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Friedrich Stock

Showing results (11-20 of 31) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|July 23, 2018
17q12 Deletion Syndrome as a Rare Cause for Diabetes Mellitus Type MODY5Natascha Roehlen, Hanna Hilger, Friedrich Stock, et al.
Ultrasonography (Seoul, Korea)|September 8, 2016
Preclinical evaluation of acoustic radiation force impulse measurements in regions of heterogeneous elasticityKatharina Hollerieth, Bernhard Gaßmann, Stefan Wagenpfeil, et al.
Acta Orthopaedica|May 20, 2008
Assessment of leech therapy for knee osteoarthritis: a randomized studyStefan Andereya, Sven Stanzel, Uwe Maus, et al.
BMC Psychiatry|August 4, 2018
Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case reportKathrin Nickel, Ludger Tebartz van Elst, Katharina Domschke, et al.
Abdominal Imaging|March 26, 2015
Comparison of a pocket-size ultrasound device with a premium ultrasound machine: diagnostic value and time required in bedside ultrasound examinationKonrad Friedrich Stock, Bettina Klein, Dominik Steubl, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 16, 2023
Pulmonary Findings in Hospitalized COVID-19 Patients Assessed by Lung Ultrasonography (LUS) - A Prospective Registry StudyAnna Barner, Egon Burian, Alexander Simon, et al.
Clinical Hemorheology and Microcirculation|December 20, 2018
Sonography of the renal allograft: Correlation between doppler sonographic resistance index (RI) and histopathologyStephanie Preuss, Charlotte Rother, Lutz Renders, et al.
Frontiers in Pediatrics|September 22, 2025
The role of <i>LSR</i> gene variants in early onset intrahepatic cholestasis: a case series with treatment optionsSinja Ohlsson, Alex Zaufel, Natalia Qvartskhava, et al.
Neuromuscular Disorders : NMD|January 8, 2021
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2PPeter Reilich, Beate Schlotter, Federica Montagnese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 22, 2016
Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndromeMarc-Alexander Rauschendorf, Meike Jost, Friedrich Stock, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
The Journal of Clinical Endocrinology and Metabolism|July 23, 2018
17q12 Deletion Syndrome as a Rare Cause for Diabetes Mellitus Type MODY5Natascha Roehlen, Hanna Hilger, Friedrich Stock, et al.
Ultrasonography (Seoul, Korea)|September 8, 2016
Preclinical evaluation of acoustic radiation force impulse measurements in regions of heterogeneous elasticityKatharina Hollerieth, Bernhard Gaßmann, Stefan Wagenpfeil, et al.
Acta Orthopaedica|May 20, 2008
Assessment of leech therapy for knee osteoarthritis: a randomized studyStefan Andereya, Sven Stanzel, Uwe Maus, et al.
BMC Psychiatry|August 4, 2018
Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case reportKathrin Nickel, Ludger Tebartz van Elst, Katharina Domschke, et al.
Abdominal Imaging|March 26, 2015
Comparison of a pocket-size ultrasound device with a premium ultrasound machine: diagnostic value and time required in bedside ultrasound examinationKonrad Friedrich Stock, Bettina Klein, Dominik Steubl, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 16, 2023
Pulmonary Findings in Hospitalized COVID-19 Patients Assessed by Lung Ultrasonography (LUS) - A Prospective Registry StudyAnna Barner, Egon Burian, Alexander Simon, et al.
Clinical Hemorheology and Microcirculation|December 20, 2018
Sonography of the renal allograft: Correlation between doppler sonographic resistance index (RI) and histopathologyStephanie Preuss, Charlotte Rother, Lutz Renders, et al.
Frontiers in Pediatrics|September 22, 2025
The role of <i>LSR</i> gene variants in early onset intrahepatic cholestasis: a case series with treatment optionsSinja Ohlsson, Alex Zaufel, Natalia Qvartskhava, et al.
Neuromuscular Disorders : NMD|January 8, 2021
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2PPeter Reilich, Beate Schlotter, Federica Montagnese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 22, 2016
Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndromeMarc-Alexander Rauschendorf, Meike Jost, Friedrich Stock, et al.
Pageof 4