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Annals of Neurology
|
November 26, 2013
GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy
Johannes R Lemke, Rik Hendrickx, Kirsten Geider, et al.
The Journal of Experimental Medicine
|
May 9, 2007
Lysosomal integral membrane protein 2 is a novel component of the cardiac intercalated disc and vital for load-induced cardiac myocyte hypertrophy
Blanche Schroen, Joost J Leenders, Arie van Erk, et al.
Brain & Spine
|
August 12, 2025
The age of Artificial Intelligence in neurosurgical practice and educational paradigms - Considerations from the EANS Ethico-Legal and Young Neurosurgeons' committees
Felix C Stengel, Stefan Motov, Cesare Zoia, et al.
Brain & Spine
|
April 26, 2024
The prevalence of imposter syndrome among neurosurgeons in Europe: An EANS YNC survey
Cesare Zoia, Martin N Stienen, Ismail Zaed, et al.
Brain & Spine
|
June 3, 2024
A spotlight on cadaveric dissection in neurosurgical training: The perspective of the EANS young neurosurgeons committee
Fabio Torregrossa, Maria Peris-Celda, Toma Spiriev, et al.
Brain & Spine
|
October 17, 2022
Transformation of neurosurgical training from "see one, do one, teach one" to AR/VR & simulation - A survey by the EANS Young Neurosurgeons
Felix C Stengel, Maria L Gandia-Gonzalez, Cristina C Aldea, et al.
American Journal of Human Genetics
|
May 10, 2011
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia
Mark A Corbett, Michael Schwake, Melanie Bahlo, et al.
Human Molecular Genetics
|
January 9, 2013
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis
Katherine R Smith, Hans-Henrik M Dahl, Laura Canafoglia, et al.
Nature Aging
|
April 28, 2023
Aging is associated with a systemic length-associated transcriptome imbalance
Thomas Stoeger, Rogan A Grant, Alexandra C McQuattie-Pimentel, et al.
The Journal of Experimental Medicine
|
November 12, 2017
Mutations in the X-linked <i>ATP6AP2</i> cause a glycosylation disorder with autophagic defects
Maria A Rujano, Magda Cannata Serio, Ganna Panasyuk, et al.
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Search research articles
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Showing results (101-110 of 117) with videos related to
Sort By:
Page
of 12
Annals of Neurology
|
November 26, 2013
GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy
Johannes R Lemke, Rik Hendrickx, Kirsten Geider, et al.
The Journal of Experimental Medicine
|
May 9, 2007
Lysosomal integral membrane protein 2 is a novel component of the cardiac intercalated disc and vital for load-induced cardiac myocyte hypertrophy
Blanche Schroen, Joost J Leenders, Arie van Erk, et al.
Brain & Spine
|
August 12, 2025
The age of Artificial Intelligence in neurosurgical practice and educational paradigms - Considerations from the EANS Ethico-Legal and Young Neurosurgeons' committees
Felix C Stengel, Stefan Motov, Cesare Zoia, et al.
Brain & Spine
|
April 26, 2024
The prevalence of imposter syndrome among neurosurgeons in Europe: An EANS YNC survey
Cesare Zoia, Martin N Stienen, Ismail Zaed, et al.
Brain & Spine
|
June 3, 2024
A spotlight on cadaveric dissection in neurosurgical training: The perspective of the EANS young neurosurgeons committee
Fabio Torregrossa, Maria Peris-Celda, Toma Spiriev, et al.
Brain & Spine
|
October 17, 2022
Transformation of neurosurgical training from "see one, do one, teach one" to AR/VR & simulation - A survey by the EANS Young Neurosurgeons
Felix C Stengel, Maria L Gandia-Gonzalez, Cristina C Aldea, et al.
American Journal of Human Genetics
|
May 10, 2011
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia
Mark A Corbett, Michael Schwake, Melanie Bahlo, et al.
Human Molecular Genetics
|
January 9, 2013
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis
Katherine R Smith, Hans-Henrik M Dahl, Laura Canafoglia, et al.
Nature Aging
|
April 28, 2023
Aging is associated with a systemic length-associated transcriptome imbalance
Thomas Stoeger, Rogan A Grant, Alexandra C McQuattie-Pimentel, et al.
The Journal of Experimental Medicine
|
November 12, 2017
Mutations in the X-linked <i>ATP6AP2</i> cause a glycosylation disorder with autophagic defects
Maria A Rujano, Magda Cannata Serio, Ganna Panasyuk, et al.
Page
of 12