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Annals of Clinical and Translational Neurology
|
January 7, 2016
Suppression of agrin-22 production and synaptic dysfunction in Cln1 (-/-) mice
Shiyong Peng, Jianhua Xu, Kenneth A Pelkey, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 1, 2018
Membrane Stabilization by Modified Steroid Offers a Potential Therapy for Muscular Dystrophy Due to Dysferlin Deficit
Sen Chandra Sreetama, Goutam Chandra, Jack H Van der Meulen, et al.
Ageing Research Reviews
|
February 27, 2026
An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine
Sakeena Asmi, Anand Krishnan, Sneha Mary Alexander, et al.
Cell Death Discovery
|
July 26, 2019
Dysregulated calcium homeostasis prevents plasma membrane repair in Anoctamin 5/TMEM16E-deficient patient muscle cells
Goutam Chandra, Aurelia Defour, Kamel Mamchoui, et al.
Zootaxa
|
October 14, 2018
Systematics of the frogs allocated to Sarcohyla bistincta sensu lato (Cope, 1877), with description of a new species from Western Mexico
Jonathan A Campbell, Edmund D Jr Brodie, Itzue W Caviedes-Solis, et al.
The Lancet. Neurology
|
July 7, 2014
Oral cysteamine bitartrate and N-acetylcysteine for patients with infantile neuronal ceroid lipofuscinosis: a pilot study
Sondra W Levin, Eva H Baker, Wadih M Zein, et al.
Annals of Neurosciences
|
July 14, 2025
Prevalence Estimates of Neurodevelopmental Disorders (NDD) in a South Indian Population
Krishna S Nair, Roana Liz George, V R Remya, et al.
Annals of Neurology
|
May 14, 2020
GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome
A Reghan Foley, Yaqun Zou, James E Dunford, et al.
Page
of 10
Search research articles
Search
Showing results (91-100 of 98) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 98 results.
Annals of Clinical and Translational Neurology
|
January 7, 2016
Suppression of agrin-22 production and synaptic dysfunction in Cln1 (-/-) mice
Shiyong Peng, Jianhua Xu, Kenneth A Pelkey, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 1, 2018
Membrane Stabilization by Modified Steroid Offers a Potential Therapy for Muscular Dystrophy Due to Dysferlin Deficit
Sen Chandra Sreetama, Goutam Chandra, Jack H Van der Meulen, et al.
Ageing Research Reviews
|
February 27, 2026
An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine
Sakeena Asmi, Anand Krishnan, Sneha Mary Alexander, et al.
Cell Death Discovery
|
July 26, 2019
Dysregulated calcium homeostasis prevents plasma membrane repair in Anoctamin 5/TMEM16E-deficient patient muscle cells
Goutam Chandra, Aurelia Defour, Kamel Mamchoui, et al.
Zootaxa
|
October 14, 2018
Systematics of the frogs allocated to Sarcohyla bistincta sensu lato (Cope, 1877), with description of a new species from Western Mexico
Jonathan A Campbell, Edmund D Jr Brodie, Itzue W Caviedes-Solis, et al.
The Lancet. Neurology
|
July 7, 2014
Oral cysteamine bitartrate and N-acetylcysteine for patients with infantile neuronal ceroid lipofuscinosis: a pilot study
Sondra W Levin, Eva H Baker, Wadih M Zein, et al.
Annals of Neurosciences
|
July 14, 2025
Prevalence Estimates of Neurodevelopmental Disorders (NDD) in a South Indian Population
Krishna S Nair, Roana Liz George, V R Remya, et al.
Annals of Neurology
|
May 14, 2020
GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome
A Reghan Foley, Yaqun Zou, James E Dunford, et al.
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of 10