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Maria Gieron-Korthals

Showing results (1-10 of 8) with videos related to

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Fetal and Pediatric Pathology|October 26, 2005
Hypoxic-ischemic encephalopathy in infants: new challengesMaria Gieron-Korthals, José Colón
Journal of Child Neurology|October 8, 2009
Early testing for Huntington disease in children: pros and consMegan Toufexis, Maria Gieron-Korthals
Fetal and Pediatric Pathology|March 12, 2011
Spinal muscular atrophy: an updateTracy Chang, Maria Gieron-Korthals
Advances in Pediatrics|July 8, 2023
Challenges in Diagnosing and Treating Myasthenia Gravis in Infants and Children with Presentation of CasesOrnella Bricoune, Bailey Hamner, Maria Gieron-Korthals
Case Reports in Pediatrics|January 7, 2014
Neuromyelitis optica in child: diagnostic and therapeutic challengesKarolina Dembinski, Maria Gieron-Korthals, Carlos R Martinez, et al.
Journal of Medical Case Reports|February 4, 2016
A novel mutation in GLUD1 causing hyperinsulinism-hyperammonemia in a patient with high density of homozygosity on microarray: a case reportJohn Odom, Maria Gieron-Korthals, Dorothy Shulman, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Pontine hypoplasia in Carey-Fineman-Ziter (CFZ) syndromeAkhil Maheshwari, Darlene A Calhoun, Atilano Lacson, et al.
BMC Neurology|December 11, 2014
An open-label pilot trial of minocycline in children as a treatment for Angelman syndromeJoseph C Grieco, Stephanie L Ciarlone, Maria Gieron-Korthals, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Fetal and Pediatric Pathology|October 26, 2005
Hypoxic-ischemic encephalopathy in infants: new challengesMaria Gieron-Korthals, José Colón
Journal of Child Neurology|October 8, 2009
Early testing for Huntington disease in children: pros and consMegan Toufexis, Maria Gieron-Korthals
Fetal and Pediatric Pathology|March 12, 2011
Spinal muscular atrophy: an updateTracy Chang, Maria Gieron-Korthals
Advances in Pediatrics|July 8, 2023
Challenges in Diagnosing and Treating Myasthenia Gravis in Infants and Children with Presentation of CasesOrnella Bricoune, Bailey Hamner, Maria Gieron-Korthals
Case Reports in Pediatrics|January 7, 2014
Neuromyelitis optica in child: diagnostic and therapeutic challengesKarolina Dembinski, Maria Gieron-Korthals, Carlos R Martinez, et al.
Journal of Medical Case Reports|February 4, 2016
A novel mutation in GLUD1 causing hyperinsulinism-hyperammonemia in a patient with high density of homozygosity on microarray: a case reportJohn Odom, Maria Gieron-Korthals, Dorothy Shulman, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Pontine hypoplasia in Carey-Fineman-Ziter (CFZ) syndromeAkhil Maheshwari, Darlene A Calhoun, Atilano Lacson, et al.
BMC Neurology|December 11, 2014
An open-label pilot trial of minocycline in children as a treatment for Angelman syndromeJoseph C Grieco, Stephanie L Ciarlone, Maria Gieron-Korthals, et al.
Pageof 1