Diabetes with Hypertrophic Cirrhosis of Liver

por Innes, A.
Publicado 1897

Introduction to superconductivity

por Rose-Innes, A C, Rhoderick, E H
Publicado 1978

Are We Missing Post-Thrombotic Syndrome Syndrome? An Orthopaedic Perspective in Lower Limb Arthroplasty

por Reidy, M., MacInnes, A., Pillai, A.
Publicado 2012

Up for grabs: prey herding by penguins facilitates shallow foraging by volant seabirds

por McInnes, A. M., Pistorius, P. A.
Publicado 2019

Spatiotemporal evolution of urban populations and housing: A dynamic utility-driven market-mediated model

por Robinson, P. A., McInnes, A., Sarkar, Somwrita
Publicado 2023

Neuropathy due to impaired axonal transport of non-fragmented mitochondria in MYH14 mutation carriers—Authors’ reply

por Pfeffer, Gerald, Innes, A. Micheil, Shutt, Timothy E.
Publicado 2019

Semiconducting III-V compounds

por Hilsum, C, Rose-Innes, A C, Henisch, Heinz R
Publicado 1961

Primary lymphoma of the pituitary gland: an unusual cause of hemianopia in an immunocompetent patient

por Rainsbury, PG, Mitchell-Innes, A, Clifton, NJ, Khalil, HS
Publicado 2012

An unusual tumor spectrum in Lynch syndrome caused by MSH6 mutation

por Perrier, Renee L, Van Galen, Paulein, Pasieka, Janice L, Magliocco, Tony, Innes, A Micheil
Publicado 2010

The de novo CACNA1A pathogenic variant Y1384C associated with hemiplegic migraine, early onset cerebellar atrophy and developmental delay leads to a loss of Cav2.1 channel function

por Gandini, Maria A., Souza, Ivana A., Ferron, Laurent, Innes, A. Micheil, Zamponi, Gerald W.
Publicado 2021

Skeletal Phenotypes Due to Abnormalities in Mitochondrial Protein Homeostasis and Import

por Zhao, Tian, Goedhart, Caitlin, Pfeffer, Gerald, Greenway, Steven C, Lines, Matthew, Khan, Aneal, Innes, A Micheil, Shutt, Timothy E
Publicado 2020

Foot care education in patients with diabetes at low risk of complications: a consensus statement

por McInnes, A, Jeffcoate, W, Vileikyte, L, Game, F, Lucas, K, Higson, N, Stuart, L, Church, A, Scanlan, J, Anders, J
Publicado 2011

Efficacy and safety of certolizumab pegol monotherapy every 4 weeks in patients with rheumatoid arthritis failing previous disease-modifying antirheumatic therapy: the FAST4WARD st...

por Fleischmann, R, Vencovsky, J, van Vollenhoven, R F, Borenstein, D, Box, J, Coteur, G, Goel, N, Brezinschek, H-P, Innes, A, Strand, V
Publicado 2008

Development of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite population

por Triggs‐Raine, Barbara, Dyck, Tamara, Boycott, Kym M., Innes, A. Micheil, Ober, Carole, Parboosingh, Jillian S., Botkin, Alexis, Greenberg, Cheryl R., Spriggs, Elizabeth L.
Publicado 2016

Bolus/infusional 5-fluorouracil and folinic acid. A report on two prospective, consecutive phase II studies with 5-fluorouracil dose escalation.

por Mackean, M. J., Cassidy, J., Jodrell, D. I., Paul, J., Reed, N. S., Canney, P. A., Yosef, H., Habeshaw, T., Robertson, A. G., McInnes, A., Twelves, C. J.
Publicado 1998

Hnrnpul1 controls transcription, splicing, and modulates skeletal and limb development in vivo

por Blackwell, Danielle L, Fraser, Sherri D, Caluseriu, Oana, Vivori, Claudia, Tyndall, Amanda V, Lamont, Ryan E, Parboosingh, Jillian S, Innes, A Micheil, Bernier, François P, Childs, Sarah J
Publicado 2022

From “ACAN” to “I CAN”: Restoring wellness in a boy with severe osteochondritis dissecans through diagnostic precision combined with optimal medical, surgical and rehabilitation ma...

por Ochoa, Maria, Yang, Ashlee, Kollias, Carrie, Bakir, Christina, Carsen, Sasha, Lazier, Joanna, Innes, A. Micheil, Pagé, Marika, Dawrant, Jonathan, Robinson, Marie-Eve, Koujok, Khaldoun, Shenouda, Nazih, Rauch, Frank, Ward, Leanne M.
Publicado 2023

De novo substitutions of TRPM3 cause intellectual disability and epilepsy

por Dyment, David A., Terhal, Paulien A., Rustad, Cecilie F., Tveten, Kristian, Griffith, Christopher, Jayakar, Parul, Shinawi, Marwan, Ellingwood, Sara, Smith, Rosemarie, van Gassen, Koen, McWalter, Kirsty, Innes, A. Micheil, Lines, Matthew A.
Publicado 2019

PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes

por Zhao, Tian, Goedhart, Caitlin M, Sam, Pingdewinde N, Sabouny, Rasha, Lingrell, Susanne, Cornish, Adam J, Lamont, Ryan E, Bernier, Francois P, Sinasac, David, Parboosingh, Jillian S, Vance, Jean E, Claypool, Steven M, Innes, A Micheil, Shutt, Timothy E
Publicado 2019

Intellectual disability associated with a homozygous missense mutation in THOC6

por Beaulieu, Chandree L, Huang, Lijia, Innes, A Micheil, Akimenko, Marie-Andree, Puffenberger, Erik G, Schwartz, Charles, Jerry, Paul, Ober, Carole, Hegele, Robert A, McLeod, D Ross, Schwartzentruber, Jeremy, Majewski, Jacek, Bulman, Dennis E, Parboosingh, Jillian S, Boycott, Kym M
Publicado 2013