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Monia B Hammer

Showing results (1-10 of 6) with videos related to

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JAMA Neurology|April 2, 2019
Common Premutations in the General PopulationMonia B Hammer, Andrew B Singleton
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
JAMA Neurology|February 27, 2018
Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia GenesMarie Coutelier, Monia B Hammer, Giovanni Stevanin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a changeHeidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
JAMA Neurology|April 2, 2019
Common Premutations in the General PopulationMonia B Hammer, Andrew B Singleton
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
JAMA Neurology|February 27, 2018
Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia GenesMarie Coutelier, Monia B Hammer, Giovanni Stevanin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a changeHeidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
Pageof 1