Resultats de la cerca - Patrick MacLeod
- Mostrar 1 - 8 resultats de 8
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1
Interaction of Gustatory and Lingual Somatosensory Perceptions at the Cortical Level in the Human: a Functional Magnetic Resonance Imaging Study per Barbara Cerf-Ducastel, Pierre‐François Van de Moortele, Patrick MacLeod, Denis Le Bihan, Annick Faurion
Publicat 2001Artigo -
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3
Early Gastric Cancer in Young, Asymptomatic Carriers of Germ-Line E-Cadherin Mutations per David G. Huntsman, Fátima Carneiro, Frank R. Lewis, Patrick MacLeod, Allen Hayashi, Kristin G. Monaghan, Raymond Maung, Raquel Seruca, Charles E. Jackson, Carlos Caldas
Publicat 2001Artigo -
4
Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia per Paul N. Valdmanis, Inge A. Meijer, Annie Reynolds, Adrienne Lei, Patrick MacLeod, David Schlesinger, Mayana Zatz, Evan Reid, Patrick A. Dion, Pierre Drapeau, Guy A. Rouleau
Publicat 2006Artigo -
5
Molecular characterization of L-CPT I deficiency in six patients: insights into function of the native enzyme per Nicholas F. Brown, Rashmi Mullur, Indhu Subramanian, Victoria Esser, Michael J. Bennett, Jean‐Marie Saudubray, Annette S. Feigenbaum, Joyce A. Kobari, Patrick MacLeod, Julie McGarry, Jonathan C. Cohen
Publicat 2001Artigo -
6
Inherited Mutations in PTEN That Are Associated with Breast Cancer, Cowden Disease, and Juvenile Polyposis per Eric D. Lynch, Elizabeth Ostermeyer, Ming K. Lee, J. Fernando Arena, Hanlee P. Ji, Jamie L. Dann, Karen Swisshelm, David Suchard, Patrick MacLeod, Stener Kvinnsland, Bjørn Tore Gjertsen, Ketil Heimdal, Herb Lubs, Pål Møller, Mary‐Claire King
Publicat 1997Artigo -
7
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum per Matthis Synofzik, Anne S. Soehn, Janina Gburek‐Augustat, Julia Schicks, Kathrin N. Karle, Rebecca Schüle, Tobias B. Haack, M. Schöning, Saskia Biskup, Sabine Rudnik–Schöneborn, Jan Senderek, Karl‐Titus Hoffmann, Patrick MacLeod, Johannes Schwarz, Benjamin Bender, Stefan Krüger, Friedmar R. Kreuz, Peter Bauer, Lüdger Schöls
Publicat 2013Artigo -
8
Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations per Jennifer J. Johnston, Isabelle Olivos‐Glander, Christina Killoran, Emma Elson, Joyce Turner, Kathryn F. Peters, Margaret H. Abbott, David J. Aughton, Arthur S. Aylsworth, Michael J. Bamshad, Carol Booth, Cynthia J. Curry, Albert David, Mary Beth Dinulos, David B. Flannery, Michelle Fox, John M. Graham, Dorothy K. Grange, Alan E. Guttmacher, Mark C. Hannibal, Wolfram Henn, RaoulC.M. Hennekam, Lewis B. Holmes, H. Eugene Hoyme, Kathleen A. Leppig, Angela E. Lin, Patrick MacLeod, David K. Manchester, Carlo Marcelis, Laura Mazzanti, Emma McCann, Marie McDonald, Nancy J. Mendelsohn, John B. Moeschler, Billur Moghaddam, Giovanni Neri, Ruth Newbury‐Ecob, Roberta A Pagon, John A. Phillips, Laurie S. Sadler, Joan M. Stoler, David Tilstra, Catherine M. Walsh Vockley, Elaine H. Zackai, Touran M. Zadeh, Louise Brueton, Graeme Black, Leslie G. Biesecker
Publicat 2005Artigo
Eines de cerca:
Matèries relacionades
Biology
Genetics
Medicine
Gene
Internal medicine
Phenotype
Pathology
Cancer
Chemistry
Neuroscience
Oncology
Amino acid
Anatomy
Asymptomatic
Asymptomatic carrier
Ataxia
Audiology
Beta oxidation
Biochemistry
Blot
Botany
Breast cancer
CDH1
Cadherin
Cancer research
Carnitine
Carnitine palmitoyltransferase I
Cell
Cerebellar ataxia
Cerebral palsy