نتائج البحث - Robson, Caroline D.

TEMPORAL BONE ABNORMALITIES IN CHILDREN WITH GJB2 MUTATIONS حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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? حسب 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) حسب 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 حسب 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 حسب 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 حسب 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 حسب 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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Novel variants in TUBA1A cause congenital fibrosis of the extraocular muscles with or without malformations of cortical brain development حسب Jurgens, Julie A., Barry, Brenda J., Lemire, Gabrielle, Chan, Wai-Man, Whitman, Mary C., Shaaban, Sherin, Robson, Caroline D., MacKinnon, Sarah, England, Eleina M., McMillan, Hugh J., Kelly, Christopher, Pratt, Brandon M., O’Donnell-Luria, Anne, MacArthur, Daniel G., Boycott, Kym M., Hunter, David G., Engle, Elizabeth C.

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