Ngā hua rapu - Doris A. Trauner
- E whakaatu ana i te 1 - 9 hua o te 9
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Dyspraxia, motor function and visual–motor integration in autism mā Michael Miller, Leanne Chukoskie, Marla Zinni, Jeanne Townsend, Doris A. Trauner
I whakaputaina 2014Artigo -
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From first words to grammar in children with focal brain injury mā Elizabeth Bates, Donna Thal, Doris A. Trauner, Judi Fenson, Dorit Aram, Julie A. Eisele, Ruth Nass
I whakaputaina 1997Artigo -
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Nephropathic cystinosis: an international consensus document mā Francesco Emma, Galina Nesterova, Craig B. Langman, Antoine Labbé, Stéphanie Cherqui, Paul Goodyer, Mirian C. H. Janssen, Marcella Greco, Rezan Topaloĝlu, Ewa Elenberg, Ranjan Dohil, Doris A. Trauner, Corinne Antignac, Pierre Cochat, Frederick J. Kaskel, Aude Servais, Elke Wühl, Patrick Niaudet, William van’t Hoff, William A. Gahl, Elena Levtchenko
I whakaputaina 2014Artigo -
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Controversies and research agenda in nephropathic cystinosis: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference mā Craig B. Langman, Bruce A. Barshop, Georges Deschênes, Francesco Emma, Paul Goodyer, Graham Lipkin, Julian Midgley, Chris Ottolenghi, Aude Servais, Neveen A. Soliman, Jess G. Thoene, Elena Levtchenko, Oliver Amon, Gema Ariceta, Maryan Basurto, Leticia Belmont‐Martínez, Aurélia Bertholet‐Thomas, Marjolein Bos, Thomas Brown, Stéphanie Cherqui, Marlies Cornelissen, Monte A. Del Monte, Jie Ding, Ranjan Dohil, Maya Doyle, Ewa Elenberg, William A. Gahl, Víctor Aguado Gómez, Marcella Greco, Christy Greeley, Larry A. Greenbaum, Paul C. Grimm, Katharina Hohenfellner, Teresa M. Holm, Valerie Hotz, Mirian C. H. Janssen, Frederick J. Kaskel, Rita Magriço, Galina Nesterova, Philip Newsholme, Patrick Niaudet, Patrice Rioux, Minnie Sarwal, Jerry A. Schneider, Rezan Topaloĝlu, Doris A. Trauner, María Helena Vaisbich, Lambertus P. van den Heuvel, William van’t Hoff
I whakaputaina 2016Artigo -
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Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy mā Anne O’Donnell‐Luria, Lynn Pais, Víctor Faúndes, Jordan C. Wood, Abigail Sveden, Victor Luria, Rami Abou Jamra, Andrea Accogli, Kimberly Amburgey, Britt‐Marie Anderlid, Silvia Azzarello‐Burri, Alice Basinger, Claudia Bianchini, Lynn M Bird, Rebecca Buchert, Wilfrid Carré, Sophia Ceulemans, Perrine Charles, Helen Cox, Lisa Culliton, Aurora Currò, Florence Démurger, James J. Dowling, Bénédicte Duban‐Bedu, Christèle Dubourg, Luis F Escobar, Alessandra Ferrarini, Tobias B. Haack, Mona Hashim, Solveig Heide, Katherine L. Helbig, Ingo Helbig, Raúl Jiménez Heredia, Delphine Héron, Bertrand Isidor, Amy R. Jonasson, Pascal Joset, Boris Keren, Fernando Kok, Hester Y. Kroes, Alinoë Lavillaureix, Xin Lü, Saskia M. Maas, Gustavo Maegawa, Carlo Marcelis, Saga Elise Eiset, Paul R. Mark, Mercelo R Masruha, Heather M. McLaughlin, Kirsty McWalter, Esther U. Melchinger, Saadet Mercimek‐Andrews, Caroline Nava, Manuela Pendziwiat, Richard Person, Gian Paolo Ramelli, Luiza LP Ramos, Anita Rauch, Caitlin Reavey, Alessandra Renieri, Angelika Rie szlig, Amarilis Sanchez‐Valle, Shifteh Sattar, Carol J. Saunders, Niklas Schwarz, Thomas Smol, Myriam Srour, Katharina Steindl, Steffen Syrbe, Jenny C Taylor, Aida Telegrafi, Isabelle Thiffault, Doris A. Trauner, Hélio van der Linden, Silvana van Koningsbruggen, Laurent Villard, Ida Vogel, Julie A. Vogt, Yvonne G. Weber, Ingrid M. Wentzensen, Elysa Widjaja, Jaroslav Žák, Samantha Baxter, Siddharth Banka, Lance H. Rodan
I whakaputaina 2019Pré-impressão -
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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy mā Anne O’Donnell‐Luria, Lynn Pais, Víctor Faúndes, Jordan C. Wood, Abigail Sveden, Victor Luria, Rami Abou Jamra, Andrea Accogli, Kimberly Amburgey, Britt Marie Anderlid, Silvia Azzarello‐Burri, Alice Basinger, Claudia Bianchini, Lynne M. Bird, Rebecca Buchert, Wilfrid Carré, Sophia Ceulemans, Perrine Charles, Helen Cox, Lisa Culliton, Aurora Currò, Florence Démurger, James J. Dowling, Bénédicte Duban‐Bedu, Christèle Dubourg, Saga Elise Eiset, Luis Escobar, Alessandra Ferrarini, Tobias B. Haack, Mona Hashim, Solveig Heide, Katherine L. Helbig, Ingo Helbig, Raúl Jiménez Heredia, Delphine Héron, Bertrand Isidor, Amy R. Jonasson, Pascal Joset, Boris Keren, Fernando Kok, Hester Y. Kroes, Alinoë Lavillaureix, Xin Lü, Saskia M. Maas, Gustavo Maegawa, Carlo Marcelis, Paul R. Mark, Marcelo Rodrigues Masruha, Heather M. McLaughlin, Kirsty McWalter, Esther U. Melchinger, Saadet Mercimek‐Andrews, Caroline Nava, Manuela Pendziwiat, Richard Person, Gian Paolo Ramelli, Luiza Ramos, Anita Rauch, Caitlin Reavey, Alessandra Renieri, Angelika Rieß, Amarilis Sanchez‐Valle, Shifteh Sattar, Carol J. Saunders, Niklas Schwarz, Thomas Smol, Myriam Srour, Katharina Steindl, Steffen Syrbe, Jenny C. Taylor, Aida Telegrafi, Isabelle Thiffault, Doris A. Trauner, Hélio van der Linden, Silvana van Koningsbruggen, Laurent Villard, Ida Vogel, Julie Vogt, Yvonne G. Weber, Ingrid M. Wentzensen, Elysa Widjaja, Jaroslav Žák, Samantha Baxter, Siddharth Banka, Lance H. Rodan, Jeremy F. McRae, Stephen Clayton, Tomas Fitzgerald, Joanna Kaplanis, Elena Prigmore, Diana Rajan, Alejandro Sifrim, Stuart Aitken, Nadia Akawi, Mohsan Alvi, Kirsty Ambridge, Daniel M. Barrett, Tanya Bayzetinova, Philip Jones, Wendy D. Jones
I whakaputaina 2019Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Medicine
Psychology
Neuroscience
Biology
Psychiatry
Autism
Pediatrics
Anatomy
Autism spectrum disorder
Biochemistry
Brain size
Central nervous system
Cerebral cortex
Cerebrum
Cysteamine
Cysteine
Cystine
Cystinosis
Developmental disorder
Developmental psychology
Enzyme
Epilepsy
Fanconi syndrome
Gene
Genetics
Grey matter
Haploinsufficiency
Hypotonia
Intellectual disability
Intensive care medicine