Martina Bebin - Concepedia

Author

Martina Bebin

University of Alabama at Birmingham

Also Known As

M Bebin, M. Bebin, Margarita Kirschner, Martina Bebin

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

University of Alabama at Birmingham Cincinnati Children's Hospital Medical Center Boston Children's Hospital The University of Texas Health Science Center at Houston Harvard University

About

Martina Bebin is an author at University of Alabama at Birmingham specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	564
2	Education	1	1	21
3	Health Sciences	1	1	10
4	Language Studies	1	1	21
5	Natural Sciences	1	1	88

Martina Bebin

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Intrinsic epileptogenesis of hypothalamic hamartomas in gelastic epilepsy Ruben Kuzniecky, Barthon Guthrie, James M. Mountz, Annals of Neurology	1997	322
Epilepsy surgery outcome Frank Gilliam, Elaine Wyllie, JODY KASHDEN, Neurology NeuropsychologyInterdisciplinary NeurosurgeryIntractable EpilepsySurgeryStroke	1997	151
Magnetic resonance imaging abnormalities associated with vigabatrin in patients with epilepsy James W. Wheless, Lionel Carmant, Martina Bebin, Epilepsia	2008	111
Everolimus for treatment-refractory seizures in TSC David Neal Franz, John A. Lawson, Hiroko Ikeda, Neurology Clinical Practice	2018	104
Pharmacokinetics of Levetiracetam in Infants and Young Children with Epilepsy Tracy A. Glauser, Wendy G. Mitchell, Arie Weinstock, Epilepsia	2007	89
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus Patricia Blanchet, Martina Bebin, Shaam Bruet, PLoS Genetics Metabolic DisorderGeneticsDisease Gene IdentificationZebrafish KnockdownVariable Obesity	2017	88
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism Frederike L. Harms, Katta M. Girisha, Andrew A. Hardigan, The American Journal of Human Genetics Facial DysmorphismGenetic DisorderCause Intellectual DisabilityGeneticsMolecular Genetics	2016	84
Congenital porencephaly: MR features and relationship to hippocampal sclerosis. S. Ho, Ruben Kuzniecky, Frank Gilliam, PubMed	1998	71
Cortical reorganization in malformations of cortical development Jorge G. Burneo, Ruben Kuzniecky, Martina Bebin, Neurology	2004	70
<i>UBQLN2</i> mutation causing heterogeneous X‐linked dominant neurodegeneration Akl C. Fahed, Barbara McDonough, Cynthia M. Gouvion, Annals of Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMendelian DisorderGenetic DisorderDominant Neurodegeneration	2014	62

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