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C Voermans

Showing results (251-260 of 344) with videos related to

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Neuromuscular Disorders : NMD|June 26, 2023
Respiratory features of centronuclear myopathy in the NetherlandsSietse Bouma, Nicolle Cobben, Karlijn Bouman, et al.
Neurology. Genetics|December 9, 2024
Nemaline Myopathy Type 6 Caused by Variants in the <i>KBTBD13</i> Gene: A Cross-Sectional Study of 24 PatientsEsmee S B van Kleef, Karlijn Bouman, Joery P F Molenaar, et al.
Neuromuscular Disorders : NMD|February 14, 2017
PGM1 deficiency: Substrate use during exercise and effect of treatment with galactoseN C Voermans, N Preisler, K L Madsen, et al.
Neuromuscular Disorders : NMD|July 8, 2022
Respiratory muscle function in patients with nemaline myopathyEsmee S B van Kleef, Jeroen L M van Doorn, Michael A Gaytant, et al.
Muscle & Nerve|April 23, 2015
Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samplesChiara S M Straathof, Dave Van Heusden, Pieternella F Ippel, et al.
Neuromuscular Disorders : NMD|October 3, 2022
Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataractI E A Karnebeek, H T M Boon, A M P Huis, et al.
Open Forum Infectious Diseases|January 1, 2025
Novel Dolutegravir and Lenacapavir Resistance Patterns in Human Immunodeficiency Virus Type 2 Infection: A Case ReportJeroen J A van Kampen, Els van Nood, Rizwan Mahmud, et al.
Neurology|May 20, 2021
Spectrum of Clinical Features in X-Linked Myotubular Myopathy Carriers: An International Questionnaire StudyStacha F I Reumers, Frederik Braun, Jennifer E Spillane, et al.
Clinical Genetics|July 23, 2021
Facioscapulohumeral muscular dystrophy-Reproductive counseling, pregnancy, and delivery in a complex multigenetic diseaseSanne C C Vincenten, Nienke Van Der Stoep, Aimée D C Paulussen, et al.
Journal of Neurology|October 28, 2020
Characterizing the face in facioscapulohumeral muscular dystrophyT G J Loonen, C G C Horlings, S C C Vincenten, et al.
Pageof 35

Showing results (251-260 of 344) with videos related to

Sort By:
Pageof 35
Neuromuscular Disorders : NMD|June 26, 2023
Respiratory features of centronuclear myopathy in the NetherlandsSietse Bouma, Nicolle Cobben, Karlijn Bouman, et al.
Neurology. Genetics|December 9, 2024
Nemaline Myopathy Type 6 Caused by Variants in the <i>KBTBD13</i> Gene: A Cross-Sectional Study of 24 PatientsEsmee S B van Kleef, Karlijn Bouman, Joery P F Molenaar, et al.
Neuromuscular Disorders : NMD|February 14, 2017
PGM1 deficiency: Substrate use during exercise and effect of treatment with galactoseN C Voermans, N Preisler, K L Madsen, et al.
Neuromuscular Disorders : NMD|July 8, 2022
Respiratory muscle function in patients with nemaline myopathyEsmee S B van Kleef, Jeroen L M van Doorn, Michael A Gaytant, et al.
Muscle & Nerve|April 23, 2015
Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samplesChiara S M Straathof, Dave Van Heusden, Pieternella F Ippel, et al.
Neuromuscular Disorders : NMD|October 3, 2022
Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataractI E A Karnebeek, H T M Boon, A M P Huis, et al.
Open Forum Infectious Diseases|January 1, 2025
Novel Dolutegravir and Lenacapavir Resistance Patterns in Human Immunodeficiency Virus Type 2 Infection: A Case ReportJeroen J A van Kampen, Els van Nood, Rizwan Mahmud, et al.
Neurology|May 20, 2021
Spectrum of Clinical Features in X-Linked Myotubular Myopathy Carriers: An International Questionnaire StudyStacha F I Reumers, Frederik Braun, Jennifer E Spillane, et al.
Clinical Genetics|July 23, 2021
Facioscapulohumeral muscular dystrophy-Reproductive counseling, pregnancy, and delivery in a complex multigenetic diseaseSanne C C Vincenten, Nienke Van Der Stoep, Aimée D C Paulussen, et al.
Journal of Neurology|October 28, 2020
Characterizing the face in facioscapulohumeral muscular dystrophyT G J Loonen, C G C Horlings, S C C Vincenten, et al.
Pageof 35