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Water Research
|
February 25, 2024
Inoculation with adapted bacterial communities promotes development of full scale slow sand filters for drinking water production
Tage Rosenqvist, Sandy Chan, Jon Ahlinder, et al.
STAR Protocols
|
January 21, 2022
Protocol for single-cell isolation and genome amplification of environmental microbial eukaryotes for genomic analysis
Doina Ciobanu, Sandy Chan, Steven Ahrendt, et al.
BMJ Supportive & Palliative Care
|
October 11, 2018
Palliative care clinicians and online education in India: a survey
Tayler Kiss-Lane, Odette Spruijt, Thomas Day, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 31, 2012
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia
Brent L Fogel, Ji Yong Lee, Jessica Lane, et al.
Journal of Palliative Medicine
|
October 19, 2022
Top Ten Tips Palliative Care Clinicians Should Know About Caring for Chinese American Patients
Cynthia X Pan, Esther J Luo, Eric Wang, et al.
Acta Neuropathologica Communications
|
April 9, 2015
A novel mutation P112H in the TARDBP gene associated with frontotemporal lobar degeneration without motor neuron disease and abundant neuritic amyloid plaques
Fermin Moreno, Gil D Rabinovici, Anna Karydas, et al.
Iscience
|
April 19, 2021
A single-cell genomics pipeline for environmental microbial eukaryotes
Doina Ciobanu, Alicia Clum, Steven Ahrendt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 2, 2013
TDP-43 frontotemporal lobar degeneration and autoimmune disease
Zachary A Miller, Katherine P Rankin, Neill R Graff-Radford, et al.
European Journal of Human Genetics : EJHG
|
June 30, 2018
Primary brain calcification: an international study reporting novel variants and associated phenotypes
Eliana Marisa Ramos, Miryam Carecchio, Roberta Lemos, et al.
Neurogenetics
|
January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Sandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Water Research
|
February 25, 2024
Inoculation with adapted bacterial communities promotes development of full scale slow sand filters for drinking water production
Tage Rosenqvist, Sandy Chan, Jon Ahlinder, et al.
STAR Protocols
|
January 21, 2022
Protocol for single-cell isolation and genome amplification of environmental microbial eukaryotes for genomic analysis
Doina Ciobanu, Sandy Chan, Steven Ahrendt, et al.
BMJ Supportive & Palliative Care
|
October 11, 2018
Palliative care clinicians and online education in India: a survey
Tayler Kiss-Lane, Odette Spruijt, Thomas Day, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 31, 2012
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia
Brent L Fogel, Ji Yong Lee, Jessica Lane, et al.
Journal of Palliative Medicine
|
October 19, 2022
Top Ten Tips Palliative Care Clinicians Should Know About Caring for Chinese American Patients
Cynthia X Pan, Esther J Luo, Eric Wang, et al.
Acta Neuropathologica Communications
|
April 9, 2015
A novel mutation P112H in the TARDBP gene associated with frontotemporal lobar degeneration without motor neuron disease and abundant neuritic amyloid plaques
Fermin Moreno, Gil D Rabinovici, Anna Karydas, et al.
Iscience
|
April 19, 2021
A single-cell genomics pipeline for environmental microbial eukaryotes
Doina Ciobanu, Alicia Clum, Steven Ahrendt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 2, 2013
TDP-43 frontotemporal lobar degeneration and autoimmune disease
Zachary A Miller, Katherine P Rankin, Neill R Graff-Radford, et al.
European Journal of Human Genetics : EJHG
|
June 30, 2018
Primary brain calcification: an international study reporting novel variants and associated phenotypes
Eliana Marisa Ramos, Miryam Carecchio, Roberta Lemos, et al.
Neurogenetics
|
January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Sandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Page
of 2