Publications by authors named "Alisa Gutman"

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Effect of Varenicline on Tardive Dyskinesia: A Pilot Study.
Stanley N Caroff, Alisa R Gutman, John Northrop, Shirley H Leong, Rosalind M Berkowitz

Clin Psychopharmacol Neurosci· May 2021

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Balancing Vulnerability and Resilience in Damage Prognostication.
Kenneth J Weiss, Alisa R Gutman

J Am Acad Psychiatry Law· March 2021

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Testifying About Trauma: A Call for Science and Civility.
Kenneth J Weiss, Alisa R Gutman

J Am Acad Psychiatry Law· March 2017

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Violent Extremism, Community-Based Violence Prevention, and Mental Health Professionals.
Stevan M Weine, Andrew Stone, Aliya Saeed, Stephen Shanfield, John Beahrs, Alisa Gutman

J Nerv Ment Dis· January 2017

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The effect of resilience on posttraumatic stress disorder in trauma-exposed inner-city primary care patients.
Glenda L Wrenn, Aliza P Wingo, Renee Moore, Tiffany Pelletier, Alisa R Gutman

J Natl Med Assoc· July 2011

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Moderating effects of resilience on depression in individuals with a history of childhood abuse or trauma exposure.
Aliza P Wingo, Glenda Wrenn, Tiffany Pelletier, Alisa R Gutman, Bekh Bradley

J Affect Disord· November 2010

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Functional interactions between endocannabinoid and CCK neurotransmitter systems may be critical for extinction learning.
Jasmeer P Chhatwal, Alisa R Gutman, Kimberly A Maguschak, Michael E Bowser, Yong Yang

Neuropsychopharmacology· January 2009

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The role of neuropeptide Y in the expression and extinction of fear-potentiated startle.
Alisa R Gutman, Yong Yang, Kerry J Ressler, Michael Davis

J Neurosci· November 2008

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A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C.
Avraham Zeharia, Merel S Ebberink, Ronald J A Wanders, Hans R Waterham, Alisa Gutman

J Hum Genet· August 2007

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Glutaric aciduria type 1: clinical, biochemical and molecular findings in patients from Israel.
Stanley H Korman, Cornelis Jakobs, Patricia S Darmin, Alisa Gutman, Marjo S van der Knaap

Eur J Paediatr Neurol· March 2007

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A novel SLC25A20 splicing mutation in patients of different ethnic origin with neonatally lethal carnitine-acylcarnitine translocase (CACT) deficiency.
Stanley H Korman, James J Pitt, Avihu Boneh, Imad Dweikat, Mokhtar Zater, Alisa Gutman

Mol Genet Metab· December 2006

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Treatment from birth of nonketotic hyperglycinemia due to a novel GLDC mutation.
Stanley H Korman, Isaiah D Wexler, Alisa Gutman, Marie-Odile Rolland, Junko Kanno

Ann Neurol· February 2006

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Central oxytocin, vasopressin, and corticotropin-releasing factor receptor densities in the basal forebrain predict isolation potentiated startle in rats.
Hemanth P Nair, Alisa R Gutman, Michael Davis, Larry J Young

J Neurosci· December 2005

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Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency.
Stanley H Korman, Hans R Waterham, Alisa Gutman, Cornelis Jakobs, Ronald J A Wanders

Mol Genet Metab· November 2005

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2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency: application to diagnosis and implications for the R-pathway of isoleucine oxidation.
Stanley H Korman, Brage S Andresen, Avraham Zeharia, Alisa Gutman, Avihu Boneh

Clin Chem· March 2005

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Prenatal diagnosis for arginase deficiency by second-trimester fetal erythrocyte arginase assay and first-trimester ARG1 mutation analysis.
Stanley H Korman, Alisa Gutman, Edia Stemmer, Barrie S Kay, Ziva Ben-Neriah

Prenat Diagn· November 2004

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N-acetyl tyrosyluria caused by parenteral or enteral administration of N-acetyl-L-tyrosine: differentiation from hereditary and acquired tyrosinemias.
Stanley H Korman, Alisa Gutman

J Pediatr Gastroenterol Nutr· July 2004

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Persistent NKH with transient or absent symptoms and a homozygous GLDC mutation.
Stanley H Korman, Avihu Boneh, Akiko Ichinohe, Kanako Kojima, Kenichi Sato, Alisa Gutman

Ann Neurol· July 2004

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Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3-1G > C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging from sudden neonatal death to asymptomatic status.
Stanley H Korman, Alisa Gutman, Rivka Brooks, Thayline Sinnathamby, Niels Gregersen

Mol Genet Metab· June 2004

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Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome with evidence of mitochondrial dysfunction due to a novel SLC25A15 (ORNT1) gene mutation in a Palestinian family.
Stanley H Korman, Naomi Kanazawa, Bassam Abu-Libdeh, Alisa Gutman, Seiichi Tsujino

J Neurol Sci· March 2004

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Pitfalls in the diagnosis of glycine encephalopathy (non-ketotic hyperglycinemia).
Stanley H Korman, Alisa Gutman

Dev Med Child Neurol· October 2002

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Hypocarnitinemia in lysinuric protein intolerance.
Stanley H Korman, Annick Raas-Rothschild, Orly Elpeleg, Alisa Gutman

Mol Genet Metab· May 2002

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A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.
Annick Raas-Rothschild, Ronald J A Wanders, Petra A W Mooijer, Jeannette Gootjes, Hans R Waterham, Alisa Gutman

Am J Hum Genet· April 2002

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