Résultats de la recherche - Chitra Prasad
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CHARGE syndrome par Kim Blake, Chitra Prasad
Publié 2006Revisão -
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Retraction notice to “Performance comparison of vibration devices on orthodontic tooth movement - A systematic review and meta-analysis”[J Oral Biol Craniofac Res. 10 (2020) 814–82... par Keerthana, Pasupureddi, Diddige, Rajasri, Chitra, Prasad
Publié 2021Texte -
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In vivo investigation of gingival health and oxidative stress changes in patients undergoing orthodontic treatment with and without fluoride use par Chitra, Prasad, Prashantha, Govinakovi Shivamurthy, Rao, Arun
Publié 2022Texte -
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Heterozygous De Novo UBTF Gain-of-Function Variant Is Associated with Neurodegeneration in Childhood par Simon Edvardson, Claudia M. Nicolae, Pankaj B. Agrawal, Cyril Mignot, Katelyn Payne, Asuri N. Prasad, Chitra Prasad, Laurie S. Sadler, Caroline Nava, Thomas E. Mullen, Amber Begtrup, Berivan Baskin, Zöe Powis, Avraham Shaag, Boris Keren, George‐Lucian Moldovan, Orly Elpeleg
Publié 2017Artigo -
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Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathy par Sietske H. Kevelam, Marianna Bugiani, Gajja S. Salomons, Annette Feigenbaum, Susan Blasér, Chitra Prasad, Johannes Häberle, Ivo Barić, Ingrid Bakker, Nienke L. Postma, Warsha A. Kanhai, Nicole I. Wolf, Truus E. M. Abbink, Quinten Waisfisz, Peter Heutink, Marjo S. van der Knaap
Publié 2013Artigo -
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Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups par Sara D. Khangura, Kylie Tingley, Pranesh Chakraborty, Doug Coyle, Jonathan B. Kronick, Anne‐Marie Laberge, Julian Little, Fiona A. Miller, John J. Mitchell, Chitra Prasad, Shabnaz Siddiq, Komudi Siriwardena, Rebecca Sparkes, Kathy N. Speechley, Sylvia Stöckler, Yannis Trakadis, Brenda J. Wilson, Kumanan Wilson, Beth K. Potter
Publié 2015Artigo -
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<i>PMPCA</i>mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia par Rebekah Jobling, Mirna Assoum, Oleksandr Gakh, Susan Blasér, Julian Raiman, Cyril Mignot, Emmanuel Roze, Alexandra Dürr, Alexis Brice, Nicolas Lévy, Chitra Prasad, Tara Paton, Andrew D. Paterson, Nicole M. Roslin, Christian R. Marshall, Jean-Pierre Desvignes, Nathalie Roëckel-Trevisiol, Stephen W. Scherer, Guy A. Rouleau, André Mégarbané, Grazia Isaya, Valérie Delague, Grace Yoon
Publié 2015Artigo -
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CODAS Syndrome Is Associated with Mutations of LONP1, Encoding Mitochondrial AAA+ Lon Protease par Kevin A. Strauss, Robert N. Jinks, Erik G. Puffenberger, Sundararajan Venkatesh, Kamalendra Singh, Iteen Cheng, Natalie Mikita, Jayapalraja Thilagavathi, Jae Lee, Stefan G. Sarafianos, Abigail R. Benkert, Alanna E. Koehler, Anni Zhu, Victoria Trovillion, Madeleine McGlincy, Thierry Morlet, Matthew A. Deardorff, A. Micheil Innes, Chitra Prasad, Albert E. Chudley, Irene Lee, Carolyn K. Suzuki
Publié 2015Artigo
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Psychiatry
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DNA methylation
Family medicine
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Genome
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CHARGE syndrome
Cell biology
Cerebellum
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DNA
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Exome sequencing
Fetus
Health care
Methylation
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