Search Results - 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... by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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? by 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) by 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 by 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 by 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 by 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 by 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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