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There are 198854 results for: content related to: PHACE Syndrome: A Retrospective Review of 23 Patients

  1. Lipofibromatosis: An Institutional and Literature Review of an Uncommon Entity

    Pediatric Dermatology

    Volume 31, Issue 3, May/June 2014, Pages: 298–304, Markus D. Boos, Kudakwashe R. Chikwava, John P. Dormans, Nancy A. Chauvin and Melinda Jen

    Version of Record online : 24 APR 2014, DOI: 10.1111/pde.12335

  2. Association between exposure to nonactionable physiologic monitor alarms and response time in a children's hospital

    Journal of Hospital Medicine

    Volume 10, Issue 6, June 2015, Pages: 345–351, Christopher P. Bonafide, Richard Lin, Miriam Zander, Christian Sarkis Graham, Christine W. Paine, Whitney Rock, Andrew Rich, Kathryn E. Roberts, Margaret Fortino, Vinay M. Nadkarni, A. Russell Localio and Ron Keren

    Version of Record online : 15 APR 2015, DOI: 10.1002/jhm.2331

  3. Unique Familial MLL(KMT2A)-Rearranged Precursor B-Cell Infant Acute Lymphoblastic Leukemia in Non-twin Siblings

    Pediatric Blood & Cancer

    Volume 63, Issue 7, July 2016, Pages: 1175–1180, Karen A. Urtishak, Blaine W. Robinson, Eric F. Rappaport, Margaret D. Sarezky, Jaclyn A. Biegel, Kim E. Nichols, Donna M. Wilmoth, Li-San Wang, Julie W. Stern and Carolyn A. Felix

    Version of Record online : 21 MAR 2016, DOI: 10.1002/pbc.25957

  4. Using electronic medical record data to report laboratory adverse events

    British Journal of Haematology

    Volume 177, Issue 2, April 2017, Pages: 283–286, Tamara P. Miller, Yimei Li, Kelly D. Getz, Jesse Dudley, Evanette Burrows, Jeffrey Pennington, Azada Ibrahimova, Brian T. Fisher, Rochelle Bagatell, Alix E. Seif, Robert Grundmeier and Richard Aplenc

    Version of Record online : 1 FEB 2017, DOI: 10.1111/bjh.14538

  5. Angiolymphoid Hyperplasia with Eosinophilia: A Previously Unreported Complication of Ear Piercing

    Pediatric Dermatology

    Volume 31, Issue 6, November/December 2014, Pages: 738–741, Jonathan S. Okman, Tricia R. Bhatti, Oksana A. Jackson and Adam I. Rubin

    Version of Record online : 25 NOV 2014, DOI: 10.1111/pde.12410

  6. EPHB4 Mutation Implicated in Capillary Malformation–Arteriovenous Malformation Syndrome: A Case Report

    Pediatric Dermatology

    JiaDe Yu, Jenna L. Streicher, Livija Medne, Ian D. Krantz and Albert C. Yan

    Version of Record online : 21 JUL 2017, DOI: 10.1111/pde.13208

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    Acquired copy number neutral loss of heterozygosity of chromosome 7 associated with clonal haematopoiesis in a patient with Shwachman-Diamond syndrome

    British Journal of Haematology

    Volume 159, Issue 4, November 2012, Pages: 480–482, Shefali Parikh, Nieves Perdigones, Michelle Paessler, Barbara Greenbaum, Laura S. Tooke, Jaclyn A. Biegel, Philip J. Mason and Monica Bessler

    Version of Record online : 31 AUG 2012, DOI: 10.1111/bjh.12032

  8. Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low-Level Uniparental Disomy

    American Journal of Medical Genetics Part A

    Volume 161, Issue 5, May 2013, Pages: 993–1001, Jennifer M. Kalish, Laura K. Conlin, Sogol Mostoufi-Moab, Alisha B. Wilkens, Surabhi Mulchandani, Kristin Zelley, Megan Kowalski, Tricia R. Bhatti, Pierre Russo, Peter Mattei, William G. Mackenzie, Virginia LiVolsi, Kim E. Nichols, Jaclyn A. Biegel, Nancy B. Spinner and Matthew A. Deardorff

    Version of Record online : 26 MAR 2013, DOI: 10.1002/ajmg.a.35831

  9. Achromobacter xylosoxidans Bacteremia and Cellulitis: A Report of a Case

    Pediatric Dermatology

    Volume 32, Issue 4, July/August 2015, Pages: e186–e187, Julia Dai, Auris O. Huen, Lori A. Kestenbaum, Margaret D. Sarezky, Carrie C. Coughlin and Albert C. Yan

    Version of Record online : 14 MAY 2015, DOI: 10.1111/pde.12608

  10. Complications preceding early deaths in Black and White children with acute myeloid leukemia

    Pediatric Blood & Cancer

    Lena E. Winestone, Kelly D. Getz, Tamara P. Miller, Yimei Li, Yuan-Shung Huang, Alix E. Seif, Brian T. Fisher and Richard Aplenc

    Version of Record online : 20 JUL 2017, DOI: 10.1002/pbc.26712

  11. Zoonotic infections in pediatric patients with acute leukemia

    Pediatric Blood & Cancer

    Volume 60, Issue 12, December 2013, Pages: E160–E162, Katherine Lothstein, Brian Fisher, Yimei Li, Alix Seif, Tracey Harris, Kari Torp, Marko Kavcic, Yuan-Shung V. Huang, Susan R. Rheingold and Richard Aplenc

    Version of Record online : 19 AUG 2013, DOI: 10.1002/pbc.24596

  12. Research consent capacity varies with executive function and memory in Parkinson's disease

    Movement Disorders

    Volume 31, Issue 3, March 2016, Pages: 414–417, Stephen T. Moelter, Daniel Weintraub, Lauren Mace, Mark Cary, Elizabeth Sullo, Sharon X. Xie and Jason Karlawish

    Version of Record online : 10 FEB 2016, DOI: 10.1002/mds.26469

  13. You have free access to this content
    Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes

    British Journal of Haematology

    Volume 164, Issue 1, January 2014, Pages: 73–82, Daria V. Babushok, Hongbo M. Xie, Jacquelyn J. Roth, Nieves Perdigones, Timothy S. Olson, Joshua D. Cockroft, Xiaowu Gai, Juan C. Perin, Yimei Li, Michele E. Paessler, Hakon Hakonarson, Gregory M. Podsakoff, Philip J. Mason, Jaclyn A. Biegel and Monica Bessler

    Version of Record online : 14 OCT 2013, DOI: 10.1111/bjh.12603

  14. Predictors of antiemetic alteration in pediatric acute myeloid leukemia

    Pediatric Blood & Cancer

    Volume 61, Issue 10, October 2014, Pages: 1798–1805, Jason L. Freedman, Jennifer Faerber, Tammy I. Kang, Dingwei Dai, Brian T. Fisher, Yuan-Shung Huang, Yimei Li, Richard Aplenc and Chris Feudtner

    Version of Record online : 17 JUN 2014, DOI: 10.1002/pbc.25108

  15. Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy

    American Journal of Medical Genetics Part A

    Volume 161, Issue 8, August 2013, Pages: 1929–1939, Jennifer M. Kalish, Laura K. Conlin, Tricia R. Bhatti, Holly A. Dubbs, Mary Catherine Harris, Kosuke Izumi, Sogol Mostoufi-Moab, Surabhi Mulchandani, Sulagna Saitta, Lisa J. States, Daniel T. Swarr, Alisha B. Wilkens, Elaine H. Zackai, Kristin Zelley, Marisa S. Bartolomei, Kim E. Nichols, Andrew A. Palladino, Nancy B. Spinner and Matthew A. Deardorff

    Version of Record online : 26 JUN 2013, DOI: 10.1002/ajmg.a.36045

  16. Iatrogenic Necrolytic Migratory Erythema in an Infant with Congenital Hyperinsulinism

    Pediatric Dermatology

    Volume 33, Issue 2, March/April 2016, Pages: e43–e47, Carrie C. Coughlin, Sani M. Roy, Lisa M. Arkin, N. Scott Adzick, Albert C. Yan, Diva D. De León and Adam I. Rubin

    Version of Record online : 9 DEC 2015, DOI: 10.1111/pde.12741

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    Multidisciplinary Perinatal Palliative Care Plan for a Pregnant Woman Carrying a Fetus with Trisomy-13 and Her Family

    Journal of Obstetric, Gynecologic, & Neonatal Nursing

    Volume 44, Issue s1, June 2015, Page: S79, Joanna C. M. Cole, Tyra Jones, Elizabeth Shaughnessy, Sara Chadwick, Dave Munson and Julie Moldenhauer

    Version of Record online : 4 JUN 2015, DOI: 10.1111/1552-6909.12583

  18. You have free access to this content
    In Reply

    Academic Emergency Medicine

    Volume 23, Issue 1, January 2016, Page: 109, Mark R. Zonfrillo, Konny H. Kim and Kristy B. Arbogast

    Version of Record online : 15 DEC 2015, DOI: 10.1111/acem.12852

  19. Exome sequencing reveals compound heterozygous mutations in ATP8B1 in a JAG1/NOTCH2 mutation-negative patient with clinically diagnosed Alagille syndrome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 4, April 2015, Pages: 891–893, Christopher M. Grochowski, Ramakrishnan Rajagopalan, Alexandra M. Falsey, Kathleen M. Loomes, David A. Piccoli, Ian D. Krantz, Marcella Devoto and Nancy B. Spinner

    Version of Record online : 3 MAR 2015, DOI: 10.1002/ajmg.a.36946

  20. Integrative genomic analysis identifies ancestry-related expression quantitative trait loci on DNA polymerase β and supports the association of genetic ancestry with survival disparities in head and neck squamous cell carcinoma

    Cancer

    Volume 123, Issue 5, March 1, 2017, Pages: 849–860, Meganathan P. Ramakodi, Karthik Devarajan, Elizabeth Blackman, Denise Gibbs, Danièle Luce, Jacqueline Deloumeaux, Suzy Duflo, Jeffrey C. Liu, Ranee Mehra, Rob J. Kulathinal and Camille C. Ragin

    Version of Record online : 1 DEC 2016, DOI: 10.1002/cncr.30457