, Doug M., Whittaker, Roger G.
Publicado en 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

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