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Showing results (1051-1060 of 1,089) with videos related to
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Annals of Clinical and Translational Neurology
|
April 22, 2026
Prodromal Lewy Body Disorder Features in REM Sleep Behavior Disorder With Biomarker-Defined Synucleinopathy
Daniel Weintraub, Michele K York, Roseanne Dobkin, et al.
Annals of Clinical and Translational Neurology
|
December 15, 2020
Dopamine transporter imaging predicts clinically-defined α-synucleinopathy in REM sleep behavior disorder
Lana M Chahine, Michael C Brumm, Chelsea Caspell-Garcia, et al.
JACC. Clinical Electrophysiology
|
July 22, 2023
Left Ventricular Abnormal Substrate in Brugada Syndrome
Ghassen Cheniti, Michel Haissaguerre, Christian Dina, et al.
Breast Cancer Research and Treatment
|
April 6, 2012
Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predisposition
E Rouleau, B Jesson, A Briaux, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 5, 2010
Two doses of sclerostin antibody in cynomolgus monkeys increases bone formation, bone mineral density, and bone strength
Michael S Ominsky, Fay Vlasseros, Jacquelin Jolette, et al.
Cardiovascular Research
|
August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants
Taisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.
International Journal of Molecular Sciences
|
March 27, 2025
Exploring the Potential of Optical Genome Mapping in the Diagnosis and Prognosis of Soft Tissue and Bone Tumors
Alejandro Berenguer-Rubio, Esperanza Such, Neus Torres Hernández, et al.
Clinical Genetics
|
January 17, 2021
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium
Flavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, et al.
Human Molecular Genetics
|
February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome
Solena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
Annals of Neurology
|
April 10, 2018
The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant
Nicolas Chatron, Rikke S Møller, Neena L Champaigne, et al.
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of 109
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Showing results (1051-1060 of 1,089) with videos related to
Sort By:
Page
of 109
Annals of Clinical and Translational Neurology
|
April 22, 2026
Prodromal Lewy Body Disorder Features in REM Sleep Behavior Disorder With Biomarker-Defined Synucleinopathy
Daniel Weintraub, Michele K York, Roseanne Dobkin, et al.
Annals of Clinical and Translational Neurology
|
December 15, 2020
Dopamine transporter imaging predicts clinically-defined α-synucleinopathy in REM sleep behavior disorder
Lana M Chahine, Michael C Brumm, Chelsea Caspell-Garcia, et al.
JACC. Clinical Electrophysiology
|
July 22, 2023
Left Ventricular Abnormal Substrate in Brugada Syndrome
Ghassen Cheniti, Michel Haissaguerre, Christian Dina, et al.
Breast Cancer Research and Treatment
|
April 6, 2012
Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predisposition
E Rouleau, B Jesson, A Briaux, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 5, 2010
Two doses of sclerostin antibody in cynomolgus monkeys increases bone formation, bone mineral density, and bone strength
Michael S Ominsky, Fay Vlasseros, Jacquelin Jolette, et al.
Cardiovascular Research
|
August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants
Taisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.
International Journal of Molecular Sciences
|
March 27, 2025
Exploring the Potential of Optical Genome Mapping in the Diagnosis and Prognosis of Soft Tissue and Bone Tumors
Alejandro Berenguer-Rubio, Esperanza Such, Neus Torres Hernández, et al.
Clinical Genetics
|
January 17, 2021
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium
Flavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, et al.
Human Molecular Genetics
|
February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome
Solena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
Annals of Neurology
|
April 10, 2018
The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant
Nicolas Chatron, Rikke S Møller, Neena L Champaigne, et al.
Page
of 109