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Lance H Rodan

Showing results (1-10 of 76) with videos related to

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JIMD Reports|May 1, 2016
N-Acetylcysteine Therapy in an Infant with Transaldolase Deficiency Is Well Tolerated and Associated with Normalization of Alpha Fetoprotein LevelsLance H Rodan, Gerard T Berry
Neurology|October 9, 2013
Clinical reasoning: a case of abnormal eye movements in an infant: more than meets the eyeLance H Rodan, Ingrid Tein, Ray Buncic
Clinical Chemistry|November 2, 2017
Ethylmalonic Aciduria in an Infant with Neurological and Skin PresentationRoy W A Peake, Lance H Rodan
American Journal of Medical Genetics. Part A|November 10, 2020
Homozygous deletion of 21q22.2 in a patient with hypotonia, developmental delay, cortical visual impairment, and retinopathyClara Hildebrandt, Anne Fulton, Lance H Rodan
Clinical Chemistry|May 28, 2017
Raised Anion Gap Metabolic Acidosis in a 4-Day-Old ChildRoy W A Peake, Lance H Rodan
Neurology|March 6, 2013
MR spectroscopy in pediatric Wernicke encephalopathyLance H Rodan, Navin Mishra, Ingrid Tein
Pediatric Neurology|July 22, 2015
Clinical Use of CSF NeurotransmittersLance H Rodan, K Michael Gibson, Phillip L Pearl
Pediatrics|June 22, 2025
Genetic Evaluation of the Child With Intellectual Disability or Global Developmental Delay: Clinical ReportLance H Rodan, Joan Stoler, Emily Chen, et al.
Clinical Chemistry|April 29, 2018
Serine Deficiency in a Child with Neurological Presentation, Hearing Loss, and Multiple Congenital AnomaliesNaif A M Almontashiri, Lance H Rodan, Roy W A Peake
Pediatric Emergency Care|March 30, 2017
Acute Illness Protocol for Fatty Acid Oxidation and Carnitine DisordersSaud H Aldubayan, Lance H Rodan, Gerard T Berry, et al.
Pageof 8

Showing results (1-10 of 76) with videos related to

Sort By:
Pageof 8
JIMD Reports|May 1, 2016
N-Acetylcysteine Therapy in an Infant with Transaldolase Deficiency Is Well Tolerated and Associated with Normalization of Alpha Fetoprotein LevelsLance H Rodan, Gerard T Berry
Neurology|October 9, 2013
Clinical reasoning: a case of abnormal eye movements in an infant: more than meets the eyeLance H Rodan, Ingrid Tein, Ray Buncic
Clinical Chemistry|November 2, 2017
Ethylmalonic Aciduria in an Infant with Neurological and Skin PresentationRoy W A Peake, Lance H Rodan
American Journal of Medical Genetics. Part A|November 10, 2020
Homozygous deletion of 21q22.2 in a patient with hypotonia, developmental delay, cortical visual impairment, and retinopathyClara Hildebrandt, Anne Fulton, Lance H Rodan
Clinical Chemistry|May 28, 2017
Raised Anion Gap Metabolic Acidosis in a 4-Day-Old ChildRoy W A Peake, Lance H Rodan
Neurology|March 6, 2013
MR spectroscopy in pediatric Wernicke encephalopathyLance H Rodan, Navin Mishra, Ingrid Tein
Pediatric Neurology|July 22, 2015
Clinical Use of CSF NeurotransmittersLance H Rodan, K Michael Gibson, Phillip L Pearl
Pediatrics|June 22, 2025
Genetic Evaluation of the Child With Intellectual Disability or Global Developmental Delay: Clinical ReportLance H Rodan, Joan Stoler, Emily Chen, et al.
Clinical Chemistry|April 29, 2018
Serine Deficiency in a Child with Neurological Presentation, Hearing Loss, and Multiple Congenital AnomaliesNaif A M Almontashiri, Lance H Rodan, Roy W A Peake
Pediatric Emergency Care|March 30, 2017
Acute Illness Protocol for Fatty Acid Oxidation and Carnitine DisordersSaud H Aldubayan, Lance H Rodan, Gerard T Berry, et al.
Pageof 8