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Turro

Showing results (481-490 of 532) with videos related to

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Blood|September 2, 2018
<i>GNE</i> variants causing autosomal recessive macrothrombocytopenia without associated muscle wastingShoshana Revel-Vilk, Ela Shai, Ernest Turro, et al.
Obesity Surgery|May 7, 2020
Correction to: The Procedureless Elipse Gastric Balloon Program: Multicenter Experience in 1770 Consecutive PatientsR Ienca, Mohammed Al Jarallah, Adelardo Caballero, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene <i>RNU2-2P</i> cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Blood|September 15, 2018
A mutation of the human Eliane Berrou, Christelle Soukaseum, Rémi Favier, et al.
Haematologica|March 12, 2026
Thyroid hormones induce an acute platelet release mechanism via integrin αVβ3Holly R Foster, Nina Herbert, Christian A Di Buduo, et al.
Obesity Surgery|April 13, 2020
The Procedureless Elipse Gastric Balloon Program: Multicenter Experience in 1770 Consecutive PatientsR Ienca, Mohammed Al Jarallah, Adelardo Caballero, et al.
Obesity Surgery|September 2, 2020
Correction to: The Procedureless Elipse Gastric Balloon Program: Multicenter Experience in 1770 Consecutive PatientsR Ienca, Mohammed Al Jarallah, Adelardo Caballero, et al.
Haematologica|November 24, 2018
Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopeniaTadbir K Bariana, Veerle Labarque, Jessica Heremans, et al.
Blood|January 20, 2026
Understanding how a highly prevalent GRK5 polymorphism affects platelets and enhances thrombotic riskYanki Yarman, Xuefei Zhao, Hyunsook Ahn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2024
Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorderAndrea Accogli, Young N Park, Guy M Lenk, et al.
Pageof 54

Showing results (481-490 of 532) with videos related to

Sort By:
Pageof 54
Blood|September 2, 2018
<i>GNE</i> variants causing autosomal recessive macrothrombocytopenia without associated muscle wastingShoshana Revel-Vilk, Ela Shai, Ernest Turro, et al.
Obesity Surgery|May 7, 2020
Correction to: The Procedureless Elipse Gastric Balloon Program: Multicenter Experience in 1770 Consecutive PatientsR Ienca, Mohammed Al Jarallah, Adelardo Caballero, et al.
Medrxiv : the Preprint Server for Health Sciences|September 16, 2024
Mutations in the U2 snRNA gene <i>RNU2-2P</i> cause a severe neurodevelopmental disorder with prominent epilepsyDaniel Greene, Koenraad De Wispelaere, Jon Lees, et al.
Blood|September 15, 2018
A mutation of the human Eliane Berrou, Christelle Soukaseum, Rémi Favier, et al.
Haematologica|March 12, 2026
Thyroid hormones induce an acute platelet release mechanism via integrin αVβ3Holly R Foster, Nina Herbert, Christian A Di Buduo, et al.
Obesity Surgery|April 13, 2020
The Procedureless Elipse Gastric Balloon Program: Multicenter Experience in 1770 Consecutive PatientsR Ienca, Mohammed Al Jarallah, Adelardo Caballero, et al.
Obesity Surgery|September 2, 2020
Correction to: The Procedureless Elipse Gastric Balloon Program: Multicenter Experience in 1770 Consecutive PatientsR Ienca, Mohammed Al Jarallah, Adelardo Caballero, et al.
Haematologica|November 24, 2018
Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopeniaTadbir K Bariana, Veerle Labarque, Jessica Heremans, et al.
Blood|January 20, 2026
Understanding how a highly prevalent GRK5 polymorphism affects platelets and enhances thrombotic riskYanki Yarman, Xuefei Zhao, Hyunsook Ahn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2024
Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorderAndrea Accogli, Young N Park, Guy M Lenk, et al.
Pageof 54