Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Lisa Kratz

Showing results (1-10 of 30) with videos related to

Pageof 3
Sort By:
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 9, 2012
Disorders of sterol synthesis: beyond Smith-Lemli-Opitz syndromeGail E Herman, Lisa Kratz
American Journal of Medical Genetics|November 29, 2002
Desmosterolosis presenting with multiple congenital anomalies and profound developmental delayHans C Andersson, Lisa Kratz, Richard Kelley
Journal of Ethnicity in Substance Abuse|June 17, 2011
Academics and substance use among Latino adolescents: results from a national studyEllen L Vaughan, Lisa Kratz, Julie d'Argent
Clinical Case Reports|September 8, 2017
Severe phenotype of X-linked dominant chondrodysplasia punctataNadirah Damseh, Karen Chong, Christian Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 12, 2019
Laboratory diagnosis of disorders of peroxisomal biogenesis and function: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Irene De Biase, Silvia Tortorelli, Lisa Kratz, et al.
Annals of Indian Academy of Neurology|April 1, 2022
Child with D-2-Hydroxyglutaric Aciduria Type II: A Rare Neurometabolic DisorderRangan Srinivasaraghavan, Suvasini Sharma, Lisa Kratz, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 29, 2006
Abnormalities of cholesterol metabolism in autism spectrum disordersElaine Tierney, Irena Bukelis, Richard E Thompson, et al.
Annals of Indian Academy of Neurology|February 15, 2020
Metabolic Stroke: A Novel Presentation in a Child with Succinic Semialdehyde Dehydrogenase DeficiencySangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1Sangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental DisorderSangeetha Yoganathan, Rangan Srinivasaraghavan, Mahalakshmi Chandran, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 9, 2012
Disorders of sterol synthesis: beyond Smith-Lemli-Opitz syndromeGail E Herman, Lisa Kratz
American Journal of Medical Genetics|November 29, 2002
Desmosterolosis presenting with multiple congenital anomalies and profound developmental delayHans C Andersson, Lisa Kratz, Richard Kelley
Journal of Ethnicity in Substance Abuse|June 17, 2011
Academics and substance use among Latino adolescents: results from a national studyEllen L Vaughan, Lisa Kratz, Julie d'Argent
Clinical Case Reports|September 8, 2017
Severe phenotype of X-linked dominant chondrodysplasia punctataNadirah Damseh, Karen Chong, Christian Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 12, 2019
Laboratory diagnosis of disorders of peroxisomal biogenesis and function: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Irene De Biase, Silvia Tortorelli, Lisa Kratz, et al.
Annals of Indian Academy of Neurology|April 1, 2022
Child with D-2-Hydroxyglutaric Aciduria Type II: A Rare Neurometabolic DisorderRangan Srinivasaraghavan, Suvasini Sharma, Lisa Kratz, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 29, 2006
Abnormalities of cholesterol metabolism in autism spectrum disordersElaine Tierney, Irena Bukelis, Richard E Thompson, et al.
Annals of Indian Academy of Neurology|February 15, 2020
Metabolic Stroke: A Novel Presentation in a Child with Succinic Semialdehyde Dehydrogenase DeficiencySangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1Sangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, et al.
Annals of Indian Academy of Neurology|July 5, 2021
Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental DisorderSangeetha Yoganathan, Rangan Srinivasaraghavan, Mahalakshmi Chandran, et al.
Pageof 3