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Daniela Karall

Showing results (91-100 of 129) with videos related to

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Molecular Genetics and Metabolism|May 19, 2026
Progressive short stature in Pearson syndrome and the impact of organ failureAyami Yoshimi, Holger Cario, Kirsten Timmermann, et al.
Journal of Inherited Metabolic Disease|October 1, 2021
100 years of inherited metabolic disorders in Austria-A national registry of minimal birth prevalence, diagnosis, and clinical outcome of inborn errors of metabolism in Austria between 1921 and 2021Gabriele Ramoser, Federica Caferri, Bernhard Radlinger, et al.
Journal of Inherited Metabolic Disease|December 16, 2024
Diagnosis, treatment, management and monitoring of patients with tyrosinaemia type 1: Consensus group recommendations from the German-speaking countriesAnibh M Das, Diana Ballhausen, Dorothea Haas, et al.
British Journal of Haematology|April 10, 2021
Haematological characteristics and spontaneous haematological recovery in Pearson syndromeAyami Yoshimi, Sarah C Grünert, Holger Cario, et al.
Nutrients|November 27, 2025
Newborn Screening Alone Cannot Prevent Most Cases of Severe Vitamin B12 Deficiency in the First Year of LifeChristina Kaufman, Julian Margreitter, Marion Herle, et al.
Journal of Inherited Metabolic Disease|November 18, 2016
Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revisionNikolas Boy, Chris Mühlhausen, Esther M Maier, et al.
Journal of Inherited Metabolic Disease|June 8, 2026
Prevalence, Disease Onset and Clinical Outcome in Arginase 1 Deficiency: Cross-Border Surveillance in Germany, Austria, and SwitzerlandSvenja Scharre, Annette L Hess, Florian Gleich, et al.
International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|September 21, 2020
Stereotactic radiofrequency ablation of a variety of liver masses in childrenBenjamin Hetzer, Georg-Friedrich Vogel, Andreas Entenmann, et al.
Annals of Clinical and Translational Neurology|July 30, 2019
KCNC1-related disorders: new de novo variants expand the phenotypic spectrumJoohyun Park, Mahmoud Koko, Ulrike B S Hedrich, et al.
Journal of Inherited Metabolic Disease|December 23, 2015
Impact of age at onset and newborn screening on outcome in organic aciduriasJana Heringer, Vassili Valayannopoulos, Allan M Lund, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Molecular Genetics and Metabolism|May 19, 2026
Progressive short stature in Pearson syndrome and the impact of organ failureAyami Yoshimi, Holger Cario, Kirsten Timmermann, et al.
Journal of Inherited Metabolic Disease|October 1, 2021
100 years of inherited metabolic disorders in Austria-A national registry of minimal birth prevalence, diagnosis, and clinical outcome of inborn errors of metabolism in Austria between 1921 and 2021Gabriele Ramoser, Federica Caferri, Bernhard Radlinger, et al.
Journal of Inherited Metabolic Disease|December 16, 2024
Diagnosis, treatment, management and monitoring of patients with tyrosinaemia type 1: Consensus group recommendations from the German-speaking countriesAnibh M Das, Diana Ballhausen, Dorothea Haas, et al.
British Journal of Haematology|April 10, 2021
Haematological characteristics and spontaneous haematological recovery in Pearson syndromeAyami Yoshimi, Sarah C Grünert, Holger Cario, et al.
Nutrients|November 27, 2025
Newborn Screening Alone Cannot Prevent Most Cases of Severe Vitamin B12 Deficiency in the First Year of LifeChristina Kaufman, Julian Margreitter, Marion Herle, et al.
Journal of Inherited Metabolic Disease|November 18, 2016
Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revisionNikolas Boy, Chris Mühlhausen, Esther M Maier, et al.
Journal of Inherited Metabolic Disease|June 8, 2026
Prevalence, Disease Onset and Clinical Outcome in Arginase 1 Deficiency: Cross-Border Surveillance in Germany, Austria, and SwitzerlandSvenja Scharre, Annette L Hess, Florian Gleich, et al.
International Journal of Hyperthermia : the Official Journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group|September 21, 2020
Stereotactic radiofrequency ablation of a variety of liver masses in childrenBenjamin Hetzer, Georg-Friedrich Vogel, Andreas Entenmann, et al.
Annals of Clinical and Translational Neurology|July 30, 2019
KCNC1-related disorders: new de novo variants expand the phenotypic spectrumJoohyun Park, Mahmoud Koko, Ulrike B S Hedrich, et al.
Journal of Inherited Metabolic Disease|December 23, 2015
Impact of age at onset and newborn screening on outcome in organic aciduriasJana Heringer, Vassili Valayannopoulos, Allan M Lund, et al.
Pageof 13