Resultats de la cerca - Robson, Caroline

Mechanism of Gram-positive Shock: Identification of Peptidoglycan and Lipoteichoic Acid Moieties Essential in the Induction of Nitric Oxide Synthase, Shock, and Multiple Organ Fail... per Kengatharan, Ken M., De Kimpe, Sjef, Robson, Caroline, Foster, Simon J., Thiemermann, Christoph

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TEMPORAL BONE ABNORMALITIES IN CHILDREN WITH GJB2 MUTATIONS per Kenna, Margaret A., Rehm, Heidi L., Frangulov, Anna, Feldman, Henry A., Robson, Caroline D.

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Magnetic Resonance Imaging Features and Clinical Findings in Pediatric Idiopathic Intracranial Hypertension: A Case–Control Study per Gilbert, Aubrey L., Vaughn, Jennifer, Whitecross, Sarah, Robson, Caroline D., Zurakowski, David, Heidary, Gena

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Nontuberculous Mycobacterial Infection of the Head and Neck in Immunocompetent Children: CT and MR Findings per Robson, Caroline D., Hazra, Rohan, Barnes, Patrick D., Robertson, Richard L., Jones, Dwight, Husson, Robert N.

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Fast Three-Point Dixon MR Imaging of the Retrobulbar Space with Low-Resolution Images for Phase Correction: Comparison with Fast Spin-Echo Inversion Recovery Imaging per Rybicki, Frank J., Mulkern, Robert V., Robertson, Richard L., Robson, Caroline D., Chung, Taylor, Ma, Jingfei

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MR Line-scan Diffusion Imaging of the Spinal Cord in Children per Robertson, Richard L., Maier, Stephan E., Mulkern, Robert V., Vajapayam, Sridhar, Robson, Caroline D., Barnes, Patrick D.

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Level of In Utero Cocaine Exposure and Neonatal Ultrasound Findings per Frank, Deborah A., McCarten, Kathleen M., Robson, Caroline D., Mirochnick, Mark, Cabral, Howard, Park, Henry, Zuckerman, Barry

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MR Line Scan Diffusion Imaging of the Brain in Children per Robertson, Richard L., Maier, Stephan E., Robson, Caroline D., Mulkern, Robert V., Karas, Palagia M., Barnes, Patrick D.

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Neuroimaging in Kabuki syndrome and another KMT2D-related disorder per Stadelmaier, Rachel T., Kenna, Margaret A., Barrett, Devon, Mullen, Thomas E., Bodamer, Olaf, Agrawal, Pankaj B., Robson, Caroline D., Wojcik, Monica H.

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The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management per Tan, Wen‐Hann, Baris, Hagit N, Burrows, Patricia E, Robson, Caroline D, Alomari, Ahmad I, Mulliken, John B, Fishman, Steven J, Irons, Mira B

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Prominent Basal Emissary Foramina in Syndromic Craniosynostosis: Correlation with Phenotypic and Molecular Diagnoses per Robson, Caroline D., Mulliken, John B., Robertson, Richard L., Proctor, Mark R., Steinberger, Daniela, Barnes, Patrick D., McFarren, Alicia, Müller, Ulrich, Zurakowski, David

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MR Line-Scan Diffusion-Weighted Imaging of Term Neonates with Perinatal Brain Ischemia per Robertson, Richard L., Ben-Sira, Liat, Barnes, Patrick D., Mulkern, Robert V., Robson, Caroline D., Maier, Stephan E., Rivkin, Michael J., du Plessis, Adre J.

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Altered White Matter Organization in the TUBB3 E410K Syndrome per Grant, P Ellen, Im, Kiho, Ahtam, Banu, Laurentys, Cynthia T, Chan, Wai-Man, Brainard, Maya, Chew, Sheena, Drottar, Marie, Robson, Caroline D, Drmic, Irene, Engle, Elizabeth C

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Volumetric MRI Study of Brain in Children With Intrauterine Exposure to Cocaine, Alcohol, Tobacco, and Marijuana per Rivkin, Michael J., Davis, Peter E., Lemaster, Jennifer L., Cabral, Howard J., Warfield, Simon K., Mulkern, Robert V., Robson, Caroline D., Rose-Jacobs, Ruth, Frank, Deborah A.

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How Accurately Does Current Fetal Imaging Identify Posterior Fossa Anomalies? per Limperopoulos, Catherine, Robertson, Richard L., Khwaja, Omar S., Robson, Caroline D., Estroff, Judy A., Barnewolt, Carole, Levine, Deborah, Morash, Donna, Nemes, Luanne, Zaccagnini, Linda, du Plessis, Adré J.

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Frequency and Cause of Disagreements in Diagnoses for Fetuses Referred for Ventriculomegaly(1) per Levine, Deborah, Feldman, Henry A., Kazan Tannus, João F., Estroff, Judy A., Magnino, Melissa, Robson, Caroline D., Poussaint, Tina Y., Barnewolt, Carol E., Mehta, Tejas S., Robertson, Richard L.

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Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies per Di Gioia, Silvio Alessandro, Shaaban, Sherin, Tüysüz, Beyhan, Elcioglu, Nursel H., Chan, Wai-Man, Robson, Caroline D., Ecklund, Kirsten, Gilette, Nicole M., Hamzaoglu, Azmi, Tayfun, Gulsen Akay, Traboulsi, Elias I., Engle, Elizabeth C.

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Cerebral vein malformations result from loss of Twist1 expression and BMP signaling from skull progenitor cells and dura per Tischfield, Max A., Robson, Caroline D., Gilette, Nicole M., Chim, Shek Man, Sofela, Folasade A., DeLisle, Michelle M., Gelber, Alon, Barry, Brenda J., MacKinnon, Sarah, Dagi, Linda R., Nathans, Jeremy, Engle, Elizabeth C.

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Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects per Park, Jong G., Tischfield, Max A., Nugent, Alicia A., Cheng, Long, Di Gioia, Silvio Alessandro, Chan, Wai-Man, Maconachie, Gail, Bosley, Thomas M., Summers, C. Gail, Hunter, David G., Robson, Caroline D., Gottlob, Irene, Engle, Elizabeth C.

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HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1(−/−) Mice per Webb, Bryn D., Shaaban, Sherin, Gaspar, Harald, Cunha, Luis F., Schubert, Christian R., Hao, Ke, Robson, Caroline D., Chan, Wai-Man, Andrews, Caroline, MacKinnon, Sarah, Oystreck, Darren T., Hunter, David G., Iacovelli, Anthony J., Ye, Xiaoqian, Camminady, Anne, Engle, Elizabeth C., Jabs, Ethylin Wang

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