खोज परिणाम - Caroline D. Robson

  • प्रदर्शित 1 - 15 परिणाम 15
परिणाम को परिष्कृत करें
  1. 1
    Morning Glory Disc Anomaly: Characteristic MR Imaging Findings

    Morning Glory Disc Anomaly: Characteristic MR Imaging Findings द्वारा Shehanaz Ellika, Caroline D. Robson, Gena Heidary, Michael J. Paldino

    प्रकाशित 2013
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  2. 2
    Lymphadenitis Due to Nontuberculous Mycobacteria in Children: Presentation and Response to Therapy

    Lymphadenitis Due to Nontuberculous Mycobacteria in Children: Presentation and Response to Therapy द्वारा Rohan Hazra, Caroline D. Robson, Antonio R. Pérez‐Atayde, Robert N. Husson

    प्रकाशित 1999
    पूर्ण पाठ प्राप्त करें
    Revisão
    सूची में सहेजें
    में बचाया:
  3. 3
    Mechanism of Gram-positive Shock: Identification of Peptidoglycan and Lipoteichoic Acid Moieties Essential in the Induction of Nitric Oxide Synthase, Shock, and Multiple Organ Failure

    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... द्वारा Ken M. Kengatharan, S. de Kimpe, Caroline D. Robson, Simon J. Foster, Christoph Thiemermann

    प्रकाशित 1998
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  4. 4
    Pediatric Chronic Nonbacterial Osteomyelitis of the Jaw: Clinical, Radiographic, and Histopathologic Features

    Pediatric Chronic Nonbacterial Osteomyelitis of the Jaw: Clinical, Radiographic, and Histopathologic Features द्वारा Bonnie L. Padwa, Kelley M. Dentino, Caroline D. Robson, Sook Bin Woo, Kyle C. Kurek, Cory M. Resnick

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  5. 5
    The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management

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

    प्रकाशित 2007
    पूर्ण पाठ प्राप्त करें
    Carta
    सूची में सहेजें
    में बचाया:
  6. 6
    Volumetric MRI Study of Brain in Children With Intrauterine Exposure to Cocaine, Alcohol, Tobacco, and Marijuana

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

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  7. 7
    How Accurately Does Current Fetal Imaging Identify Posterior Fossa Anomalies?

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

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  8. 8
    Neurodevelopmental outcome of fetuses referred for ventriculomegaly

    Neurodevelopmental outcome of fetuses referred for ventriculomegaly द्वारा Marjorie Beeghly, Janice Ware, Janet S. Soul, Adré du Plessis, Omar Khwaja, Gunjan M. Senapati, Caroline D. Robson, Richard L. Robertson, Tina Young Poussaint, Carol E. Barnewolt, Henry A. Feldman, Judy A. Estroff, Deborah Levine

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  9. 9
    Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura

    Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura द्वारा Max A. Tischfield, Caroline D. Robson, Nicole M. Gilette, Shek Man Chim, Folasade A. Sofela, Michelle M. DeLisle, Alon Gelber, Brenda J. Barry, Sarah MacKinnon, Linda R. Dagi, Jeremy Nathans, Elizabeth C. Engle

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  10. 10
    Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects

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

    प्रकाशित 2016
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  11. 11
    HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1 Mice

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

    प्रकाशित 2012
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  12. 12
    Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes

    Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes द्वारा Sibel Kantarci, Lihadh Al‐Gazali, R. Sean Hill, Dian Donnai, Graeme Black, Éric Bieth, Nicolas Chassaing, Didier Lacombe, Koenraad Devriendt, Ahmad S. Teebi, Marı́a Loscertales, Caroline D. Robson, Tianming Liu, David T. MacLaughlin, Kristin Noonan, Meaghan Russell, Christopher A. Walsh, Patricia K. Donahoe, Barbara R. Pober

    प्रकाशित 2007
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  13. 13
    Biallelic mutations in human DCC cause developmental split-brain syndrome

    Biallelic mutations in human DCC cause developmental split-brain syndrome द्वारा Saumya Shekhar Jamuar, Klaus Schmitz‐Abe, Alissa M. D’Gama, Marie Drottar, Wai‐Man Chan, Maya Peeva, Sarah Servattalab, Anh-Thu N. Lam, Mauricio R. Delgado, Nancy J. Clegg, Zayed Al Zayed, Mohammad Asif Dogar, Ibrahim A. Alorainy, Abdullah Abu Jamea, Khaled K. Abu‐Amero, May L. Griebel, Wendy L. Ward, Ed S. Lein, Kyriacos Markianos, A. James Barkovich, Caroline D. Robson, P. Ellen Grant, Thomas M. Bosley, Elizabeth C. Engle, Christopher A. Walsh, Timothy W. Yu

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  14. 14
    Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis

    Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis द्वारा Alan P. Tenney, Silvio Alessandro Di Gioia, Bryn D. Webb, Wai‐Man Chan, Elke de Boer, Sarah J. Garnai, Brenda J. Barry, Tammy Ray, Michael Kosicki, Caroline D. Robson, Zhongyang Zhang, Thomas E. Collins, Alon Gelber, Brandon M. Pratt, Yuko Fujiwara, Arushi Varshney, Monkol Lek, Peter E. Warburton, Carol Van Ryzin, Tanya Lehky, Christopher Zalewski, Kelly King, Carmen C. Brewer, Audrey Thurm, Joseph Snow, Flavia M. Facio, Narisu Narisu, Lori L. Bonnycastle, Amy J. Swift, Peter S. Chines, Jessica Bell, Suresh Mohan, Mary C. Whitman, Sandra E. Staffieri, James E. Elder, Joseph L. Demer, Alcy Torres, Elza Rachid, Christiane Al‐Haddad, Rose‐Mary Boustany, David A. Mackey, Angela F. Brady, María Fenollar‐Cortés, Mélanie Fradin, Tjitske Kleefstra, George W. Padberg, Salmo Raskin, Mário Teruo Sato, Stuart H. Orkin, Stephen C. J. Parker, Tessa A. Hadlock, Lisenka E.L.M. Vissers, Hans van Bokhoven, Ethylin Wang Jabs, Francis S. Collins, L Pennacchio, Irini Manoli, Elizabeth C. Engle

    प्रकाशित 2023
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  15. 15
    A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome

    A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome द्वारा Silvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, Jessica Cannavino, Matthew F. Rose, Nicole M. Gilette, Pietro Artoni, Nara Sobreira, Wai‐Man Chan, Bryn D. Webb, Caroline D. Robson, Long Cheng, Carol Van Ryzin, Andres Ramirez-Martinez, Payam Mohassel, Mark Leppert, Mary Beth Scholand, Christopher Grunseich, Carlos R. Ferreira, Tyler Hartman, Ian Hayes, Tim Morgan, David Markie, Michela Fagiolini, Amy J. Swift, Peter S. Chines, Carlos E. Speck‐Martins, Francis S. Collins, Ethylin Wang Jabs, Carsten G. Bönnemann, Eric N. Olson, Caroline Andrews, Brenda J. Barry, David G. Hunter, Sarah MacKinnon, Sherin Shaaban, Mónica Erazo, Tamiesha Frempong, Ke Hao, Thomas P. Naidich, Janet C. Rucker, Zhongyang Zhang, Barbara B. Biesecker, Lori L. Bonnycastle, Carmen C. Brewer, Brian P. Brooks, John A. Butman, Wade W. Chien, Kathleen Farrell, Edmond J. FitzGibbon, Andrea Gropman, Elizabeth Hutchinson, Minal S. Jain, Kelly King, Tanya Lehky, Janice Lee, Denise K. Liberton, Narisu Narisu, Scott M. Paul, Neda Sadeghi, Joseph Snow, Beth Solomon, Angela C. Summers, Camilo Toro, Audrey Thurm, Christopher Zalewski, John C. Carey, Stephen P. Robertson, Irini Manoli, Elizabeth C. Engle

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:

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