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Marina Siebert

Showing results (21-30 of 46) with videos related to

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Autopsy & Case Reports|August 30, 2021
Histomorphometric analysis of liver biopsies of treated patients with Gaucher disease type 1Rodrigo Tzovenos Starosta, Marina Siebert, Filippo Pinto E Vairo, et al.
Blood Cells, Molecules & Diseases|November 10, 2016
Use of a multiplex ligation-dependent probe amplification method for the detection of deletions/duplications in the GBA1 gene in Gaucher disease patientsSuelen P Basgalupp, Marina Siebert, Filippo Pinto E Vairo, et al.
BMC Rheumatology|December 9, 2020
Urinary soluble VCAM-1 is a useful biomarker of disease activity and treatment response in lupus nephritisAndrese Aline Gasparin, Nicole Pamplona Bueno de Andrade, Vanessa Hax, et al.
Epilepsy & Behavior : E&B|May 28, 2017
Tyrosine receptor kinase B gene variants (NTRK2 variants) are associated with depressive disorders in temporal lobe epilepsyCarolina Machado Torres, Marina Siebert, Hugo Bock, et al.
Molecular Genetics and Metabolism Reports|December 5, 2019
Rare <i>GBA1</i> genotype associated with severe bone disease in Gaucher disease type 1Livia d'Avila Paskulin, Rodrigo Tzovenos Starosta, Vitória Schütt Zizemer, et al.
Clinical Genetics|December 20, 2022
Copy number variations in SPAST and ATL1 are rare among BraziliansHelena Fussiger, Bruna Letícia da Silva Pereira, Janice Pacheco Dias Padilha, et al.
Photodermatology, Photoimmunology & Photomedicine|July 20, 2024
Modulation of gene expression in skin wound healing by photobiomodulation therapy: A systematic review in vivo studiesEmily Ferreira Salles Pilar, Fernanda Thomé Brochado, Tuany Rafaeli Schmidt, et al.
Genetics and Molecular Biology|April 16, 2019
Sensitivity, advantages, limitations, and clinical utility of targeted next-generation sequencing panels for the diagnosis of selected lysosomal storage disordersDiana Rojas Málaga, Ana Carolina Brusius-Facchin, Marina Siebert, et al.
Cytokine|December 3, 2022
Cytokine profiling in patients with hepatic glycogen storage disease: Are there clues for unsolved aspects?Karina Colonetti, Filippo Pinto E Vairo, Marina Siebert, et al.
Journal of the Neurological Sciences|December 17, 2017
Clinical and molecular characterization of hereditary spastic paraplegias: A next-generation sequencing panel approachDaniela Burguez, Márcia Polese-Bonatto, Laís Alves Jacinto Scudeiro, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Autopsy & Case Reports|August 30, 2021
Histomorphometric analysis of liver biopsies of treated patients with Gaucher disease type 1Rodrigo Tzovenos Starosta, Marina Siebert, Filippo Pinto E Vairo, et al.
Blood Cells, Molecules & Diseases|November 10, 2016
Use of a multiplex ligation-dependent probe amplification method for the detection of deletions/duplications in the GBA1 gene in Gaucher disease patientsSuelen P Basgalupp, Marina Siebert, Filippo Pinto E Vairo, et al.
BMC Rheumatology|December 9, 2020
Urinary soluble VCAM-1 is a useful biomarker of disease activity and treatment response in lupus nephritisAndrese Aline Gasparin, Nicole Pamplona Bueno de Andrade, Vanessa Hax, et al.
Epilepsy & Behavior : E&B|May 28, 2017
Tyrosine receptor kinase B gene variants (NTRK2 variants) are associated with depressive disorders in temporal lobe epilepsyCarolina Machado Torres, Marina Siebert, Hugo Bock, et al.
Molecular Genetics and Metabolism Reports|December 5, 2019
Rare <i>GBA1</i> genotype associated with severe bone disease in Gaucher disease type 1Livia d'Avila Paskulin, Rodrigo Tzovenos Starosta, Vitória Schütt Zizemer, et al.
Clinical Genetics|December 20, 2022
Copy number variations in SPAST and ATL1 are rare among BraziliansHelena Fussiger, Bruna Letícia da Silva Pereira, Janice Pacheco Dias Padilha, et al.
Photodermatology, Photoimmunology & Photomedicine|July 20, 2024
Modulation of gene expression in skin wound healing by photobiomodulation therapy: A systematic review in vivo studiesEmily Ferreira Salles Pilar, Fernanda Thomé Brochado, Tuany Rafaeli Schmidt, et al.
Genetics and Molecular Biology|April 16, 2019
Sensitivity, advantages, limitations, and clinical utility of targeted next-generation sequencing panels for the diagnosis of selected lysosomal storage disordersDiana Rojas Málaga, Ana Carolina Brusius-Facchin, Marina Siebert, et al.
Cytokine|December 3, 2022
Cytokine profiling in patients with hepatic glycogen storage disease: Are there clues for unsolved aspects?Karina Colonetti, Filippo Pinto E Vairo, Marina Siebert, et al.
Journal of the Neurological Sciences|December 17, 2017
Clinical and molecular characterization of hereditary spastic paraplegias: A next-generation sequencing panel approachDaniela Burguez, Márcia Polese-Bonatto, Laís Alves Jacinto Scudeiro, et al.
Pageof 5