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Michael Mull

Showing results (21-30 of 28) with videos related to

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Journal of Child Neurology|June 15, 2011
Aicardi-Goutières syndrome and systemic lupus erythematosus (SLE) in a 12-year-old boy with SAMHD1 mutationsGeorgia Ramantani, Martin Häusler, Pascal Niggemann, et al.
Stroke|October 30, 2004
Do normal D-dimer levels reliably exclude cerebral sinus thrombosis?Christoph M Kosinski, Michael Mull, Michael Schwarz, et al.
Pediatric Blood & Cancer|January 4, 2019
Ectopic intracranial retinoblastoma in a 3.5-month-old infant without eye involvement and without evidence of heritabilityTristan Römer, Petra Temming, Dietmar R Lohmann, et al.
Molecular Genetics & Genomic Medicine|November 6, 2018
Familial NEDD4L variant in periventricular nodular heterotopia and in a fetus with hypokinesia and flexion contracturesMiriam Elbracht, Florian Kraft, Matthias Begemann, et al.
Brain and Behavior|April 19, 2016
Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?Friederike Werheid, Hamid Azzedine, Eva Zwerenz, et al.
Neuroimaging Clinics of North America|May 12, 2007
Imaging in spinal vascular diseaseTimo Krings, Pierre L Lasjaunias, Franz J Hans, et al.
The Journal of Clinical Investigation|January 9, 2019
DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humansGergely Karsai, Florian Kraft, Natja Haag, et al.
The Journal of Clinical Investigation|May 4, 2021
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammationEva Lausberg, Sebastian Gießelmann, Joseph P Dewulf, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Journal of Child Neurology|June 15, 2011
Aicardi-Goutières syndrome and systemic lupus erythematosus (SLE) in a 12-year-old boy with SAMHD1 mutationsGeorgia Ramantani, Martin Häusler, Pascal Niggemann, et al.
Stroke|October 30, 2004
Do normal D-dimer levels reliably exclude cerebral sinus thrombosis?Christoph M Kosinski, Michael Mull, Michael Schwarz, et al.
Pediatric Blood & Cancer|January 4, 2019
Ectopic intracranial retinoblastoma in a 3.5-month-old infant without eye involvement and without evidence of heritabilityTristan Römer, Petra Temming, Dietmar R Lohmann, et al.
Molecular Genetics & Genomic Medicine|November 6, 2018
Familial NEDD4L variant in periventricular nodular heterotopia and in a fetus with hypokinesia and flexion contracturesMiriam Elbracht, Florian Kraft, Matthias Begemann, et al.
Brain and Behavior|April 19, 2016
Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?Friederike Werheid, Hamid Azzedine, Eva Zwerenz, et al.
Neuroimaging Clinics of North America|May 12, 2007
Imaging in spinal vascular diseaseTimo Krings, Pierre L Lasjaunias, Franz J Hans, et al.
The Journal of Clinical Investigation|January 9, 2019
DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humansGergely Karsai, Florian Kraft, Natja Haag, et al.
The Journal of Clinical Investigation|May 4, 2021
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammationEva Lausberg, Sebastian Gießelmann, Joseph P Dewulf, et al.
Pageof 3