Zobrazeno 1 - 10
of 55
pro vyhledávání: '"David E, Mandelbaum"'
Autor:
David E. Mandelbaum, Hedy S. Wald
Publikováno v:
Pediatric neurology. 117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33e746445a1ff50edd0655d335365d32
https://pubmed.ncbi.nlm.nih.gov/33652338
https://pubmed.ncbi.nlm.nih.gov/33652338
Autor:
David E. Mandelbaum
Publikováno v:
Epilepsia. 61(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b8fe94b585b12e54546255968b54901
https://pubmed.ncbi.nlm.nih.gov/32623711
https://pubmed.ncbi.nlm.nih.gov/32623711
Autor:
Lisa J Strug, Laura Addis, Theodore Chiang, Zeynep Baskurt, Weili Li, Tara Clarke, Huntley Hardison, Steven L Kugler, David E Mandelbaum, Edward J Novotny, Steven M Wolf, Deb K Pal
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e40696 (2012)
BackgroundReading disability (RD) is a common neurodevelopmental disorder with genetic basis established in families segregating "pure" dyslexia. RD commonly occurs in neurodevelopmental disorders including Rolandic Epilepsy (RE), a complex genetic d
Externí odkaz:
https://doaj.org/article/abfb5ed79ddd4be28e2b968ea47c8eab
Autor:
Ann Tilton, Mark Mintz, David E. Mandelbaum, Peter B. Kang, William H. Trescher, Mary L. Zupanc, Bruce H. Cohen, Jonathan Mink
Publikováno v:
Neurology. 94(2)
In September 2017, the Child Neurology Society (CNS) convened a special task force to review the practice of child neurology in the United States. This was deemed a necessity by our membership, as our colleagues expressed discouragement and burnout b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c6d75886005cbe5a75c9cae73cf5615
https://pubmed.ncbi.nlm.nih.gov/33318161
https://pubmed.ncbi.nlm.nih.gov/33318161
Autor:
David McCormick, Steven L. Kugler, Deb K. Pal, Jacqueline Taylor, Jennifer Crosbie, Tara Clarke, Steven M. Wolf, Russell Schachar, John Trounce, Cigdem I. Akman, Elaine C. Wirrell, Michael D. Wilson, David E. Mandelbaum, Laura Addis, Roberto Caraballo, Lisa J. Strug, Stéphane Auvin, Paul Arnold, Caroline Oren, Maria Kinali, Naim Panjwani, Patricia McGoldrick
Publikováno v:
Annals of Clinical and Translational Neurology
Objective Rolandic epilepsy is a common genetic focal epilepsy of childhood characterized by centrotemporal sharp waves on electroencephalogram. In previous genome‐wide analysis, we had reported linkage of centrotemporal sharp waves to chromosome 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d37dbe2495d7ef0609a1afbb7f3fb6b5
http://europepmc.org/articles/PMC4931716
http://europepmc.org/articles/PMC4931716
Autor:
David E. Mandelbaum
Publikováno v:
Child Neurology Open, Vol 8 (2021)
Artist-critic Clive James said: “Common sense and a sense of humor are the same thing, moving at different speeds. A sense of humor is just common sense, dancing. Those who lack humor are without judgment and should be trusted with nothing.”
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::509de655d24000d627c26458948fb230
https://doi.org/10.1177/2329048x211012831
https://doi.org/10.1177/2329048x211012831
Autor:
Laura, Addis, William, Sproviero, Sanjeev V, Thomas, Roberto H, Caraballo, Stephen J, Newhouse, Kumudini, Gomez, Elaine, Hughes, Maria, Kinali, David, McCormick, Siobhan, Hannan, Silvia, Cossu, Jacqueline, Taylor, Cigdem I, Akman, Steven M, Wolf, David E, Mandelbaum, Rajesh, Gupta, Rick A, van der Spek, Dario, Pruna, Deb K, Pal
Publikováno v:
Journal of Medical Genetics
Background Rolandic epilepsy (RE) is the most common genetic childhood epilepsy, consisting of focal, nocturnal seizures and frequent neurodevelopmental impairments in speech, language, literacy and attention. A complex genetic aetiology is presumed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::544ab0666bbf8b1c16d08be657cc4374
https://pubmed.ncbi.nlm.nih.gov/29789371
https://pubmed.ncbi.nlm.nih.gov/29789371
Autor:
David E. Mandelbaum
Publikováno v:
Pediatric Neurology. 96:1-2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b6989f1ee850b6c7e4a7c4eec10d552
https://doi.org/10.1016/j.pediatrneurol.2019.03.025
https://doi.org/10.1016/j.pediatrneurol.2019.03.025
Autor:
David McCormick, Tara Clarke, Shan Tang, Rajesh Gupta, Steven L. Kugler, Lisa J. Strug, Marisa Pina, Sushma Goyal, Cigdem I. Akman, Caroline Oren, Anna B. Smith, John Trounce, Elaine Hughes, Hannah Cockerill, Steven M Wolf, John Jackman, David E. Mandelbaum, Kumudini Gomez, Colm J. McGinnity, Zaloa Agirre-Arrizubieta, Patricia McGoldrick, Nicola Jolleff, Jacqueline Taylor, Yaiza Hernández Vega, David Scott, Deb K. Pal
Publikováno v:
Epilepsy & Behavior. 53:174-179
Objective The high prevalence and impact of neurodevelopmental comorbidities in childhood epilepsy are now well known, as are the increased risks and familial aggregation of reading disability (RD) and speech sound disorder (SSD) in rolandic epilepsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a2946e77f34f7b7d901a846353303b6
https://doi.org/10.1016/j.yebeh.2015.10.016
https://doi.org/10.1016/j.yebeh.2015.10.016
Autor:
David E. Mandelbaum, Suzanne M. de la Monte, Stefan Kostadinov, Amanda B. Arsenault, Barbara S. Stonestreet
Publikováno v:
The Journal of pediatrics. 197
A pregnant woman with new-onset type 1 diabetes and ketoacidosis delivered an infant at 28 weeks of gestation who died with multiple organ failure and severe cerebral vasculopathy with extensive hemorrhage, diffuse microgliosis, and edema. This illus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21040a661279b9be022c9d544af3b92c
https://pubmed.ncbi.nlm.nih.gov/29555093
https://pubmed.ncbi.nlm.nih.gov/29555093