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Neurogenetics
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January 29, 2024
A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review
Fumikazu Kojima, Yuji Okamoto, Masahiro Ando, et al.
Neurogenetics
|
September 12, 2024
The role of gut-derived short-chain fatty acids in Parkinson's disease
Mohamed J Saadh, Anfal Nabeel Mustafa, Mohammed Ahmed Mustafa, et al.
Neurogenetics
|
October 21, 2024
Impact of flexible assertive community treatment model (FACT) on community rehabilitation of schizophrenia in Southern China
Yinglin Zhao, Shaoxiong Zheng, Handi Zhang, et al.
Neurogenetics
|
May 29, 2024
Hitting Epstein Barr virus where it hurts: computational methods exploration for siRNA therapy in alleviating Epstein Barr virus-induced multiple sclerosis
Taiwo Ooreoluwa Ojo, Oluwabamise Emmanuel Elegbeleye, Olawale Quadri Bolaji, et al.
Neurogenetics
|
May 22, 2024
Identification of established and novel extracellular matrix components in glioblastoma as targets for angiogenesis and prognosis
Lucas Cunha Barbosa, Gabriel Cardoso Machado, Manoela Heringer, et al.
Neurogenetics
|
April 15, 2024
Identification of a Novel Homozygous GLS Gene Variant Associated with Developmental and Epileptic Encephalopathy (DEE) Type 71
Afsaneh Bazgir, Mehdi Agha Gholizadeh, Seyyed Mohammad Kahani, et al.
Neurogenetics
|
January 8, 2024
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review
Raffaele Falsaperla, Vincenzo Sortino, Giovanna Vitaliti, et al.
Neurogenetics
|
June 23, 2026
Behavioral variant frontotemporal dementia associated with a NEK1 missense variant: exploring a possible phenotypic association
Ozlem Totuk, Sevki Sahin
Neurogenetics
|
June 30, 2026
Charcot-Marie-Tooth type 4 C misdiagnosed as CIDP: electrodiagnostic pitfalls and genetic confirmation
Ali Asghar Okhovat, Hamed Shahriyari, Aida Ghasemi, et al.
Neurogenetics
|
August 29, 2001
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
C F Boerkoel, H Takashima, C A Bacino, et al.
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of 95
Search research articles
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Showing results (691-700 of 949) with videos related to
Sort By:
Page
of 95
Neurogenetics
|
January 29, 2024
A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review
Fumikazu Kojima, Yuji Okamoto, Masahiro Ando, et al.
Neurogenetics
|
September 12, 2024
The role of gut-derived short-chain fatty acids in Parkinson's disease
Mohamed J Saadh, Anfal Nabeel Mustafa, Mohammed Ahmed Mustafa, et al.
Neurogenetics
|
October 21, 2024
Impact of flexible assertive community treatment model (FACT) on community rehabilitation of schizophrenia in Southern China
Yinglin Zhao, Shaoxiong Zheng, Handi Zhang, et al.
Neurogenetics
|
May 29, 2024
Hitting Epstein Barr virus where it hurts: computational methods exploration for siRNA therapy in alleviating Epstein Barr virus-induced multiple sclerosis
Taiwo Ooreoluwa Ojo, Oluwabamise Emmanuel Elegbeleye, Olawale Quadri Bolaji, et al.
Neurogenetics
|
May 22, 2024
Identification of established and novel extracellular matrix components in glioblastoma as targets for angiogenesis and prognosis
Lucas Cunha Barbosa, Gabriel Cardoso Machado, Manoela Heringer, et al.
Neurogenetics
|
April 15, 2024
Identification of a Novel Homozygous GLS Gene Variant Associated with Developmental and Epileptic Encephalopathy (DEE) Type 71
Afsaneh Bazgir, Mehdi Agha Gholizadeh, Seyyed Mohammad Kahani, et al.
Neurogenetics
|
January 8, 2024
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review
Raffaele Falsaperla, Vincenzo Sortino, Giovanna Vitaliti, et al.
Neurogenetics
|
June 23, 2026
Behavioral variant frontotemporal dementia associated with a NEK1 missense variant: exploring a possible phenotypic association
Ozlem Totuk, Sevki Sahin
Neurogenetics
|
June 30, 2026
Charcot-Marie-Tooth type 4 C misdiagnosed as CIDP: electrodiagnostic pitfalls and genetic confirmation
Ali Asghar Okhovat, Hamed Shahriyari, Aida Ghasemi, et al.
Neurogenetics
|
August 29, 2001
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy
C F Boerkoel, H Takashima, C A Bacino, et al.
Page
of 95