Rezultati pretrage - Haim Bassan
- Prikaz rezultata 1 – 12 od 12
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1
Diagnosis of inferior vermian hypoplasia by fetal magnetic resonance imaging: Potential pitfalls and neurodevelopmental outcome od Catherine Limperopoulos, Richard L. Robertson, Judy A. Estroff, Carol E. Barnewolt, Deborah Levine, Haim Bassan, Adré J. du Plessis
Izdano 2006Artigo -
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Identification of Pressure Passive Cerebral Perfusion and Its Mediators after Infant Cardiac Surgery od Haim Bassan, Kimberlee Gauvreau, Jane W. Newburger, Miles Tsuji, Catherine Limperopoulos, Janet S. Soul, Gene Walter, Peter C. Laussen, Richard A. Jonas, Adré J. du Plessis
Izdano 2004Artigo -
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Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy od Shir Quinn, Nan Zhang, Timothy A. Fenton, Marina Brusel, Preethi Muruganandam, Yoav Peleg, Moshe Giladi, Yoni Haitin, Holger Lerche, Haim Bassan, Yuanyuan Liu, Roy Ben‐Shalom, Moran Rubinstein
Izdano 2024Artigo -
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Fluctuating Pressure-Passivity Is Common in the Cerebral Circulation of Sick Premature Infants od Janet S. Soul, Peter E. Hammer, Miles Tsuji, J. Philip Saul, Haim Bassan, Catherine Limperopoulos, D N DiSalvo, Marianne Moore, Patricia Akins, Steven A. Ringer, Joseph J. Volpe, Felicia Trachtenberg, Adré J. du Plessis
Izdano 2007Artigo -
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Cranial Ultrasound Lesions in the NICU Predict Cerebral Palsy at Age 2 Years in Children Born at Extremely Low Gestational Age od Karl Kuban, Elizabeth N. Allred, T. Michael O’Shea, Nigel Paneth, Michele Pagano, Olaf Dammann, Alan Leviton, Adré du Plessis, Sjirk J. Westra, Cindy Miller, Haim Bassan, Kalpathy Krishnamoorthy, Joseph Junewick, Nicholas Olomu, Elaine Romano, Joanna J. Seibert, Steve Engelke, Padmani Karna, Daniel G. Batton, Sunila E. O’Connor, Cecelia Keller
Izdano 2009Artigo -
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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome od Sarah E. Heron, Bronwyn E. Grinton, Sara Kivity, Zaid Afawi, Sameer M. Zuberi, James N. Hughes, Clair Pridmore, Bree Hodgson, Xenia Iona, Lynette G. Sadleir, James T. Pelekanos, Eric Herlenius, Hadassa Goldberg‐Stern, Haim Bassan, Eric Haan, Amos D. Korczyn, Alison Gardner, Mark Corbett, Jozef Gécz, Paul Q. Thomas, John C. Mulley, Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens
Izdano 2012Artigo -
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<scp><i>SCN3A</i></scp>‐Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation od Tariq Zaman, Katherine L. Helbig, Jérôme Clatot, Christopher H. Thompson, Seok Kyu Kang, Katrien Stouffs, Anna Jansen, Lieve Verstraete, Adeline Jacquinet, Elena Parrini, Renzo Guerrini, Yuh Fujiwara, Satoko Miyatake, Bruria Ben‐Zeev, Haim Bassan, Orit Reish, Daphna Marom, Natalie Hauser, Thuy‐Anh Vu, Sally Ackermann, Careni Spencer, Natalie Lippa, Shraddha Srinivasan, Agnieszka Charzewska, Dorota Hoffman‐Zacharska, David Fitzpatrick, Victoria Harrison, Pradeep Vasudevan, Shelagh Joss, Daniela T. Pilz, Katherine A. Fawcett, Ingo Helbig, Naomichi Matsumoto, Jennifer A. Kearney, Andrew E. Fry, Ethan M. Goldberg
Izdano 2020Artigo -
11
Refining the phenotype associated with <i>GNB1</i> mutations: Clinical data on 18 newly identified patients and review of the literature od Parisa Hemati, Anya Revah‐Politi, Haim Bassan, Slavé Petrovski, Colleen G. Bilancia, Keri Ramsey, Nicole G. Griffin, Louise Bier, Megan T. Cho, Mónica Roselló, Sally Ann Lynch, Sophie Colombo, Astrid Weber, Marte G. Haug, Erin L. Heinzen, Tristan T. Sands, Vinodh Narayanan, Michelle Primiano, Vimla S. Aggarwal, Francisca Millan, Shannon G. Sattler‐Holtrop, Alfonso Caro‐Llopis, Nir Pillar, Janice Baker, Rebecca Freedman, Hester Y. Kroes, Stephanie Sacharow, Nicholas Stong, Pablo Lapunzina, Michael C. Schneider, Nancy J. Mendelsohn, Amanda Singleton, Valerie Loik Ramey, Karen Wou, Alla Kuzminsky, Sandra Monfort, Monika Weisz Hubshman, Samantha Doyle, Alejandro Iglesias, Francisco Martı́nez, F. Ellis McKenzie, Carmen Orellana, Koen L.I. van Gassen, María Palomares‐Bralo, Lily Bazak, Andy Lee, Ana Bircher, Lina Basel‐Vanagaite, Maria Hafström, Gunnar Houge, David B. Goldstein, Kwame Anyane‐Yeboa
Izdano 2018Revisão -
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Genotype-phenotype correlations in <i>SCN8A</i>-related disorders reveal prognostic and therapeutic implications od Katrine M. Johannesen, Yuanyuan Liu, Mahmoud Koko, Cathrine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert, Christina Fenger, Ahmed Eltokhi, Maert Rannap, Nils A. Koch, Stephan Lauxmann, Johanna Krüger, Josua Kegele, Laura Canafoglia, Silvana Franceschetti, Patrick May, Johannes Rebstock, Pia Zacher, Susanne Ruf, Michael Alber, Katalin Štěrbová, Petra Laššuthová, Markéta Vlčková, Johannes R. Lemke, Konrad Platzer, Ilona Krey, Constanze Heine, Dagmar Wieczorek, Judith Kroell-Seger, Caroline Lund, Karl Martin Klein, P Y Billie Au, Jong M. Rho, Alice Ho, Silvia Masnada, Pierangelo Veggiotti, Lucio Giordano, Patrizia Accorsi, Christina Engel Hoei‐Hansen, Pasquale Striano, Federico Zara, Hélène Verhelst, J. Verhoeven, Hilde M. H. Braakman, Bert van der Zwaag, Aster V. E. Harder, Eva H. Brilstra, Manuela Pendziwiat, Sebastian Lebon, María Vaccarezza, Ngọc Minh Lê, Jakob Christensen, Sabine Grønborg, Stephen W. Scherer, Jennifer Howe, Walid Fazeli, Katherine B. Howell, Richard J. Leventer, Chloe Stutterd, Sonja Walsh, Marion Gérard, Bénédicte Gérard, Sara Matricardi, Claudia Bonardi, Stefano Sartori, Andrea Berger, Dorota Hoffman‐Zacharska, Massimo Mastrangelo, Francesca Darra, Arve Vøllo, M. Mahdi Motazacker, Phillis Lakeman, Mathilde Nizon, Cornelia Betzler, Cécilia Altuzarra, Roseline Caume, Agathe Roubertie, Philippe Gélisse, Carla Marini, Renzo Guerrini, Frédéric Bilan, Daniel Tibussek, Margarete Koch‐Hogrebe, Μ. Scott Perry, Shoji Ichikawa, Е. Л. Дадали, Artem Sharkov, Irina Mishina, M. O. Abramov, Ilya Kanivets, С. А. Коростелев, Sergey I. Kutsev, Karen E. Wain, Nancy Eisenhauer, Monisa Wagner, Juliann M. Savatt, Karen Müller‐Schlüter, Haim Bassan, Artem Borovikov, Marie‐Cécile Nassogne
Izdano 2021Artigo
Alati za pretragu:
Povezani predmeti
Medicine
Biology
Genetics
Pregnancy
Gestational age
Anesthesia
Cardiology
Pediatrics
Epilepsy
Gene
Phenotype
Psychology
Autoregulation
Birth weight
Blood pressure
Cerebral autoregulation
Cerebral blood flow
Cerebral perfusion pressure
Fetus
Genotype
Hemodynamics
Internal medicine
Intracranial pressure
Intraventricular hemorrhage
Neuroscience
Psychiatry
Radiology
Anatomy
Angiography
Autism